Delaware
|
6770
|
85-1914700
|
||
(State or other jurisdiction of
incorporation or organization) |
(Primary Standard Industrial
Classification Code Number) |
(I.R.S. Employer
Identification No.)
|
Steven B. Stokdyk
Brian Duff
Brent T. Epstein
Latham & Watkins LLP
355 South Grand Avenue, Suite 100
Los Angeles, California 90071-1560
Tel: (213)
485-1234
|
David A. Broadwin
Adrienne Ellman
John D. Hancock
Foley Hoag LLP
155 Seaport Boulevard
Boston, Massachusetts 02210
Tel: (617)
832-1000
|
Large accelerated filer | ☐ | Accelerated filer | ☐ | |||
Non-accelerated
filer
|
☒ | Smaller reporting company | ☒ | |||
Emerging growth company | ☒ |
|
•
|
|
Proposal No.
1: The Business Combination Proposal
Business Combination Proposal
”).
|
|
•
|
|
Proposal No.
2: The Public Benefit Corporation Proposal
Public Benefit Corporation Proposal
”).
|
|
•
|
|
Proposal No.
3: The Charter Amendment Proposal
Proposed Charter
”) to be in effect following the Business Combination, which, if approved, would take effect at the effective time of the Merger, as further described in this proxy statement/prospectus (the “
Charter Amendment Proposal
”).
|
|
•
|
|
Proposal No. 4(A)-(C): Advisory Charter Amendment Proposals
non-binding
advisory basis, each of the following governance proposals regarding the Proposed Charter (such proposals, collectively, the “
Advisory Charter Amendment Proposals
”) and the following material differences between the Amended and Restated Certificate of Incorporation of ENVI currently in effect (the “
Existing Charter
”) and the Proposed Charter (the “
Advisory Charter Amendment Proposals
”):
|
|
•
|
|
Proposal No. 4(A): Advisory Charter Amendment Proposal A
|
|
•
|
|
Proposal No. 4(B): Advisory Charter Amendment Proposal B
|
|
•
|
|
Proposal No. 4(C): Advisory Charter Amendment Proposal C
|
|
•
|
|
Proposal No.
5: The Nasdaq Proposal
Nasdaq Proposal
”).
|
|
•
|
|
Proposal No.
6: The Incentive Award Plan Proposal—
New GreenLight 2021 Plan
”), a copy of which is attached to this proxy statement/prospectus as Annex H (the “
Incentive Award Plan Proposal
”).
|
|
•
|
|
Proposal No.
7: The Employee Stock Purchase Plan Proposal—
New GreenLight ESPP
”), a copy of which is attached to this proxy statement/prospectus as Annex J (the “
Employee Stock Purchase Plan Proposal
”).
|
|
•
|
|
Proposal No.
8: The Director Election Proposal—
Director Election Proposal
”).
|
|
•
|
|
Proposal No.
9: The Adjournment Proposal—
|
|
Business Combination that the aggregate cash proceeds to be received by ENVI from the trust account in connection with the Business Combination, together with the aggregate gross proceeds from the PIPE Financing, equal no less than $105.0 million (after deducting ENVI’s unpaid expenses, liabilities, and any amounts paid to ENVI stockholders that exercise their redemption rights in connection with the Business Combination) would not be satisfied (the “
Adjournment Proposal
”).
|
• |
“50% Redemption Scenario” are to a scenario in which it is assumed that 10,187,589 shares of ENVI Class A Common Stock are redeemed by public stockholders for an aggregate payment of approximately $101.9 million (based on the estimated per share redemption price of approximately $10.00 per share) from the Trust Account;
|
• |
“Aggregate Transaction Proceeds” are to the amount equal to (a) the sum of (i) the aggregate cash proceeds available to ENVI from the Trust Account in connection with the Business Combination (calculated after giving effect to any redemption of shares of ENVI Class A Common Stock) and (ii) the aggregate proceeds from the PIPE Financing, less (b) unpaid expenses and liabilities of ENVI;
|
• |
“Aggregate Transaction Proceeds Condition” are to an amount of Aggregate Transaction Proceeds no less than $105.0 million;
|
• |
“Business Combination” are to the Merger and the other transactions contemplated by the Business Combination Agreement, collectively, including the PIPE Financing;
|
• |
“Business Combination Agreement” are to that certain Business Combination Agreement, dated August 9, 2021, by and among ENVI, Merger Sub and GreenLight;
|
• |
“Canaccord” are to Canaccord Genuity LLC, our financial advisor and an affiliate of the Sponsor;
|
• |
“Closing” are to the closing of the Business Combination;
|
• |
“Closing Date” are to that date that is in no event later than the third (3rd) business day following the satisfaction (or, to the extent permitted by applicable law, waiver) of the conditions described under the sections titled “
Business Combination Proposal
—
Business Combination Agreement
Business Combination Proposal
—
Conditions to Closing of the Business Combination
|
• |
“Condition Precedent Proposals” are to the Business Combination Proposal, the Charter Amendment Proposal, the Nasdaq Proposal, the Incentive Award Plan Proposal, the Employee Stock Purchase Plan Proposal and the Director Election Proposal, collectively;
|
• |
“Continental” are to Continental Stock Transfer & Trust Company;
|
• |
“DGCL” are to the Delaware General Corporation Law;
|
• |
“Effective Time” are to the time at which the Merger becomes effective;
|
• |
“ENVI,” “we,” “us” or “our” are to Environmental Impact Acquisition Corp., a Delaware corporation, prior to the consummation of the Business Combination;
|
• |
“ENVI Acquisition Proposal” are to (a) any direct or indirect acquisition (or other business combination), in one or a series of related transactions under which ENVI or any of its controlled affiliates, directly or indirectly, (i) acquires or otherwise purchases any other person(s), (ii) engages in a business combination with any other person(s) or (iii) acquires or otherwise purchases all or a material portion of the assets, equity securities or businesses of any other Persons(s) (in the case of each of clause (i), (ii) and (iii), whether by merger, consolidation, recapitalization, purchase or issuance of equity securities, tender offer or otherwise), (b) any equity, debt or similar investment in ENVI or any of its controlled affiliates or (c) any other Business Combination;
|
• |
“ENVI Board” are to ENVI’s board of directors;
|
• |
“ENVI Class A Common Stock” are to the Class A common stock, par value $0.0001 per share, of ENVI, which will automatically convert, on a
one-for-one
|
• |
“ENVI Class B Common Stock” or “founder shares” are to the Class B common stock, par value $0.0001 per share, of ENVI outstanding as of the date of this proxy statement/prospectus that were initially issued to the Sponsor, HB Strategies, and certain directors of ENVI in private placement transactions prior to and in connection with our initial public offering;
|
• |
“ENVI common stock” are to the ENVI Class A Common Stock and the ENVI Class B Common Stock;
|
• |
“ENVI Parties” are to, collectively, ENVI and Merger Sub;
|
• |
“ENVI Units” are to the units offered at ENVI’s initial public offering at a price of $10.00 per unit, with each unit consisting of one share of ENVI Class A Common Stock and
one-half
of one redeemable warrant entitling the holder of such warrant to purchase one share of ENVI Class A Common Stock at a price of $11.50 per share;
|
• |
“Exchange Act” are to the Securities Exchange Act of 1934, as amended;
|
• |
“Existing Bylaws” are to ENVI’s Bylaws currently in effect as of the date of this proxy statement/prospectus;
|
• |
“Existing Charter” are to ENVI’s Amended and Restated Certificate of Incorporation currently in effect as of the date of this proxy statement/prospectus;
|
• |
“Existing Organizational Documents” are to the Existing Charter and the Existing Bylaws;
|
• |
“GreenLight” are to GreenLight Biosciences, Inc., a Delaware corporation, prior to the consummation of the Business Combination and, following the consummation of the Business Combination, are to the surviving company in the Merger;
|
• |
“GreenLight 2012 Equity Plan” are to the GreenLight Biosciences, Inc. 2012 Stock Incentive Plan;
|
• |
“GreenLight Acquisition Proposal” are to (a) any direct or indirect acquisition (or other business combination), in one or a series of related transactions, (i) of the equity securities of GreenLight, in each case, that, if consummated, would result in a person acquiring beneficial ownership of 15% or more of any class of outstanding voting equity securities of GreenLight or 15% or more of the outstanding voting equity securities of GreenLight (regardless of class) or (ii) of all or a portion of assets or businesses of GreenLight which constitute 15% or more of the fair market value of GreenLight, taken as a whole (in the case of each of clause (i) and (ii), whether by merger, consolidation, recapitalization, purchase or issuance of equity securities, tender offer or otherwise), or (b) any direct or indirect acquisition, in one or a series of related transactions, of 15% or more of any class of outstanding voting equity securities of GreenLight or 15% or more of the outstanding voting equity securities of the GreenLight (regardless of class) (in each case of clauses (a) and (b) other than pursuant to the exercise or conversion of any GreenLight options or warrants in accordance with the terms of the GreenLight 2012 Equity Plan, the underlying grant, award or similar agreement or GreenLight’s warrant agreement (as applicable));
|
• |
“GreenLight Common Stock” are to shares of common stock, par value $0.001 per share, of GreenLight;
|
• |
“GreenLight Preferred Stock” are to the GreenLight Series A Preferred Stock, GreenLight Series B Preferred Stock, GreenLight Series C Preferred Stock and GreenLight Series D Preferred Stock;
|
• |
“GreenLight Series A Preferred Stock” are to shares of Series A-1 Preferred Stock, Series A-2 Preferred Stock and Series A-3 Preferred Stock, in each case with a par value $0.001 per share, of GreenLight;
|
• |
“GreenLight Series B Preferred Stock” are to shares of Series B Preferred Stock, par value $0.001 per share, of GreenLight;
|
• |
“GreenLight Series C Preferred Stock” are to shares of Series C Preferred Stock, par value $0.001 per share, of GreenLight;
|
• |
“GreenLight Series D Preferred Stock” are to shares of Series D Preferred Stock, par value $0.001 per share, of GreenLight;
|
• |
“GreenLight Shares” are, as the context requires, to the GreenLight Common Stock, GreenLight Series A Preferred Stock, GreenLight Series B Preferred Stock, GreenLight Series C Preferred Stock and GreenLight Series D Preferred Stock;
|
• |
“GreenLight stockholders” are to holders of GreenLight capital stock prior to the consummation of the Business Combination;
|
• |
“HB Strategies” are to HB Strategies, LLC, a Delaware limited liability company and an affiliate of Hudson Bay Capital Management, LP;
|
• |
“initial public offering” are to ENVI’s initial public offering that was consummated on January 19, 2021;
|
• |
“initial stockholders” are to the Sponsor, HB Strategies and any other holders of ENVI Class B Common Stock prior to the consummation of ENVI’s initial public offering;
|
• |
“Insider Warrants” are to the 750,000 private placement warrants issued simultaneously with the closing of ENVI’s initial public offering, of which 600,000 warrants were issued to the Sponsor and 50,000 warrants were issued to each of Gov. Patrick and Messrs. Brewster and Seavers, entitling such warrant holder the right to purchase one share of ENVI Class A Common Stock on terms identical to the warrants included in the ENVI Units;
|
• |
“Merger” are to the merger of Merger Sub with and into GreenLight pursuant to the Business Combination Agreement, with GreenLight as the surviving company in the Merger and, after giving effect to such Merger, GreenLight becoming a wholly owned subsidiary of ENVI, which itself will be renamed “GreenLight Biosciences, Inc.”;
|
• |
“Merger Sub” are to Honey Bee Merger Sub, Inc., a Delaware corporation and wholly owned subsidiary of ENVI prior to the consummation of the Business Combination;
|
• |
“Nasdaq” are to the Nasdaq Capital Market;
|
• |
“New GreenLight” are to Environmental Impact Acquisition Corp. following the filing of the Proposed Charter or the PBC Proposed Charter, as applicable, the consummation of the Business Combination and the change of ENVI’s name to “GreenLight Biosciences, Inc.” or “GreenLight Biosciences, PBC”, as applicable;
|
• |
“New GreenLight Board” are to the board of directors of New GreenLight;
|
• |
“New GreenLight Common Stock” are to the common stock, par value $0.0001 per share, of New GreenLight upon the effectiveness of the Proposed Charter;
|
• |
“New GreenLight Equity Plan” are to the New GreenLight Biosciences, Inc. 2021 Equity and Incentive Plan to be considered for adoption and approval by the stockholders pursuant to the Incentive Award Plan Proposal, a form of which is attached to this proxy statement / prospectus as Annex H;
|
• |
“New GreenLight ESPP” are to the New GreenLight 2021 Employee Stock Purchase Plan, a form of which is attached to this proxy statement/prospectus as Annex I, to be considered for adoption and approval by the stockholders pursuant to the Employee Stock Purchase Plan Proposal;
|
• |
“PBC” are to a public benefit corporation;
|
• |
“PBC Purpose” are to the public benefit corporation purpose of ENVI, as provided in the PBC Proposed Charter;
|
• |
“PBC Proposed Charter” are to the proposed second amended and restated certificate of incorporation, to be approved and adopted by the ENVI stockholders pursuant to the Public Benefit Corporation Proposal, and attached as Annex J hereto;
|
• |
“PIPE Financing” are to the transactions contemplated by the Subscription Agreements, pursuant to which the PIPE Investors have collectively committed to subscribe for an aggregate of 12,425,000 shares of ENVI Class A Common Stock for an aggregate purchase price of $124,250,000 to be consummated in connection with the Closing;
|
• |
“PIPE Investors” are to the investors party to the Subscription Agreements who have agreed to subscribe for and purchase on the date of the Closing a number of shares of ENVI Class A Common Stock set forth in the applicable Subscription Agreement;
|
• |
“private placement warrants” are to the warrants entitling such warrant holder the right to purchase one share of ENVI Class A Common Stock on terms identical to the warrants included in the ENVI Units offered in ENVI’s initial public offering;
|
• |
“pro forma” are to giving pro forma effect to the Business Combination, including the Merger and the PIPE Financing;
|
• |
“Proposed Bylaws” are to the proposed bylaws of New GreenLight attached to this proxy statement/prospectus as Annex C;
|
• |
“Proposed Charter” are to the proposed second amended and restated certificate of incorporation of New GreenLight to be effective upon the Closing, a copy of which is attached to this proxy statement/prospectus as Annex B and, except where the context otherwise requires, the PBC Proposed Charter;
|
• |
“Proposed Organizational Documents” are to the Proposed Charter and the Proposed Bylaws;
|
• |
“public common stock” are to the 20,700,000 shares of ENVI Class A Common Stock outstanding as of the date of this proxy statement/prospectus, whether acquired in ENVI’s initial public offering or acquired in the secondary market;
|
• |
“public stockholders” are to holders of public common stock, whether acquired in ENVI’s initial public offering or acquired in the secondary market;
|
• |
“public warrants” are to the currently outstanding warrants to purchase 10,350,000 shares of ENVI Class A Common Shares for an exercise price of $11.50 per share;
|
• |
“redemption” are to each redemption of public common stock for cash pursuant to the Existing Organizational Documents;
|
• |
“SEC” are to the Securities and Exchange Commission;
|
• |
“Securities Act” are to the Securities Act of 1933, as amended;
|
• |
“special meeting” are to the special meeting of ENVI at 9:00 a.m., Eastern Time, held virtually at 9:00 a.m., Eastern Time, on , 2021, at the following address: , or at such other time, on such other date and at such other place to which the meeting may be adjourned;
|
• |
“Sponsor” are to CG Investments Inc. VI, a Canadian corporation;
|
• |
“Subscription Agreements” are to the subscription agreements, entered into by ENVI and each of the PIPE Investors in connection with the PIPE Financing;
|
• |
“transfer agent” are to Continental, ENVI’s transfer agent; and
|
• |
“trust account” are to the trust account established at the consummation of ENVI’s initial public offering that holds the proceeds of the initial public offering and is maintained by Continental, acting as trustee.
|
Q.
|
Why am I receiving this proxy statement/prospectus?
|
A. |
ENVI stockholders are being asked to consider and vote upon, among other proposals, a proposal to approve and adopt the Business Combination Agreement and approve the transactions contemplated thereby, including the Business Combination. In accordance with the terms and subject to the conditions of the Business Combination Agreement, among other things, (i) ENVI will be renamed “GreenLight Biosciences, Inc.” if the Charter Amendment Proposal is approved (or “GreenLight Biosciences, PBC” if the Public Benefit Corporation Proposal is also approved), and (ii) each outstanding share of capital stock of GreenLight (other than treasury shares and shares with respect to which appraisal rights under the DGCL are properly exercised and not withdrawn) will be exchanged for shares of New GreenLight Common Stock and outstanding GreenLight options and warrants to purchase shares of GreenLight (whether vested or unvested) will be exchanged for comparable options or warrants, as applicable, to purchase New GreenLight Common Stock, in each case, based on an implied GreenLight equity value of $1.2 billion. See “
Business Combination Proposal
|
Q.
|
What proposals are stockholders of ENVI being asked to vote upon?
|
A. |
At the special meeting, ENVI is asking its stockholders to consider and vote upon the following separate proposals:
|
• |
a proposal to approve and adopt the Business Combination Agreement, including the Merger, and the transactions contemplated thereby;
|
• |
a proposal to adopt and approve the PBC Proposed Charter;
|
• |
a proposal to adopt and approve the Proposed Charter;
|
• |
the following governance proposals to approve, on a
non-binding
advisory basis, the following material differences between the Existing Charter and the Proposed Charter:
|
• |
to change the authorized capital stock of ENVI from (a) 121,000,000 shares, par value $0.0001 per share, consisting of 100,000,000 shares of ENVI Class A Common Stock, 20,000,000 shares of ENVI Class B Common Stock, and 1,000,000 shares of undesignated
|
preferred stock, to (b) 510,000,000 shares, par value $0.0001 per share, consisting of 500,000,000 shares of common stock of New GreenLight and 10,000,000 shares of undesignated preferred stock of New GreenLight;
|
• |
to provide that, in addition to any vote required by applicable law or the certificate of incorporation or bylaws of New GreenLight, the affirmative vote of the holders of at least seventy-five percent (75%) of the voting power of all then-outstanding shares of capital stock of New GreenLight entitled to vote generally in the election of directors, voting together as a single class, will be required for the stockholders to reduce the total number of shares of New GreenLight Preferred Stock authorized to be issued by New GreenLight or to amend, alter, change or repeal, or adopt any provision of the charter of New GreenLight inconsistent with, specified provisions of the charter of New GreenLight; and
|
• |
to provide that the bylaws of New GreenLight may be adopted, amended, altered or repealed with the approval of a majority of the New GreenLight Board or by the affirmative vote of the holders of at least 75% of the voting power of all then-outstanding shares of capital stock of New GreenLight entitled to vote generally in the election of directors, voting together as a single class, provided that the voting requirement is reduced to a majority if the New GreenLight Board recommends that stockholders approve the adoption, amendment, alteration or repeal;
|
• |
a proposal to approve the issuance of shares of New GreenLight Common Stock in connection with the Business Combination in compliance with the Nasdaq listing rules;
|
• |
a proposal to approve and adopt the New GreenLight Equity Plan;
|
• |
a proposal to approve and adopt the New GreenLight ESPP;
|
• |
to elect seven directors to serve on the New GreenLight Board, effective upon the closing of the Business Combination; and
|
• |
a proposal to approve the adjournment of the special meeting to a later date or dates, if necessary, to, among other things, permit further solicitation and voting of proxies in the event that there are insufficient votes for the approval of one or more proposals at the special meeting.
|
Q.
|
Why is ENVI proposing the Business Combination?
|
A. |
ENVI is a blank check company incorporated in Delaware on July 2, 2020 for the purpose of effecting a merger, share exchange, asset acquisition, share purchase, reorganization or similar business combination with one or more businesses. ENVI is authorized to pursue an acquisition opportunity in any business, industry, sector or geographical location for purposes of consummating an initial business combination. ENVI is not permitted under its Existing Organizational Documents to effect a business combination with a blank check company or a similar type of company with nominal operations.
|
Q.
|
Did the ENVI Board obtain a fairness opinion in determining whether or not to proceed with the Business Combination?
|
A. |
Yes. The ENVI Board obtained a fairness opinion from Duff & Phelps in connection with its determination to approve the Business Combination. See the section titled “
The Business Combination Proposal—Opinion of Duff
& Phelps
, Financial Adviser to the ENVI Board
|
Q.
|
What will GreenLight’s equityholders receive in return for the Business Combination with ENVI?
|
A. |
On the date of Closing, Merger Sub will merge with and into GreenLight, with GreenLight as the surviving company in the Merger and, after giving effect to such Merger, GreenLight will be a wholly owned subsidiary of ENVI. In accordance with the terms and subject to the conditions of the Business Combination Agreement, at the Effective Time, outstanding shares of GreenLight (other than treasury shares and shares with respect to which appraisal rights under the DGCL are properly exercised and not withdrawn) will be exchanged for shares of New GreenLight Common Stock and outstanding GreenLight options and warrants to purchase shares of GreenLight (whether vested or unvested) will be exchanged for comparable options or warrants, as applicable, to purchase New GreenLight Common Stock, in each case, based on an implied GreenLight equity value of $1.2 billion.
|
Q.
|
How will the combined company be managed following the Business Combination?
|
A. |
Following the Closing, it is expected that the current management of GreenLight will become the management of New GreenLight, and the New GreenLight Board will consist of seven (7) directors, which will be divided into three classes (Class I, II and III) with each class initially consisting of two (2) or three (3) directors. Pursuant to the Business Combination Agreement, the New GreenLight Board will consist of four (4) individuals designated by GreenLight, GreenLight’s chief executive officer and, prior to the effectiveness of the Registration Statement of which this proxy statement/prospectus forms a part, one (1) individual determined by ENVI and one (1) individual determined by GreenLight. Please see the section titled “
Management Following the Business Combination
|
Q.
|
What equity stake will current ENVI stockholders and current equityholders of GreenLight hold in New GreenLight immediately after the consummation of the Business Combination?
|
A. |
As of September 30, 2021, there were outstanding 25,875,000 shares of ENVI common stock, consisting of 20,700,000 shares of ENVI Class A Common Stock, all of which were issued in ENVI’s initial public offering, and 5,175,000 shares of ENVI Class B Common Stock, all of which were issued to ENVI’s initial stockholders. These amounts do not include 10,350,000 public warrants or 2,750,000 private placement warrants (including the Insider Warrants).
|
The following table illustrates different ownership levels in New GreenLight Common Stock immediately following the consummation of the Business Combination based on the capitalization of ENVI and GreenLight as of September 30, 2021 and either no redemptions, 50% redemptions or maximum redemptions by the public stockholders, assuming: (i) 103,470,217 shares of New GreenLight Common Stock will be issued to the holders of outstanding shares of capital stock of GreenLight at Closing (including shares issuable upon the conversion of certain notes and the exercise of certain warrants); (ii) 12,425,000 shares of ENVI Class A Common Stock will be issued in the PIPE Financing; and (iii) no outstanding
|
options to purchase New GreenLight Common Stock are exercised. If the actual facts differ from these assumptions, the ownership percentages in New GreenLight will be different. |
Assuming
No Redemption
|
Assuming
50% Redemption
|
Assuming
Maximum Redemption
|
||||||||||||||||||||||
Shares
|
%
|
Shares
|
%
|
Shares
|
%
|
|||||||||||||||||||
(percentages represent percentages of pro forma outstanding shares)
|
||||||||||||||||||||||||
Public shares
(a)
|
20,700,000 | 14 | % | 10,512,411 | 8 | % | 324,821 | * | ||||||||||||||||
Founder shares
|
5,175,000 | 4 | % | 5,175,000 | 4 | % | 5,175,000 | 4 | % | |||||||||||||||
GreenLight stockholders
(b)(c)
|
103,470,217 | 73 | % | 103,470,217 | 79 | % | 103,470,217 | 85 | % | |||||||||||||||
PIPE shares
|
12,425,000 | 9 | % | 12,425,000 | 9 | % | 12,425,000 | 10 | % | |||||||||||||||
Pro forma common stock outstanding as of September 30, 2021
(d)
|
141,770,217 | 100 | % | 131,582,628 | 100 | % | 121,395,038 | 100 | % | |||||||||||||||
|
|
|
|
|
|
|
|
|
|
|
|
|||||||||||||
Potential sources of dilution
|
||||||||||||||||||||||||
Public Warrants
|
10,350,000 | 7 | % | 10,350,000 | 8 | % | 10,350,000 | 9 | % | |||||||||||||||
Private Placement Warrants
|
2,000,000 | 1 | % | 1,500,000 | 1 | % | 1,500,000 | 1 | % | |||||||||||||||
Insider Warrants
|
750,000 | * | 600,000 | * | 600,000 | * | ||||||||||||||||||
Rollover Options
|
17,555,928 | 12 | % | 17,555,928 | 13 | % | 17,555,928 | 14 | % |
* |
Less than 1%
|
(a) |
Amount includes 1,000,000 shares of ENVI Class A Common Stock held by HB Strategies, a founder, all of which shares carry the same redemption rights as other shares of ENVI Class A Common Stock. The 50% Redemption Scenario and the Maximum Redemption Scenario assume that HB Strategies will redeem 50% and 100%, respectively, of its shares of ENVI Class A Common Stock. Amount excludes 13,100,000 warrants to purchase ENVI Class A Common Stock, which is made up of 10,350,000 public warrants, 2,000,000 private placement warrants and 750,000 Insider Warrants. Additionally, under each of the 50% Redemption Scenario and the Maximum Redemption Scenario, an aggregate of 650,000 Warrants comprised of 500,000 Private Placement Warrants owned by HB Strategies and 150,000 Insider Warrants owned by the Sponsor will be forfeited pursuant to the Sponsor Letter Agreement.
|
(b) |
In accordance with the terms and subject to the conditions of the Business Combination Agreement, each outstanding share of capital stock of GreenLight will be exchanged for shares of New GreenLight Common Stock and outstanding GreenLight Options (whether vested or unvested) will be exchanged for comparable options to purchase New GreenLight Common Stock, in each case, based on an implied GreenLight equity value of $1.2 billion. The number of shares of New GreenLight Common Stock issued to the holders of shares of capital stock of GreenLight at Closing will fluctuate based on the number of shares underlying GreenLight Options and GreenLight Warrants, whether vested or unvested (and the exercise prices of such options and warrants), outstanding at Closing.
|
(c) |
Amount includes 6,583,549 shares issuable upon conversion of the GreenLight Convertible Notes and 872,667 shares underlying GreenLight Warrants that are assumed to be exercised immediately prior to the consummation of the Business Combination and excludes 17,555,928 shares underlying Rollover Options to be issued to holders of GreenLight Options, assuming such GreenLight Options remain unexercised as of the Closing.
|
(d) |
Amount excludes 31,750,000 shares (which amount includes shares underlying Rollover Options) and 2,000,000 shares of New GreenLight Common Stock that are expected to be available for issuance under the New GreenLight Equity Plan and the New GreenLight ESPP, respectively, after the consummation of the Business Combination, assuming approval of the Condition Precedent Proposals.
|
Q.
|
Do I have redemption rights?
|
A. |
If you are a holder of shares public common stock, you have the right to request that we redeem all or a portion of your shares of public common stock for cash provided that you follow the procedures and deadlines described elsewhere in this proxy statement/prospectus.
Public stockholders may elect to redeem all or a portion of the shares of public common stock held by them regardless of whether or how they vote in respect of the Business Combination Proposal.
How do I exercise my redemption rights?
|
The initial stockholders have agreed to waive their redemption rights with respect to certain of their common stock in connection with the consummation of the Business Combination.
|
Q.
|
How do I exercise my redemption rights?
|
A. |
If you are a public stockholder and wish to exercise your right to redeem your shares of public common stock, you must:
|
(i) |
hold shares of public common stock;
|
(ii) |
submit a written request to Continental, ENVI’s transfer agent, in which you (i) request that we redeem all or a specified portion of your shares of public common stock for cash, and (ii) identify yourself as the beneficial holder of the shares of public common stock and provide your legal name, phone number and address; and
|
(iii) |
deliver your shares of public common stock to be redeemed to Continental, our transfer agent, physically or electronically through The Depository Trust Company (“
DTC
”).
|
Q.
|
What are the U.S. federal income tax consequences of exercising my redemption rights?
|
A. |
The receipt of cash by a holder of public common stock in redemption of such stock will generally be a taxable event for U.S. federal income tax purposes that could result in the recognition of income or gain in the case of a U.S. holder (as defined below), and could be a taxable event for U.S. federal income tax purposes in the case of a
Non-U.S.
holder (as defined below). Please see the discussion below under the caption “
Material U.S. Federal Income Tax Consequences
|
Q.
|
What happens to the funds deposited in the trust account after consummation of the Business Combination?
|
A. |
Following the closing of our initial public offering, an amount equal to $207,000,000 of the net proceeds from our initial public offering was placed in the trust account. As of September 30, 2021, funds in the trust account totaled approximately $207.0 million and were held in money market funds. These funds will remain in the trust account, except for the withdrawal of interest to pay taxes, if any, until the earliest of (i) the completion of a business combination (including the closing of the Business Combination) or (ii) the redemption of all of the public common stock if we are unable to complete a business combination by July 19, 2022 (or by January 19, 2023 if we, by resolution of our board, extend the period of time by an additional six months), subject to applicable law.
|
Q.
|
What happens if a substantial number of the public stockholders vote in favor of the Business Combination Proposal and exercise their redemption rights?
|
A. |
Our public stockholders are not required to vote “FOR” the Business Combination in order to exercise their redemption rights. Accordingly, the Business Combination may be consummated even though the funds available from the trust account and the number of public stockholders are reduced as a result of redemptions by public stockholders.
|
Q.
|
What conditions must be satisfied to complete the Business Combination?
|
A. |
The consummation of the Business Combination is conditioned upon, among other things, (i) the approval by our stockholders of the Condition Precedent Proposals being obtained; (ii) approval of the Business Combination Agreement and the Merger by the GreenLight stockholders; (iii) each applicable waiting period under the HSR Act relating to the Business Combination Agreement having expired or been terminated; (iv) ENVI having at least $5,000,001 of net tangible assets (as determined in accordance with Rule
3a51-1(g)(1)
of the Exchange Act) after giving effect to the transactions contemplated by the Business Combination Agreement and the PIPE Financing; (v) the Aggregate Transaction Proceeds Condition; (vi) the approval by Nasdaq of our initial listing application in connection with the Business Combination (also see “
Risk Factors—Nasdaq may not list New GreenLight’s securities on its exchange, which could limit investors’ ability to make transactions in New GreenLight’s securities and subject New GreenLight to additional trading restrictions
|
Q.
|
When do you expect the Business Combination to be completed?
|
A. |
It is currently expected that the Business Combination will be consummated in the fourth quarter of 2021. This date depends, among other things, on the approval of the proposals to be put to ENVI stockholders at the special meeting. However, such special meeting could be adjourned if the Adjournment Proposal is adopted by our stockholders at the special meeting and we elect to adjourn the special meeting to a later date or dates to consider and vote upon a proposal to approve the adjournment of the special meeting to a later date or dates (A) to the extent necessary to ensure that any required supplement or amendment to this proxy statement/prospectus is provided to ENVI stockholders, (B) if as of the time for which the special meeting is scheduled, there are insufficient shares of ENVI Class A Common Stock and ENVI Class B Common Stock represented (either in person or by proxy) to constitute a quorum necessary to conduct business at the special meeting, (C) in order to solicit additional proxies from ENVI stockholders in favor of one or more of the proposals at the special meeting or (D) if ENVI stockholders redeem an amount of public common stock such that the Aggregate Transaction Proceeds Condition would not be satisfied. For a description of the conditions for the completion of the Business Combination, see “
Business Combination Proposal—Conditions to Closing of the Business Combination.
|
Q.
|
What happens if the Business Combination is not consummated?
|
A. |
If ENVI is not able to consummate the Business Combination with GreenLight nor able to complete another business combination by July 19, 2022 (or by January 19, 2023 if the Company, by resolution of its board, extends the period of time by an additional six months), we will (i) cease all operations except for the purpose of winding up, (ii) as promptly as reasonably possible but not more than ten business days thereafter, redeem the public common stock, at a
per-share
price, payable in cash, equal to the aggregate amount then on deposit in the trust account, including interest earned on the funds held in the trust account and not previously released to pay taxes (less up to $100,000 of interest to pay dissolution expenses), divided by the number of then outstanding shares of public common stock, which redemption will completely extinguish the public stockholders’ rights as stockholders (including the right to receive further liquidating distributions, if any), and (iii) as promptly as reasonably possible following such redemption, subject to the approval of ENVI’s remaining stockholders and our board of directors, dissolve and liquidate, subject in each case to the Company’s obligations under Delaware law to provide for claims of creditors and the requirements of other applicable law.
|
Q.
|
Do I have appraisal rights in connection with the proposed Business Combination?
|
A. |
Our stockholders have no appraisal rights in connection with the Business Combination under the DGCL.
|
Q.
|
What do I need to do now?
|
A. |
We urge you to read this proxy statement/prospectus, including the Annexes and the documents referred to herein, carefully and in their entirety and to consider how the Business Combination will affect you as a stockholder. Our stockholders should then vote as soon as possible in accordance with the instructions provided in this proxy statement/prospectus and on the enclosed proxy card.
|
Q.
|
How do I vote?
|
A. |
If you are a holder of record of common stock on the record date for the special meeting, you may vote in person at the special meeting or by submitting a proxy for the special meeting. You may submit your proxy by completing, signing, dating and returning the enclosed proxy card in the accompanying
pre-addressed
postage paid envelope.
If you hold your shares in “street name,” which means your shares are held of record by a broker, bank or nominee, you should contact your broker, bank or nominee to ensure that votes related to the shares you beneficially own are properly counted. In this regard, you must provide the broker, bank or nominee with instructions on how to vote your shares or, if you wish to attend the special meeting and vote in person, obtain a proxy from your broker, bank or nominee.
|
Q.
|
If my shares are held in “street name,” will my broker, bank or nominee automatically vote my shares for me?
|
A. |
No. If your shares are held in a stock brokerage account or by a bank or other nominee, you are considered the “beneficial holder” of the shares held for you in what is known as “street name.” If this is the case, this proxy statement/prospectus may have been forwarded to you by your brokerage firm, bank or other nominee, or its agent. As the beneficial holder, you have the right to direct your broker, bank or other nominee as to how to vote your shares. If you do not provide voting instructions to your broker, bank or nominee on a particular proposal on which your broker, bank or nominee does not have discretionary authority to vote, your shares will not be voted on that proposal. This is called a “broker
non-vote.”
Abstentions and broker
non-votes
will be counted as present for the purpose of determining the presence of a quorum on all matters. Abstentions and broker non-votes will not count as votes cast at the special meeting and will have no effect on the outcome of a proposal, other than the Charter Amendment Proposal and the Public Benefit Corporation Proposal. For the Charter Amendment Proposal and the Public Benefit
|
Corporation Proposal, abstentions and broker non-votes will have the same effect as votes “AGAINST” such proposal. If you hold shares in street name and decide to vote, you should provide instructions to your broker, bank or other nominee on how to vote in accordance with the information and procedures provided to you by your broker, bank or other nominee. |
Q.
|
When and where will the special meeting be held?
|
A. |
The special meeting will be held virtually at 9:00 a.m., Eastern Time, on , 2021, at the following address: , or at such other time, on such other date and at such other place to which the meeting may be adjourned.
|
Q.
|
Will stockholders of ENVI be able to ask questions during the general meeting?
|
A. |
Stockholders of ENVI will be able to ask questions about the Business Combination during the special meeting, as time permits.
|
Q.
|
What impact will the
COVID-19
pandemic have on the Business Combination?
|
A. |
Given the ongoing and dynamic nature of the circumstances, it is difficult to predict the impact of the coronavirus pandemic on the business of ENVI and GreenLight, and there is no guarantee that efforts by ENVI and GreenLight to address the adverse impacts of the coronavirus pandemic will be effective. The extent of such impact will depend on future developments, which are highly uncertain and cannot be predicted, including new information which may emerge concerning the severity of the coronavirus and actions taken to contain the coronavirus or its impact, among others. If ENVI or GreenLight is unable to recover from a business disruption on a timely basis, the Business Combination and New GreenLight’s business, financial condition and results of operations following the completion of the Business Combination would be adversely affected. The Business Combination may also be delayed and adversely affected by the coronavirus pandemic and become more costly. Each of ENVI and GreenLight may also incur additional costs to remedy damages caused by any such disruptions, which could adversely affect its financial condition and results of operations.
|
Q.
|
Who is entitled to vote at the special meeting?
|
A. |
We have fixed December 10, 2021 as the record date for the special meeting. If you were a stockholder of ENVI at the close of business on the record date, you are entitled to vote on matters that come before the special meeting. However, a stockholder may only vote his, her or their shares if he, she or they are present in person or is represented by proxy at the special meeting.
|
Q.
|
How many votes do I have?
|
A. |
ENVI stockholders are entitled to one vote at the special meeting for each share of ENVI Class A Common Stock or ENVI Class B Common Stock held of record as of the record date. As of the close of business on the record date for the special meeting, there were 20,700,000 shares of ENVI Class A Common Stock issued and outstanding and 5,175,000 shares of ENVI Class B Common Stock issued and outstanding. Under the Existing Charter, prior to the consummation of the Business Combination, only holders of ENVI Class B Common Stock will have the right vote on the election or removal of a director of ENVI.
|
Q.
|
What constitutes a quorum?
|
A. |
A quorum of ENVI stockholders is necessary to hold a valid meeting. For each proposal, a quorum will be present at the special meeting if one or more stockholders who together hold a majority of the voting power of the outstanding shares of each class (or group of classes voting as a single class) of ENVI common stock entitled to vote on such proposal at the special meeting are represented in person or by proxy at the special meeting.
|
Q.
|
What vote is required to approve each proposal at the special meeting?
|
A. |
The proposals at the special meeting each involve a vote by holders of ENVI Class A Common Stock and holders of ENVI Class B Common Stock. As of the date of this proxy statement/prospectus, there are 20,700,000 shares of ENVI Class A Common Stock outstanding, all of which were issued in ENVI’s initial public offering, and 5,175,000 shares of ENVI Class B Common Stock outstanding, all of which were issued to ENVI’s initial stockholders. In connection with the Business Combination, ENVI’s initial stockholders have agreed to vote all shares of ENVI Class B Common Stock owned by them in favor of the proposals at the special special meeting. Thus, any approval requiring the affirmative vote of the holders of at least a majority of the shares of ENVI Class A Common Stock and ENVI Class B Common Stock issued and outstanding on the record date for the special meeting, voting as a single class, would require only 7,762,501 more shares of ENVI Class A Common Stock, or approximately 37.5% of the total outstanding shares of ENVI Class A Common Stock, voting in favor of the proposal. The following votes are required for each proposal at the special meeting:
|
(i) |
The Business Combination Proposal
|
(ii) |
The Public Benefit Corporation Proposal
|
(iii)
|
The Charter Amendment Proposal
|
(iv) |
The Advisory Charter Amendment Proposals
non-binding
advisory basis, of each of the Advisory Charter Amendment Proposals the affirmative vote (in person or by proxy) of the holders of at least a majority of the shares of ENVI Class A Common Stock and ENVI Class B Common Stock entitled to vote on such matter and actually cast thereon at the special meeting, voting as a single class.
|
(v) |
The Nasdaq Proposal
|
(vi) |
The Incentive Award Plan Proposal
|
(vii) |
The Employee Stock Purchase Plan Proposal
|
the shares of ENVI Class A Common Stock and ENVI Class B Common Stock entitled to vote and actually cast thereon at the special meeting, voting as a single class. |
(viii) |
The Director Election Proposal
The Director Election Proposal
|
(ix) |
The Adjournment Proposal
|
Q.
|
What are the recommendations of the ENVI Board?
|
A. |
The ENVI Board believes that the Business Combination Proposal and the other proposals to be presented at the special meeting are in the best interest of ENVI and its stockholders and unanimously recommends that its stockholders vote “FOR” the Business Combination Proposal, “FOR” the Public Benefit Corporation Proposal, “FOR” the Charter Amendment Proposal, “FOR” each of the separate Advisory Charter Amendment Proposals, “FOR” the Nasdaq Proposal, “FOR” the Incentive Award Plan Proposal, “FOR” the Employee Stock Purchase Plan Proposal, “FOR” the Director Election Proposal and “FOR” the Adjournment Proposal, in each case, if presented to the special meeting.
|
Q.
|
How do the Sponsor and the other initial stockholders intend to vote their shares?
|
A. |
Our initial stockholders have agreed to vote all their founders shares in favor of all the proposals being presented at the special meeting. As of the date of this proxy statement/prospectus, our initial stockholders own approximately 5% of the outstanding shares of ENVI Class A Common Stock and 100% of the shares of ENVI Class B Common Stock. As the holder of a majority of the outstanding shares of ENVI Class B Common Stock, our initial stockholders control the outcome of the Director Election Proposal. See the section titled “
The Director Election Proposal
|
Q.
|
What do I need to know about the conflicts of interest that the directors and officers of ENVI may have?
|
A. |
When you consider the recommendation of the ENVI Board in favor of approval of the Business Combination and the other proposals to be presented at the special meeting, you should keep in mind that the initial stockholders, which include the Sponsor, HB Strategies and ENVI’s directors and officers, have interests in such proposals that are different from, or in addition to, those of ENVI stockholders generally. These interests include, among other things, the fact that the initial stockholders paid an aggregate of $25,000 for the 5,175,000 shares of ENVI Class B Common Stock currently owned by them and such securities will have a significantly higher value as a result of the Business Combination and the fact that the private placement warrants purchased by HB Strategies, as well as the Insider Warrants, in connection with our initial public offering would be worthless if a business combination is not consummated by July 19, 2022 (or by January 19, 2023 if we, by resolution of the ENVI Board, elects to extend the period of time by an additional six months). As a result of the lower price paid by our initial stockholders for their shares of ENVI Class B Common Stock, the initial stockholders may generate a profit on those shares even at prices that would generate a significant loss for the public stockholders on their shares of public common stock. Additionally, at the election of the Sponsor, any amounts outstanding under any loan made by the Sponsor, any of its affiliates or HB Strategies to ENVI in an aggregate amount of up to $1,500,000 may be converted into ENVI Units in connection with the consummation of the Business Combination. For more information regarding certain conflicts of interests of ENVI and its affiliates relating to the Business Combination and the other proposals to be presented at the special meeting, see “
Summary of the Proxy Statement/Prospectus—Interests of ENVI Directors and Officers in the Business Combination
|
Q.
|
What happens if I sell my ENVI common stock before the special meeting?
|
A. |
The record date for the special meeting is earlier than the date of the special meeting and earlier than the date that the Business Combination is expected to be completed. If you transfer your public common stock after the applicable record date, but before the special meeting, unless you grant a proxy to the transferee, you will retain your right to vote at such general meeting.
|
Q.
|
May I change my vote after I have mailed my signed proxy card?
|
A. |
Yes. ENVI stockholders may send a
later-dated,
signed proxy card to our Secretary at our address set forth below so that it is received by our Secretary prior to the vote at the special meeting or attend the special meeting and vote. ENVI stockholders also may revoke their proxy by sending a notice of revocation to our Secretary, which must be received by our Secretary prior to the vote at the special meeting. However, if your shares are held in “street name” by your broker, bank or another nominee, you must contact your broker, bank or other nominee to change your vote.
|
Q.
|
What happens if I fail to take any action with respect to the special meeting?
|
A. |
If you fail to vote with respect to the special meeting and the Business Combination is approved by stockholders and the Business Combination is consummated, you will become a stockholder of New GreenLight. If you fail to vote with respect to the special meeting and the Business Combination is not approved, you will remain a stockholder of ENVI. However, if you fail to vote with respect to the special meeting, you will nonetheless be able to elect to redeem your public common stock in connection with the Business Combination in accordance with the procedures described in this proxy statement/prospectus.
|
Q.
|
What should I do if I receive more than one set of voting materials?
|
A. |
Stockholders may receive more than one set of voting materials, including multiple copies of this proxy statement/prospectus and multiple proxy cards or voting instruction cards. For example, if you hold your shares in more than one brokerage account, you will receive a separate voting instruction card for each brokerage account in which you hold shares. If you are a holder of record and your shares are registered in more than one name, you will receive more than one proxy card. Please complete, sign, date and return each proxy card and voting instruction card that you receive in order to cast a vote with respect to all of your common stock.
|
Q.
|
Who will solicit and pay the cost of soliciting proxies for the special meeting?
|
A. |
ENVI will pay the cost of soliciting proxies for the special meeting. ENVI has engaged D.F. King to assist in the solicitation of proxies for the special meeting. ENVI has agreed to pay the proxy solicitor a fee of , plus disbursements, and will reimburse the proxy solicitor for its reasonable
out-of-pocket
|
Q.
|
Where can I find the voting results of the special meeting?
|
A. |
The preliminary voting results will be announced at the special meeting. ENVI will also publish the voting results of the special meeting in a Current Report on Form
8-K
within four business days after the special meeting.
|
Q.
|
Who can help answer my questions?
|
A. |
If you have questions about the Business Combination or if you need additional copies of the proxy statement/prospectus or the enclosed proxy card you should contact:
|
• |
Advisory Charter Amendment Proposal A
|
• |
Advisory Charter Amendment Proposal B
.
|
• |
Advisory Charter Amendment Proposal C
|
• |
synthetic biology and biomanufacturing platform with flexible technology;
|
• |
leadership in
RNA-based
product development;
|
• |
near-term adoption of GreenLight’s products;
|
• |
experienced, diverse, mission-driven and multidisciplinary management team;
|
• |
development of products through a strong commitment to research and development and new partnerships and collaborations;
|
• |
efficient and scalable biomanufacturing processes;
|
• |
results of due diligence and attractive valuation;
|
• |
strong alignment with sustainability and ESG focus;
|
• |
continued participation by leading private investors and a strong balance sheet; and
|
• |
the fairness opinion of Duff & Phelps.
|
• |
the risk that the potential benefits of the Business Combination may not be fully achieved;
|
• |
the risks and costs to ENVI if the Business Combination is not completed;
|
• |
the fact that the Business Combination Agreement includes an exclusivity provision that prohibits ENVI from soliciting other business combination proposals;
|
• |
the risk that ENVI’s stockholders may fail to provide the respective votes necessary to effect the Business Combination;
|
• |
the
post-business
combination corporate governance and the terms of the Investor Rights Agreement;
|
• |
the fact that the completion of the Business Combination is conditioned on the satisfaction of certain closing conditions that are not within ENVI’s control;
|
• |
potential litigation challenging the Business Combination;
|
• |
the fees and expenses associated with completing the Business Combination; and
|
• |
various other risks associated with the Business Combination, the business of ENVI and the business of GreenLight described under the section titled “
Risk Factors
|
Assuming
No Redemption
|
Assuming
50% Redemption
|
Assuming
Maximum
Redemption |
||||||||||||||||||||||
Shares
|
%
|
Shares
|
%
|
Shares
|
%
|
|||||||||||||||||||
(percentages represent percentages of pro forma outstanding shares)
|
||||||||||||||||||||||||
Public shares
(a)
|
20,700,000 | 14 | % | 10,512,411 | 8 | % | 324,821 | * | ||||||||||||||||
Founder shares
|
5,175,000 | 4 | % | 5,175,000 | 4 | % | 5,175,000 | 4 | % | |||||||||||||||
GreenLight stockholders
(b)(c)
|
103,470,217 | 73 | % | 103,470,217 | 79 | % | 103,470,217 | 85 | % | |||||||||||||||
PIPE shares
|
12,425,000 | 9 | % | 12,425,000 | 9 | % | 12,425,000 | 10 | % | |||||||||||||||
|
|
|
|
|
|
|
|
|
|
|
|
|||||||||||||
Pro forma common stock outstanding as of September 30, 2021
(d)
|
141,770,217 | 100 | % | 131,582,628 | 100 | % | 121,395,038 | 100 | % | |||||||||||||||
Potential sources of dilution
|
||||||||||||||||||||||||
Public Warrants
|
10,350,000 | 7 | % | 10,350,000 | 8 | % | 10,350,000 | 9 | % | |||||||||||||||
Private Placement Warrants
|
2,000,000 | 1 | % | 1,500,000 | 1 | % | 1,500,000 | 1 | % | |||||||||||||||
Insider Warrants
|
750,000 | * | 600,000 | * | 600,000 | * | ||||||||||||||||||
Rollover Options
|
17,555,928 | 12 | % | 17,555,928 | 13 | % | 17,555,928 | 14 | % |
* |
Less than 1%
|
(a) |
Amount includes 1,000,000 shares of ENVI Class A Common Stock held by HB Strategies, a founder, all of which shares carry the same redemption rights as other shares of ENVI Class A Common Stock. The 50% Redemption Scenario and the Maximum Redemption Scenario assume that HB Strategies will redeem 50% and 100%, respectively, of its shares of ENVI Class A Common Stock. Amount excludes 13,100,000 warrants to purchase ENVI Class A Common Stock, which is made up of 10,350,000 public warrants, 2,000,000 private placement warrants and 750,000 Insider Warrants. Additionally, under each of the 50% Redemption Scenario and the Maximum Redemption Scenario, an aggregate of 650,000 Warrants comprised of 500,000 private placement warrants owned by HB Strategies and 150,000 Insider Warrants owned by the Sponsor will be forfeited pursuant to the Sponsor Letter Agreement.
|
(b) |
In accordance with the terms and subject to the conditions of the Business Combination Agreement, each outstanding share of capital stock of GreenLight will be exchanged for shares of New GreenLight Common Stock and outstanding GreenLight Options (whether vested or unvested) will be exchanged for comparable options to purchase New GreenLight Common Stock, in each case, based on an implied GreenLight equity value of $1.2 billion. The number of shares of New GreenLight Common Stock issued to the holders of shares of capital stock of GreenLight at Closing will fluctuate based on the number of shares underlying GreenLight Options and GreenLight Warrants, whether vested or unvested (and the exercise prices of such options and warrants), outstanding at Closing.
|
(c) |
Amount includes 6,583,549 shares issuable upon conversion of the GreenLight Convertible Notes and 872,667 shares underlying GreenLight Warrants that are assumed to be exercised immediately prior to the consummation of the Business Combination and excludes 17,555,928 shares underlying Rollover Options to be issued to holders of GreenLight Options, assuming such GreenLight Options remain unexercised as of the Closing.
|
(d) |
Amount excludes 31,750,000 shares (which amount includes shares underlying Rollover Options) and 2,000,000 shares of New GreenLight Common Stock that are expected to be available for issuance under the New GreenLight Equity Plan and the New GreenLight ESPP, respectively, after the consummation of the Business Combination, assuming approval of the Condition Precedent Proposals.
|
Assuming
No
Redemption |
Assuming
50% of
Maximum Redemption |
Assuming
Maximum Redemption |
||||||||||
Underwriting fee as % of total stockholders’ equity
|
2.5 | % | 3.6 | % | 6.8 | % | ||||||
Underwriting fee per share attributable to common stockholders
|
$ | (0.05 | ) | $ | (0.06 | ) | $ | (0.06 | ) |
(i) |
Business Combination Proposal
|
(ii) |
Public Benefit Corporation Proposal
|
(iii) |
Charter Amendment Proposal
|
(iv) |
Advisory Charter Amendment Proposals
non-binding
advisory basis, of each of the Advisory Charter Amendment Proposals the affirmative vote (in person or by proxy) of the holders of at least a majority of the shares of ENVI Class A Common Stock and ENVI Class B Common Stock entitled to vote on such matter and actually cast thereon at the special meeting, voting as a single class.
|
(v) |
Nasdaq Proposal
|
(vi) |
Incentive Award Plan Proposal
|
(vii) |
Employee Stock Purchase Plan Proposal
|
(viii) |
Director Election Proposal
The Director Election Proposal
|
(ix) |
Adjournment Proposal
|
(i) |
hold shares of public common stock;
|
(ii) |
submit a written request to Continental, ENVI’s transfer agent, in which you (i) request that New GreenLight redeem all or a specified portion of your shares of public common stock for cash, and (ii) identify yourself as the beneficial holder of the shares of public common stock and provide your legal name, phone number and address; and
|
(iii) |
deliver your shares of public common stock to be redeemed to Continental, ENVI’s transfer agent, physically or electronically through DTC.
|
• |
the fact that our initial stockholders, and in the case of HB Strategies solely with respect to their founder shares, have agreed not to redeem any founders shares or any shares of ENVI Class A Common Stock held by them in connection with a stockholder vote to approve a proposed initial business combination, including all 5,175,000 shares of ENVI Class B Common Stock held by them as of the date of this proxy statement/prospectus;
|
• |
the fact that our initial stockholders and their affiliates would receive approximately $8.3 million in aggregate proceeds comprised of (i) fees to Canaccord, an affiliate of the Sponsor, who will receive a fee of $7.8 million in connection with the closing of the proposed business combination and (ii) the repayment of a promissory note issued to HB Strategies in an aggregate principal amount of $500,000, the entire amount of which remains outstanding as of the date of this prospectus;
|
• |
the fact that the initial stockholders paid an aggregate of $25,000 for the 5,175,000 shares of ENVI Class B Common Stock currently owned by them, or approximately $0.005 per share, and such securities will have a significantly higher value at the time of the Business Combination;
|
• |
As a result of the lower price paid by our initial stockholders for their shares as compared to, for example, the price per share of our public shares of $10.00 at our initial public offering (which price is $9.995 above the price per share paid by our initial stockholders), the initial stockholders may generate a profit on their shares even at prices that would generate a significant loss for the public stockholders on their shares of public common stock;
|
• |
the fact that HB Strategies paid $2,000,000 for its private placement warrants, and that ENVI issued the 750,000 Insider Warrants, and that these private placement warrants would be worthless if a business combination is not consummated by July 19, 2022 (or by January 19, 2023 if we, by resolution of our board, extend the period of time by an additional six months);
|
• |
the fact that the initial stockholders and ENVI’s other current officers and directors have agreed to waive their rights to liquidating distributions from the trust account with respect to any common stock (other than public common stock) held by them if ENVI fails to complete an initial business combination by July 19, 2022 (or by January 19, 2023 if we elect to extend);
|
• |
the fact that the Investor Rights Agreement has been entered into by the initial stockholders;
|
• |
the fact that, at the option of the Sponsor, any amounts outstanding under any loan made by the Sponsor or any of its affiliates to ENVI in an aggregate amount of up to $1,500,000 may be converted into ENVI Units in connection with the consummation of the Business Combination;
|
• |
the fact that HB Strategies has made a $500,000 working capital loan to ENVI;
|
• |
the continued indemnification of ENVI’s directors and officers and the continuation of ENVI’s directors’ and officers’ liability insurance after the Business Combination (
i.e.
|
• |
the fact that the Sponsor and ENVI’s officers and directors will lose their entire investment in ENVI and will not be reimbursed for any
out-of-pocket
|
• |
the fact that if the trust account is liquidated, including in the event ENVI is unable to complete an initial business combination by July 19, 2022 (or by January 19, 2023 if we elect to extend), the Sponsor has agreed to indemnify ENVI to ensure that the proceeds in the trust account are not reduced below $10.00 per public share, or such lesser per public share amount as is in the trust account on the liquidation date, by the claims of prospective target businesses with which ENVI has entered into an acquisition agreement or claims of any third party for services rendered or products sold to ENVI, but only if such a vendor or target business has not executed a waiver of any and all rights to seek access to the trust account; and
|
• |
the fact that ENVI may be entitled to distribute or pay over funds held by ENVI outside the Trust Account to the Sponsor or any of its Affiliates prior to the Closing.
|
No
Redemption
(1)
|
Maximum
Redemption
(2)
|
|||||||
(
in millions)
|
||||||||
Sources
|
||||||||
Cash Held in Trust Account(3)
|
$ | 207.0 | $ | — | ||||
PIPE Financing(4)
|
124.3 | 124.3 | ||||||
Seller Rollover Equity
|
1,200.0 | 1,200.0 | ||||||
|
|
|
|
|||||
Total Sources
|
$ | 1,531.3 | $ | 1,324.3 | ||||
|
|
|
|
|||||
Uses
|
||||||||
Seller Rollover Equity
|
$ | 1,200.0 | $ | 1,200.0 | ||||
Net Cash to Balance Sheet
|
301.3 | 97.9 | ||||||
Estimated Transaction Costs
|
30.0 | 26.4 | ||||||
|
|
|
|
|||||
Total Uses
|
$ | 1,531.3 | $ | 1,324.3 | ||||
|
|
|
|
(1) |
Assumes that none of the holders of Class A Common Stock exercise their redemption rights.
|
(2) |
Assumes that holders of 20,375,179 shares of Class A Common Stock exercise their redemption rights (representing the maximum amount of public shares that can be redeemed to satisfy the Aggregate Transaction Proceeds Condition).
|
(3) |
Represents the expected amount of the cash held in ENVI’s trust account prior to the Closing (and prior to any redemption by ENVI stockholders), excluding any interest earned on the funds.
|
(4) |
Represents the proceeds from the PIPE Financing as of the consummation of the Business Combination.
|
• |
The
pre-combination
equityholders of GreenLight will hold the majority of voting rights in New GreenLight;
|
• |
The
pre-combination
equityholders of GreenLight will have the right to appoint six of the seven directors on the New GreenLight Board;
|
• |
Senior management of GreenLight will comprise the senior management of New GreenLight; and
|
• |
Operations of GreenLight will comprise the ongoing operations of New GreenLight.
|
• |
GreenLight may not be successful in its efforts to develop or bring products or services to market, to introduce new products, or to achieve market acceptance;
|
• |
GreenLight has a limited operating history and funding, which may make it difficult to evaluate its product development, product prospects and overall likelihood of success;
|
• |
GreenLight may fail to obtain regulatory approval for some or all of its products;
|
• |
GreenLight will require substantial additional funds to complete its research and development activities and fund its other operations. Its current available funds are not sufficient for all of these activities and, as a result, there is substantial doubt about its ability to continue as a going concern;
|
• |
GreenLight has identified material weaknesses in its internal controls of financial reporting, which may result in material misstatements or restatements of its consolidated financial statements or cause it to fail to meet New GreenLight’s periodic reporting obligations;
|
• |
GreenLight’s product candidates may be more complex and more difficult to manufacture than initially anticipated, and GreenLight may encounter difficulties in manufacturing, product release, shelf life, testing, storage, supply chain management or shipping of any of its product candidates;
|
• |
GreenLight depends on relationships with third parties for revenues, and for the development, regulatory approval, commercialization and marketing of certain of its products and product candidates, which are outside of its full control;
|
• |
GreenLight’s product candidates are extremely temperature sensitive, may have other attributes that lead to limited shelf life, and may pose other risks to supply, inventory and waste management and increased cost of goods;
|
• |
Even if any product candidates developed by GreenLight receives regulatory approval, GreenLight may nonetheless fail to achieve the degree of market acceptance by physicians, patients, healthcare payors, and others in the medical community necessary for commercial success;
|
• |
GreenLight faces significant competition, and its competitors may develop and market technologies or products more rapidly than it does or that are more effective, safer or less expensive;
|
• |
GreenLight’s preclinical studies may not succeed or achieve positive results, and, even if such preclinical studies are successful, the resulting clinical trials of GreenLight’s human health product candidates may nevertheless reveal significant adverse events, including negative immune system responses, and may result in a safety profile that could prevent or delay regulatory approval, licensure or market acceptance;
|
• |
The time and expense required to obtain regulatory approvals for preclinical and clinical trials could be significantly greater than for more conventional therapeutic technologies or products. If preclinical studies or clinical trials of any product candidates fail to demonstrate safety and efficacy to the satisfaction of regulatory authorities or do not otherwise produce positive results, GreenLight may incur additional costs or experience delays in completing, or ultimately be unable to complete, the development and commercialization of such product candidates;
|
• |
GreenLight, its service providers or any third-party manufacturers may fail to comply with regulatory requirements which could subject GreenLight to enforcement actions;
|
• |
If field trials are unsuccessful, GreenLight may fail to obtain regulatory approval of, or commercialize, its products on a timely basis;
|
• |
U.S. agricultural production could decline;
|
• |
GreenLight’s plant health program is susceptible to risks relating to weather conditions, seasonal variations and other factors;
|
• |
Crop protection products must be extensively tested for safety, efficacy and environmental impact before they can be registered for production, use, sale or commercialization in a given market, and there can be no guaranty that such testing will be successful;
|
• |
The agricultural products may fail to meet the criteria for desirable certifications such as
“non-GMO”
or “organic” and may cause the plants or products to which they are applied also to lose these certifications, reducing the addressable market for and value of our products;
|
• |
The honeybee ecosystem is complex and it is difficult to measure the overall efficacy of GreenLight’s product candidate since there are multiple factors other than Varroa mites contributing to the decline in honeybee populations;
|
• |
At the dose safety factor typically required by the EPA for approval, our Varroa mite control product causes significant bee mortality, and our dose control system may not convince the EPA to waive its customary dose safety factor requirement;
|
• |
GreenLight’s product will need to be evaluated by the EPA without a precedent product, the process of which may incur additional time needed for further field trials;
|
• |
The intellectual property related to GreenLight’s RNA honeybee product was purchased from Bayer Crop Science, a subsidiary of Bayer, which now owns Monsanto which has had significant pushback from environmental groups regarding its technology and practices, which may affect GreenLight’s ability to market its products;
|
• |
The research and development process for our Varroa mite control product is expensive with little immediate return, and the field trials associated with honeybees in general are susceptible to circumstances outside of GreenLight’s control;
|
• |
If our Varroa mite control product is used inappropriately and is consumed by invertebrates other than the Varroa destructor mite, it could be harmful to those invertebrates;
|
• |
The raw materials used in GreenLight’s manufacturing process may become difficult to obtain in the quality or quantity required for its business plans or at prices that are currently projected;
|
• |
Single or limited sources for some materials may impact GreenLight’s ability to secure supply;
|
• |
Any disruption to the supply chain for, or any malfunction of, the highly specialized equipment and consumables on which GreenLight relies may adversely impact GreenLight’s operations;
|
• |
GreenLight may be unable to protect and maintain sufficient intellectual property protection for its products, platform, methods, trademarks, and technology, or the scope of the intellectual property protection obtained may not be sufficiently broad, and as a result, competitors could develop and commercialize similar or identical products;
|
• |
GreenLight may lose its existing licenses, or may be unable to obtain licenses to patent rights it may need in the future, or if they are able to obtain such licenses, such third-party owners may not properly maintain or enforce the patents underlying such licenses; and
|
• |
GreenLight may become involved in lawsuits to enforce its intellectual property or defend against third-party claims of infringement, misappropriation or other violations of intellectual property in the U.S. or internationally.
|
• |
the risk that the transaction may not be completed in a timely manner or at all, which may adversely affect the price of ENVI’s securities;
|
• |
the failure to satisfy the conditions to the consummation of the transaction, including the approval of the business combination agreement by the stockholders of ENVI, the satisfaction of the Aggregate Transaction Proceeds Condition by ENVI following any redemptions by its public stockholders and the receipt of certain governmental and regulatory approvals;
|
• |
potential changes to the proposed structure of the business combination that may be required or appropriate to achieve the intended tax treatment or to satisfy other legal or regulatory requirements;
|
• |
the potential inability to complete the PIPE Financing;
|
• |
the occurrence of any event, change or other circumstance that could give rise to the termination of the business combination agreement;
|
• |
the potential inability to maintain the listing of ENVI’s securities with Nasdaq;
|
• |
the outcome of any legal proceedings that may be instituted against GreenLight or ENVI related to the business combination agreement or the proposed transaction;
|
• |
unanticipated costs related to the transaction and the potential failure to realize anticipated benefits of the transaction or to realize estimated pro forma results and underlying assumptions, including with respect to estimated shareholder redemptions;
|
• |
potential exercise of appraisal rights by some GreenLight stockholders, which may reduce available cash;
|
• |
the effect of the announcement or pendency of the transaction on GreenLight’s business relationships, operating results, and business generally;
|
• |
risks that the proposed transaction disrupts current plans and operations of GreenLight;
|
• |
the need to obtain regulatory approval for GreenLight’s product candidates;
|
• |
the risk that preclinical studies and any ensuing clinical trials will not demonstrate that GreenLight’s product candidates are safe and effective;
|
• |
the risk that GreenLight’s product candidates will have adverse side effects or other unintended consequences, which could impair their marketability;
|
• |
the risk that GreenLight’s product candidates do not satisfy other legal and regulatory requirements for marketability in one or more jurisdictions;
|
• |
the risks of enhanced regulatory scrutiny of solutions utilizing messenger ribonucleic acid (“
mRNA
”) as a basis;
|
• |
the potential inability to achieve GreenLight’s goals regarding scalability, affordability and speed of commercialization of its product candidates;
|
• |
the anticipated need for additional capital to achieve GreenLight’s business goals;
|
• |
changes in the industries in which GreenLight operates;
|
• |
changes in laws and regulations affecting the business of GreenLight;
|
• |
the potential inability to implement or achieve business plans, forecasts, and other expectations after the completion of the proposed transaction; and
|
• |
other factors detailed under the section titled “
Risk Factors
|
• |
the resources, time and costs required to initiate and complete our research and development and to initiate and complete studies and trials and to obtain regulatory approvals for additions to our product pipeline;
|
• |
progress in our research and development programs;
|
• |
the timing and amount of milestone, royalty and other payments; and
|
• |
costs necessary to protect any intellectual property rights.
|
• |
our products may not perform as expected;
|
• |
we may be unable to capitalize on successful innovation because we may choose not to incur the expense of patenting our discoveries in all jurisdictions or may be unable to obtain patents in the jurisdictions in which we wish to obtain patents;
|
• |
any strategy of discovering additional vertical markets beyond plant, animal and human health for the use of RNA may be infeasible, limiting our growth;
|
• |
our products may not receive necessary regulatory permits and governmental clearances in the markets in which we intend to sell them;
|
• |
our competitors may develop new products or improve existing products that may make our products uncompetitive;
|
• |
the lower cost of RNA produced by us may not translate equally or at all into lower prices for the products that use it;
|
• |
our products may be difficult to produce on a large scale;
|
• |
intellectual property and other proprietary rights of third parties may prevent us or our collaborators from making, marketing or selling our products;
|
• |
we or our collaborators may be unable to fully develop or commercialize products in a timely manner or at all; and
|
• |
third parties may develop superior or equivalent products.
|
• |
The failure to maintain a sufficient complement of personnel in our accounting and reporting department to ensure adequate segregation of duties such that appropriate review and monitoring of our financial records is executed.
|
• |
The failure to design and implemented adequate information systems controls, including access and change management controls
|
• |
the inability to control the resources such third parties devote to GreenLight’s programs, products or product candidates;
|
• |
disputes may arise under an agreement and the underlying agreement may fail to provide us with significant protection or may fail to be effectively enforced if such third parties fail to perform;
|
• |
the interests of such third parties may not always be aligned with the interests of GreenLight, and such parties may not pursue regulatory approvals or market a product in the same manner or to the same extent as GreenLight, which could adversely affect revenues, or may adopt tax strategies that could have an adverse effect on GreenLight’s business, results of operations or financial condition;
|
• |
third-party relationships require the parties to cooperate, and failure to do so effectively could adversely affect product development or the clinical development or regulatory approvals of product candidates under collaborative control, could result in termination of the research, development or commercialization of product candidates or could result in litigation or arbitration;
|
• |
any failure on the part of such third parties to comply with applicable laws, including tax laws, regulatory requirements and/or applicable contractual obligations or to fulfill any responsibilities they may have to protect and enforce any intellectual property rights underlying product candidates could have an adverse effect on revenues as well as give rise to possible legal proceedings; and
|
• |
any improper conduct or actions on the part of such third parties could subject us to civil or criminal investigations and monetary and injunctive penalties, impact the accuracy and timing of financial reporting and/or adversely impact GreenLight’s ability to conduct business, operating results and reputation.
|
• |
Risks of Reliance on Third Parties and Single Source Providers.
COVID-19
pandemic and intellectual property protection. These third parties may not perform their obligations in a timely and cost-effective manner or in compliance with applicable regulations, and they may be unable or unwilling to increase production capacity commensurate with demand for existing or future products. Finding alternative providers could take a significant amount of time and involve significant expense due to the specialized nature of the services and the need to obtain regulatory approval of any significant changes to suppliers or manufacturing methods. GreenLight cannot be certain that it could reach an agreement with alternative providers or that the FDA or other regulatory authorities would approve the use of such alternatives.
|
• |
Risks Relating to Compliance with cGMP.
|
• |
Global Supply Risks.
|
expected timelines or that there will not be any direct or indirect delays resulting from the
COVID-19
pandemic. GreenLight has had delays, and if there are additional delays, in bringing its current and planned facilities online and it may not have sufficient manufacturing capacity to meet its long-term manufacturing requirements.
|
• |
Risk of Product Loss.
|
• |
a disruption to suppliers’ operations which could leave GreenLight with no other means of continuing the research, development, or manufacturing operations for which the supplier provides inputs;
|
• |
the inability to locate a suitable replacement on acceptable terms or on a timely basis, if at all;
|
• |
existing suppliers may cease or reduce production or deliveries, raise prices, or renegotiate terms;
|
• |
delays caused by supply issues may harm GreenLight’s reputation, frustrate customers, and cause them to turn to GreenLight’s competitors; and
|
• |
GreenLight’s ability to progress the development of existing programs and the expansion of capacity to begin future programs could be materially and adversely impacted if the single-source, limited-source or preferred suppliers upon which GreenLight relies were to experience a significant business challenge, disruption, or failure due to issues such as financial difficulties or bankruptcy, issues relating to other customers such as regulatory or quality compliance issues, or other financial, legal, regulatory, or reputational issues.
|
• |
the wider acceptance by patients of products derived from RNA manufacturing processes;
|
• |
the efficacy and safety of such product candidates as demonstrated in pivotal clinical trials published in peer-reviewed journals;
|
• |
the potential and perceived advantages compared to alternative treatments;
|
• |
the ability to offer GreenLight’s products for sale at competitive prices;
|
• |
the ability to offer appropriate patient access programs, such as
co-pay
assistance;
|
• |
the extent to which physicians recommend GreenLight’s products to their patients;
|
• |
convenience and ease of dosing and administration compared to alternative treatments;
|
• |
the clinical indications for which the product candidate is approved by the FDA, EMA or other comparable foreign regulatory agencies;
|
• |
product labeling or product insert requirements of the FDA, EMA or other comparable foreign regulatory authorities, including any limitations, contraindications or warnings contained in a product’s approved labeling;
|
• |
restrictions on how the product is distributed;
|
• |
the timing of market introduction of competitive products;
|
• |
publicity concerning GreenLight’s products or competing products and treatments;
|
• |
the effectiveness of marketing and distribution efforts by us and other licenses and distributors;
|
• |
sufficient governmental third party coverage or reimbursement; and
|
• |
the prevalence and severity of any side effects.
|
• |
difficulties and challenges relating to the building, commissioning and complying with regulatory requirements related to manufacturing facilities in foreign countries;
|
• |
the inability to obtain necessary foreign regulatory or pricing approvals of products in a timely manner;
|
• |
limitations and additional pressures on GreenLight’s ability to obtain and maintain product pricing or receive price increases, including those resulting from governmental or regulatory requirements;
|
• |
the inability to successfully complete preclinical studies or subsequent or confirmatory clinical trials in countries where GreenLight’s experience is limited;
|
• |
longer payment and reimbursement cycles and uncertainties regarding the collectability of accounts receivable;
|
• |
fluctuations in foreign currency exchange rates that may adversely impact GreenLight’s revenues, net income and value of certain of its investments;
|
• |
the imposition of governmental controls;
|
• |
diverse data privacy and protection requirements;
|
• |
increasingly complex standards for complying with foreign laws and regulations that may differ substantially from country to country and may conflict with corresponding U.S. laws and regulations;
|
• |
the
far-reaching
anti-bribery and anti-corruption legislation in the U.K., including the Bribery Act, and elsewhere and escalation of investigations and prosecutions pursuant to such laws;
|
• |
compliance with complex import and export control laws;
|
• |
changes in tax laws;
|
• |
the imposition of tariffs or embargoes and other trade restrictions;
|
• |
the impact of public health epidemics, such as the
COVID-19
pandemic, on the global economy and the delivery of healthcare treatments;
|
• |
less favorable intellectual property or other applicable laws; and
|
• |
known and unknown risks related to local and geopolitical unrest;
|
• |
developing drug candidates;
|
• |
conducting preclinical and clinical trials;
|
• |
obtaining regulatory approvals; and
|
• |
commercializing product candidates.
|
• |
regulatory authorities may withdraw licensures and/or approvals of such product;
|
• |
regulatory authorities may require additional warnings on the label, such as a “black box” warning or contraindication;
|
• |
additional restrictions may be imposed on the marketing of the particular product or the manufacturing processes for the product or any product component;
|
• |
we may be required to restrict the conductions under which the product may be distributed, including through implementation a Risk Evaluation and Mitigation Strategy, or REMS;
|
• |
we may be required to change the way a product candidate is administered or conduct additional clinical trials;
|
• |
we could be sued and held liable for harm caused to patients;
|
• |
the product may become less competitive; and
|
• |
our reputation may suffer.
|
• |
much greater experience, financial, technical and human resources than we have at every stage of the discovery, development, manufacture and commercialization process;
|
• |
more extensive experience in preclinical studies, conducting clinical trials, obtaining and maintaining regulatory approvals or licensures and manufacturing and marketing products;
|
• |
products that have been approved or licensed or are in late stages of development;
|
• |
established distribution networks;
|
• |
collaborative arrangements with leading companies and research institutions; and
|
• |
entrenched and established relationships with healthcare providers and payors.
|
• |
the patient eligibility and exclusion criteria defined in the protocol;
|
• |
the severity of the disease under investigation;
|
• |
the size of the patient population required for analysis of the trial’s primary endpoints and the process for identifying patients;
|
• |
the proximity of patients to trial sites;
|
• |
the design of the trial;
|
• |
our ability to recruit clinical study investigators with the appropriate competencies and experience;
|
• |
clinicians’ and patients’ perceptions as to the potential advantages and risks of the product candidate being studied with respect to other available therapies, including any new products that may be approved for the indications we are investigating;
|
• |
the availability of competing commercially available therapies and other competing product candidates’ clinical studies;
|
• |
the ability to monitor patients adequately during and after treatment;
|
• |
efforts to facilitate timely enrollment in clinical trials;
|
• |
our ability to obtain and maintain patient informed consents; and
|
• |
the risk that patients enrolled in clinical studies will drop out of the trials before completion.
|
• |
regulators or IRBs, or ethics committees may not authorize us or our investigators to commence a clinical study or conduct a clinical study at a prospective trial site;
|
• |
the FDA or other comparable regulatory authorities may disagree with our clinical study design, including with respect to dosing levels administered in its planned clinical studies, which may delay or prevent us from initiating its clinical studies with its originally intended trial design;
|
• |
we may experience delays in reaching, or fail to reach, agreement on acceptable terms with prospective trial sites and prospective Contract Research Organizations (CROs), which can be subject to extensive negotiation and may vary significantly among different CROs and trial sites;
|
• |
the number of subjects required for clinical studies of any product candidates may be larger than we anticipate or subjects may drop out of these clinical studies or fail to return for post-treatment
follow-up
at a higher rate than it anticipates;
|
• |
our third-party contractors may fail to comply with regulatory requirements or meet their contractual obligations to us in a timely manner, or at all, or may deviate from the clinical study protocol or drop out of the trial, which may require that we add new clinical study sites or investigators;
|
• |
we may experience delays and interruptions to clinical studies, we may experience delays or interruptions to our manufacturing supply chain, or we could suffer delays in reaching, or we may fail to reach, agreement on acceptable terms with third-party service providers on whom we rely;
|
• |
additional delays and interruptions to our clinical studies could extend the duration of the trials and increase the overall costs to finish the trials as its fixed costs are not substantially reduced during delays;
|
• |
we may elect to, or regulators, IRBs, Data Safety Monitoring Boards or ethics committees may require that it or its investigators, suspend or terminate clinical research or trials for various reasons, including noncompliance with regulatory requirements or a finding that the participants are being exposed to unacceptable health risks;
|
• |
we may need to amend or submit new clinical protocols because of changes in regulatory requirements and guidance;
|
• |
we may not have the financial resources available to begin and complete the planned trials, or the cost of clinical studies of any product candidates may be greater than it anticipates; and
|
• |
the supply or quality of our product candidates or other materials necessary to conduct clinical studies of our product candidates may be insufficient or inadequate to initiate or complete a given clinical study.
|
• |
the FDA may disagree with the design or implementation of our clinical trials;
|
• |
we may be unable to demonstrate to the satisfaction of the FDA that a product candidate is safe, pure, and potent;
|
• |
results of clinical trials may not meet the level of statistical significance required by the FDA for licensure;
|
• |
we may be unable to demonstrate that a product candidate’s clinical and other benefits outweigh its safety risks;
|
• |
the FDA may disagree with our interpretation of data from preclinical studies or clinical trials;
|
• |
data collected from clinical trials of our product candidates may not be sufficient to support the submission of a BLA to the FDA or other submission or to obtain marketing licensure in the United States;
|
• |
the FDA may find deficiencies with or fail to approve the manufacturing processes or facilities of third-party manufacturers with which we contract for clinical and commercial supplies; and
|
• |
the licensure policies or regulations of the FDA may significantly change in a manner rendering our clinical data insufficient for licensure.
|
• |
seek to enter into collaboration arrangements to fund development and commercialization of our products;
|
• |
rely on CROs to conduct key elements of research by which our products are developed;
|
• |
rely on Contract Development Organizations (“
CDOs
”) to develop key components of our products;
|
• |
retain individual contractors or contracting organizations to perform critical functions in our company, including functions associated with senior management positions.
|
• |
seek to enter into joint development agreements for the manufacture of both our RNA materials and human health products with partners outside the U.S.;
|
• |
restrictions on, or prohibitions against, marketing;
|
• |
restrictions on importation;
|
• |
suspension of review or refusal to approve new or pending applications;
|
• |
suspension or withdrawal of product approvals;
|
• |
product seizures or recalls;
|
• |
operating restrictions;
|
• |
injunctions; and
|
• |
civil and criminal penalties and fines.
|
• |
discovery efforts at identifying potential mRNA medicines may not be successful;
|
• |
nonclinical or preclinical study results may show potential mRNA medicines to be less effective than desired or to have harmful or problematic side effects;
|
• |
clinical trial results may show potential mRNA medicines to be less effective than expected (e.g., a clinical trial could fail to meet one or more endpoint(s)) or to have unacceptable side effects or toxicities;
|
• |
adverse effects in any one of our clinical programs or adverse effects relating to our mRNA, or our lipid nanoparticles (“
LNPs
”), may lead to delays in or termination of one or more of our programs;
|
• |
the insufficient ability of translational models to reduce risk or predict outcomes in humans, particularly given that each component of investigational medicines and development candidates may have a dependent or independent effect on safety, tolerability, and efficacy, which may, among other things, be species-dependent;
|
• |
manufacturing failures or insufficient supply of cGMP materials for clinical trials, or higher than expected cost could delay or set back clinical trials, or make mRNA-based medicines commercially unattractive;
|
• |
our improvements in the manufacturing processes for this new class of medicines and potential medicines may not be sufficient to satisfy the clinical or commercial demand of our investigational medicines or regulatory requirements for clinical trials;
|
• |
changes that we make to optimize our manufacturing, testing or formulating of cGMP (current good manufacturing process regulations as enforced by the FDA) materials could impact the safety, tolerability, and efficacy of our investigational medicines and development candidates;
|
• |
pricing or reimbursement issues or other factors may delay clinical trials or make any mRNA medicine uneconomical or noncompetitive with other therapies;
|
• |
failure to timely advance our programs or receive the necessary regulatory approvals or a delay in receiving such approvals, due to, among other reasons, slow or failure to complete enrollment in clinical trials, withdrawal by trial participants from trials, failure to achieve trial endpoints, additional time requirements for data analysis, data integrity issues, preparation of a BLA, or the equivalent application, discussions with the FDA or EMA, a regulatory request for additional nonclinical or clinical data, or safety formulation or manufacturing issues may lead to our inability to obtain sufficient funding; and
|
• |
the proprietary rights of others and their competing products and technologies that may prevent our mRNA medicines from being commercialized.
|
• |
Others may be able to develop or make products , platform, methods or technology that are similar to products, platform, methods or technology we have developed or will develop, but that are not covered by the claims of the patents that we own or have licensed and are not protectable through trade secret law.
|
• |
We or our licensors or strategic partners might not have been the first to make the inventions covered by the issued patent or pending patent application that we own or have exclusively licensed, and therefore our patents may be found to be invalid or our patent applications may be rejected.
|
• |
We or our licensors or strategic partners might not have been the first to file patent applications covering certain of our inventions, and therefore our patents may be found to be invalid or our patent applications may be rejected.
|
• |
Others may independently develop or make similar or alternative products, platform, methods or technology or duplicate any of our products, platform, methods or technology without infringing our intellectual property rights. For example, independent development of such products, platform, methods or technology would make it impossible for us to assert trade secret rights against such third parties. If such third parties publish the details of such independently developed products, platform, methods or technology, then we could lose any trade secret protection even as against others.
|
• |
It is possible that our pending patent applications will not lead to issued patents.
|
• |
Issued patents that we own or have exclusively licensed may not provide us with any competitive advantages, or may be held invalid or unenforceable, as a result of legal challenges by our competitors.
|
• |
Our competitors might conduct research and development activities in countries where we do not have patent rights and then use the information learned from such activities to develop competitive products for sale in our major commercial markets.
|
• |
Our competitors may use our manufacturing methods to produce products in jurisdictions in which we do not have patent protection on our manufacturing methods and may export such products for sale other jurisdictions, including our major commercial markets for us. Patents on such methods in our major commercial markets may not protect against such product sales.
|
• |
We may not develop additional proprietary technologies that are patentable or protectible through other intellectual property rights.
|
• |
The intellectual property rights of others may have an adverse effect on our business.
|
• |
the need to obtain regulatory approval for New GreenLight’s product candidates;
|
• |
the risk that clinical trials will not demonstrate that New GreenLight’s therapeutic product candidates are safe and effective;
|
• |
the risk that New GreenLight’s product candidates will have adverse side effects or other unintended consequences, which could impair their marketability;
|
• |
the risk that New GreenLight’s product candidates do not satisfy other legal and regulatory requirements for marketability in one or more jurisdictions;
|
• |
the risks of enhanced regulatory scrutiny of RNA-based products, including mRNA and dsRNA;
|
• |
the potential inability to achieve New GreenLight’s goals regarding scalability, affordability and speed of commercialization of its product candidates;
|
• |
the anticipated need for additional capital to achieve New GreenLight’s business goals;
|
• |
changes in the industries in which New GreenLight operates; changes in laws and regulations affecting the business of New GreenLight;
|
• |
the potential inability to implement or achieve business plans, forecasts, and other expectations after the completion of the proposed transaction;
|
• |
actual or anticipated fluctuations in New GreenLight’s operating results, including fluctuations in its quarterly and annual results;
|
• |
operating expenses being more than anticipated;
|
• |
the failure or discontinuation of any of New GreenLight’s product development and research programs;
|
• |
the success of existing or new competitive businesses or technologies;
|
• |
announcements about new research programs or products of New GreenLight’s competitors;
|
• |
developments or disputes concerning patent applications, issued patents or other proprietary rights;
|
• |
the recruitment or departure of key personnel;
|
• |
litigation and governmental investigations involving New GreenLight, its industry or both;
|
• |
investor perceptions of New GreenLight or its industry;
|
• |
negative perceptions of publicly traded companies that have gone public through business combinations with publicly traded special purpose acquisition companies;
|
• |
sales of New GreenLight’s common stock by New GreenLight or by its insiders or other stockholders;
|
• |
the expiration of market standoff or
lock-up
agreements;
|
• |
general economic, industry and market conditions; and
|
• |
the
COVID-19
pandemic, natural disasters or major catastrophic events.
|
• |
reduced liquidity;
|
• |
a limited availability of market quotations for New GreenLight Common Stock;
|
• |
a potential determination that New GreenLight Common Stock is a “penny stock,” which will require brokers trading in New GreenLight Common Stock to adhere to more stringent rules, possibly resulting in a reduced level of trading activity in the secondary trading market for shares of New GreenLight Common Stock;
|
• |
a limited amount of analyst coverage; and
|
• |
a decreased ability to issue additional securities or obtain additional financing in the future.
|
• |
New GreenLight’s board of directors will be classified into three classes of directors with staggered
three-year
terms, and directors will only be able to be removed from office for cause by the affirmative vote of holders of a majority of the voting power of New GreenLight’s then-outstanding capital stock;
|
• |
certain amendments to New GreenLight’s certificate of incorporation will require the approval of stockholders holding three-fourths of the voting power of its
then-outstanding
capital stock;
|
• |
any
stockholder-proposed
amendment to the Proposed Bylaws that is not recommended by the New GreenLight Board will require the approval of stockholders holding three-fourths of the voting power of its
then-outstanding
capital stock;
|
• |
New GreenLight’s stockholders will only be able to take action at a meeting of stockholders and will not be able to take action by written consent for any matter;
|
• |
vacancies on New GreenLight’s board of directors will be able to be filled only by New GreenLight’s board of directors and not by stockholders;
|
• |
only the New GreenLight Board, pursuant to a written resolution adopted by a majority of the New GreenLight Board is authorized to call a special meeting of stockholders;
|
• |
certain litigation against New GreenLight can only be brought in Delaware;
|
• |
the Proposed Charter authorizes undesignated preferred stock, the terms of which may be established by the New GreenLight Board, which shares may be issued without the approval of the holders of New GreenLight’s capital stock; and
|
• |
advance notice procedures apply for stockholders to nominate candidates for election as directors or to bring matters before an annual meeting of stockholders.
|
• |
the fact that our initial stockholders, and in the case of HB Strategies, solely with respect to their founder shares, have agreed not to redeem any founder shares or any shares of ENVI Class A Common Stock held by them in connection with a stockholder vote to approve the Business Combination, including all 5,175,000 shares of ENVI Class B Common Stock held by them as of the date of this proxy statement/prospectus;
|
• |
the fact that our initial stockholders and their affiliates would receive approximately $8.3 million in aggregate proceeds comprised of (i) fees to Canaccord, an affiliate of the Sponsor, who will receive a fee of $7.8 million in connection with the closing of the proposed business combination and (ii) the repayment of a promissory note issued to HB Strategies in an aggregate principal amount of $500,000, the entire amount of which remains outstanding as of the date of this prospectus;
|
• |
the fact that the initial stockholders paid an aggregate of $25,000 for the 5,175,000 shares of ENVI Class B Common Stock currently owned by them, or approximately $0.005 per share, and such securities will have a significantly higher value at the time of the Business Combination;
|
• |
As a result of the lower price paid by our initial stockholders for their shares of ENVI Class B Common Stock as compared to, for example, the price per share of our public shares of $10.00 at our initial public offering (which price is $9.995 above the price per share paid by our initial stockholders), the initial stockholders may generate a profit on their shares even at prices that would generate a significant loss for the public stockholders on their shares of public common stock;
|
• |
the fact that HB Strategies paid $2,000,000 for its private placement warrants, and that ENVI issued the 750,000 Insider Warrants, and that these private placement warrants will be worthless if a business combination is not consummated by July 19, 2022 (or by January 19, 2023 if we, by resolution of our board, extend the period of time by an additional six months);
|
• |
the fact that the initial stockholders and ENVI’s other current officers and directors have agreed to waive their rights to liquidating distributions from the trust account with respect to any common stock (other than public common stock) held by them if ENVI fails to complete an initial business combination by July 19, 2022 (or by January 19, 2023 if we elect to extend);
|
• |
the fact that the Investor Rights Agreement has been entered into by the initial stockholders;
|
• |
the fact that, at the option of the Sponsor, any amounts outstanding under any loan made by the Sponsor or any of its affiliates to ENVI in an aggregate amount of up to $1,500,000 may be converted into ENVI’s warrants in connection with the consummation of the Business Combination;
|
• |
the fact that HB Strategies has made a $500,000 working capital loan to ENVI;
|
• |
the continued indemnification of ENVI’s directors and officers and the continuation of ENVI’s directors’ and officers’ liability insurance after the Business Combination (i.e., a “tail policy”);
|
• |
the fact that the Sponsor and ENVI’s officers and directors will lose their entire investment in ENVI and will not be reimbursed for any
out-of-pocket
|
• |
the fact that if the trust account is liquidated, including in the event ENVI is unable to complete an initial business combination by July 19, 2022 (or by January 19, 2023 if we elect to extend), the Sponsor has agreed to indemnify ENVI to ensure that the proceeds in the trust account are not reduced below $10.00 per public share, or such lesser per public share amount as is in the trust account on the liquidation date, by the claims of prospective target businesses with which ENVI has entered into an acquisition agreement or claims of any third party for services rendered or products sold to ENVI, but only if such a vendor or target business has not executed a waiver of any and all rights to seek access to the trust account; and
|
• |
the fact that ENVI may be entitled to distribute or pay over funds held by ENVI outside the Trust Account to the Sponsor or any of its Affiliates prior to the Closing.
|
• |
a proposal to approve and adopt the Business Combination Agreement, including the Merger, and the transactions contemplated thereby;
|
• |
a proposal to adopt and approve the PBC Proposed Charter;
|
• |
a proposal to adopt and approve the Proposed Charter;
|
• |
the following governance proposals to approve, on a
non-binding
advisory basis, the following material differences between the Existing Charter and the Proposed Charter:
|
• |
to change the authorized capital stock of ENVI from 121,000,000 shares, par value $0.0001 per share, consisting of (a) 100,000,000 shares of ENVI Class A Common Stock, 20,000,000 shares of ENVI Class B Common Stock, and 1,000,000 shares of undesignated preferred stock, to (b) 510,000,000 shares, par value $0.0001 per share, consisting of 500,000,000 shares of common stock of New GreenLight and 10,000,000 shares of undesignated preferred stock of New GreenLight;
|
• |
to provide that, in addition to any vote required by applicable law or the certificate of incorporation or bylaws of New GreenLight, the affirmative vote of the holders of at least seventy-five percent (75%) of the voting power of all then-outstanding shares of capital stock of New GreenLight entitled to vote generally in the election of directors, voting together as a single class, will be required for the stockholders to reduce the total number of shares of New GreenLight Preferred Stock authorized to be issued by New GreenLight or to amend, alter, change or repeal, or adopt any provision of the charter of New GreenLight inconsistent with, specified provisions of the charter of New GreenLight; and
|
• |
to provide that the bylaws of New GreenLight may be adopted, amended, altered or repealed with the approval of a majority of the New GreenLight Board or by the affirmative vote of the holders of at least 75% of the voting power of all then-outstanding shares of capital stock of New GreenLight entitled to vote generally in the election of directors, voting together as a single class, provided that the voting requirement is reduced to a majority if the New GreenLight Board recommends that stockholders approve the adoption, amendment, alteration or repeal;
|
• |
a proposal to approve the issuance of shares of New GreenLight Common Stock in connection with the Business Combination in compliance with the Nasdaq listing rules;
|
• |
a proposal to approve and adopt the New GreenLight Equity Plan;
|
• |
a proposal to approve and adopt the New GreenLight ESPP;
|
• |
to elect seven directors to serve on the New GreenLight Board, effective upon the closing of the Business Combination; and
|
• |
a proposal to approve the adjournment of the special meeting to a later date or dates, if necessary, to, among other things, permit further solicitation and voting of proxies in the event that there are insufficient votes for the approval of one or more proposals at the special meeting.
|
• |
You can vote by signing and returning the enclosed proxy card. If you vote by proxy card, your “proxy,” whose name is listed on the proxy card, will vote your shares as you instruct on the proxy card. If you sign and return the proxy card but do not give instructions on how to vote your shares, your shares will be voted as recommended by the ENVI Board “FOR” the Business Combination Proposal, “FOR” the Charter Amendment Proposal, “FOR” each of the separate Advisory Charter Amendment Proposals, “FOR” the Nasdaq Proposal, “FOR” the Incentive Award Plan Proposal, “FOR” the Employee Stock Purchase Plan Proposal, “FOR” the Director Election Proposal and “FOR” the Adjournment Proposal, in each case, if presented to the special meeting. Votes received after a matter has been voted upon at the special meeting will not be counted.
|
• |
You can attend the special meeting and vote in person. You will receive a ballot when you arrive. However, if your shares are held in the name of your broker, bank or another nominee, you must get a valid legal proxy from the broker, bank or other nominee. That is the only way ENVI can be sure that the broker, bank or nominee has not already voted your shares.
|
• |
you may send another proxy card with a later date;
|
• |
you may notify ENVI’s Secretary in writing before the special meeting that you have revoked your proxy; or
|
• |
you may attend the special meeting, revoke your proxy, and vote at the meeting, as indicated above.
|
(i) |
hold shares of public common stock;
|
(ii) |
submit a written request to Continental, ENVI’s transfer agent, in which you (i) request that New GreenLight redeem all or a specified portion of your shares of public common stock for cash, and (ii) identify yourself as the beneficial holder of the shares of public common stock and provide your legal name, phone number and address; and
|
(iii) |
deliver your shares of public common stock to be redeemed to Continental, ENVI’s transfer agent, physically or electronically through DTC.
|
(a) |
on the Closing Date, the parties to the Business Combination Agreement will cause a certificate of merger to be executed and filed with the Secretary of State of the State of Delaware, pursuant to which Merger Sub will merge with and into GreenLight, with GreenLight being the surviving company in the Merger and, after giving effect to such merger, GreenLight will be a wholly owned subsidiary of New GreenLight;
|
(b) |
at the Effective Time, each outstanding share of capital stock of GreenLight (other than treasury shares and shares with respect to which appraisal rights under the DGCL are properly exercised and not withdrawn) (each, a “
Company Share
”) shall be automatically cancelled and extinguished and converted into a number of shares of New GreenLight Common Stock equal to the product of (x) the conversion ratio applicable to such Company Share, if any, multiplied by (y) the quotient obtained by dividing (a) 120,000,000 by (b) the number of Fully-Diluted Shares (as defined in the Business Combination Agreement) (such quotient, the “
Exchange Ratio
”);
|
(c) |
each option to purchase shares of capital stock of GreenLight (each, a “
GreenLight Option
”) that is outstanding and unexercised immediately prior to the Effective Time shall be converted into an option issued under the New GreenLight Equity Plan to purchase a number of shares of New GreenLight Common Stock (each, a “
Rollover Option
”) equal to the product (rounded down to the nearest whole number) of (x) the number of Company Shares subject to such GreenLight Option immediately prior to the Effective Time, multiplied by (y) the Exchange Ratio, at an exercise price per share (rounded up to the nearest whole cent) equal to the quotient of (i) the exercise price per share of such GreenLight Option immediately prior to the Effective Time divided by (ii) the Exchange Ratio. Each Rollover Option shall be subject to the same terms and conditions (including applicable vesting, expiration and forfeiture provisions) that applied to the corresponding GreenLight Option immediately prior to the Effective Time, except (I) as specifically provided above, or (II) as to (1) terms rendered inoperative by reason of the transactions contemplated by the Business Combination Agreement (including any anti-dilution or other similar provisions that may have adjusted or may adjust the number of underlying shares that are subject to any such option until the effective time of the Merger), or (2) such other immaterial administrative or ministerial changes as the ENVI Board (or the compensation committee of the ENVI Board) may determine in good faith are appropriate to effectuate the administration of the Rollover Options;
|
(d) |
shares of New GreenLight Common Stock issued in respect of shares of GreenLight common stock that are subject to vesting or forfeiture (the “
GreenLight Restricted Shares
”), shall be subject to the same terms and conditions (including applicable vesting, expiration and forfeiture provisions) that applied to the corresponding GreenLight Restricted Share immediately prior to the Effective Time;
|
(e) |
each warrant of GreenLight (“
GreenLight Warrant
”), to the extent outstanding and unexercised, shall automatically, without any action of any party or any other person (including the holder thereof), be assumed by New GreenLight and converted into a warrant to acquire shares of New GreenLight Common Stock (such warrants, the “
New GreenLight Warrants
”) equal to the product (rounded down to the nearest whole number) of (x) the number of GreenLight Shares (on an
as-converted
basis) subject to such GreenLight Warrant immediately prior to the Effective Time, multiplied by (y) the Exchange Ratio, at an exercise price per share (rounded up to the nearest whole cent) equal to the quotient of (i) the exercise price per share of such GreenLight Warrant immediately prior to the Effective Time, divided by (ii) the Exchange Ratio. Each New GreenLight Warrant will be subject to the same terms and conditions as were applicable to the GreenLight Warrant other than for terms rendered inoperative by reason of the transactions contemplated by the Business Combination Agreement, including any anti-dilution or other similar adjustment provisions;
|
(f) |
at the Effective Time, each of the treasury shares of GreenLight will be cancelled and extinguished for no additional consideration;
|
(g) |
at the Effective Time, each ENVI Class A Share and ENVI Class B Share that is issued and outstanding immediately prior to the Merger shall become one share of New GreenLight Common Stock;
|
(h) |
at the Effective Time, each share of capital stock of the Merger Sub shall be converted into one share of common stock, par value $0.0001 per share of Honey Bee Merger Sub, Inc.; and
|
(i) |
at the Effective Time, ENVI will change its name to “GreenLight Biosciences, Inc.” (or if the Public Benefit Corporation Proposal is also approved, ENVI will instead change its name to “GreenLight Biosciences, PBC”.)
|
• |
each applicable waiting period under the HSR Act relating to the Business Combination having expired or been terminated;
|
• |
no order or law issued or enacted by any court of competent jurisdiction or other governmental entity of competent jurisdiction enjoining or prohibiting the Merger shall be in effect;
|
• |
the Registration Statement becoming effective in accordance with the provisions of the Securities Act, no stop order being issued by the SEC and remaining in effect with respect to the Registration Statement, of which this proxy statement/prospectus forms a part, and no proceeding seeking such a stop order being threatened or initiated by the SEC and remaining pending;
|
• |
the approval of the Business Combination Agreement and the transactions contemplated thereby (including the Merger) being obtained by (a) a majority of the voting power of the outstanding shares of capital stock of GreenLight, voting together on an
as-converted
to common stock basis, (b) a majority of the outstanding commons stock of GreenLight, (c) a majority of the outstanding shares of preferred stock of GreenLight, voting together on an
as-converted
to common stock basis, (d) a majority of the outstanding shares of GreenLight Series C Preferred Stock, voting as a separate class, and (e) a majority of the outstanding shares of GreenLight Series D Preferred, voting as a separate class (clauses (a)-(e), the “
GreenLight Required Shareholder Approval
”);
|
• |
the approval of each Condition Precedent Proposal by the affirmative vote of the requisite percentage of holders of common stock of ENVI entitled to vote thereon being obtained, under and in accordance with the DGCL and the Existing Organizational Documents;
|
• |
New GreenLight’s initial listing application with Nasdaq in connection with the transactions contemplated by the Business Combination Agreement being approved and, immediately following the Effective Time and after giving effect to any redemption of shares of ENVI Class A Common Stock in accordance with the Existing Organizational Documents, ENVI satisfying any applicable initial and continuing listing requirements of Nasdaq, and ENVI not having received any notice of
non-compliance
in connection therewith (and there is no basis for Nasdaq to provide such a notice of
non-compliance)
that has not been cured or would not be cured at or immediately following the Effective Time, and the shares of New GreenLight Common Stock (including the shares of New GreenLight Common Stock to be issued in connection with the Merger), being approved for listing on Nasdaq; and
|
• |
after giving effect to the transactions contemplated by the Business Combination Agreement (including the PIPE Financing and any redemptions of shares of ENVI Class A Common Stock in accordance with the Existing Organizational Documents), ENVI having at least $5,000,001 of net tangible assets (as determined in accordance with Rule
3a51-1(g)(1)
of the Exchange Act) immediately after the Effective Time of the Merger.
|
• |
the representations and warranties of GreenLight regarding its organization and qualification, certain representations and warranties regarding its capitalization, the absence of change in control payments
|
or declaration of dividends or other distributions, the authority of GreenLight to execute and deliver the Business Combination Agreement and each of the ancillary documents thereto to which it is or will be a party and to consummate the transactions contemplated thereby and GreenLight brokers’ fees being true and correct (without giving effect to any limitation of “materiality” or “GreenLight Material Adverse Effect” (as defined below) or any similar limitation set forth in the Business Combination Agreement) in all material respects as of the date of the Business Combination Agreement and the Closing Date as though made on and as of the Closing Date (or, if given as of an earlier date, as of such earlier date);
|
• |
the representation and warranty regarding the absence of a “GreenLight Material Adverse Effect” since January 1, 2021 being true and correct in all respects as of the date of the Business Combination Agreement and the Closing Date, as though made on and as of the Closing Date (or, if given as of an earlier date, as of such earlier date), provided that this condition will be deemed satisfied if there is no GreenLight Material Adverse Effect that is continuing;
|
• |
the other representations and warranties of GreenLight being true and correct (without giving effect to any limitation as to “materiality” or “GreenLight Material Adverse Effect” or any similar limitation set forth in the Business Combination Agreement) in all respects as of the date of the Business Combination Agreement and the Closing Date, as though made on and as of the Closing Date (or, if given as of an earlier date, as of such earlier date), except where the failure of such representations and warranties to be true and correct, taken as a whole, does not cause a GreenLight Material Adverse Effect;
|
• |
GreenLight having performed and complied in all material respects with the covenants and agreements required to be performed or complied with by it under the Business Combination Agreement at or prior to the Closing;
|
• |
since the date of the Business Combination Agreement, no GreenLight Material Adverse Effect has occurred that is continuing;
|
• |
GreenLight having secured the requisite written consent and approval of note holders necessary to cause the promissory notes issued pursuant to that certain Convertible Note Purchase Agreement, dated as of April 9, 2020 by and between a subsidiary of GreenLight and the other parties thereto, as amended to date, to convert concurrently with (or immediately prior to) the Closing into shares of GreenLight Series D Preferred Stock;
|
• |
ENVI must have received a certificate executed by an authorized officer of GreenLight confirming that the conditions set forth in the first five bullet points in this section have been satisfied.
|
• |
ENVI must have received the Investor Rights Agreement, duly executed by certain stockholders of GreenLight.
|
• |
the representations and warranties regarding the organization and qualification of the ENVI Parties, the authority of each ENVI Party to execute and deliver the Business Combination Agreement and each of the ancillary documents thereto to which it is or will be a party and to consummate the transactions contemplated thereby, certain representations and warranties regarding the capitalization of the ENVI Parties, the absence of change in control payments and ENVI brokers’ fees being true and correct (without giving effect to any limitation of “materiality” or “ENVI Material Adverse Effect” (as defined below) or any similar limitation set forth in the Business Combination Agreement) in all material respects as of the date of the Business Combination Agreement and the Closing Date, as though made on and as of the Closing Date (or, if given as of an earlier date, as of such earlier date);
|
• |
certain other representations and warranties regarding the absence of an ENVI Material Adverse Effect since December 31, 2020 being true and correct in all respects, as of the date of the Business Combination Agreement and the Closing Date, as though made on and as of the Closing Date (or, if given as of an earlier date, as of such earlier date), provided that this condition will be deemed satisfied if there is no ENVI Material Adverse Effect that is continuing;
|
• |
the other representations and warranties of the ENVI Parties being true and correct (without giving effect to any limitation of “materiality” or “ENVI Material Adverse Effect” or any similar limitation set forth in the Business Combination Agreement) in all respects as of the date of the Business Combination Agreement and the Closing Date, as though made on and as of the Closing Date (or, if given as of an earlier date, as of such earlier date), except where the failure of such representations and warranties to be true and correct, taken as a whole, does not cause an ENVI Material Adverse Effect;
|
• |
the ENVI Parties having performed and complied in all material respects with the covenants and agreements required to be performed or complied with by them under the Business Combination Agreement at or prior to the Closing;
|
• |
since the date of the Business Combination Agreement, no ENVI Material Adverse Effect has occurred that is continuing;
|
• |
the Aggregate Transaction Proceeds being equal to or greater than $105,000,000;
|
• |
the New GreenLight Board consisting of the number of directors, and comprising the individuals, determined pursuant to Section 5.18(a)(i) and (ii) of the Business Combination Agreement;
|
• |
(i) the Proposed Charter having been filed with the Secretary of State of the State of Delaware and becoming effective or providing that the Proposed Certificate of Incorporation will become effective no later than the Effective Time and (ii) the Proposed Bylaws having become effective or providing that the Proposed Bylaws will become effective no later than the Effective Time;
|
• |
the initial stockholders having complied in all material respects with their respective covenants and agreements to be performed or complied with by them under the Sponsor Letter Agreement at or prior to Closing;
|
• |
ENVI must maintain its Nasdaq listing in good standing;
|
• |
GreenLight must have received a certificate executed by an authorized officer of ENVI confirming that the conditions set forth in the first five bullet points of this section have been satisfied; and
|
• |
GreenLight must have received the Investor Rights Agreement, duly executed by ENVI and the initial stockholders.
|
• |
subject to certain exceptions or as consented to in writing by ENVI (such consent not to be unreasonably withheld, conditioned or delayed), prior to the Closing, GreenLight will and will cause its subsidiaries to, use commercially reasonable efforts to operate the business of GreenLight and its subsidiaries in the ordinary course in all material respects and use commercially reasonable efforts to maintain and preserve intact in all material respects the business organization, assets, properties and material business relations of GreenLight and its subsidiaries, taken as a whole.
|
• |
subject to certain exceptions, prior to the Closing, GreenLight will and will cause its subsidiaries to, except as expressly contemplated in the Business Combination Agreement or the ancillary documents, as required by applicable law, as set forth on Section 5.1(b) of the GreenLight disclosure schedules or as consented to by ENVI (such consent not to be unreasonably withheld, conditioned or delayed except in the case of the first, second, fourth, twelfth, fifteenth and sixteenth
sub-bullets
below), not do any of the following:
|
• |
declare, set aside, make or pay any dividends or distribution or payment in respect of, any equity securities of GreenLight and its subsidiaries or repurchase or redeem any outstanding equity securities of GreenLight and its subsidiaries, other than dividends or distributions, declared, set aside or paid by any of GreenLight’s subsidiaries to GreenLight or any subsidiary that is, directly or indirectly, wholly owned by GreenLight;
|
• |
merge, consolidate, combine or amalgamate GreenLight or any of its subsidiaries with any person or purchase or otherwise acquire any corporation, partnership, association or other business entity or organization or division thereof;
|
• |
adopt any amendments, supplements, restatements or modifications to GreenLight or its subsidiaries’ governing documents or the GreenLight stockholders agreement;
|
• |
subject to certain exceptions, sell, assign, exclusively license or otherwise dispose of any material assets or properties of GreenLight or its subsidiaries;
|
• |
subject any material assets or properties of GreenLight to any lien (other than any permitted liens);
|
• |
transfer, issue, sell, grant, or otherwise dispose of, or subject to a lien, (i) any equity interests of GreenLight or its subsidiaries or (ii) any options warrants, rights of conversion or other rights, agreements, arrangements or commitments obligating GreenLight or its subsidiaries to issue, deliver or sell any equity securities of GreenLight or its subsidiaries, other than, in each case, (x) the issuance of
|
shares of common stock of GreenLight upon the exercise of any options outstanding in accordance with the terms of the GreenLight 2012 Equity Plan and each other plan that provides for the award to any current or former director, manager, officer, employee, individual, independent contractor or other service provider of GreenLight and the underlying grant, award or similar agreement, (y) the issuance of shares of GreenLight Series A Preferred Stock or GreenLight Series D Preferred Stock upon the exercise of any warrants outstanding in accordance with the terms of the applicable agreement governing the terms of such warrants and (z) the issuance of shares of common stock of GreenLight upon conversion of shares of preferred stock of GreenLight in accordance with the governing documents of GreenLight;
|
• |
incur, create or assume any indebtedness other than ordinary course trade payables or guarantee any liability of any person;
|
• |
amend or modify, in either case in a manner materially adverse to GreenLight, or terminate certain material contracts of GreenLight, waive any material benefit or right under any such material contracts or enter into, amend or modify any contract that would have been a certain type of material contract had such contract been entered into, amended or modified prior to the date of the Business Combination Agreement;
|
• |
subject to certain exceptions, make any loans, advances or capital contributions to, or guarantees for the benefit of, or any investments in, any person;
|
• |
subject to certain exceptions, amend or modify in any material respect, or adopt or enter into any collective bargaining agreement, benefit or compensation plan, policy, program or contract that would have been an employee benefit plan had such plan been entered into as of the date of the Business Combination Agreement or materially increase the compensation or benefits payable to any current or former director, manager, officer, employee, individual, independent contractor or other service provider or take any action to accelerate any payments or benefit payable to any such person;
|
• |
waive or release any noncompetition,
non-solicitation,
no-hire,
nondisclosure or other restrictive covenant obligation of any current or former director, manager, officer, employee, individual independent contractor or other service provider;
|
• |
make, change or revoke any material tax election other than in the ordinary course of business consistent with past practice, change any annual tax accounting period, surrender any right to claim a material tax refund, materially amend any filed material tax return, file any material tax return inconsistent with past practice in any material respect, enter into any tax allocation, tax sharing, tax indemnity or similar agreement (other than one that is in a contract entered into in the ordinary course of business that is not primarily related to taxes), enter into any tax closing agreement, settle any material tax claim or assessment, or consent to any extension or waiver of the limitation period applicable to or relating to any material tax claim or assessment, other than any such extension of waiver that is obtained in the ordinary course of business;
|
• |
enter into any settlements, conciliation or similar contracts which would involve the payment by GreenLight or any of its subsidiaries in excess of a certain threshold or that impose any material
non-monetary
obligations on GreenLight or any of its subsidiaries;
|
• |
subject to certain exceptions, authorize, recommend, propose or announce an intention to adopt a plan, or otherwise effect, a plan of complete or partial liquidation, dissolution, restructuring, recapitalization, reorganization or similar transaction;
|
• |
make any material changes to the methods of accounting of GreenLight or any of its subsidiaries, other changes that are made in accordance with Public Company Accounting Oversight Board standard;
|
• |
enter into any contract with any broker, finder, investment banker or other person providing for the payment of any brokerage fee, finders’ fee or other commission in connection with the transactions contemplated by the Business Combination Agreement or ancillary documents;
|
• |
make any change of control payment that is not disclosed to ENVI on the GreenLight disclosure schedules or make any material payments with respect to a GreenLight affiliated party arrangement that is not disclosed to ENVI on the GreenLight disclosure schedules; or
|
• |
enter into any contract to do, or cause to be taken, any of the above actions prohibited under the Business Combination Agreement.
|
• |
GreenLight shall terminate certain affiliate contracts as set forth on the GreenLight disclosure schedules effective as of the Closing.
|
• |
as promptly as reasonably practicable (and in any event within five (5) business days) following the time at which this registration statement of which this proxy statement/prospectus forms a part, is declared effective under the Securities Act, GreenLight is required to obtain and deliver to ENVI a true and correct copy of a written consent of the GreenLight stockholders adopting and approving the Business Combination Agreement and the transactions contemplated thereby (including the Merger), duly executed by (i) the requisite number of stockholders of GreenLight in accordance with the DGCL and (ii) at least that number of shares equal to the GreenLight Required Shareholder Approval (the “
GreenLight Stockholder Written Consent
”).
|
• |
at least two (2) business days prior to the Closing Date, GreenLight is required to deliver an allocation schedule setting forth certain capitalization information of GreenLight for purposes of allocating New GreenLight Common Stock, options to purchase New GreenLight Common Stock or the number of New GreenLight Common Stock subject to the Assumed Warrants, as applicable, among the GreenLight equityholders.
|
• |
subject to certain exceptions, prior to the Closing, each of ENVI and GreenLight will purchase a “tail” policy providing liability insurance coverage for directors and officers of ENVI and GreenLight, respectively, with respect to matters occurring on or prior to the Closing, with such “tail” policies to be maintained by New GreenLight following the Closing.
|
• |
subject to certain exceptions, prior to the Closing, ENVI will and will cause its subsidiaries to, except as expressly contemplated in the Business Combination Agreement or the ancillary documents, as required by applicable law, as set forth on Section 5.11 of the ENVI disclosure schedules or as consented to in writing by GreenLight (such consent not to be unreasonably withheld, conditioned or delayed except in the case of the first, second, third, fourth, fifth, ninth, and eleventh
sub-bullets
below), not do any of the following:
|
• |
adopt any amendments, supplements, restatements or modifications to the ENVI trust agreement or the governing documents of any ENVI Party;
|
• |
create or form a subsidiary;
|
• |
acquire (including by merger, consolidation, or acquisition of stock or assets or any other business combination) any corporation, partnership, other business organization or enter into any strategic joint ventures, partnerships or alliances with any other person, or make any loans, advances or capital contributions to, or guarantees for the benefit of, or any investments in, any person;
|
• |
declare, set aside, make or pay any dividends or distribution or payment in respect of, any equity securities of ENVI and its subsidiaries or repurchase or redeem or otherwise acquire any outstanding equity securities of ENVI and its subsidiaries;
|
• |
authorize, recommend, propose or announce an intention to adopt, or otherwise effect, a plan of complete or partial liquidation, dissolution, restructuring, recapitalization, reorganization or similar transaction involving ENVI or its subsidiaries;
|
• |
split, combine or reclassify any ENVI’s or its subsidiaries capital stock or other equity securities or issue any other security in respect of, in lieu of or in substitution for shares of ENVI’s or its subsidiaries capital stock;
|
• |
incur, create or assume any indebtedness or guarantee liability of any person;
|
• |
make any loans or advances to, or capital contributions in, any other person, other than to, or in, ENVI or any of its subsidiaries;
|
• |
issue any equity securities of ENVI or grant any additional options, warrants or stock appreciation rights with respect to its equity securities;
|
• |
subject to certain exceptions, amend, modify or renew any ENVI related party transaction or make any material payment to any ENVI related party or enter into any contract that would constitute an ENVI related party transaction;
|
• |
engage in any activities or business, or incur any liabilities, other than activities or business or liabilities (i) in connection with or incidental or related to Merger Sub’s organization, incorporation or formation, as applicable, or ENVI’s or its subsidiaries continuing corporate (or similar) existence, (ii) expressly permitted pursuant to or in accordance with Section 5.11 of the Business Combination Agreement (including those actions expressly contemplated by the Business Combination Agreement, any ancillary document thereto, the performance of covenants or agreements thereunder or the consummation of the transactions contemplated thereby) or (iii) those that are administrative or ministerial in nature and less than $100,000 individually, or in the aggregate;
|
• |
enter into, or amend or modify any material term of (in a manner adverse to ENVI or its subsidiaries), terminate (excluding any expiration in accordance with its terms), or waive or release any material rights, claims or benefits under, any contract of a type required to be listed on Section 4.9 of the ENVI disclosure schedules (or any contract, that if existing on the date hereof, would have been required to be listed on Section 4.9 of the ENVI disclosure schedules);
|
• |
adopt or amend any benefit plan, enter into any employment contract or collective bargaining agreement or hire any person as an employee of ENVI or Merger Sub;
|
• |
make, change or revoke any material tax election other than in the ordinary course of business consistent with past practice, change any annual tax accounting period, surrender any right to claim a material tax refund, materially amend any filed material tax return, file any material tax return inconsistent with past practice in any material respect, enter into any tax allocation, tax sharing, tax indemnity or similar agreement (other than one that is in a contract entered into in the ordinary course of business that is not primarily related to taxes), enter into any tax closing agreement, settle any material tax claim or assessment, or consent to any extension or waiver of the limitation period applicable to or relating to any material tax claim or assessment, other than any such extension of waiver that is obtained in the ordinary course of business;
|
• |
change the methods of accounting of ENVI or any of its subsidiaries in any material respect, other changes that are made in accordance with Public Company Accounting Oversight Board standard;
|
• |
authorize, recommend, propose or announce an intention to adopt a plan of complete or partial liquidation or dissolution;
|
• |
enter into any contract with any broker, finder, investment banker or other person providing for the payment of any brokerage fee, finders’ fee or other commission in connection with the transactions contemplated by the Business Combination Agreement;
|
• |
make any change of control payment that is not disclosed to GreenLight on the ENVI disclosure schedules;
|
• |
amend, modify, alter, change or waive any of the terms, conditions and other provisions of any warrants, including any reduction, adjustment or other alteration of the warrant price; or
|
• |
enter into any contract to do, or cause to be taken, any of the above actions prohibited under the Business Combination Agreement.
|
• |
As promptly as reasonably practicable (and in any event within one business day) following the date of the Business Combination Agreement, ENVI, as the sole stockholder of Merger Sub, will approve and adopt the Business Combination Agreement, the ancillary documents to which Merger Sub is or will be a party and the transactions contemplated hereby and thereby (including the Merger).
|
• |
As promptly as reasonably practicable following the effectiveness of this registration statement of which this proxy statement/prospectus forms a part, ENVI will, among other things, (i) duly give notice
|
of and duly convene a meeting of its stockholders for purposes of obtaining the approval of the ENVI stockholders of the Condition Precedent Proposals and the Advisory Charter Amendment Proposals, (ii) cause the registration statement of which this proxy statement/prospectus forms a part to be mailed to the ENVI stockholders, use commercially reasonable efforts to solicit proxies from the holders of ENVI’s outstanding shares to vote in favor of the Condition Precedent Proposals, the Advisory Charter Amendment Proposals and the Adjournment Proposal, and (iii) provide ENVI stockholders with the opportunity to elect to effect an ENVI Stockholder redemption in accordance with the Existing Organizational Documents.
|
• |
the ENVI Board shall (i) unanimously approve and recommend to the ENVI Stockholders each of the Condition Precedent Proposals, and (ii) include such recommendation by the ENVI Board in this proxy statement/prospectus.
|
• |
none of the ENVI Board, ENVI or any committee of the ENVI Board shall, except as otherwise determined by the ENVI Board in good faith, based on written advice from outside counsel, that, in response to an ENVI Intervening Event (as defined in the Business Combination Agreement), a failure to change, withdraw, withhold, qualify, amend or modify its recommendation would violate the ENVI Board’s fiduciary duties under applicable Law, effect an ENVI Change in Recommendation (as defined in the Business Combination Agreement).
|
• |
ENVI shall use its commercially reasonable efforts to cause: (i) New GreenLight’s initial listing application with Nasdaq to have been approved; (ii) New GreenLight Common Stock issuable in accordance with the Business Combination Agreement, including the Merger, to be approved for listing on Nasdaq; and ENVI to satisfy all applicable initial and continuing listing requirements of Nasdaq.
|
• |
Prior to the special meeting of the ENVI stockholders, the ENVI Board will approve and adopt the New GreenLight Equity Plan with any changes or modifications thereto as GreenLight and ENVI may mutually agree (such agreement not to be unreasonably withheld, conditioned or delayed by either GreenLight or ENVI, as applicable), and ENVI will initially reserve 31,750,000 shares of New GreenLight Common Stock for grant thereunder plus such additional New GreenLight Common Stock as may become available for issuance under the terms and subject to the conditions of the New GreenLight Equity Plan.
|
• |
Prior to the special meeting of the ENVI stockholders, the ENVI Board will approve and adopt the New GreenLight ESPP with any changes or modifications thereto as GreenLight and ENVI may mutually agree (such agreement not to be unreasonably withheld, conditioned or delayed by either GreenLight or ENVI, as applicable), and ENVI will initially reserve 2,000,000 shares of New GreenLight Common Stock for grant thereunder plus such additional shares of New GreenLight Common Stock that may become available for issuance under the terms and subject to the conditions of the New GreenLight ESPP.
|
• |
Prior to the Effective Time, ENVI shall maintain the indemnification, exculpation and advancement of expenses provisions in favor of the current or former directors or officers of ENVI or its subsidiaries for a period of six years after the Closing Date and shall, subject to certain exceptions, prior to the Closing, obtain a “tail” policy providing liability insurance coverage for ENVI directors and officers with respect to matters occurring on or prior to the Closing. Prior to the earlier of the Closing or termination of the Business Combination Agreement in accordance with its terms, ENVI and its subsidiaries shall not, and shall cause its respective officers, and directors not to, and shall cause the Sponsor and its controlled affiliates not to, and shall use their commercially reasonable efforts to cause their other affiliates and representatives of ENVI and its subsidiaries, the Sponsor and their controlled affiliates not to, directly or indirectly: (i) solicit, initiate, knowingly induce, knowingly encourage, knowingly facilitate, discuss or negotiate, directly or indirectly, any inquiry, proposal or offer (written or oral) that constitutes or could reasonably be expected to lead to, an ENVI Acquisition Proposal (as defined below); (ii) furnish or disclose any
non-public
information to any person in connection with, or that could reasonably be expected to lead to, an ENVI Acquisition Proposal; (iii) enter into any contract
|
or other arrangement or understanding regarding an ENVI Acquisition Proposal; (iv) make any filings or submissions with the SEC in connection with an offering of any securities of ENVI or its subsidiaries, other than such filings or submissions required or otherwise expressly contemplated by the Business Combination Agreement; or (v) otherwise cooperate in any way with, or assist or participate in, any negotiations of discussion with any person in connection with an ENVI Acquisition Proposal or a transaction of the type in clause (iv). An “
ENVI Acquisition Proposal
” is defined as (a) any direct or indirect acquisition (or other business combination), in one or a series of related transactions under which ENVI or any of its controlled Affiliates, directly or indirectly, (i) acquires or otherwise purchases any other person(s), (ii) engages in a business combination with any other person(s) or (iii) acquires or otherwise purchases all or a material portion of the assets, Equity Securities or businesses of any other Persons(s) (in the case of each of clause (i), (ii) and (iii), whether by merger, consolidation, recapitalization, purchase or issuance of Equity Securities, tender offer or otherwise), (b) any equity, debt or similar investment in ENVI or any of its controlled Affiliates or (c) any other “Business Combination” as defined in this proxy statement/prospectus. Notwithstanding the foregoing or anything to the contrary herein, none of the Business Combination Agreement, the ancillary documents or the transactions contemplated thereby shall constitute an ENVI Acquisition Proposal. ENVI shall use its commercially reasonable efforts to obtain the PIPE financing, enforce the obligations of the PIPE investors and satisfy and comply with all the conditions to each Subscription Agreement.
|
• |
Subject to certain exceptions, ENVI shall not amend, modify or waive any provision of any Subscription Agreement without prior written consent of GreenLight.
|
• |
ENVI shall also promptly notify GreenLight of any material breach or termination under any Subscription Agreement and shall deliver a Closing Notice (as defined in the Subscription Agreements) to the PIPE Investors promptly (and in any event within two (2) business days) following GreenLight’s reasonable request once all the conditions to closing the Business Combination have been satisfied.
|
• |
ENVI shall take all such actions as may be necessary or reasonably appropriate such that effective as of the Effective Time the ENVI Board shall consist of seven (7) board members as agreed to in Section 5.18 of the Business Combination Agreement described under the section titled
“-Board
of Directors.”
|
• |
Upon the satisfaction or waiver of the conditions to closing, ENVI shall deliver to the trustee all documents, certificates or other notices required to be delivered to the trustee and shall cause the trustee to (i) pay all amounts (if any) payable to the public stockholders of ENVI pursuant to the redemption, (ii) pay the deferred underwriting expenses as set forth in the Trust Agreement, (iii) deposit all remaining amounts to New GreenLight and (iv) terminate the trust account following the completion of the actions described in clauses (i) through (iii).
|
• |
At or prior to the Effective Time, the amended and restated bylaws of ENVI shall have become effective.
|
• |
using commercially reasonable efforts to consummate the Business Combination and the transactions contemplated thereby;
|
• |
notifying the other parties in writing promptly after learning of any event which would reasonably be expected to cause the closing conditions to the Business Combination Agreement to fail or any stockholder demands or other stockholder proceedings relating to the Business Combination Agreement, any ancillary document or any matters relating thereto and reasonably cooperate with one
|
another in connection therewith, including not settling any such proceedings without the consent of the other party;
|
• |
keeping certain information confidential in accordance with the existing
non-disclosure
agreements;
|
• |
making public announcements with the written consent of GreenLight and ENVI;
|
• |
providing each party reasonable access to the other party’s books, records and management;
|
• |
using commercially reasonable efforts to cause the Merger to constitute a transaction treated as a “reorganization” within the meaning of Section 368 of the Code or otherwise use commercially reasonable efforts to restructure the Merger to so qualify;
|
• |
cooperating in connection with certain tax matters and filings; and
|
• |
making any appropriate filings pursuant to the HSR Act with respect to the transactions contemplated by the Business Combination Agreement promptly (and in any event within ten (10) Business Days) following the date the Business Combination Agreement.
|
• |
by the mutual written consent of ENVI and GreenLight;
|
• |
by ENVI, subject to certain exceptions, if any of the representations or warranties made by GreenLight are not true and correct or if GreenLight fails to perform any of its respective covenants or agreements under the Business Combination Agreement (including an obligation to consummate the Closing) such that certain conditions to the obligations of ENVI, as described in the section titled
“
-Conditions
to Closing of the Business Combination”
Termination Date
”) unless otherwise extended pursuant to the terms of the Business Combination Agreement;
|
• |
by GreenLight, subject to certain exceptions, if any of the representations or warranties made by the ENVI Parties are not true and correct or if any ENVI Party fails to perform any of its covenants or agreements under the Business Combination Agreement (including an obligation to consummate the Closing) such that the condition to the obligations of GreenLight, as described in the section titled
“
-Conditions
to Closing of the Business Combination”
|
• |
by either ENVI or GreenLight, subject to certain exceptions, if the transactions contemplated by the Business Combination Agreement are not consummated on or prior to the Termination Date;
|
• |
by either ENVI or GreenLight,
|
• |
if any governmental entity of competent jurisdiction shall have issued an order or enacted or promulgated a law permanently enjoining or prohibiting the transactions contemplated by the Business Combination Agreement and, in the case of an order, such order shall have become final and nonappealable;
|
• |
if the approval of the Condition Precedent Proposals by ENVI stockholders is not obtained at the special meeting (including any adjournment thereof); and
|
• |
by ENVI, if GreenLight does not deliver, or cause to be delivered to ENVI, the GreenLight Stockholder Written Consent when required under the Business Combination Agreement.
|
Assuming
No Redemption
|
Assuming
50% Redemption
|
Assuming
Maximum Redemption
|
||||||||||||||||||||||
Shares
|
%
|
Shares
|
%
|
Shares
|
%
|
|||||||||||||||||||
(percentages represent percentages of pro forma outstanding shares)
|
||||||||||||||||||||||||
Public shares
(a)
|
20,700,000 | 14 | % | 10,512,411 | 8 | % | 324,821 | * | ||||||||||||||||
Founder shares
|
5,175,000 | 4 | % | 5,175,000 | 4 | % | 5,175,000 | 4 | % | |||||||||||||||
GreenLight stockholders
(b)(c)
|
103,470,217 | 73 | % | 103,470,217 | 79 | % | 103,470,217 | 85 | % | |||||||||||||||
PIPE shares
|
12,425,000 | 9 | % | 12,425,000 | 9 | % | 12,425,000 | 10 | % | |||||||||||||||
|
|
|
|
|
|
|
|
|
|
|
|
|||||||||||||
Pro forma common stock outstanding as of September 30, 2021
(d)
|
141,770,217 | 100 | % | 131,582,628 | 100 | % | 121,395,038 | 100 | % | |||||||||||||||
Potential sources of dilution
|
||||||||||||||||||||||||
Public Warrants
|
10,350,000 | 7 | % | 10,350,000 | 8 | % | 10,350,000 | 9 | % | |||||||||||||||
Private Placement Warrants
|
2,000,000 | 1 | % | 1,500,000 | 1 | % | 1,500,000 | 1 | % | |||||||||||||||
Insider Warrants
|
750,000 | * | 600,000 | * | 600,000 | * | ||||||||||||||||||
Rollover Options
|
17,555,928 | 12 | % | 17,555,928 | 13 | % | 17,555,928 | 14 | % |
* |
Less than 1%
|
(a) |
Amount includes 1,000,000 shares of ENVI Class A Common Stock held by HB Strategies, a founder, all of which shares carry the same redemption rights as other shares of ENVI Class A Common Stock. The 50% Redemption Scenario and the Maximum Redemption Scenario assume that HB Strategies will redeem 50% and 100%, respectively, of its shares of ENVI Class A Common Stock. Amount excludes 13,100,000 warrants to purchase ENVI Class A Common Stock, which is made up of 10,350,000 public warrants, 2,000,000 private placement warrants and 750,000 Insider Warrants. Additionally, under each of the 50% Redemption Scenario and the a Maximum Redemption Scenario, an aggregate of 650,000 Warrants
|
comprised of 500,000 private placement warrants owned by HB Strategies and 150,000 Insider Warrants owned by the Sponsor will be forfeited pursuant to the Sponsor Letter Agreement. |
(b) |
In accordance with the terms and subject to the conditions of the Business Combination Agreement, each outstanding share of capital stock of GreenLight will be exchanged for shares of New GreenLight Common Stock and outstanding GreenLight Options (whether vested or unvested) will be exchanged for comparable options to purchase New GreenLight Common Stock, in each case, based on an implied GreenLight equity value of $1.2 billion. The number of shares of New GreenLight Common Stock issued to the holders of shares of capital stock of GreenLight at Closing will fluctuate based on the number of shares underlying GreenLight Options and GreenLight Warrants, whether vested or unvested (and the exercise prices of such options and warrants), outstanding at Closing.
|
(c) |
Amount includes 6,583,549 shares issuable upon conversion of the GreenLight Convertible Notes and 872,667 shares underlying GreenLight Warrants that are assumed to be exercised immediately prior to the consummation of the Business Combination and excludes 17,555,928 shares underlying Rollover Options to be issued to holders of GreenLight Options, assuming such GreenLight Options remain unexercised as of the Closing.
|
(d) |
Amount excludes 31,750,000 shares (which amount includes shares underlying Rollover Options) and 2,000,000 shares of New GreenLight Common Stock that are expected to be available for issuance under the New GreenLight Equity Plan and the New GreenLight ESPP, respectively, after the consummation of the Business Combination, assuming approval of the Condition Precedent Proposals.
|
• |
Synthetic biology and biomanufacturing platform with flexible technology
|
• |
Leadership in
RNA-based
product development
RNA-based
synthetic biology. GreenLight has consulted with well-established companies, industry experts, academic institutions and research organizations to inform its product development plans and address its target customer needs. The ENVI Board believes that GreenLight’s novel synthetic biology platform has the potential to allow GreenLight to develop a broad set of
RNA-based
products for numerous applications across large addressable markets. The ENVI Board believes that GreenLight is well positioned to continue to innovate through its platform, with an ongoing strong commitment to research and development and pursuit of new collaborations to complement existing collaborations.
|
• |
Near-term adoption of GreenLight’s products
RNA-based
biological products continue to mature, the GreenLight platform can transfer well into the clinical setting which should drive collaborations along with milestone and royalty revenue. The ENVI Board believes that GreenLight’s mission to positively impact certain populations with limited or
at-risk
access to quality food and healthcare will result in meaningful opportunities in the future to scale revenues and deliver profitable financial results.
|
• |
Experienced, diverse, mission-driven and multidisciplinary management team
|
• |
Efficient biomanufacturing processes
|
• |
Development and commercialization platform that could enable the discovery of additional products
|
• |
Results of due diligence and attractive valuation
Certain Company Projected Financial Information.
|
• |
Strong alignment with Sustainability and ESG focus.
|
• |
Continued participation by leading private investors and a strong balance sheet
.
|
• |
Fairness opinion of Duff
& Phelps.
|
• |
Benefits Not Achieved
|
• |
Liquidation of ENVI
|
• |
Exclusivity
|
• |
Stockholder vote
|
• |
Post
-Business
Combination corporate governance; terms of the Investor Rights Agreement
“—The Business Combination Agreement”, “—Related Agreements
—
Investor Rights Agreement
“
Advisory Charter Amendment Proposals
|
• |
Closing conditions
|
• |
Litigation
|
• |
Fees and expenses
|
• |
Other risks
Risk Factors
|
• |
reviewed ENVI’s audited balance sheet as of January 19, 2021 included in ENVI’s Form
8-K
filed with the SEC on January 25, 2021, ENVI’s audited balance sheet as of December 31, 2020 and the related statements of operations, changes in stockholder’s equity and cash flows for the period from July 2,
|
2020 (inception) through December 31, 2020 included in ENVI’s Form
10-K
filed with the SEC on March 26, 2021, and ENVI’s unaudited interim financial statements as of and for the three months ended March 31, 2021 included in ENVI’s Form
10-Q
filed with the SEC on May 24, 2021;
|
• |
reviewed audited financial statements of GreenLight as of and for the year ended December 31, 2019, unaudited financial information of GreenLight as of and for the year ended December 31, 2020 and for the three months ended March 31, 2021 and the six months ended June 30, 2021, which GreenLight’s management identified as being the most current financial statements available;
|
• |
reviewed other internal documents relating to the history, current operations, and probable future outlook of GreenLight, including financial projections of GreenLight for the years ended December 31, 2021 through December 31, 2025, prepared by GreenLight and provided to us by the management of ENVI (the “
Financial Projections
”);
|
• |
reviewed a letter dated August 9, 2021 from the management of ENVI and GreenLight which made certain representations as to historical financial statements, the Financial Projections and the assumptions underlying the Financial Projections, for ENVI and GreenLight, respectively;
|
• |
reviewed industry reports that Duff & Phelps deemed relevant;
|
• |
reviewed the GreenLight PIPE Investor Deck, dated August 9, 2021;
|
• |
reviewed a draft of the Business Combination Agreement, by and among ENVI, Merger Sub, and GreenLight, dated August 8, 2021;
|
• |
discussed the information referred to above and the background and other elements of the Business Combination with the management of ENVI and with the management of GreenLight;
|
• |
discussed with ENVI management and GreenLight’s management team the plans and intentions with respect to the management and operation of ENVI following the completion of the Business Combination
|
• |
reviewed the historical trading price and trading volume of ENVI’s common stock, and the publicly traded securities of certain other companies that Duff & Phelps deemed relevant;
|
• |
performed certain valuation and comparative analyses using generally accepted valuation and analytical techniques, including a discounted cash flow analysis, an analysis of selected public companies that Duff & Phelps deemed relevant and an analysis of selected transactions that Duff & Phelps deemed relevant, as further described below in this section titled “
The Business Combination Proposal—Opinion of Duff
& Phelps, Financial Advisor
to the ENVI Board
|
• |
conducted such other analyses and considered such other factors as Duff & Phelps deemed appropriate.
|
• |
relied upon the accuracy, completeness, and fair presentation of all information, data, advice, opinions and representations obtained from public sources or provided to it from private sources, including ENVI management, and did not independently verify such information;
|
• |
relied upon the fact that the ENVI Board and ENVI have been advised by counsel as to all legal matters with respect to the Business Combination, including whether all procedures required by law to be taken in connection with the Business Combination have been duly, validly and timely taken;
|
• |
assumed that any estimates, evaluations, forecasts and projections, including the Financial Projections, furnished to Duff & Phelps were reasonably prepared and based upon the best currently available information and good faith judgment of the person furnishing the same, and Duff & Phelps expresses no opinion with respect to such estimates, evaluations, forecasts and projections or the underlying assumptions;
|
• |
assumed that information supplied by and representations made by ENVI management are substantially accurate regarding ENVI, GreenLight and the Business Combination;
|
• |
assumed that the representations and warranties made in the Business Combination Agreement are substantially accurate;
|
• |
assumed that the final versions of all documents reviewed by Duff & Phelps in draft form conform in all material respects to the drafts reviewed;
|
• |
assumed that there has been no material change in the assets, liabilities, financial condition, results of operations, business, or prospects of ENVI or GreenLight since the date of the most recent financial statements and other information made available to Duff & Phelps, and that there is no information or facts that would make the information reviewed by Duff & Phelps incomplete or misleading;
|
• |
assumed that all of the conditions required to implement the Business Combination will be satisfied and that the Business Combination will be completed substantially in accordance with the Business Combination Agreement without any material amendments thereto or any material waivers of any terms or conditions thereof;
|
• |
assumed that all governmental, regulatory or other consents and approvals necessary for the consummation of the Business Combination will be obtained without any adverse effect on ENVI, GreenLight, or the contemplated benefits expected to be derived in the Business Combination;
|
• |
assumed a value of $10.00 per share of ENVI Class A Common Stock and ENVI Class B Common Stock, with such $10.00 value being based on the sale price of the ENVI Units sold in ENVI’s initial public offering of ENVI Units and the approximate amount of cash contained in ENVI’s trust account per outstanding share of ENVI Class A Common Stock (excluding, for the avoidance of doubt, any dilutive impact of the shares of ENVI Class B Common Stock, any warrants of ENVI or any other securities); and
|
• |
assumed that ENVI Class A Common Stock and ENVI Class B Common Stock are identical in all respects.
|
(i) |
Revenue-Generating Human Health Biotechnology Companies. Duff & Phelps used this group of publicly traded companies to derive a range of revenue multiples to apply to GreenLight’s Human Health platform projected revenue in 2025. The resulting range of values was the first component of the Terminal Values in the DCF Analysis.
|
(ii) |
Synthetic Biotechnology Companies. Duff & Phelps used this group of publicly traded companies to derive a range of revenue multiples to apply to GreenLight’s Plant Health platform projected revenue in 2025. The resulting range of values was the second component of the Terminal Values in the DCF Analysis.
|
(iii) |
Pre-Revenue
Human Health Biotechnology Companies. Duff & Phelps used this group of publicly traded companies to compare the multiples of enterprise
value-to-projected
|
(iv) |
De-SPAC
transactions involving companies with businesses involved in comparable aspects of biotechnology. Duff & Phelps also used this group of companies to compare the multiples of enterprise
value-to-projected
de-SPAC
targets to similar multiples Duff & Phelps calculated for GreenLight.
|
ENTERPRISE VALUE AS A MULTIPLE OF: | ||||||||||||||||||||||||
LTM
Revenue |
2021
Revenue |
2022
Revenue |
2023
Revenue |
2024
Revenue |
2025
Revenue |
|||||||||||||||||||
Revenue Generating Human Health Biotechnology
|
||||||||||||||||||||||||
Alnylam Pharmaceuticals, Inc.
|
33.76x | 27.50x | 17.89x | 12.20x | 8.91x | 7.07x | ||||||||||||||||||
Arrowhead Pharmaceuticals, Inc.
|
60.57x | 42.15x | 27.99x | 24.59x | 13.44x | NA | ||||||||||||||||||
BioNTech SE
|
31.74x | 6.31x | 7.92x | 9.90x | 18.84x | 23.21x | ||||||||||||||||||
Dicerna Pharmaceuticals, Inc.
|
9.89x | 7.94x | 10.65x | 11.43x | 9.35x | 6.28x | ||||||||||||||||||
Genmab A/S
|
15.75x | 22.39x | 16.82x | 13.13x | 11.16x | 8.77x | ||||||||||||||||||
Ionis Pharmaceuticals, Inc.
|
6.96x | 7.77x | 7.39x | 7.10x | 5.89x | 3.68x |
ENTERPRISE VALUE AS A MULTIPLE OF: | ||||||||||||||||||||||||
LTM
Revenue |
2021
Revenue |
2022
Revenue |
2023
Revenue |
2024
Revenue |
2025
Revenue |
|||||||||||||||||||
Laboratorios Farmaceuticos Rovi, S.A.
|
6.30x | 5.71x | 4.65x | 4.41x | 4.34x | 4.06x | ||||||||||||||||||
Lonza Group Ltd
|
NM | 10.84x | 9.61x | 8.66x | 7.94x | 6.80x | ||||||||||||||||||
Maravai LifeSciences Holdings, Inc.
|
NA | 9.28x | 8.93x | 8.59x | 7.32x | 6.76x | ||||||||||||||||||
Moderna, Inc.
|
23.98x | 8.31x | 9.93x | 19.53x | 32.80x | 28.65x | ||||||||||||||||||
Myriad Genetics, Inc.
|
NM | 4.16x | 4.23x | 4.06x | 3.61x | 3.40x | ||||||||||||||||||
NeoGenomics, Inc.
|
11.86x | 11.56x | 9.93x | 8.58x | NA | NA | ||||||||||||||||||
Pharma Mar, S.A.
|
5.49x | 5.26x | 4.74x | 3.64x | 4.41x | 3.80x | ||||||||||||||||||
PTC Therapeutics, Inc.
|
NM | 4.75x | 3.45x | 2.74x | 2.21x | 2.26x | ||||||||||||||||||
Sarepta Therapeutics, Inc.
|
9.78x | 8.90x | 7.50x | 6.08x | 4.38x | 3.78x | ||||||||||||||||||
Translate Bio, Inc.
(1)
|
11.11x | 17.30x | 17.58x | 16.58x | 25.00x | 21.91x | ||||||||||||||||||
Revenue-Generating Human Health Biotechnology Mean
|
18.93x | 12.51x | 10.58x | 10.07x | 10.64x | 9.32x | ||||||||||||||||||
Revenue-Generating Human Health Biotechnology Median
|
11.48x | 8.60x | 9.27x | 8.62x | 7.94x | 6.52x | ||||||||||||||||||
Synthetic Biotechnology
|
||||||||||||||||||||||||
Amyris, Inc.
|
13.63x | 11.86x | 11.53x | 8.46x | 6.78x | 5.35x | ||||||||||||||||||
Codexis, Inc.
|
19.37x | 15.78x | 13.71x | 10.98x | 8.98x | 7.26x | ||||||||||||||||||
Twist Bioscience Corporation
|
41.53x | 40.11x | 28.10x | 20.65x | 18.61x | NA | ||||||||||||||||||
Zymergen Inc.
|
70.34x | 44.50x | 9.47x | 3.14x | 2.07x | 1.53x | ||||||||||||||||||
Synthetic Biotechnology Mean
|
36.22x | 28.06x | 15.70x | 10.81x | 9.11x | 4.71x | ||||||||||||||||||
Synthetic Biotechnology Median
|
30.45x | 27.95x | 12.62x | 9.72x | 7.88x | 5.35x | ||||||||||||||||||
Pre-Revenue
Human Health Biotechnology
|
||||||||||||||||||||||||
Aldeyra Therapeutics, Inc.
|
NM | NM | NM | 6.00x | 2.77x | 1.49x | ||||||||||||||||||
Arcturus Therapeutics Holdings Inc.
|
NM | 27.32x | 3.46x | 2.79x | 1.96x | 2.37x | ||||||||||||||||||
Clene Inc.
|
NM | NM | NM | 30.38x | 5.13x | 2.63x | ||||||||||||||||||
CureVac N.V.
|
NM | NM | 18.95x | 3.53x | 6.14x | 6.45x | ||||||||||||||||||
Evelo Biosciences, Inc.
|
NM | NM | NM | NM | 38.29x | 5.84x | ||||||||||||||||||
IGM Biosciences, Inc.
|
NM | NM | NM | NM | 24.22x | 7.75x | ||||||||||||||||||
Inhibrx, Inc.
|
NM | NM | NM | NM | NM | 15.61x | ||||||||||||||||||
Krystal Biotech, Inc.
|
NM | NM | 36.14x | 10.21x | 4.42x | 2.70x | ||||||||||||||||||
Mind Medicine (MindMed) Inc.
|
NA | NM | NM | NM | NM | 34.39x | ||||||||||||||||||
Nautilus Biotechnology, Inc.
|
NA | NM | NM | NM | 15.67x | 7.07x | ||||||||||||||||||
Precision BioSciences, Inc.
|
12.60x | 10.54x | 16.95x | 15.70x | 3.24x | 1.29x | ||||||||||||||||||
Replimune Group, Inc.
|
NM | NM | NM | 24.66x | 7.83x | 4.01x | ||||||||||||||||||
Seer, Inc.
|
NA | NM | NM | NM | 25.03x | 14.12x | ||||||||||||||||||
Silence Therapeutics plc
|
NM | 30.47x | 18.08x | 16.29x | NM | NA | ||||||||||||||||||
VBI Vaccines Inc.
|
NM | NM | 45.53x | 9.69x | 3.98x | 2.06x | ||||||||||||||||||
Vera Therapeutics, Inc.
|
NA | NM | NM | NM | NM | 24.94x | ||||||||||||||||||
Pre-Revenue
Human Health Biotechnology Mean
|
NM | NM | NM | 13.25x | 11.56x | 8.85x | ||||||||||||||||||
Pre-Revenue
Human Health Biotechnology Median
|
NM | NM | NM | 10.21x | 5.63x | 5.84x |
(1) |
On August 3, 2021 Translate Bio, Inc. announced it will be acquired by Sanofi for $38 per share
|
De-SPAC
Current Value
(1)
|
||||||||||||||||||||
Benson Hill Biosystems, Inc. (Star Peak Corp II)
|
10.48x | 8.27x | 5.30x | 3.82x | 2.37x | |||||||||||||||
Ginkgo Bioworks, Inc. (Soaring Eagle Acquisition Corp.)
|
NM | NM | 44.52x | 24.17x | 13.81x | |||||||||||||||
Humacyte, Inc. (Alpha Healthcare Acquisition Corp.)
|
NM | 16.28x | 6.61x | 4.03x | 3.07x | |||||||||||||||
Jasper Therapeutics, Inc. (Amplitude Healthcare Acquisition Corporation)
|
NA | NA | NA | 20.44x | 3.94x | |||||||||||||||
Nuvation Bio Inc. (Panacea Acquisition Corp.)
|
NA | NA | NA | NA | 23.84x | |||||||||||||||
Vincerx Pharma, Inc. (LifeSci Acquisition Corp.)
|
NA | NA | 13.46x | 3.95x | NA | |||||||||||||||
Mean
|
NM | NM | 17.47x | 11.28x | 9.41x | |||||||||||||||
Median
|
NM | NM | 10.04x | 4.03x | 3.94x | |||||||||||||||
De-SPAC
Transaction Value
(2)
|
||||||||||||||||||||
Benson Hill Biosystems, Inc.
|
10.64x | 8.39x | 5.38x | 3.88x | 2.41x | |||||||||||||||
Ginkgo Bioworks, Inc.
|
NM | NM | 44.47x | 24.15x | 13.80x | |||||||||||||||
Humacyte, Inc.
|
NM | 16.32x | 6.63x | 4.04x | 3.07x | |||||||||||||||
Jasper Therapeutics, Inc.
|
NA | NA | NA | 20.71x | 3.99x | |||||||||||||||
Nuvation Bio Inc.
|
NA | NA | NA | NA | 31.30x | |||||||||||||||
Vincerx Pharma, Inc.
|
NA | NA | 9.37x | 2.75x | NA | |||||||||||||||
Mean
|
NM | NM | 16.46x | 11.11x | 10.91x | |||||||||||||||
Median
|
NM | NM | 8.00x | 4.04x | 3.99x |
(1) |
Enterprise Value calculated based on current price of SPAC Vehicle
|
(2) |
Enterprise Value calculated based on pro forma transaction value
|
Source: |
S&P Capital IQ, SEC Filings, Annual and Interim Reports, Investor Presentations
|
REVENUE GROWTH | ||||||||||||||||||||||||||||
2021-2024
CAGR |
LTM | 2021 | 2022 | 2023 | 2024 | 2025 | ||||||||||||||||||||||
Revenue Generating Human Health Biotechnology
|
||||||||||||||||||||||||||||
Alnylam Pharmaceuticals, Inc.
|
45.6 | % | 99.2 | % | 71.2 | % | 53.7 | % | 46.7 | % | 36.8 | % | 26.0 | % | ||||||||||||||
Arrowhead Pharmaceuticals, Inc.
|
46.4 | % | -13.0 | % | 93.8 | % | 50.6 | % | 13.8 | % | 83.0 | % | NA | |||||||||||||||
BioNTech SE
|
554.0 | % | 2172.7 | % | 2510.6 | % | -20.3 | % | -20.0 | % | -47.5 | % | -18.8 | % | ||||||||||||||
Dicerna Pharmaceuticals, Inc.
|
-5.3 | % | 224.5 | % | 34.9 | % | -25.5 | % | -6.8 | % | 22.2 | % | 48.8 | % | ||||||||||||||
Genmab A/S
|
26.1 | % | 90.6 | % | -24.9 | % | 33.1 | % | 28.2 | % | 17.6 | % | 27.3 | % | ||||||||||||||
Ionis Pharmaceuticals, Inc.
|
9.6 | % | -26.9 | % | -15.5 | % | 5.2 | % | 4.1 | % | 20.4 | % | 60.4 | % | ||||||||||||||
Laboratorios Farmaceuticos Rovi, S.A.
|
9.6 | % | 31.4 | % | 36.2 | % | 22.7 | % | 5.6 | % | 1.6 | % | 6.9 | % | ||||||||||||||
Lonza Group Ltd
|
11.0 | % | NM | 14.4 | % | 12.8 | % | 11.0 | % | 9.1 | % | 16.8 | % | |||||||||||||||
Maravai LifeSciences Holdings, Inc.
|
8.2 | % | NA | 151.5 | % | 4.0 | % | 4.0 | % | 17.2 | % | 8.3 | % | |||||||||||||||
Moderna, Inc.
|
-36.7 | % | 6515.8 | % | 2421.9 | % | -16.4 | % | -49.1 | % | -40.5 | % | 14.5 | % | ||||||||||||||
Myriad Genetics, Inc.
|
4.8 | % | NM | 15.4 | % | -1.7 | % | 4.2 | % | 12.3 | % | 6.2 | % | |||||||||||||||
NeoGenomics, Inc.
|
NM | 20.8 | % | 12.8 | % | 16.4 | % | 15.8 | % | NA | NA | |||||||||||||||||
Pharma Mar, S.A.
|
6.0 | % | -6.5 | % | -23.0 | % | 11.1 | % | 30.3 | % | -17.6 | % | 16.1 | % | ||||||||||||||
PTC Therapeutics, Inc.
|
29.2 | % | NM | 28.6 | % | 37.8 | % | 25.8 | % | 24.3 | % | -2.5 | % | |||||||||||||||
Sarepta Therapeutics, Inc.
|
26.7 | % | 33.3 | % | 22.0 | % | 18.8 | % | 23.4 | % | 38.7 | % | 16.0 | % | ||||||||||||||
Translate Bio, Inc.
|
-11.5 | % | 761.4 | % | 4.1 | % | -1.6 | % | 6.0 | % | -33.7 | % | 14.1 | % | ||||||||||||||
Revenue Generating Human Health Biotechnology Mean
|
48.2 | % | 825.3 | % | 334.6 | % | 12.5 | % | 8.9 | % | 9.6 | % | 17.1 | % | ||||||||||||||
Revenue Generating Human Health Biotechnology Median
|
9.6 | % | 61.9 | % | 25.3 | % | 12.0 | % | 8.5 | % | 17.2 | % | 15.2 | % |
REVENUE GROWTH | ||||||||||||||||||||||||||||
2021-2024
CAGR |
LTM | 2021 | 2022 | 2023 | 2024 | 2025 | ||||||||||||||||||||||
Synthetic Biotechnology
|
||||||||||||||||||||||||||||
Amyris, Inc.
|
140.5 | % | 154.9 | % | 127.9 | % | 2.8 | % | 36.3 | % | 24.7 | % | 26.7 | % | ||||||||||||||
Codexis, Inc.
|
20.7 | % | 18.1 | % | 47.3 | % | 15.2 | % | 24.8 | % | 22.3 | % | 23.6 | % | ||||||||||||||
Twist Bioscience Corporation
|
103.0 | % | 72.8 | % | 29.9 | % | 42.8 | % | 36.0 | % | 11.0 | % | NA | |||||||||||||||
Zymergen Inc.
|
178.1 | % | 10.4 | % | 102.5 | % | 369.9 | % | 202.0 | % | 51.5 | % | 35.4 | % | ||||||||||||||
Synthetic Biotechnology Mean
|
110.6 | % | 64.0 | % | 76.9 | % | 107.7 | % | 74.8 | % | 27.4 | % | 28.6 | % | ||||||||||||||
Synthetic Biotechnology Median
|
121.8 | % | 45.4 | % | 74.9 | % | 29.0 | % | 36.2 | % | 23.5 | % | 26.7 | % | ||||||||||||||
Pre-Revenue
Human Health Biotechnology
|
||||||||||||||||||||||||||||
Aldeyra Therapeutics, Inc.
|
NM | NM | NM | NM | NM | 116.4 | % | 86.2 | % | |||||||||||||||||||
Arcturus Therapeutics Holdings Inc.
|
20.5 | % | -52.7 | % | 245.9 | % | 689.8 | % | 23.9 | % | 42.2 | % | -17.3 | % | ||||||||||||||
Clene Inc.
|
-30.6 | % | 398.6 | % | 96.1 | % | -35.6 | % | 7232.3 | % | 492.8 | % | 94.9 | % | ||||||||||||||
CureVac N.V.
|
202.5 | % | 74.4 | % | -1.2 | % | 796.9 | % | 436.9 | % | -42.5 | % | -4.8 | % | ||||||||||||||
Evelo Biosciences, Inc.
|
NM | NM | NM | NM | NM | NM | 555.2 | % | ||||||||||||||||||||
IGM Biosciences, Inc.
|
NM | NM | NM | NM | NM | NM | 212.6 | % | ||||||||||||||||||||
Inhibrx, Inc.
|
63.0 | % | 132.0 | % | -76.7 | % | 0.0 | % | 36.7 | % | 217.1 | % | 384.6 | % | ||||||||||||||
Krystal Biotech, Inc.
|
NM | NM | NM | NM | 253.8 | % | 130.9 | % | 63.9 | % | ||||||||||||||||||
Mind Medicine (MindMed) Inc.
|
NM | NA | NM | NM | NM | NM | NM | |||||||||||||||||||||
Nautilus Biotechnology, Inc.
|
NM | NA | NM | NM | 302.5 | % | 295.6 | % | 121.7 | % | ||||||||||||||||||
Precision BioSciences, Inc.
|
48.2 | % | 41.5 | % | 65.5 | % | -37.8 | % | 8.0 | % | 384.9 | % | 151.6 | % | ||||||||||||||
Replimune Group, Inc.
|
NM | NM | NM | NM | NM | 214.8 | % | 95.3 | % | |||||||||||||||||||
Seer, Inc.
|
155.5 | % | NA | 491.2 | % | 265.2 | % | 128.6 | % | 99.7 | % | 77.3 | % | |||||||||||||||
Silence Therapeutics plc
|
-21.8 | % | 2145.5 | % | 224.9 | % | 68.5 | % | 11.0 | % | -74.5 | % | NA | |||||||||||||||
VBI Vaccines Inc.
|
327.8 | % | -50.3 | % | 107.4 | % | 583.9 | % | 369.9 | % | 143.5 | % | 92.9 | % | ||||||||||||||
Vera Therapeutics, Inc.
|
NM | NA | NM | NM | NM | NM | NM | |||||||||||||||||||||
Pre-Revenue
Human Health Biotechnology Mean
|
95.6 | % | 384.1 | % | 144.1 | % | 291.4 | % | 880.4 | % | 168.4 | % | 147.2 | % | ||||||||||||||
Pre-Revenue
Human Health Biotechnology Median
|
55.6 | % | 74.4 | % | 101.7 | % | 166.9 | % | 191.2 | % | 137.2 | % | 94.9 | % | ||||||||||||||
De-SPAC
Transactions
|
||||||||||||||||||||||||||||
Benson Hill Biosystems, Inc.
|
39.9 | % | NA | 24.5 | % | 26.8 | % | 55.9 | % | 38.6 | % | 61.2 | % | |||||||||||||||
Ginkgo Bioworks, Inc.
|
61.2 | % | NA | 94.8 | % | 16.7 | % | 94.9 | % | 84.2 | % | 75.0 | % | |||||||||||||||
Humacyte, Inc.
|
371.8 | % | NA | NM | 2500.0 | % | 146.2 | % | 64.1 | % | 31.4 | % | ||||||||||||||||
Jasper Therapeutics, Inc.
|
NM | NA | NM | NM | NM | NM | 419.3 | % | ||||||||||||||||||||
Nuvation Bio Inc.
|
NM | NA | NM | NM | NM | NM | NM | |||||||||||||||||||||
Vincerx Pharma, Inc.
|
NM | NA | NM | NM | NM | 240.5 | % | NM | ||||||||||||||||||||
De-SPAC
Transactions Mean
|
157.6 | % | NM | NM | 847.8 | % | 99.0 | % | 106.8 | % | 146.7 | % | ||||||||||||||||
De-SPAC
Transactions Median
|
61.2 | % | NM | NM | 26.8 | % | 94.9 | % | 74.1 | % | 68.1 | % |
LTM |
= Latest Twelve Months
|
CAGR |
= Compounded Annual Growth Rate
|
($ in millions)
|
2021E
|
2022E
|
2023E
|
2024E
|
2025E
|
|||||||||||||||
Revenue
|
$ | 2 | $ | 41 | $ | 186 | $ | 231 | $ | 849 | ||||||||||
EBITDA
|
(114 | ) | (190 | ) | (11 | ) | (23 | ) | 235 | |||||||||||
Capital expenditures
|
14 | 71 | 52 | 104 | 32 | |||||||||||||||
Working capital investment
|
— | 69 | 64 | 61 | 51 |
• |
Development of the revenue estimates for plant health relied on calculations of the total addressable market available to pesticide products controlling a given target pest or disease. In most instances, we calculated this by defining a relevant active ingredient market for the crop or crops where we intend to market our products and then making an assumption as to the percentage of that market that is spent on controlling the target pest or disease. The projections assumed that revenue build for our products would take between three and five years from launch, and penetration estimates were built by product given the effectiveness and safety profiles of current products in the market along with other factors. Estimated revenue at year five of each of our programs except Varroa mite ranged from 2% to 10% penetration of current markets with an average penetration rate of 6.5%. Our Varroa mite product was assumed to have higher penetration in the market at 35% in light of performance expectations compared to existing products available to beekeepers.
|
• |
Our programs for human health are all in the preclinical stages of development and, as such, we recognize that these programs may or may not ultimately result in revenues. We projected revenue only for our COVID-19 and influenza programs due to the expected commencement of clinical trials for those programs in 2022. A key assumption was that COVID-19 becomes and remains an endemic disease similar to influenza. The revenue forecast assumed that regulatory approval in countries outside the United States and Europe will be available through Emergency Use Authorization at the time of regulatory submission, which would provide an expedited regulatory review and marketing pathway. The revenue forecast also assumed that there will be a shortage of vaccines in Africa/Middle East, South East Asia, South Asia, Latin America, and China, and that, as a result, one or more companies in those regions will be seeking a partnership with a company like GreenLight. GreenLight plans to seek partnerships to make its COVID-19 vaccine available in each of these regions. Partnering financial terms reflected our understanding of general market terms in the mRNA industry and included assumptions relating to an upfront payment, clinical and commercial milestones, and royalties on net sales. In addition to partnering clinical stage assets, we will strive to establish research collaborations with pharmaceutical/biotechnology companies if our mRNA platform is validated in the clinic.
|
• |
Revenue in 2021 of $2 million was projected to include grant revenue from the Bill & Melinda Gates Foundation, which is to be used for the sole purpose of research for in vivo gene therapy for sickle cell disease and to explore new,
low-cost
capabilities for the in vivo functional cure of sickle cell and or durable suppression of HIV in developing countries.
|
• |
In 2022, the financial projections provided to ENVI included estimated revenue from plant health programs of $1 million generated from a future research and development collaboration with a strategic partner. The financial projections provided to ENVI also estimated that we would generate revenue of $40 million in 2022 from a future collaboration on our COVID-19 vaccine program with a single strategic partner. As noted above, because of developments in the COVID-19 market since June 30, 2021, we now expect to seek future collaborations on our COVID-19 vaccine program with multiple strategic partners and expect to generate revenue from our human health programs that may fall within the broader range of approximately $20 million to $60 million. This projected range of potential revenue assumed that in 2022 we will enter into one partnership for Africa/Middle East and another for COVID-19 vaccine distribution in one additional developing region, such as South Asia. All of these projections assumed that the commercial partner will bear the late-stage clinical and commercialization costs. Our projections for these arrangements were benchmarked against the 2020 CureVac-GSK transaction, which included an upfront payment of $30 million per target and milestones (development and commercial) of $170 million per target for worldwide rights to preclinical-stage assets. The projections assumed that we would receive lower revenue from partners because we plan to target transactions for underserved geographic territories instead of global partnering arrangements. In 2022, if we attain positive Phase 1 results for our COVID-19 vaccine, we also plan to seek multi-target research, development, and commercialization agreements, and the projections assumed that we will have one world-wide agreement and one regional agreement in place in 2022. The assumed terms of
|
these projected agreements were also benchmarked against the 2020 CureVac-GSK transaction. We assumed lower amounts to reflect the fact that any such arrangement would be the first collaboration agreement signed by GreenLight and would involve only one target.
|
• |
In 2023, the financial projections provided to ENVI included estimated revenue from plant health programs of $5 million, which was expected to be generated from the commercial launch of our first plant health product addressing the Colorado potato beetle pest in the U.S. as well as research and development collaboration revenue. The financial projections provided to ENVI also estimated that we would generate human health revenue of $181 million from clinical milestone accomplishments on the COVID-19 program initiated in 2022. As noted above, because of developments in the COVID-19 market since June 30, 2021, we now expect to seek future collaborations with multiple strategic partners and expect to generate revenue from our human health programs that may fall within the broader range of approximately $160 million to $181 million. The financial projections also assumed that we would obtain partnerships for COVID-19 and multi-target partnerships in 2023, including COVID-19 partnerships in two additional developing country regions, such as Latin America and Southeast Asia, as well as a 2-target world-wide partnership agreement, which were estimated using the same benchmarks described above. In 2023, the financial projections assumed that we would establish a partnering agreement in China, with that agreement benchmarked against the 2021 Everest-Providence pre-clinical Asia COVID-19 transaction. The upfront payment was assumed to be lower because we assumed that the GreenLight agreement will not include Pakistan. Because we do not expect that the agreement would include initial profit-sharing similar to the Everest-Providence transaction, the projections assumed instead that development milestones would be paid. Also in 2023, if our Phase 1 clinical trial for our influenza vaccine generates positive results, we expect to seek a world-wide partnership for our influenza program. The assumed terms of this transaction were benchmarked against the 2018 Pfizer-BioNTech agreement for worldwide rights to a research-stage program, which included $120 million upfront in cash, equity, and near-term milestones. GreenLight’s estimated payments were assumed to be lower to reflect the fact that GreenLight’s platform is not expected to have as much clinical validation data as BioNTech and that GreenLight may be unable to find a partner with Pfizer’s extensive global commercial reach. We cannot assure you that any of the benchmark transactions for other companies are indicative of the actual terms, if any, that we will be able to achieve.
|
• |
The projections estimated that we will generate revenue of $19 million in 2024 from plant health products as we expand US sales of our product for the Colorado potato beetle pest, and assumed we will launch our product for the Varroa mite pest in that year. In human health, the projections estimated that we will generate revenue of $212 million from our COVID-19 program through additional milestone payments on assumed agreements and royalties on first commercial sales of COVID-19 vaccine sales in South Africa.
|
• |
The projections assumed that we will launch four additional plant health products against Botrytis, Diamondback Moth, Fusarium and Powdery Mildew in 2025, contributing to the plant health revenue estimate of $120 million in that year.
|
• |
The projections assumed that GreenLight will complete development of all programs in the pipeline and obtain all required regulatory approvals on time. The projections provided to ENVI did not factor in or otherwise consider the possibility that any of our product candidates will not successfully complete field or clinical trials on our projected timelines or at all because ENVI, a financially sophisticated business enterprise, was aware of the risks and uncertainties associated with early-stage product candidates and could conduct its own assessment of both the likelihood that these risks and uncertainties might lead to unanticipated delays in, or failure to obtain, regulatory approval for our product candidates and any resulting impact on our projected financial information. There is no guarantee that we will successfully receive timely regulatory approval for any of our products according to our projected timelines, or at all. If we fail to achieve approval or if we encounter
|
significant delays in approval for any of these applications, our ability to achieve our prospective financial information set forth above could be materially and adversely affected.
|
• |
The projections assumed that GreenLight will be able to build sufficient manufacturing capacity to support anticipated commercial product demand.
|
• |
The projections assumed that GreenLight will be able to obtain sufficient incremental funding, whether by debt, equity, strategic partners, or other sources, or a combination of these sources.
|
• |
the fact that our initial stockholders, and in the case of HB Strategies solely with respect to their founder shares, have agreed not to redeem any shares of ENVI Class A Common Stock held by them in connection with a stockholder vote to approve a proposed initial business combination, including all 5,175,000 shares of ENVI Class B Common Stock held by them as of the date of this proxy statement/prospectus;
|
• |
the fact that Canaccord, an affiliate of the Sponsor, will receive a fee of $7.8 million in connection with the closing of the proposed business combination;
|
• |
the fact that the initial stockholders paid an aggregate of $25,000 for the 5,175,000 shares of ENVI Class B Common Stock currently owned by them and such securities will have a significantly higher value at the time of the Business Combination and that, as a result of the lower price paid by our initial stockholders for their shares of ENVI Class B Common Stock, the initial stockholders may generate a profit on those shares even at prices that would generate a significant loss for the public stockholders on their shares of public common stock;
|
• |
the fact that HB Strategies paid $2,000,000 for its private placement warrants, and that ENVI issued the 750,000 Insider Warrants, and that these private placement warrants would be worthless if a business combination is not consummated by July 19, 2022 (or by January 19, 2023 if we, by resolution of our board, extend the period of time by an additional six months);
|
• |
the fact that the initial stockholders and ENVI’s other current officers and directors have agreed to waive their rights to liquidating distributions from the trust account with respect to any common stock (other than public common stock) held by them if ENVI fails to complete an initial business combination by July 19, 2022 (or by January 19, 2023 if we elect to extend);
|
• |
the fact that the Investor Rights Agreement has been entered into by the initial stockholders;
|
• |
the fact that, at the option of the Sponsor, any amounts outstanding under any loan made by the Sponsor, HB Strategies or any of their affiliates to ENVI in an aggregate amount of up to $1,500,000 may be converted into ENVI Units in connection with the consummation of the Business Combination;
|
• |
the fact that HB Strategies has made a $500,000 working capital loan to ENVI;
|
• |
the continued indemnification of ENVI’s directors and officers and the continuation of ENVI’s directors’ and officers’ liability insurance after the Business Combination (
i.e.
|
• |
the fact that the Sponsor and ENVI’s officers and directors will lose their entire investment in ENVI and will not be reimbursed for any
out-of-pocket
|
• |
the fact that if the trust account is liquidated, including in the event ENVI is unable to complete an initial business combination by July 19, 2022 (or by January 19, 2023 if we elect to extend), the Sponsor has agreed to indemnify ENVI to ensure that the proceeds in the trust account are not reduced below $10.00 per public share, or such lesser per public share amount as is in the trust account on the liquidation date, by the claims of prospective target businesses with which ENVI has entered into an acquisition agreement or claims of any third party for services rendered or products sold to ENVI, but only if such a vendor or target business has not executed a waiver of any and all rights to seek access to the trust account; and
|
• |
the fact that ENVI may be entitled to distribute or pay over funds held by ENVI outside the Trust Account to the Sponsor or any of its Affiliates prior to the Closing.
|
• |
the fact that certain of GreenLight’s directors are expected to become directors of New GreenLight upon the Closing and will receive compensation under New GreenLight’s director compensation practices described in the section titled “
GreenLight Director Compensation
|
• |
the fact that each of GreenLight’s executive officers are expected to become executive officers of New GreenLight upon the Closing, serving in the same position they are currently serving with GreenLight, in each case on substantially the terms described in the sections entitled “
GreenLight Executive Compensation
GreenLight Director Compensation
|
• |
the substantial number of shares of New GreenLight to be issued to GreenLight’s directors, executive officers and/or their affiliated entities, as set forth in the section titled “
Beneficial Ownership of
Securities,
GreenLight Executive Compensation
GreenLight Director Compensation
|
• |
the fact that the Investor Rights Agreement has been entered into by certain of GreenLight’s directors or their affiliated entities, as set forth in the section titled “
Certain Relationships and Related Person Transactions
|
• |
the fact that certain of GreenLight’s directors or their affiliated entities have entered into subscription agreements for the PIPE Financing, as set forth in the section titled “
Certain Relationships and Related Person Transactions
|
• |
the continued indemnification of GreenLight’s directors and officers, as set forth in the section titled “
Certain Relationships and Related Person Transactions
i.e.
|
1. |
The objectives the board of directors has established to promote such public benefit or public benefits and interests;
|
2. |
The standards the board of directors has adopted to measure the corporation’s progress in promoting such public benefit or public benefits and interests;
|
3. |
Objective factual information based on those standards regarding the corporation’s success in meeting the objectives for promoting such public benefit or public benefits and interests; and
|
4. |
An assessment of the corporation’s success in meeting the objectives and promoting such public benefit or public benefits and interests.
|
Provision
|
Traditional Delaware Corporations
|
Delaware PBCs
|
||
General
|
Subject in all respects to the provisions of the DGCL. | Same as a traditional Delaware corporation, except to the extent subchapter XV imposes additional or different requirements, in which case such requirements shall apply. | ||
Purpose
|
Usually incorporated as a
for-profit
corporation that may engage in any lawful act or activity for which corporations may be organized and incorporated under the DGCL.
|
Same as a traditional Delaware corporation; in addition, a Delaware PBC is intended to produce a public benefit or public benefits and to operate in a responsible and sustainable manner. Accordingly, a Delaware PBC shall: identify within its statement of business or purpose one or more specific “public benefits,” i.e., a positive effect (or reduction of negative effects) on one or more categories of persons, entities, communities or interests (other than stockholders in their capacities as stockholders), to be promoted by the corporation; and state within its heading that it is a PBC. | ||
Name
|
Must include in its name one of the following words: “association,” “company,” “corporation,” “club,” “foundation,” “fund,” “incorporated,” “institute,” “society,” “union,” “syndicate,” or “limited,” (or abbreviations thereof, with or without punctuation), or words (or abbreviations thereof, with or without punctuation) of like import of foreign countries or jurisdictions (provided they are written in roman characters or letters). | Must state within its heading that it is a public benefit corporation and may also include in its name the identifier of “PBC” or “public benefit corporation”. Additionally, such identifier must also appear on the company’s stock certificate. |
Provision
|
Traditional Delaware Corporations
|
Delaware PBCs
|
||
Duties of Directors
|
Manage in the best interests of the corporation and its stockholders. | Manage in a manner that balances the pecuniary interests of the stockholders, the best interests of those materially affected by the corporation’s conduct, and the specific public benefit or public benefits identified in its certificate of incorporation. | ||
Director Liability for Public Benefit Purpose
|
Not applicable. | A director of a PBC shall not, by virtue of the public benefit provisions of the DGCL, have any duty to any person on account of any interest of such person in the public benefit or public benefits identified in the certificate of incorporation or on account of any interest materially affected by the corporation’s conduct and, with respect to a decision implicating the balance requirement described in “Duties of Directors” above, will be deemed to satisfy such director’s fiduciary duties to stockholders and the corporation if such director’s decision is both informed and disinterested and not such that no person of ordinary, sound judgment would approve. | ||
Conflicts of Interest for Public Benefit Duties of Directors
|
Not applicable. | A director’s ownership of or other interest in the stock of the PBC shall not alone create a conflict of interest on the part of the director with respect to the director’s decision implicating the balancing requirement described in “Duties of Directors” above, except to the extent that such ownership or interest would create a conflict of interest if the corporation were not a PBC. In the absence of a conflict of interest, no failure to satisfy that balancing requirement shall, for the purposes of §102(b)(7) or §145 of the DGCL, constitute an act or omission not in good faith, or a breach of the duty of loyalty, unless the certificate of incorporation so provides. |
Provision
|
Traditional Delaware Corporations
|
Delaware PBCs
|
||
Suits to Enforce Public Benefit Duties of Directors
|
Not applicable. | Any action to enforce the balancing requirement described in “Duties of Directors” above, including any individual, derivative or any other type of action, may not be brought unless the plaintiffs in such action own individually or collectively, as of the date of instituting such action, at least 2% of the corporation’s outstanding shares or, in the case of a corporation with shares listed on a national securities exchange, the lesser of such percentage or shares of the corporation with a market value of at least $2,000,000 as of the date the action is instituted. The provisions of subchapter XV do not relieve the plaintiffs from complying with any other conditions applicable to filing a derivative action including §327 of the DGCL and any rules of the court in which the action is filed. | ||
Public Benefit Notices
|
Not applicable. | A PBC shall include in every notice of a meeting of stockholders a statement to the effect that it is a PBC formed pursuant to subchapter XV. | ||
Biennial PBC Reporting
|
Not applicable. | A PBC shall no less than biennially provide its stockholders with a statement as to the corporation’s promotion of the public benefit or public benefits identified in the certificate of incorporation and of the best interests of those materially affected by the corporation’s conduct. The statement shall include items specified in subchapter XV. | ||
Common law fiduciary duties in transactions for corporate control
|
In the context of certain transactions implicating a sale of control of a company, Delaware common law may impose on directors of a traditional corporation a duty to maximize short-term stockholder value (the “
Revlon Rule
”)
|
In response to all sale transactions, the directors of a PBC are required to adhere to the balancing requirement described in “Duties of Directors” above. Additionally, the directors of a PBC are not subject to the constraints of the Revlon Rule. |
• |
change the name of ENVI to “GreenLight Biosciences, Inc.” (or, if the Public Benefit Corporation Proposal is also approved, ENVI will instead change its name to “GreenLight Biosciences, PBC”.);
|
• |
remove the provisions of the Existing Charter relating to ENVI’s status as a special purpose acquisition company that will no longer be relevant following the Closing, including provisions relating to the trust account and the redemption rights of the holders of ENVI Class A Common Stock (which removal shall not affect any such redemption rights that shall have been exercised in accordance with the procedures described in this proxy statement/prospectus);
|
• |
remove the provisions of the Existing Charter relating to the ENVI Class B Common Stock that will no longer be relevant following the Closing, including the right of the holders of ENVI Class B Common Stock to appoint directors and to act by written consent, because no shares of ENVI Class B Common Stock will remain outstanding after the Closing;
|
• |
remove the “Class A” designation from the remaining shares of New GreenLight Common Stock and increase the number of shares of New GreenLight Common Stock that New GreenLight is authorized to issue from 120,000,000 shares to 500,000,000 shares;
|
• |
increase the number of undesignated shares of New GreenLight Preferred Stock that New GreenLight is authorized to issue from 1,000,000 shares to 10,000,000 shares;
|
• |
require the vote of at least 75% of the voting power of the
then-outstanding
shares of capital stock of New GreenLight, rather than a simple majority, to adopt, amend or repeal certain provisions of the Proposed Charter, including (a) to reduce the number of authorized shares of preferred stock, (b) Section 4.2 relating to the authorization and designation of new classes of preferred stock of New GreenLight (c) Article V, which relates to the number, powers and term of the New GreenLight Board and the removal of directors, (d) Article VI, which relates to the amendment, alteration, repeal or adoption of the Proposed Bylaws, (e) Article VII, which relates to the calling of meetings of stockholders, notice requirements for stockholder proposals and director nominations, and the prohibition on actions by written consent by stockholders, and (f) Article X, which relates to exclusive forum provisions for certain lawsuits; and
|
• |
require that special meetings of stockholders may only be called by a resolution of the New GreenLight Board and not merely by certain individuals, subject to any special rights of the holders of preferred stock.
|
Existing Charter
|
Proposed Charter
|
|||
Authorized Shares
Advisory Charter Amendment Proposal A
|
The Existing Charter authorizes the issuance of 121,000,000 shares, par value $0.0001 per share, consisting of 120,000,000 shares of common stock, including 100,000,000 shares of ENVI Class A Common Stock and 20,000,000 shares of ENVI Class B Common Stock, and 1,000,000 shares of undesignated preferred stock. | The Proposed Charter authorizes the issuance of 510,000,000 shares, par value $0.0001 per share, consisting of 500,000,000 shares of New GreenLight Common Stock and 10,000,000 shares of undesignated New GreenLight Preferred Stock. | ||
See Section 4.1 of the Existing Charter.
|
See Section 4.1 of the Proposed Charter.
|
|||
Required Vote to Amend or Repeal Certain Provisions of the Charter
Advisory Charter Amendment Proposal B
|
The Existing Charter does not modify the requirements of the Delaware General Corporation Law to amend the Existing Charter, other than certain provisions relating to the rights of the holders of ENVI Class B Common Stock that will cease to apply at the Effective Time. Under the Delaware General Corporation Law, amendments to the Existing Charter generally require the affirmative vote of a majority of the outstanding stock entitled to | The Proposed Charter provides that, in addition to any vote required by applicable law or the certificate of incorporation or bylaws of New GreenLight, the affirmative vote of the holders of at least seventy-five percent (75%) of the voting power of the then-outstanding shares of capital stock of New GreenLight entitled to vote generally in the election of directors, voting together as a single class, will be required for the stockholders to reduce the total |
• |
The New GreenLight Equity Plan will continue until terminated by the New GreenLight Board or New GreenLight’s compensation committee.
|
• |
The New GreenLight Equity Plan provides for the grant of stock options, both incentive stock options and nonstatutory stock options, stock appreciation rights, restricted stock, unrestricted stock, restricted stock units, dividend equivalent rights, and cash awards.
|
• |
A number of shares of New GreenLight Common Stock will be authorized for issuance pursuant to awards under the New GreenLight Equity Plan equal to 31,750,000 shares of New GreenLight Common Stock.
|
• |
The New GreenLight Equity Plan provides for an automatic share reserve increase feature, whereby the share reserve will be increased automatically on the first day of each fiscal year beginning with the 2022 fiscal year, in an amount equal to 4% of the total number of shares of New GreenLight Common Stock outstanding on the last day of the immediately preceding fiscal year, or a lesser number of shares as determined by the administrator. The automatic share reserve feature will cease immediately after the increase on the first day of the 2031 fiscal year.
|
• |
The New GreenLight Equity Plan will be administered by the New GreenLight Board or, if designated by the New GreenLight Board, the compensation committee of the New GreenLight Board.
|
• |
Eric O’Brien
|
• |
|
• |
Matthew Walker
|
• |
|
• |
Andrey Zarur
|
• |
Charles Cooney
|
• |
Ganesh Kishore
|
• |
financial institutions or financial services entities;
|
• |
broker-dealers;
|
• |
governments or agencies or instrumentalities thereof;
|
• |
regulated investment companies;
|
• |
real estate investment trusts;
|
• |
expatriates or former long-term residents of the United States;
|
• |
individual retirement or other
tax-deferred
accounts;
|
• |
persons that actually or constructively own five percent or more of our voting shares;
|
• |
insurance companies;
|
• |
dealers or traders subject to a
mark-to-market
|
• |
persons holding GreenLight Capital Stock or ENVI Class A Common Stock as part of a “straddle,” constructive sale, hedge, conversion or other integrated transaction or similar transaction;
|
• |
holders of ENVI Class A Common Stock that own (actually or constructively) any GreenLight Capital Stock;
|
• |
U.S. holders (as defined below) whose functional currency is not the U.S. dollar;
|
• |
partnerships or other pass-through entities for U.S. federal income tax purposes and any beneficial owners of such entities;
|
• |
controlled foreign corporations;
|
• |
a person required to accelerate the recognition of any item of gross income as a result of such income being recognized on an applicable financial statement;
|
• |
the Sponsor and persons related to the Sponsor;
|
• |
passive foreign investment companies; and
|
• |
tax-exempt
entities.
|
• |
an individual who is a citizen or resident of the United States;
|
• |
a corporation (or other entity taxable as a corporation) organized in or under the laws of the United States, any state thereof or the District of Columbia;
|
• |
an estate the income of which is includible in gross income for U.S. federal income tax purposes regardless of its source; or
|
• |
a trust, if (i) a court within the United States is able to exercise primary supervision over the administration of the trust and one or more “United States persons” (as defined in the Code) have authority to control all substantial decisions of the trust or (ii) it has a valid election in effect under Treasury Regulations to be treated as a United States person.
|
• |
a
non-resident
alien individual (other than certain former citizens and residents of the United States subject to U.S. tax as expatriates);
|
• |
a corporation (or other entity taxable as a corporation) that is not organized in or under the laws of the United States, any state thereof or the District of Columbia; or
|
• |
an estate or trust that is not a U.S. holder;
|
• |
the gain is effectively connected with the conduct of a trade or business by the
Non-U.S.
holder within the United States (and, under certain income tax treaties, is attributable to a United States permanent establishment or fixed base maintained by the
Non-U.S.
holder); or
|
• |
we are or have been a “United States real property holding corporation” for U.S. federal income tax purposes at any time during the shorter of the five-year period ending on the date of disposition or the period that the
Non-U.S.
holder held ENVI Class A Common Stock, and, in the case where shares of ENVI Class A Common Stock are regularly traded on an established securities market, the
Non-U.S.
holder has owned, directly or constructively, more than 5% of ENVI Class A Common Stock at any time within the shorter of the five-year period preceding the disposition or such
Non-U.S.
holder’s holding period for the shares of ENVI Class A Common Stock. There can be no assurance that ENVI Class A Common Stock will be treated as regularly traded on an established securities market for this purpose.
|
• |
the subsidiary of ENVI will merge with and into GreenLight, with GreenLight being the surviving company in the Merger and, after giving effect to such merger, GreenLight will be a wholly owned subsidiary of New GreenLight.
|
• |
each issued and outstanding share of capital stock of GreenLight will be converted into a number of shares of New GreenLight Common Stock equal to the product of (x) the conversion ratio applicable to such share multiplied by (y) the quotient obtained by dividing (a) 120,000,000, by (b) the number of “Fully-Diluted Shares” as defined in the Business Combination Agreement (such ratio, the “
Exchange Ratio
”);
|
• |
each GreenLight Option will be converted into an option to purchase a number of shares of New GreenLight Common Stock in accordance with the terms and subject to the conditions of the Business Combination Agreement;
|
• |
each GreenLight Warrant, to the extent outstanding and unexercised, will be converted into a warrant to acquire shares of New GreenLight Common Stock in accordance with the terms and subject to the conditions of the Business Combination Agreement; and
|
• |
each share of ENVI Class A Common Stock and ENVI Class B Common Stock that is issued and outstanding immediately prior to the Merger shall become one share of New GreenLight Common Stock;
|
• |
immediately prior to the consummation of the Merger, ENVI will issue and sell 12,425,000 shares of ENVI Class A Common Stock for a purchase price of $10.00 per share and aggregate gross proceeds of $124.3 million in the PIPE Financing pursuant to the Subscription Agreements;
|
• |
immediately prior to the consummation of the Merger, the GreenLight Convertible Notes will convert into GreenLight Series D Preferred Stock equal to the quotient of (a) the face value of the note plus all accrued but unpaid interest thereon divided by (b) the price of GreenLight Series D Preferred Stock;
|
• |
it is assumed that, immediately prior to the consummation of the Merger, GreenLight Warrants that are issued and outstanding prior to the Closing Date will be exercised in full on a cash basis. As all of the GreenLight Warrants have exercise prices substantially below the value of the estimated per share consideration to be paid in the Merger, it is deemed probable that all outstanding GreenLight Warrants will be cash exercised and therefore, the unaudited pro forma condensed combined balance sheet and statement of operations include adjustments related to the cash exercise of all the GreenLight Warrants,
|
and concurrently, the conversion of the GreenLight Preferred Stock and GreenLight Common Stock received on exercise directly into New GreenLight Common Stock pursuant to the terms of the Business Combination Agreement; and
|
• |
immediately prior to the consummation of the Merger, the ENVI Related Party Loan will be repaid.
|
• |
GreenLight’s existing stockholders will have the greater voting interest in New GreenLight with an estimated 73% voting interest under a No Redemption scenario as of immediately following the Closing;
|
• |
by virtue of such estimated voting interest upon the Closing, GreenLight’s existing stockholders will have the ability to control decisions regarding the election and removal of directors and officers of New GreenLight following the Closing;
|
• |
the New GreenLight Board will consist of seven members, of which five will be appointed by GreenLight, one will be appointed by GreenLight and approved by ENVI and one will be appointed by ENVI;
|
• |
senior management of GreenLight will comprise the senior management of New GreenLight; and
|
• |
Operations of GreenLight will comprise the ongoing operations of New GreenLight.
|
• |
the accompanying notes to the unaudited pro forma condensed combined financial statements;
|
• |
the historical audited financial statements of ENVI as of December 31, 2020 and for the period from July 2, 2020 (inception) through December 31, 2020, and the related notes, which are included elsewhere in this proxy statement/ prospectus;
|
• |
the historical unaudited financial statements of ENVI as of and for the nine months ended September 30, 2021 and the related notes, which are included elsewhere in this proxy statement/prospectus;
|
• |
the historical audited consolidated financial statements of GreenLight as of and for the year ended December 31, 2020 and the related notes, which are included elsewhere in this proxy statement/ prospectus;
|
• |
the historical unaudited condensed consolidated financial statements of GreenLight as of and for the nine months ended September 30, 2021 and the related notes, which are included elsewhere in this proxy statement/ prospectus; and
|
• |
other information relating to ENVI and GreenLight contained in this proxy statement/prospectus, including the Business Combination Agreement and the description of certain terms thereof set forth in the section titled “
The Business Combination
The Business Combination Agreement
Risk Factors
|
• |
No Redemption
|
• |
Maximum Redemption
|
Assuming
No Redemption
|
Assuming
Maximum Redemption
|
|||||||||||||||
Shares
|
%
|
Shares
|
%
|
|||||||||||||
Public shares
(a)
|
20,700,000 | 14 | % | 324,821 | * | |||||||||||
Founder shares
|
5,175,000 | 4 | % | 5,175,000 | 4 | % | ||||||||||
GreenLight Equityholders
(b)(c)
|
103,470,217 | 73 | % | 103,470,217 | 86 | % | ||||||||||
PIPE shares
|
12,425,000 | 9 | % | 12,425,000 | 10 | % | ||||||||||
|
|
|
|
|
|
|
|
|||||||||
Pro forma common stock outstanding at September 30, 2021
(d)
|
141,770,217 | 100 | % | 121,395,038 | 100 | % | ||||||||||
Potential sources of dilution
|
||||||||||||||||
Public Warrants
|
10,350,000 | 7 | % | 10,350,000 | 9 | % | ||||||||||
Private Placement Warrants
|
2,000,000 | 1 | % | 1,500,000 | 1 | % | ||||||||||
Insider Warrants
|
750,000 | * | 600,000 | * | ||||||||||||
Rollover options
|
17,555,928 | 12 | % | 17,555,928 | 14 | % |
* |
Certain amounts adjusted for rounding
|
(a) |
Amount includes 1,000,000 shares of ENVI Class A Common Stock held by HB Strategies, an affiliate of our sponsor, all of which shares carry the same redemption rights as other shares of ENVI Class A Common Stock. The Maximum Redemption Scenario assume that HB Strategies will redeem 100%, respectively, of its shares of ENVI Class A Common Stock. Amount excludes 13,100,000 warrants to purchase ENVI Class A Common Stock, which is made up of 10,350,000 public warrants, 2,000,000 private placement warrants and 750,000 Insider Warrants. Additionally, under the Maximum Redemption Scenario, an aggregate of 650,000 Warrants comprised of 500,000 Private Placement Warrants owned by HB Strategies and 150,000 Insider Warrants owned by the Sponsor will be forfeited pursuant to the Sponsor Letter Agreement.
|
(b) |
In accordance with the terms and subject to the conditions of the Business Combination Agreement, each outstanding share of capital stock of GreenLight will be exchanged for shares of New GreenLight Common Stock and outstanding GreenLight Options (whether vested or unvested) will be exchanged for comparable options to purchase New GreenLight Common Stock, in each case, based on an implied GreenLight equity value of $1.2 billion. The number of shares of New GreenLight Common Stock issued to the holders of shares of capital stock of GreenLight at Closing will fluctuate based on the number of shares underlying GreenLight Options and GreenLight Warrants, whether vested or unvested (and the exercise prices of such options and warrants), outstanding at Closing.
|
(c) |
Amount includes 6,583,549 shares issuable upon conversion of the GreenLight Convertible Notes and 872,667 shares underlying GreenLight Warrants that are assumed to be exercised immediately prior to the consummation of the Merger and excludes 17,555,928 shares underlying Rollover Options to be issued to holders of GreenLight Options, assuming such GreenLight Options remain unexercised as of the Closing.
|
(d) |
Amount excludes 31,750,000 shares (which amount includes shares underlying Rollover Options) and
|
As of September 30, 2021
|
Assuming No Redemption
|
Assuming Maximum
Redemption |
||||||||||||||||||||||||||||||
Environmental
Impact Acquisition Corp.* |
GreenLight
Biosciences, Inc. |
Pro Forma
Adjustments |
Pro Forma
Condensed Combined |
Additional
Pro Forma Adjustments |
Pro Forma
Condensed Combined |
|||||||||||||||||||||||||||
ASSETS
|
||||||||||||||||||||||||||||||||
Current Assets
|
||||||||||||||||||||||||||||||||
Cash and cash equivalents
|
$ | 158 | $ | 34,754 | $ | 207,009 |
|
(A
|
)
|
$ | 337,711 | $ | (203,760 | ) |
|
(L
|
)
|
$ | 138,187 | |||||||||||||
(500 | ) |
|
(D
|
)
|
4,236 |
|
(N
|
)
|
||||||||||||||||||||||||
231 |
|
(F
|
)
|
|||||||||||||||||||||||||||||
1,683 |
|
(G
|
)
|
|||||||||||||||||||||||||||||
(29,874 | ) |
|
(I
|
)
|
||||||||||||||||||||||||||||
124,250 |
|
(J
|
)
|
|||||||||||||||||||||||||||||
Prepaid expenses and other current assets
|
698 | 2,781 | — | 3,479 | — | 3,479 | ||||||||||||||||||||||||||
|
|
|
|
|
|
|
|
|
|
|
|
|||||||||||||||||||||
Total Current Assets
|
856 | 37,535 | 302,799 | 341,190 | (199,524 | ) | 141,666 | |||||||||||||||||||||||||
Restricted Cash
|
— | 167 | 167 | — | 167 | |||||||||||||||||||||||||||
Property and equipment, net
|
— | 21,744 | 21,744 | — | 21,744 | |||||||||||||||||||||||||||
Deferred offering costs
|
— | 2,590 | (2,590 | ) |
|
(I
|
)
|
— | — | — | ||||||||||||||||||||||
Security deposits
|
— | 1,256 | 1,256 | — | 1,256 | |||||||||||||||||||||||||||
Marketable securities held in Trust Account
|
207,009 | — | (207,009 | ) |
|
(A
|
)
|
— | — | — | ||||||||||||||||||||||
|
|
|
|
|
|
|
|
|
|
|
|
|||||||||||||||||||||
TOTAL ASSETS
|
$
|
207,865
|
|
$
|
63,292
|
|
$
|
93,200
|
|
$
|
364,357
|
|
$
|
(199,524
|
)
|
$
|
164,833
|
|
||||||||||||||
|
|
|
|
|
|
|
|
|
|
|
|
|||||||||||||||||||||
Current liabilities
|
||||||||||||||||||||||||||||||||
Accrued expenses
|
$ | 3,016 | $ | 9,351 | $ | (2,881 | ) |
|
(I
|
)
|
$ | 9,486 | $ | — | $ | 9,486 | ||||||||||||||||
Accounts payable
|
— | 6,559 | (2,085 | ) |
|
(I
|
)
|
4,474 | — | 4,474 | ||||||||||||||||||||||
Convertible debt
|
— | 17,959 | (17,959 | ) |
|
(E
|
)
|
— | — | — | ||||||||||||||||||||||
Accrued offering costs
|
119 | — | (119 | ) |
|
(I
|
)
|
— | — | — | ||||||||||||||||||||||
Promissory note - related party
|
500 | (500 | ) |
|
(D
|
)
|
— | — | — | |||||||||||||||||||||||
Deferred revenue
|
— | 1,378 | 1,378 | — | 1,378 | |||||||||||||||||||||||||||
Long term debt, current portion
|
— | 5,844 | 5,844 | — | 5,844 | |||||||||||||||||||||||||||
Other current liabilities
|
— | 585 | (314 | ) |
|
(F
|
)
|
271 | — | 271 | ||||||||||||||||||||||
|
|
|
|
|
|
|
|
|
|
|
|
|||||||||||||||||||||
Total Current Liabilities
|
3,635 | 41,676 | (23,858 | ) | 21,453 | — | 21,453 | |||||||||||||||||||||||||
Warrant liability
|
13,341 | 1,293 | (1,293 | ) |
|
(F
|
)
|
13,341 | (683 | ) |
|
(M
|
)
|
12,658 | ||||||||||||||||||
Long term debt, net of current portion
|
— | 15,013 | 15,013 | — | 15,013 | |||||||||||||||||||||||||||
Other liabilities
|
— | 1,355 | 1,355 | — | 1,355 | |||||||||||||||||||||||||||
|
|
|
|
|
|
|
|
|
|
|
|
|||||||||||||||||||||
TOTAL LIABILITIES
|
|
16,976
|
|
|
59,337
|
|
|
(25,151
|
)
|
|
51,162
|
|
|
(683
|
)
|
|
50,479
|
|
||||||||||||||
|
|
|
|
|
|
|
|
|
|
|
|
|||||||||||||||||||||
Commitments
|
||||||||||||||||||||||||||||||||
Class A Common stock subject to possible redemption
|
207,000 | — | (207,000 | ) |
|
(B
|
)
|
— | — | — |
* |
certain amounts adjusted for rounding.
|
As of September 30, 2021
|
Assuming No Redemption
|
Assuming Maximum
Redemption |
||||||||||||||||||||||||||||||
Environmental
Impact Acquisition Corp.* |
GreenLight
Biosciences, Inc. |
Pro Forma
Adjustments |
Pro Forma
Condensed Combined |
Additional
Pro Forma Adjustments |
Pro Forma
Condensed Combined |
|||||||||||||||||||||||||||
Redeemable Convertible Preferred Stock
|
— | 218,787 | (218,787 | ) |
|
(H
|
)
|
— | — | — | ||||||||||||||||||||||
Stockholders’ Equity (Deficit)
|
||||||||||||||||||||||||||||||||
Common Stock, $0.0001 par value
|
— | — | 2 |
|
(B
|
)
|
14 | (2 | ) |
|
(L
|
)
|
12 | |||||||||||||||||||
1 |
|
(C
|
)
|
|||||||||||||||||||||||||||||
1 |
|
(E
|
)
|
|||||||||||||||||||||||||||||
9 |
|
(H
|
)
|
|||||||||||||||||||||||||||||
1 |
|
(J
|
)
|
|||||||||||||||||||||||||||||
Class A Common Stock, $0.001 par value
|
— | 3 | (3 | ) |
|
(H
|
)
|
— | — | |||||||||||||||||||||||
Class B Common Stock, $0.0001 par value
|
1 | — | (1 | ) |
|
(C
|
)
|
— | — | |||||||||||||||||||||||
Additional paid-in capital
|
— | 4,062 | 206,998 |
|
(B
|
)
|
532,117 | (203,758 | ) |
|
(L
|
)
|
333,278 | |||||||||||||||||||
17,997 |
|
(E
|
)
|
|||||||||||||||||||||||||||||
1,838 |
|
(F
|
)
|
683 |
|
(M
|
)
|
|||||||||||||||||||||||||
1,683 |
|
(G
|
)
|
4,236 |
|
(N
|
)
|
|||||||||||||||||||||||||
218,781 |
|
(H
|
)
|
|||||||||||||||||||||||||||||
(27,379 | ) |
|
(I
|
)
|
||||||||||||||||||||||||||||
124,249 |
|
(J
|
)
|
|||||||||||||||||||||||||||||
(16,112 | ) |
|
(K
|
)
|
||||||||||||||||||||||||||||
Accumulated Deficit
|
(16,112 | ) | (218,897 | ) | (39 | ) |
|
(E
|
)
|
(218,936 | ) | — | (218,936 | ) | ||||||||||||||||||
16,112 |
|
(K
|
)
|
|||||||||||||||||||||||||||||
|
|
|
|
|
|
|
|
|
|
|
|
|||||||||||||||||||||
Total Stockholders’ Equity (Deficit)
|
(16,111 | ) | (214,832 | ) | 544,138 | 313,195 | (198,841 | ) | 114,354 | |||||||||||||||||||||||
|
|
|
|
|
|
|
|
|
|
|
|
|||||||||||||||||||||
TOTAL LIABILITIES AND STOCKHOLDERS’ EQUITY (DEFICIT)
|
$
|
207,865
|
|
$
|
63,292
|
|
$
|
93,200
|
|
$
|
364,357
|
|
$
|
(199,524
|
)
|
$
|
164,833
|
|
||||||||||||||
|
|
|
|
|
|
|
|
|
|
|
|
* |
certain amounts adjusted for rounding.
|
For the nine months ended
September 30, 2021 |
Assuming No Redemption
|
Assuming Maximum Redemption
|
||||||||||||||||||||||||||||||
Environmental
Impact Acquisition Corp. |
GreenLight
Biosciences, Inc. |
Pro Forma
Adjustments |
Pro Forma
Condensed Combined |
Additional
Pro Forma Adjustments |
Pro Forma
Condensed Combined |
|||||||||||||||||||||||||||
Revenues:
|
||||||||||||||||||||||||||||||||
Collaboration Revenue
|
$ | — | $ | — | $ | — | $ | — | ||||||||||||||||||||||||
Grant Revenue
|
— | 1,180 | 1,180 | 1,180 | ||||||||||||||||||||||||||||
|
|
|
|
|
|
|
|
|
|
|
|
|||||||||||||||||||||
Total revenues
|
$ | — | $ | 1,180 | $ | — | $ | 1,180 | $ | — | $ | 1,180 | ||||||||||||||||||||
|
|
|
|
|
|
|
|
|
|
|
|
|||||||||||||||||||||
Operating expenses
|
||||||||||||||||||||||||||||||||
Research and development
|
— | 62,081 | — | 62,081 | — | 62,081 | ||||||||||||||||||||||||||
General and administrative
|
4,084 | 13,943 | 18,027 | — | 18,027 | |||||||||||||||||||||||||||
Operating and formation costs
|
— | — | — | — | — | — | ||||||||||||||||||||||||||
|
|
|
|
|
|
|
|
|
|
|
|
|||||||||||||||||||||
Total operating expenses
|
4,084 | 76,024 | — | 80,108 | — | 80,108 | ||||||||||||||||||||||||||
|
|
|
|
|
|
|
|
|
|
|
|
|||||||||||||||||||||
Operating loss:
|
$
|
(4,084
|
)
|
$
|
(74,844
|
)
|
$
|
—
|
|
$
|
(78,928
|
)
|
$
|
—
|
|
$
|
(78,928
|
)
|
||||||||||||||
|
|
|
|
|
|
|
|
|
|
|
|
|||||||||||||||||||||
Interest income
|
9 | 20 | (9 | ) |
|
(AA
|
)
|
20 | — | 20 | ||||||||||||||||||||||
Loss in initial issuance of Private Placement Warrants
|
(1,273 | ) | — | — | (1,273 | ) | 301 |
|
(EE
|
)
|
(972 | ) | ||||||||||||||||||||
Interest expense
|
— | (1,471 | ) | 687 |
|
(CC
|
)
|
(784 | ) | — | (784 | ) | ||||||||||||||||||||
Change in fair value of warrant liability
|
1,840 | (1,343 | ) | 1,343 |
|
(DD
|
)
|
1,840 | (91 | ) |
|
(EE
|
)
|
1,749 | ||||||||||||||||||
|
|
|
|
|
|
|
|
|
|
|
|
|||||||||||||||||||||
Loss before benefit for income taxes
|
(3,508 | ) | (77,638 | ) | 2,021 | (79,125 | ) | 210 | (78,915 | ) | ||||||||||||||||||||||
|
|
|
|
|
|
|
|
|
|
|
|
|||||||||||||||||||||
Net loss
|
$
|
(3,508
|
)
|
$
|
(77,638
|
)
|
$
|
2,021
|
|
$
|
(79,125
|
)
|
$
|
210
|
|
$
|
(78,915
|
)
|
||||||||||||||
|
|
|
|
|
|
|
|
|
|
|
|
|||||||||||||||||||||
Loss per Share
|
||||||||||||||||||||||||||||||||
Weighted average shares of common stock outstanding
|
141,770,217 | (20,375,179 | ) | 121,395,038 | ||||||||||||||||||||||||||||
Loss per share (basic and diluted) attributable to common stockholders
|
$ | (0.56 | ) | $ | (0.65 | ) |
For the period
from July 2, 2020 (inception) through December 31, 2020 |
For the year
ended December 31, 2020 |
Assuming No Redemption
|
Assuming Maximum
Redemption |
|||||||||||||||||||||||||
Environmental
Impact Acquisition Corp. |
GreenLight
Biosciences, Inc. |
Pro Forma
Adjustments |
Pro Forma
Condensed Combined |
Additional
Pro Forma Adjustments |
Pro Forma
Condensed Combined |
|||||||||||||||||||||||
Revenues:
|
||||||||||||||||||||||||||||
Collaboration Revenue
|
$ | — | $ | 962 | $ | 962 | $ | 962 | ||||||||||||||||||||
Grant Revenue
|
— | 785 | 785 | 785 | ||||||||||||||||||||||||
|
|
|
|
|
|
|
|
|
|
|
|
|||||||||||||||||
Total revenues
|
$ | — | $ | 1,747 | $ | — | $ | 1,747 | $ | — | $ | 1,747 | ||||||||||||||||
|
|
|
|
|
|
|
|
|
|
|
|
|||||||||||||||||
Operating expenses
|
||||||||||||||||||||||||||||
Research and development
|
— | 42,866 | 42,866 | — | 42,866 | |||||||||||||||||||||||
General and administrative
|
— | 11,165 | 260 |
|
(BB
|
)
|
11,425 | — | 11,425 | |||||||||||||||||||
Operating and formation costs
|
3 | — | — | 3 | — | 3 | ||||||||||||||||||||||
|
|
|
|
|
|
|
|
|
|
|
|
|||||||||||||||||
Total operating expenses
|
3 | 54,031 | 260 | 54,294 | — | 54,294 | ||||||||||||||||||||||
|
|
|
|
|
|
|
|
|
|
|
|
|||||||||||||||||
Operating loss:
|
$
|
(3
|
)
|
$
|
(52,284
|
)
|
$
|
(260
|
)
|
$
|
(52,547
|
)
|
$
|
—
|
|
$
|
(52,547
|
)
|
||||||||||
|
|
|
|
|
|
|
|
|
|
|
|
|||||||||||||||||
Interest income
|
— | 83 | — | 83 | — | 83 | ||||||||||||||||||||||
Interest expense
|
— | (1,028 | ) | 575 |
|
(CC
|
)
|
(453 | ) | — | (453 | ) | ||||||||||||||||
Change in fair value of warrant liability
|
— | (22 | ) | 22 |
|
(DD
|
)
|
— | — | — | ||||||||||||||||||
|
|
|
|
|
|
|
|
|
|
|
|
|||||||||||||||||
Loss before benefit for income taxes
|
(3 | ) | (53,251 | ) | 337 | (52,917 | ) | — | (52,917 | ) | ||||||||||||||||||
|
|
|
|
|
|
|
|
|
|
|
|
|||||||||||||||||
Net loss
|
$
|
(3
|
)
|
$
|
(53,251
|
)
|
$
|
337
|
|
$
|
(52,917
|
)
|
$
|
—
|
|
$
|
(52,917
|
)
|
||||||||||
|
|
|
|
|
|
|
|
|
|
|
|
|||||||||||||||||
Loss per Share
|
||||||||||||||||||||||||||||
Weighted average shares of common stock outstanding
|
141,770,217 | (20,375,179 | ) | 121,395,038 | ||||||||||||||||||||||||
Loss per share (basic and diluted) attributable to common stockholders
|
$ | (0.37 | ) | $ | (0.44 | ) |
• |
ENVI’s unaudited condensed balance sheet as of September 30, 2021, and the related notes, which is included elsewhere in this proxy statement/ prospectus; and
|
• |
GreenLight’s unaudited condensed consolidated balance sheet as of September 30, 2021, and the related notes, which is included elsewhere in this proxy statement/prospectus.
|
• |
ENVI’s audited statement of operations for the year ended December 31, 2020 and the related notes, which is included elsewhere in this proxy statement/prospectus; and
|
• |
GreenLight’s audited consolidated statement of operations for the year ended December 31, 2020, and the related notes, which is included elsewhere in this proxy statement/ prospectus.
|
• |
ENVI’s unaudited condensed statement of operations for the nine months ended September 30, 2021 and the related notes, which is included elsewhere in this proxy statement/prospectus; and
|
• |
GreenLight’s unaudited condensed consolidated statement of operations for the nine months ended September 30, 2021, and the related notes, which is included elsewhere in this proxy statement/prospectus.
|
1. |
Represents pro forma adjustments to the condensed combined balance sheet:
|
2. |
The pro forma adjustments included in the unaudited pro forma condensed combined statements of operations for the year ended December 31, 2020 and the nine months ended September 30, 2021 are as follows:
|
For the year ended
December 31, 2020 |
For the nine months ended
September 30, 2021 |
|||||||||||||||
(Amounts in thousands, except per share data)
|
Assuming No
Redemption |
Assuming
Maximum Redemption |
Assuming No
Redemption |
Assuming
Maximum Redemption |
||||||||||||
Pro forma net loss
|
$ | (52,917 | ) | $ | (52,917 | ) | $ | (79,125 | ) | $ | (78,915 | ) | ||||
Weighted average shares calculation, basic and diluted
|
||||||||||||||||
Public shares
(a)
|
20,700,000 | 20,700,000 | 20,700,000 | 20,700,000 | ||||||||||||
Founder Shares
|
5,175,000 | 5,175,000 | 5,175,000 | 5,175,000 | ||||||||||||
GreenLight Equityholders
(b)(c)
|
103,470,217 | 103,470,217 | 103,470,217 | 103,470,217 | ||||||||||||
PIPE Shares
|
12,425,000 | 12,425,000 | 12,425,000 | 12,425,000 | ||||||||||||
Redemptions
|
— | (20,375,179 | ) | — | (20,375,179 | ) | ||||||||||
|
|
|
|
|
|
|
|
|||||||||
Weighted average common stock outstanding
(d)
|
141,770,217 | 121,395,038 |
|
141,770,217
|
|
121,395,038 | ||||||||||
|
|
|
|
|
|
|
|
|||||||||
Loss per share, basic and diluted, attributable to common stockholders
|
$ | (0.37 | ) | $ | (0.44 | ) | $ | (0.56 | ) | $ | (0.65 | ) | ||||
|
|
|
|
|
|
|
|
(a) |
Amount includes 1,000,000 shares of ENVI Class A Common Stock held by HB Strategies, a founder, all of which shares carry the same redemption rights as other shares of ENVI Class A Common Stock. The Maximum Redemption Scenario assume that HB Strategies will redeem 100% of its shares of ENVI Class A Common Stock. Excludes a total of 13,100,000 shares related to 10,350,000 public warrants, 2,000,000 private placement warrants and 750,000 Insider Warrants. Under a Maximum Redemption Scenario, an aggregate of 650,000 warrants comprised of 500,000 private placement warrants and 150,000 Insider Warrants owned by the Sponsor and HB Strategies will be forfeited pursuant to the Sponsor Letter Agreement.
|
(b) |
In accordance with the terms and subject to the conditions of the Business Combination Agreement, each outstanding share of capital stock of GreenLight will be exchanged for shares of New GreenLight Common Stock and outstanding GreenLight Options (whether vested or unvested) will be exchanged for comparable options to purchase New GreenLight Common Stock, in each case, based on an implied GreenLight equity
|
value of $1.2 billion. The number of shares of New GreenLight Common Stock issued to the holders of shares of capital stock of GreenLight at Closing will fluctuate based on the number of shares underlying GreenLight Options and GreenLight Warrants, whether vested or unvested (and the exercise prices of such options and warrants), outstanding at Closing. |
(c) |
Amount includes 6,583,549 shares issuable upon conversion of the GreenLight Convertible Notes and 872,667 shares underlying GreenLight Warrants that are assumed to be exercised immediately prior to the consummation of the Merger and excludes 17,555,928 shares underlying Rollover Options to be issued to holders of GreenLight Options, assuming such GreenLight Options remain unexercised as of the Closing.
|
(d) |
Amount excludes 31,750,000 shares (which amount includes shares underlying Rollover Options) and 2,000,000 shares of New GreenLight Common Stock that are expected to be available for issuance under the New GreenLight Equity Plan and the New GreenLight ESPP, respectively, after the consummation of the Business Combination, assuming approval of the Condition Precedent Proposals.
|
• |
Assuming No Redemption—assumes that none of the holders of shares of ENVI Class A Common Stock will exercise redemption rights with respect to their public shares for a pro rata share of the funds in the trust account;
|
• |
Assuming 50% Redemption—assumes that holders of 10,187,589 shares of ENVI Class A Common Stock will exercise their redemption rights for their pro rata share (approximately $10.00 per share) of the funds in the trust account, which is 50% of the number of shares that would be redeemed in the Maximum Redemption Scenario, as described below; and
|
• |
Assuming Maximum Redemption—assumes that holders of 20,375,179 shares of ENVI Class A Common Stock will exercise their redemption rights for their pro rata share (approximately $10.00 per share) of the funds in the trust account, which is the estimated maximum number of redemptions that could occur without a failure to satisfy the Aggregate Transaction Proceeds Condition set forth in the Business Combination Agreement. See the unaudited pro forma condensed combined financial statements included elsewhere in this proxy statement/prospectus.
|
Pro Forma Condensed Combined
|
||||||||||||||||||||
GreenLight
(Historical) |
ENVI
(Historical) |
Assuming No
Redemption |
Assuming 50%
Redemption |
Assuming
Maximum Redemption |
||||||||||||||||
As of and for the nine months ended September 30, 2021
|
||||||||||||||||||||
Book value per share (1)
|
$ | (64.62 | ) | $ | (0.66 | ) | $ | 2.21 | $ | 1.64 | $ | 0.94 | ||||||||
Weighted average shares outstanding of common stock—basic and diluted
|
3,324,547 | — | 141,770,217 | 131,582,628 | 121,395,038 | |||||||||||||||
Weighted average shares outstanding of ENVI Class A Common Stock—basic and diluted
|
19,335,165 |
Pro Forma Condensed Combined
|
||||||||||||||||||||
GreenLight
(Historical) |
ENVI
(Historical) |
Assuming No
Redemption |
Assuming 50%
Redemption |
Assuming
Maximum Redemption |
||||||||||||||||
Weighted average shares outstanding of ENVI Class B Common Stock—basic and diluted
|
5,130,495 | |||||||||||||||||||
Net loss per share of common stock—basic and diluted
|
$ | (27.27 | ) | $ | (0.56 | ) | $ | (0.60 | ) | $ | (0.65 | ) | ||||||||
Net loss per share of ENVI Class A Common Stock—basic and diluted
|
$ | — | ||||||||||||||||||
Net loss per share of ENVI Class B Common Stock—basic and diluted
|
$ | (0.58 | ) |
(1) |
Book value per share = (Total equity excluding preferred shares)/shares outstanding.
|
• |
subject us to negative economic, competitive and regulatory developments, any or all of which may have a substantial adverse impact on the particular industry in which we operate after our initial business combination; and
|
• |
cause us to depend on the marketing and sale of a single product or limited number of products or services.
|
Name
|
Age
|
Position
|
||
Daniel Coyne | 49 | Chief Executive Officer, President and Director | ||
Marc Marano | 49 | Chief Financial Officer and Treasurer | ||
Andrew Viles | 58 | Secretary | ||
Jennifer E. Pardi | 39 | Director | ||
Deval L. Patrick | 64 | Director | ||
David Brewster | 50 | Director | ||
Dean Seavers | 60 | Director |
• |
assisting board oversight of (1) the integrity of our financial statements, (2) our compliance with legal and regulatory requirements, (3) our independent auditor’s qualifications and independence, and (4) the performance of our internal audit function and independent auditors; the appointment, compensation, retention, replacement, and oversight of the work of the independent auditors and any other independent registered public accounting firm engaged by us;
|
• |
pre-approving
all audit and
non-audit
services to be provided by the independent auditors or any other registered public accounting firm engaged by us, and establishing
pre-approval
policies and procedures; reviewing and discussing with the independent auditors all relationships the auditors have with us in order to evaluate their continued independence;
|
• |
setting clear policies for audit partner rotation in compliance with applicable laws and regulations; obtaining and reviewing a report, at least annually, from the independent auditors describing (1) the independent auditor’s internal quality-control procedures and (2) any material issues raised by the most recent internal quality-control review, or peer review, of the audit firm, or by any inquiry or investigation by governmental or professional authorities, within the preceding five years respecting one or more independent audits carried out by the firm and any steps taken to deal with such issues;
|
• |
meeting to review and discuss our annual audited financial statements and quarterly financial statements with management and the independent auditor, including reviewing our specific disclosures under “ENVI Management’s Discussion and Analysis of Financial Condition and Results of Operations”; reviewing and approving any related party transaction required to be disclosed pursuant to Item 404 of Regulation
S-K
promulgated by the SEC prior to us entering into such transaction; and
|
• |
reviewing with management, the independent auditors, and our legal advisors, as appropriate, any legal, regulatory or compliance matters, including any correspondence with regulators or government agencies and any employee complaints or published reports that raise material issues regarding our financial statements or accounting policies and any significant changes in accounting standards or rules promulgated by the Financial Accounting Standards Board, the SEC or other regulatory authorities.
|
• |
reviewing and approving on an annual basis the corporate goals and objectives relevant to our Chief Executive Officer’s compensation evaluating our Chief Executive Officer’s performance in light of such goals and objectives and determining and approving the remuneration (if any) of our Chief Executive Officer based on such evaluation;
|
• |
reviewing and making recommendations to our board of directors with respect to the compensation, and any incentive compensation and equity based plans that are subject to board approval of all of our other officers;
|
• |
reviewing our executive compensation policies and plans;
|
• |
implementing and administering our incentive compensation equity-based remuneration plans;
|
• |
assisting management in complying with our proxy statement and annual report disclosure requirements;
|
• |
approving all special perquisites, special cash payments and other special compensation and benefit arrangements for our officers and employees;
|
• |
producing a report on executive compensation to be included in our annual proxy statement; and
|
• |
reviewing, evaluating and recommending changes, if appropriate, to the remuneration for directors.
|
• |
None of our officers or directors is required to commit his, her or their full time to our affairs and, accordingly, may have conflicts of interest in allocating his, her or their time among various business activities.
|
• |
In the course of their other business activities, our officers and directors may become aware of investment and business opportunities which may be appropriate for presentation to us as well as the other entities with which they are affiliated. Our management may have conflicts of interest in determining to which entity a particular business opportunity should be presented.
|
• |
Our initial stockholders have agreed to waive their redemption rights with respect to any founder shares and any public shares held by them in connection with the consummation of our initial business combination. HB Strategies has agreed to waive its redemption rights with respect to its founder shares. Additionally, our initial stockholders have agreed to waive their redemption rights with respect to any founder shares held by them if we fail to consummate our initial business combination within 18 months from the closing of the initial public offering (or up to 24 months from the closing of the initial public offering if we, by resolution of our board, extend the period of time by an additional six months). With certain limited exceptions, the founder shares will not be transferable, assignable by our initial stockholders until the earlier of: (A) six months after the completion of our initial business combination or (B) subsequent to our initial business combination, (x) if the last sale price of our ENVI Class A Common Stock equals or exceeds $12.00 per share (as adjusted for stock splits, stock dividends, reorganizations, recapitalizations and the like) for any 20 trading days within any
30-trading
day period commencing at least 60 days after our initial business combination, or (y) the date on which we complete a liquidation, merger, capital stock exchange, reorganization or other similar transaction
|
that results in all of our stockholders having the right to exchange their shares of common stock for cash, securities or other property. Since the Sponsor and officers and directors may directly or indirectly own common stock and warrants following the initial public offering, our officers and directors may have a conflict of interest in determining whether a particular target business is an appropriate business with which to effectuate our initial business combination.
|
• |
Our officers and directors may have a conflict of interest with respect to evaluating a particular business combination if the retention or resignation of any such officers and directors was included by a target business as a condition to any agreement with respect to our initial business combination.
|
• |
The Sponsor, officers or directors may have a conflict of interest with respect to evaluating a business combination and financing arrangements as we may obtain loans from the Sponsor or an affiliate of the Sponsor or any of our officers or directors to finance transaction costs in connection with an intended initial business combination. Up to $1,500,000 of such working capital loans (including working capital loans that we obtain from HB Strategies) may be convertible into private placement-equivalent warrants, at the option of the lender.
|
• |
The Sponsor, officers or directors may have a conflict of interest with respect to evaluating a business combination and financing arrangements on account of the cash fee that may be due to Canaccord in an amount equal to 3.76% of the gross proceeds of the initial public offering (or $7,783,200), for certain advisory services in connection with our business combination. Pursuant to the terms of the Business Combination Marketing Agreement, no fee will be due if we do not complete an business combination.
|
• |
the corporation could financially undertake the opportunity;
|
• |
the opportunity is within the corporation’s line of business; and
|
• |
it would not be fair to our company and its stockholders for the opportunity not to be brought to the attention of the corporation.
|
INDIVIDUAL
|
ENTITY
|
ENTITY’S BUSINESS
|
AFFILIATION
|
|||
Daniel Coyne | Canaccord Genuity LLC | Financial Services |
Managing Director,
Co-Head
of U.S. Investment Banking and Global Head of Sustainability Investment Banking
|
|||
Marc Marano | Canaccord Genuity LLC | Managing Director | ||||
Andrew Viles | Canaccord Genuity Group Inc. | Executive Vice President, Chief Legal Officer and US General Counsel | ||||
Jennifer E. Pardi | Canaccord Genuity LLC | Global Head of Equity Capital Markets | ||||
Deval Patrick | Together Fund | Politics | Founder | |||
David Brewster |
EnerNOC
Vicinity Energy
Line Vision
Mantis Innovation Group
|
Energy
Energy
Energy
Facility Management
|
Co-Founder
Director
Director
Director
|
|||
Dean Seavers |
PG&E Corporation
Albermarle Corporation
|
Energy
Chemical
|
Director
Director
|
• |
may significantly dilute the equity interest of investors in our initial public offering, which dilution would increase if the
anti-dilution
provisions in the ENVI Class B Common Stock resulted in the issuance of ENVI Class A Common Stock on a greater than
one-to-one
|
• |
may subordinate the rights of holders of ENVI Class A Common Stock if preference shares are issued with rights senior to those afforded our ENVI Class A Common Stock;
|
• |
could cause a change in control if a substantial number of our ENVI Class A Common Stock are issued, which may affect, among other things, our ability to use our net operating loss carry forwards, if any, and could result in the resignation or removal of our present officers and directors;
|
• |
may have the effect of delaying or preventing a change of control of us by diluting the share ownership or voting rights of a person seeking to obtain control of us; and
|
• |
may adversely affect prevailing market prices for our ENVI Class A Common Stock.
|
• |
default and foreclosure on our assets if our operating revenues after an initial business combination are insufficient to repay our debt obligations;
|
• |
acceleration of our obligations to repay the indebtedness even if we make all principal and interest payments when due if we breach certain covenants that require the maintenance of certain financial ratios or reserves without a waiver or renegotiation of that covenant;
|
• |
our immediate payment of all principal and accrued interest, if any, if the debt is payable on demand;
|
• |
our inability to obtain necessary additional financing if the debt contains covenants restricting our ability to obtain such financing while the debt security is outstanding;
|
• |
our inability to pay dividends on our common stock;
|
• |
using a substantial portion of our cash flow to pay principal and interest on our debt, which will reduce the funds available for dividends on our common stock, if declared, expenses, capital expenditures, acquisitions and other general corporate purposes;
|
• |
limitations on our flexibility in planning for and reacting to changes in our business and in the industry in which we operate;
|
• |
increased vulnerability to adverse changes in general economic, industry and competitive conditions and adverse changes in government regulation; and
|
• |
limitations on our ability to borrow additional amounts for expenses, capital expenditures, acquisitions, debt service requirements, execution of our strategy and other purposes and other disadvantages compared to our competitors who have less debt.
|
• |
Human and animal health—where messenger RNA, or mRNA, can be used to express proteins which form the basis of vaccines as well as other therapies.
|
• |
Plant health—where dsRNA can be leveraged to regulate the expression of a target protein by interfering with its message. Such RNA-mediated interference can form the basis for highly targeted pesticides or protection against parasites.
|
• |
Wide range of applications: mRNA can produce any encoded protein (intracellular, membrane-bound, or secreted), giving it many uses in vaccines, gene therapy, or for therapeutic proteins.
|
• |
Transient expression: The body has mechanisms to degrade mRNA, allowing for repeat dosing and a dose response which can be tailored for the needs of the pharmaceutical product.
|
• |
Fast development: Relatively simple changes to the mRNA molecule are needed to produce different therapeutic proteins, enabling a fast turnaround from gene selection to product with little need for manufacturing changes. For instance, if a booster vaccine is needed for a new variant, no changes will need to be made except to the mRNA sequence itself.
|
• |
Flexible manufacturing: A single manufacturing facility can produce different vaccines and therapies, as the process is essentially the same regardless of the product.
|
• |
Cell-based fermentation does not achieve the quality required for human health uses or the cost considerations for broadacre coverage in agriculture applications.
|
• |
Conventional cell-free processes, such as in vitro transcription (IVT), are cost prohibitive for agricultural applications and require complex specialty input supply chains.
|
• |
a proprietary cell-free methodology that enables production at less than $1/gram for the production of technical grade active ingredient dsRNA.
|
• |
a flexible architecture that accommodates the manufacturing of a wide variety of products.
|
1. |
Identification: Machine learning and proprietary algorithms are key tools as we work to identify the best gene target candidates. We become more efficient and innovative as we accumulate data, and our algorithms learn.
|
2. |
Develop and optimize: We run parallel trials on thousands of distinct RNA sequences to design our agricultural products, which gives us many more opportunities to develop the best products.
|
3. |
Manufacturing: We can produce dsRNA products through our proprietary cell-free system. Our current production capacity is 2,000 liters per batch, and we are planning to build the capacity to produce dsRNA at a rate of at least 10,000 liters per batch. Production at larger capacities will allow us to achieve economies of scale by reducing labor costs and the fixed costs that we allocate to each liter of RNA that we produce.
|
1. |
Fast development of agricultural products. Our Colorado potato beetle product will, if approved in 2022, have taken four years from start to market compared to a typical
10-year
cycle at major agribusinesses.
|
2. |
Rapid integration of acquisitions. We acquired Bayer’s topical RNA treatment for honeybees in December 2020. By May 2021, we were conducting further field trials and intend to be ready for regulatory submission in 2022.
|
3. |
Validation of our mRNA platform. We are working toward clinical proof of concept of our
COVID-19
and influenza mRNA vaccines.
|
4. |
Innovative approaches to gene editing. We have the potential to tackle grave diseases such as sickle cell, for which we received a $3.3 million grant from the Bill & Melinda Gates Foundation.
|
5. |
Expansion of production capabilities. Our Rochester RNA manufacturing facility can produce 500 kg of dsRNA per year with the capability to expand to 1,000 kg. It currently provides samples for our field trials.
|
1. |
Insecticides ($17 billion)
|
2. |
Fungicides ($16.5 billion)
|
3. |
Vaccines ($93 billion)
|
4. |
Gene therapies ($3 billion)
|
• |
Colorado potato beetle, 2022
|
• |
Varroa mite, 2024
|
• |
Botrytis, 2025
|
• |
Diamondback moth, 2025
|
• |
Fusarium, 2025
|
• |
Powdery mildew, 2025
|
• |
Two-spotted
spider mite, 2026
|
• |
COVID-19 vaccine, 2022 (currently in animal toxicity studies)
|
• |
Seasonal flu vaccine, late 2022/early 2023 (currently in pre-toxicity study development)
|
• |
Supra-seasonal flu, 2024 (currently in early stages of concept evaluation)
|
• |
Antibody therapy, 2024 (currently in early stages of concept evaluation)
|
• |
Sickle cell disease product concept, 2025 (currently in early stages of concept evaluation)
|
• |
The key raw material for dsRNA can be obtained in large quantities from such sources as industrial fermentation processes (e.g., derived from yeast).
|
• |
Our proprietary process allows us to energize naturally occurring nucleoside monophosphates at low cost using inorganic polyphosphate, which is readily available and affordable.
|
• |
Thermophilic enzymes are employed to facilitate the production of high-energy nucleotides. The utilization of thermally stable enzymes allows high temperature to be incorporated in their preparation, providing a way to mitigate undesirable contaminating activities (e.g., RNA-degrading enzymes, DNA-degrading enzymes, nucleotide-degrading/altering enzymes, protein-degrading enzymes) from entering the RNA synthesis portion of the process and affecting quality and yield.
|
• |
We believe our process know-how and the technology we developed can be leveraged for our mRNA platform.
|
• |
The manufacturing process used to produce the product (described above)
|
• |
The mRNA molecule
|
• |
The delivery vehicle it uses to reach the target tissue
|
• |
Prophylactic vaccines for infectious diseases
|
• |
Gene therapies
|
• |
The antigen expressed is a true match to the protein present in the pathogen, thus increasing the potential for quality of the immune response as compared to vaccines produced through other methods, in which manufacturing processes may result in changes to the antigen.
|
• |
The short development time from antigen selection to clinical trials makes mRNA ideal for emerging epidemics or pandemic response. This is why mRNA vaccines have been among the fastest developed for
COVID-19.
|
• |
The same manufacturing plant can be used to produce different mRNA vaccines.
|
*: |
p<0.05
|
***: |
p<0.001
|
ns: |
p=0.0523 (not significant)
|
• |
Accessible: Based on our cost-competitive RNA platform and with an in vivo administration, we believe our therapy will enable us to to bypass the need for facilities required to edit the cells ex vivo.
|
• |
Targeted: The delivery technology targets specific cells in tissue.
|
• |
One dose and done: Our strategy is to target precursor stem cells to provide long-lasting expression.
|
• |
Versatile: Our therapy has the potential to encode for full-length genes and address genetic indications that require therapy in nondividing cells.
|
• |
Care for everyone
|
• |
Courage to achieve the impossible
|
• |
Collaboration to propel our success
|
• |
Commitment to science and doing the right thing, always
|
• |
completion of preclinical laboratory tests and animal studies performed in accordance with the FDA’s Good Laboratory Practice requirements (“
GLPs
”);
|
• |
submission to the FDA of an investigational new drug application (“
IND
”), which must become effective before clinical trials may begin;
|
• |
approval by an institutional review board (“
IRB
”) or ethics committee at each clinical site before the trial is commenced;
|
• |
performance of adequate and well-controlled human clinical trials to establish the safety, purity and potency of the proposed biologic product candidate for its intended purpose;
|
• |
preparation of and submission to the FDA of a biologics license application (“
BLA
”), after completion of all pivotal clinical trials;
|
• |
satisfactory completion of an FDA Advisory Committee review, if applicable;
|
• |
a determination by the FDA within 60 days of its receipt of a BLA to file the application for review;
|
• |
satisfactory completion of an FDA
pre-approval
inspection of the manufacturing facility or facilities at which the proposed product is produced to assess compliance with cGMP, and to assure that the facilities, methods and controls are adequate to preserve the biological product’s continued safety, purity and potency, and of selected clinical investigation sites to assess compliance with Good Clinical Practices (“
GCPs
”); and
|
• |
FDA review and approval of the BLA to permit commercial marketing of the product for particular indications for use in the United States.
|
• |
Phase 1—The investigational product is initially introduced into healthy human subjects or patients with the target disease or condition. These studies are designed to test the safety, dosage tolerance, absorption, metabolism and distribution of the investigational product in humans, the side effects associated with increasing doses, and, if possible, to gain early evidence on effectiveness.
|
• |
Phase 2—The investigational product is administered to a limited patient population with a specified disease or condition to evaluate the preliminary efficacy, optimal dosages and dosing schedule and to identify possible adverse side effects and safety risks. Multiple Phase 2 clinical trials may be conducted to obtain information prior to beginning larger and more expensive Phase 3 clinical trials.
|
• |
Phase 3—The investigational product is administered to an expanded patient population to further evaluate dosage, to provide statistically significant evidence of clinical efficacy and to further test for safety, generally at multiple geographically dispersed clinical trial sites. These clinical trials are intended to establish the overall risk/benefit ratio of the investigational product and to provide an adequate basis for product approval.
|
• |
restrictions on the marketing or manufacturing of the product, complete withdrawal of the product from the market or product recalls;
|
• |
fines, warning letters, or untitled letters;
|
• |
clinical holds on clinical studies;
|
• |
refusal of the FDA to approve pending applications or supplements to approved applications, or suspension or revocation of product license approvals;
|
• |
product seizure or detention, or refusal to permit the import or export of products;
|
• |
consent decrees, corporate integrity agreements, debarment or exclusion from federal healthcare programs;
|
• |
mandated modification of promotional materials and labeling and the issuance of corrective information;
|
• |
the issuance of safety alerts, Dear Healthcare Provider letters, press releases and other communications containing warnings or other safety information about the product; or
|
• |
injunctions or the imposition of civil or criminal penalties.
|
• |
the applicant must first conduct specified studies to evaluate mammalian toxicology, toxicological effects to non-target organisms in the environment (ecotoxicological exposures), and the product’s physical and chemical properties;
|
• |
the applicant must then submit to the EPA a registration dossier that includes data demonstrating that the product does not pose unreasonable risks;
|
• |
the EPA will conduct both scientific and administrative reviews of the dossier, including a thorough evaluation of submitted safety data and completion of risk assessments for human dietary and ecotoxicological exposures;
|
• |
if the EPA identifies any risks that appear to exceed regulatory standards or any other deficiencies in the dossier, it will ordinarily issue a letter identifying the deficiencies;
|
• |
the applicant will have one or more opportunities to address any deficiencies, including the submission of factors that mitigate any risks identified in the EPA’s risk assessments; this process may involve ongoing submissions and coordination with the EPA to address any unresolved concerns; and
|
• |
the EPA will undertake various stages of internal review prior to making a final decision on the application.
|
• |
conduct field and clinical trials for our product candidates;
|
• |
continue to develop additional product candidates;
|
• |
maintain, expand and protect our intellectual property portfolio;
|
• |
hire additional clinical, scientific manufacturing and commercial personnel;
|
• |
expand external and/or establish internal commercial manufacturing sources and secure supply chain capacity sufficient to provide commercial quantities of any product candidates for which we may obtain regulatory approval;
|
• |
acquire or in-license other product candidates and technologies;
|
• |
seek regulatory approvals for any product candidates that successfully complete field trials or clinical trials;
|
• |
establish a sales, marketing and distribution infrastructure to commercialize any products for which we may obtain regulatory approval; and
|
• |
add operational, financial and management information systems and personnel to support our product development, clinical execution and planned future commercialization efforts, as well as to support our transition to operating as a public company.
|
• |
external research and development expenses incurred under agreements with CMOs, CROs, universities and research laboratories that conduct our field trials, preclinical studies and development services;
|
• |
costs related to manufacturing material for our field trials and preclinical studies;
|
• |
laboratory supplies and research materials;
|
• |
payments made in cash or equity securities under third-party licensing agreements and acquisition agreements;
|
• |
costs to fulfill our obligations under the grant agreement with the Bill & Melinda Gates Foundation; and
|
• |
costs related to compliance with regulatory requirements;
|
• |
employee-related expenses, including salaries, bonuses, benefits, stock-based compensation, and other related costs for employees involved in research and development efforts;
|
• |
costs of outside consultants engaged in research and development functions, including their fees and travel expenses; and
|
• |
facilities, depreciation, and other allocated expenses, which include direct and allocated expenses for rent, utilities, and insurance.
|
NINE MONTHS ENDED
SEPTEMBER 30, |
INCREASE /
(DECREASE) |
|||||||||||
Dollars (in thousands)
|
2020
|
2021
|
||||||||||
Collaboration Revenue
|
$ | 962 | $ | — | $ | (962 | ) | |||||
Grant Revenue
|
513 | 1,180 | 667 | |||||||||
|
|
|
|
|
|
|||||||
Total Revenue
|
1,475 | 1,180 | (295 | ) | ||||||||
Operating Expenses:
|
||||||||||||
Research and development
|
28,901 | 62,081 | 33,180 | |||||||||
General and administrative
|
7,699 | 13,943 | 6,244 | |||||||||
|
|
|
|
|
|
|||||||
Total operating expenses
|
36,600 | 76,024 | 39,424 | |||||||||
|
|
|
|
|
|
|||||||
Loss from operations
|
(35,125 | ) | (74,844 | ) | (39,719 | ) | ||||||
|
|
|
|
|
|
|||||||
Other income (expense):
|
||||||||||||
Interest income
|
74 | 20 | (54 | ) | ||||||||
Interest expense
|
(704 | ) | (1,471 | ) | (767 | ) | ||||||
Change in fair value of warrant liability
|
(8 | ) | (1,343 | ) | (1,335 | ) | ||||||
|
|
|
|
|
|
|||||||
Total other income, net
|
(638 | ) | (2,794 | ) | (2,156 | ) | ||||||
|
|
|
|
|
|
|||||||
Net loss
|
$ | (35,763 | ) | $ | (77,638 | ) | $ | (41,875 | ) | |||
|
|
|
|
|
|
NINE MONTHS ENDED
SEPTEMBER 30, |
INCREASE /
(DECREASE)
|
|||||||||||
Dollars (in thousands)
|
2020
|
2021
|
||||||||||
Program expense
|
$ | 10,078 | $ | 25,671 | $ | 15,593 | ||||||
Personnel costs
|
14,014 | 24,924 | 10,910 | |||||||||
Other
|
4,809 | 11,486 | 6,677 | |||||||||
|
|
|
|
|
|
|||||||
Total research and development expenses
|
$ | 28,901 | $ | 62,081 | $ | 33,180 | ||||||
|
|
|
|
|
|
YEAR ENDED
DECEMBER 31,
|
INCREASE /
(DECREASE)
|
|||||||||||
Dollars (in thousands)
|
2019
|
2020
|
||||||||||
Collaboration Revenue
|
$ | 3,001 | $ | 962 | $ | (2,039 | ) | |||||
Grant Revenue
|
— | 785 | 785 | |||||||||
|
|
|
|
|
|
|||||||
Total Revenue
|
3,001 | 1,747 | (1,254 | ) | ||||||||
Operating Expenses:
|
||||||||||||
Research and development
|
23,489 | 42,866 | 19,377 | |||||||||
General and administrative
|
8,714 | 11,165 | 2,451 | |||||||||
|
|
|
|
|
|
|||||||
Total operating expenses
|
32,203 | 54,031 | 21,828 | |||||||||
|
|
|
|
|
|
|||||||
Loss from operations
|
(29,202 | ) | (52,284 | ) | (23,082 | ) | ||||||
|
|
|
|
|
|
|||||||
Other income (expense):
|
||||||||||||
Interest income
|
865 | 83 | (782 | ) | ||||||||
Interest expense
|
(317 | ) | (1,028 | ) | (711 | ) | ||||||
Change in fair value of warrant liability
|
5 | (22 | ) | (27 | ) | |||||||
|
|
|
|
|
|
|||||||
Total other income, net
|
553 | (967 | ) | (1,520 | ) | |||||||
|
|
|
|
|
|
|||||||
Net loss
|
$ | (28,649 | ) | $ | (53,251 | ) | $ | (24,602 | ) | |||
|
|
|
|
|
|
YEARS ENDED
DECEMBER 31, |
INCREASE /
(DECREASE)
|
|||||||||||
Dollars (in thousands)
|
2019
|
2020
|
||||||||||
Program expense
|
$ | 6,279 | $ | 16,368 | $ | 10,089 | ||||||
Personnel expense
|
12,407 | 19,645 | 7,238 | |||||||||
Facilities and other expense
|
4,803 | 6,853 | 2,050 | |||||||||
|
|
|
|
|
|
|||||||
Total research and development expenses
|
$ | 23,489 | $ | 42,866 | $ | 19,377 | ||||||
|
|
|
|
|
|
• |
the design, initiation, timing, costs, progress and results of our planned clinical trials;
|
• |
the progress of preclinical development and possible clinical trials of our current and future earlier-stage programs;
|
• |
the scope, progress, results and costs of our research programs and preclinical development of any additional product candidates that we may pursue;
|
• |
the development requirements of other product candidates that we may pursue;
|
• |
our headcount growth and associated costs as we expand our research and development and establish a commercial infrastructure;
|
• |
the timing and amount of milestone and royalty payments that we are required to make or eligible to receive under our current or future collaboration and license agreements;
|
• |
the outcome, timing and cost of meeting regulatory requirements established by the FDA, EPA and other regulatory authorities;
|
• |
the costs and timing of future commercialization activities, including product manufacturing, marketing, sales and distribution, for any of our product candidates for which we receive marketing approval;
|
• |
the cost of expanding, maintaining and enforcing our intellectual property portfolio, including filing, prosecuting, defending and enforcing our patent claims and other intellectual property rights;
|
• |
the cost of defending potential intellectual property disputes, including patent infringement actions brought by third parties against us or any of our product candidates;
|
• |
the effect of competing technological and market developments;
|
• |
the cost and timing of completion of commercial-scale manufacturing activities;
|
• |
the extent to which we partner our programs, acquire or
in-license other
product candidates and technologies or enter into additional collaborations;
|
• |
the revenue, if any, received from commercial sales of any future product candidates for which we receive marketing approval; and
|
• |
the costs of operating as a public company.
|
YEARS ENDED
DECEMBER 31, |
INCREASE /
(DECREASE) |
NINE MONTHS ENDED
SEPTEMBER 31, |
INCREASE /
(DECREASE) |
|||||||||||||||||||||
2019
|
2020
|
2020
|
2021
|
|||||||||||||||||||||
Net cash used in operating activities
|
$ | (25,636 | ) | $ | (46,599 | ) | $ | (20,963 | ) | $ | (29,971 | ) | $ | (67,241 | ) | $ | (37,270 | ) | ||||||
Net cash used in investing activities
|
(1,896 | ) | (10,047 | ) | (8,151 | ) | (7,502 | ) | (11,362 | ) | (3,860 | ) | ||||||||||||
Net cash provided by financing activities
|
13,316 | 125,848 | 112,532 | 126,039 | 18,376 | (107,663 | ) | |||||||||||||||||
|
|
|
|
|
|
|
|
|
|
|
|
|||||||||||||
Net increase (decrease) in cash, cash equivalents and restricted cash
|
$ | (14,216 | ) | $ | 69,202 | $ | 83,418 | $ | 88,566 | $ | (60,227 | ) | $ | (148,793 | ) | |||||||||
|
|
|
|
|
|
|
|
|
|
|
|
• |
the prices at which we sold shares of preferred stock and the superior rights and preferences of the preferred stock relative to our common stock at the time of each grant;
|
• |
the progress of our research and development programs, including the status and results of our product candidates;
|
• |
our stage of development and commercialization and our business strategy;
|
• |
external market conditions affecting the biotechnology industry and trends within the biotechnology industry;
|
• |
our financial position, including cash on hand, and our historical and forecasted performance and operating results;
|
• |
the lack of an active public market for our common stock and our preferred stock;
|
• |
the likelihood of achieving a liquidity event given prevailing market conditions; and
|
• |
the analysis of IPOs and the market performance of similar companies in the biotechnology industry.
|
• |
Dr. Andrey Zarur, President and Chief Executive Officer
|
• |
Carole B. Cobb, Chief Operating Officer
|
• |
Susan E. Keefe, Chief Financial Officer
|
Name and principal position
|
Year
|
Salary
($) |
Option
awards
($)
(1)
|
Non-equity
incentive plan compensation
($)
(2)
|
All other
compensation
(3)
|
Total
($) |
||||||||||||||||||
Dr. Andrey Zarur
President and Chief Executive Officer |
2020 | 450,000 | $ | 1,146,000 |
(4)
|
180,000 | 285 | 1,776,285 | ||||||||||||||||
Carole B. Cobb
Chief Operating Officer |
2020 | 350,000 | 196,000 | 105,000 | 285 | 651,285 | ||||||||||||||||||
Susan E. Keefe
Chief Financial Officer |
2020 | 325,000 | 340,000 | 97,500 | 285 | 762,785 |
(1) |
In accordance with SEC rules, this column reflects the aggregate grant date fair value of the stock option awards granted during the year ended December 31, 2020, computed in accordance with FASB ASC 718. These amounts do not reflect the actual economic value that will be realized by the named executive officer upon the vesting of the stock options, the exercise of the stock options, or the sale of the shares underlying such stock options. For a description of the determination of the fair value of the stock option awards, see “
GreenLight’s Management’s Discussion and Analysis of Financial Condition and Results of Operations — Critical Accounting Policies and Significant Judgments and Estimates — Determination of the Fair Value of Common Stock” and Note 14 to GreenLight’s audited consolidated financial statements contained elsewhere in this proxy statement/prospectus
Outstanding Equity Awards at December 31, 2020,
—Employment Arrangements with Officers
—GreenLight 2012 Stock Incentive Plan
|
(2) |
These amounts represent performance-based cash bonuses based upon the achievement of goals for 2020, which were earned in 2020 and paid in 2021. GreenLight’s bonus program is more fully described below under the section titled “
—Non-Equity
Incentive Plan Compensation
|
(3) |
These amounts represent life insurance premiums paid by GreenLight for the benefit of the named executive officers.
|
(4) |
In the year ended December 31, 2020, Dr. Zarur received two stock option awards, one of which is a performance-based award and one of which is a service-based award. At the date of grant, achievement of the conditions in the performance-based award was deemed not probable and, accordingly, the grant date fair value of the award was zero based upon the probable outcome of such conditions. Assuming achievement of the highest level of performance, the performance-based award would have had a grant date fair value of $162,681. Accordingly, the value reflected in the table represents only the grant date fair value of the service-based award.
|
Name
|
2021 Base
Salary |
|||
Dr. Andrey Zarur
|
$ | 500,000 | ||
Carole B. Cobb
|
$ | 425,000 | ||
Susan E. Keefe
|
$ | 380,000 |
Name
|
2021 Target
Bonus Amount |
|||
Dr. Andrey Zarur
|
50 | % | ||
Carole B. Cobb
|
40 | % | ||
Susan E. Keefe
|
40 | % |
(1) |
All of the outstanding stock option awards were granted under and subject to the terms of the GreenLight 2012 equity plan, described below under “
—
|
(2) |
The stock option awards were granted with a per share exercise price equal to the fair market value of one share of GreenLight Common Stock on the date of grant, as determined in good faith by the GreenLight Board.
|
(3) |
The stock option award vests as to 20% of the total number of shares subject to the award on the first anniversary of the vesting start date (which in some cases precedes the date of grant), and the remainder vests in 48 equal monthly installments thereafter.
|
(4) |
The stock option award is subject to performance-based vesting conditions. The award will vest as described in footnote (5) below, provided that GreenLight consummates a specified new investment (which for this purpose includes the Business Combination) by December 31, 2021.
|
(5) |
The stock option award vests as to 25% of the total number of shares subject to the award on the first anniversary of the vesting start date (which in some cases precedes the date of grant), and the remainder vests in 36 equal monthly installments thereafter.
|
• |
provide that such stock options will be assumed, or equivalent stock options substituted, by the acquiring or succeeding corporation (or an affiliate thereof);
|
• |
upon written notice to the optionees, provide that all unexercised stock options will terminate immediately prior to the consummation of the change in control transaction unless exercised by the optionee to the extent otherwise then exercisable within a specified period following the date of such notice;
|
• |
upon written notice to the grantees, provide that all unvested shares of restricted stock will be repurchased at cost;
|
• |
make or provide for a cash payment to the optionees equal to the difference between (x) the fair market value of the per share consideration (whether cash, securities or other property or any combination thereof) the holder of a GreenLight Common Share will receive upon consummation of the change in control transaction times the number of GreenLight Common Stock subject to outstanding vested stock options (to the extent then exercisable at prices not equal to or in excess of such per share consideration) and (y) the aggregate exercise price of such outstanding vested stock options, in exchange for the termination of such stock options; or
|
• |
provide that all or any outstanding stock options will become exercisable and all or any outstanding restricted stock awards will vest in part or in full immediately prior to the change in control transaction. To the extent that any stock options are exercisable at a price equal to or in excess of the per share consideration in the change in control transaction, the GreenLight Board may provide that such stock options will terminate immediately upon the consummation of the change in control transaction without any payment being made to the holders of such stock options.
|
Name
|
Fees earned or
paid in cash
($)
|
Total
($)
|
||||||
Dr. Charles Cooney
(1)
|
75,000 | 75,000 | ||||||
Jason Dinges
|
— | — | ||||||
Mike Liang
|
— | — | ||||||
Dr. Ganesh Kishore
|
— | — | ||||||
Eric O’Brien
|
— | — | ||||||
Dr. Martha Schlicher
(2)
|
50,000 | 50,000 | ||||||
Neil Renninger
(3)
|
39,583 | 39,583 |
(1) |
At December 31, 2020, Dr. Cooney held 10,004 shares of restricted stock acquired upon the early exercise of a stock option granted prior to 2020. These share vest in 11 equal monthly installments of 833 shares and a final installment of 841 shares.
|
(2) |
At December 31, 2020, Dr. Schlicher held 7,461 shares of restricted stock acquired upon the early exercise of a stock option granted prior to 2020. These shares vest in two parts: (a) 1,461 shares vest in 13 equal monthly installments of 104 shares and a final installment of 109 shares and (b) 6,000 shares vest in three equal annual installments, the first of which vested on June 24, 2021.
|
(3) |
During the year ended December 31, 2020, Mr. Renninger served as a member of the GreenLight Board until June 2020.
|
• |
$ per year for service as a
non-employee
director (other than the chair);
|
• |
$ per year for service as
non-employee
chair of the New GreenLight Board;
|
• |
$ per year for service as chair of the New GreenLight audit committee;
|
• |
$ per year for service as a member of the New GreenLight audit committee (other than the chair);
|
• |
$ per year for service as chair of the New GreenLight talent and compensation committee;
|
• |
$ per year for service as a member of the New GreenLight talent and compensation committee (other than the chair);
|
• |
$ per year for service as chair of the New GreenLight nominating and corporate governance committee; and
|
• |
$ per year for service as a member of the New GreenLight nominating and corporate governance committee (other than the chair).
|
Name
|
Age
|
Position
|
||
Executive Officers
|
||||
Andrey J. Zarur, Ph.D. | 51 |
Chief Executive Officer, President and Class III Director-Nominee
|
||
Carole Cobb, M.B.A. | 64 | Chief Operating Officer | ||
Charu Manocha, M.B.A. | 55 | Chief People Officer | ||
Marta Ortega-Valle, M.B.A. | 49 | Chief Business Officer, Human Health | ||
Susan Keefe, M.B.A | 49 | Chief Financial Officer | ||
David Kennedy | 60 | General Counsel | ||
Amin Khan, Ph.D. | 59 | Chief Scientific Officer | ||
Mark Singleton, Ph.D. | 54 | Senior Vice President of Technology | ||
Non-Employee
Directors
|
||||
Charles Cooney | 76 | Class III Director-Nominee | ||
Ganesh Kishore | 68 | Class III Director-Nominee | ||
Eric O’Brien | 49 | Class I Director-Nominee | ||
Matthew Walker | 39 | Class II Director-Nominee |
• |
select, retain, compensate, evaluate, oversee and, where appropriate, terminate New GreenLight’s independent registered public accounting firm;
|
• |
review and approve the scope and plans for the audits and the audit fees and approve all
non-audit
and tax services to be performed by the independent registered public accounting firm;
|
• |
evaluate the independence and qualifications of New GreenLight’s independent registered public accounting firm;
|
• |
review New GreenLight’s financial statements, and discuss with management and New GreenLight’s independent registered public accounting firm the results of the annual audit and the quarterly reviews;
|
• |
review and discuss with management and New GreenLight’s independent registered public accounting firm the quality and adequacy of New GreenLight’s internal controls and New GreenLight’s disclosure controls and procedures;
|
• |
discuss with management New GreenLight’s procedures regarding the presentation of New GreenLight’s financial information, and review earnings press releases and guidance;
|
• |
oversee the design, implementation and performance of New GreenLight’s internal audit function, if any;
|
• |
set hiring policies with regard to the hiring of employees and former employees of New GreenLight’s independent registered public accounting firm and oversee compliance with such policies;
|
• |
review, approve and monitor related party transactions;
|
• |
review and monitor compliance with New GreenLight’s Code of Business Conduct and Ethics and consider questions of actual or possible conflicts of interest of New GreenLight’s directors and officers;
|
• |
adopt and oversee procedures to address complaints regarding accounting, internal accounting controls and auditing matters, including confidential, anonymous submissions by New GreenLight’s employees of concerns regarding questionable accounting or auditing matters;
|
• |
review and discuss with management and New GreenLight’s independent registered public accounting firm the adequacy and effectiveness of New GreenLight’s legal, regulatory and ethical compliance programs; and
|
• |
review and discuss with management and New GreenLight’s independent registered public accounting firm New GreenLight’s guidelines and policies to identify, monitor and address enterprise risks.
|
• |
review and approve or recommend to the New GreenLight Board for approval the compensation for New GreenLight’s executive officers, including New GreenLight’s chief executive officer;
|
• |
review, approve and administer New GreenLight’s employee benefit and equity incentive plans;
|
• |
advise the New GreenLight Board on stockholder proposals related to executive compensation matters;
|
• |
establish and review the compensation plans and programs of New GreenLight’s employees, and ensure that they are consistent with New GreenLight’s general compensation strategy;
|
• |
oversee the management of risks relating to executive compensation plans and arrangements;
|
• |
monitor compliance with any stock ownership guidelines;
|
• |
approve the creation or revision of any clawback policy;
|
• |
review and approve or recommend to the New GreenLight Board for approval
non-employee
director compensation;
|
• |
review executive compensation disclosure in New GreenLight’s SEC filings and prepare the compensation committee report required to be included in New GreenLight’s annual proxy statement.
|
• |
review, assess and make recommendations to the New GreenLight Board regarding desired qualifications, expertise and characteristics sought of board members;
|
• |
identify, evaluate, select or make recommendations to the New GreenLight Board regarding nominees for election to the New GreenLight Board;
|
• |
develop policies and procedures for considering stockholder nominees for election to the New GreenLight Board;
|
• |
review New GreenLight’s succession planning process for New GreenLight’s chief executive officer and any other members of New GreenLight’s executive management team;
|
• |
review and make recommendations to the New GreenLight Board regarding the composition, organization and governance the New GreenLight Board and its committees;
|
• |
review and make recommendations to the New GreenLight Board regarding New GreenLight’s corporate governance guidelines and corporate governance framework;
|
• |
oversee director orientation for new directors and continuing education for New GreenLight’s directors;
|
• |
oversee New GreenLight’s Environmental, Social and Governance (“
ESG
”) programs and related disclosures and communications;
|
• |
oversee the evaluation of the performance of the New GreenLight Board and its committees; and
|
• |
administer policies and procedures for communications with the
non-management
members of the New GreenLight Board.
|
• |
each person who is the beneficial owner of more than 5% of the outstanding GreenLight Common Stock and GreenLight Preferred Stock on an
as-converted
basis;
|
• |
each of GreenLight’s directors and named executive officers; and
|
• |
all directors and executive officers of GreenLight, as a group.
|
* |
Less than 1%.
|
(1) |
Beneficial ownership of shares of GreenLight Common Stock and GreenLight Preferred Stock is based on (a) 3,535,943 shares of GreenLight Common Stock and (b) 134,952,637 shares of GreenLight Preferred Stock, which are convertible into an aggregate of 141,405,233 shares of GreenLight Common Stock, which includes (1) 2,807,571 shares of GreenLight
Series A-1
Preferred Stock, which are convertible into an aggregate of 3,550,068 shares of GreenLight Common Stock, (2) 6,993,693 shares of GreenLight Series A-2 Preferred Stock, which are convertible into an aggregate of 9,058,757 shares of GreenLight Common Stock, (3) 8,629,505 shares of GreenLight
Series A-3
Preferred Stock, which are convertible into an aggregate of 12,274,540 shares of GreenLight Common Stock, (4) 21,245,353 shares of GreenLight Series B Preferred Stock, which are convertible into an aggregate of 21,245,353 shares of GreenLight Common Stock, (5) 35,092,183 shares of GreenLight Series C Preferred Stock, which are convertible into an aggregate of 35,092,183 shares of GreenLight Common Stock, and (6) 60,184,332 shares of GreenLight Series D Preferred Stock, which are convertible into an aggregate of 60,184,332 shares of GreenLight Common Stock, in each case issued and outstanding as of the Ownership Date.
|
(2) |
Includes (a) 3,135,582 shares of GreenLight Series C Preferred Stock held by S2G Ventures Fund I, L.P., (b)(1) 4,086,398 shares of GreenLight Series B Preferred Stock, (2) 3,135,583 shares of GreenLight Series C Preferred Stock, (3) 3,863,561 shares of GreenLight Series D Preferred Stock and (4) 1,800,925 shares of GreenLight Series D Preferred Stock issuable upon conversion of a GreenLight Convertible Note having an aggregate principal amount of $3,000,000 plus accrued interest through December 31, 2021 of $262,917, in each case held by S2G Ventures Fund II, L.P.; and (c) 5,519,372 shares of GreenLight Series D Preferred Stock held by S2G Ventures Fund III, L.P. (together with S2G Ventures Fund I, L.P. and S2G Ventures Fund II, L.P., “
S2G Ventures
”). The General Partner of S2G Ventures Fund I, L.P. is S2G Ventures, LLC. The General Partner of S2G Ventures Fund II, L.P. is S2G Ventures II, LLC. The General Partner of S2G Ventures Fund III, L.P. is S2G Ventures III, LLC.
|
Mr. Matthew Walker, a director of GreenLight and a director-nominee of New GreenLight, is a Managing Director at S2G Ventures. Each of S2G Ventures, LLC, S2G Ventures II, LLC and Builders Vision, LLC has the power to vote or direct the voting of the shares of GreenLight Stock held by the S2G Ventures fund managed. By virtue of the foregoing, each of S2G Ventures LLC, S2G Ventures II, LLC and Builders Vision, LLC may be deemed to indirectly beneficially own (as that term is defined in Rule 13d-3 of the Exchange Act) the shares of GreenLight Stock held by the S2G Ventures fund managed. Mr. Walker disclaims beneficial ownership of these shares of GreenLight Stock except to the extent of any pecuniary interest therein. The business address for S2G Ventures (other than S2G Builders Food & Agriculture Fund III, L.P.) is PO Box 1860, Bentonville, AR 72712. The address for S2G Builders Food & Agriculture Fund III, L.P. is 9218 Metcalf Ave. #238, Overland Park, KS 66212. |
(3) |
Includes 19,317,805 shares of GreenLight Series D Preferred Stock held by Morningside Venture Investments Limited (“
Morningside
”). Frances Anne Elizabeth Richard, Jill Marie Franklin, Peter Stuart Allenby Edwards and Cheung Ka Ho are the directors of Morningside and have shared voting power over the securities held by Morningside. Each of these individuals disclaims beneficial ownership of the shares owned by Morningside. The address of Morningside is c/o THC Management Services S.A.M., 2nd Floor, Le Prince de Galles, 3-5 Avenue des Citronniers, MC 98000, Monaco.
|
(4) |
Includes (a)(1) 3,464,397 shares of GreenLight Series
A-1
Preferred Stock, (2) 1,831,756 shares of GreenLight Series
A-2
Preferred Stock, (3) 2,277,432 shares of GreenLight Series
A-3
Preferred Stock, (4) 4,055,242 shares of GreenLight Series B Preferred Stock and (5) 2,753,920 shares of GreenLight Series C Preferred Stock, in each case held by Kodiak Venture Partners III, L.P., and (b)(1) 85,671 shares of GreenLight Series
A-1
Preferred Stock, (2) 45,299 shares of GreenLight Series
A-2
Preferred Stock, (3) 56,319 shares of GreenLight Series
A-3
Preferred Stock, (4) 100,283 shares of GreenLight Series B Preferred Stock and (5) 68,104 shares of GreenLight Series C Preferred Stock, in each case held by Kodiak III Entrepreneurs Fund, L.P. (together with Kodiak Venture Partners III, L.P. “Kodiak”). Kodiak Ventures Management III, L.P. (“
Kodiak Ventures
”) is the General Partner for Kodiak, Kodiak Venture Management (GP), LLC is the General Partner for Kodiak Ventures and Kodiak Ventures Management Company, Inc. is the Member of Kodiak Ventures Management (GP), LLC. Mr. David Furneaux is the Chief Executive Officer of Kodiak Ventures Management Company, Inc.. Each therefore has the power to vote, or direct the voting of, the shares of GreenLight Stock held by Kodiak. By virtue of the foregoing, each of Kodiak, Kodiak Ventures, Kodiak Ventures Management (GP), LLC, Kodiak Ventures Management Company, Inc. and Mr. Furneaux may be deemed to indirectly beneficially own (as that term is defined in Rule 13d-3 of the Exchange Act) the shares of GreenLight Stock held by Kodiak. Mr. Furneaux disclaims beneficial ownership of these shares of GreenLight Stock except to the extent of any pecuniary interest therein. The business address for Kodiak and Mr. Furneaux is P.O. Box 550225, Waltham, MA 02455.
|
(5) |
Includes (a) 4,670,169 shares of GreenLight Series B Preferred Stock, (b) 3,135,583 shares of GreenLight Series C Preferred Stock, (c) 3,311,623 shares of GreenLight Series D Preferred Stock and (d) 1,200,004 shares of GreenLight Series D Preferred Stock issuable upon conversion of a GreenLight Convertible Note having any aggregate principal amount of $2,000,000 and accrued but unpaid interest of $174,167 through December 31, 2021, in each case held by Fall Line Endurance Fund, LP (“
Fall Line
”). Mr. Eric O’Brien, a director of GreenLight, is the
co-founder
and Managing Director of Fall Line and has the power to vote, or to direct the voting of, the shares of GreenLight Stock held by Fall Line. By virtue of the foregoing, Mr. O’Brien may be deemed to indirectly beneficially own (as that term is defined in Rule
13d-3
of the Exchange Act) the shares of GreenLight Stock held by Fall Line. Mr. O’Brien disclaims beneficial ownership of these shares of GreenLight Stock except to the extent of any pecuniary interest therein. The business address of Fall Line and Mr. O’Brien is 119 South B Street, Suite B, San Mateo, CA 94401.
|
(6) |
Includes (a) 3,680,982 shares of GreenLight Series
A-3
Preferred Stock, (b) 1,962,964 shares of GreenLight Series B Preferred Stock, (c) 1,881,350 shares of GreenLight Series C Preferred Stock and (d) 1,103,874 shares of GreenLight Series D Preferred Stock, in each case held by MLS Capital Fund II, LP (“
MLS
”). Mr. Kishore, a director of GreenLight, is the Manager of MLS and has the power to vote, or to direct the voting of, the shares of GreenLight Stock held by MLS. By virtue of the foregoing, Mr. Kishore may be deemed to indirectly beneficially own (as that term is defined in Rule
13d-3
of the Exchange Act) the shares of GreenLight Stock held by MLS. Mr. Kishore disclaims beneficial ownership of these shares of
|
GreenLight Stock except to the extent of any pecuniary interest therein. The business address of MLS and Mr. Kishore is 100 Montgomery Street, Suite 2190, San Francisco, CA 94104. |
(7) |
Includes (a)(1) 308,284 shares of GreenLight Series C Preferred Stock, (2) 203,495 shares of GreenLight Series D Preferred Stock and (3) 104,177 shares of GreenLight Series D Preferred Stock issuable upon conversion of a GreenLight Convertible Note having an aggregate principal amount of $174,006 and accrued but unpaid interest of $14,742 as of December 31, 2021, in each case held by BVP V Affiliates Fund Limited Partnership, (b)(1) 327,367 shares of GreenLight Series C Preferred Stock, (2) 216,090 shares of GreenLight Series D Preferred Stock and (3) 98,105 shares of GreenLight Series D Preferred Stock issuable upon conversion of a GreenLight Convertible Note having an aggregate principal amount of $163,864 and accrued but unpaid interest of $13,883 as of December 31, 2021, in each case held by BVP V Special Affiliates Limited Partnership, and (c)(1) 3,127,048 shares of GreenLight Series C Preferred Stock, (2) 2,064,131 shares of GreenLight Series D Preferred Stock and (3) 995,115 shares of GreenLight Series D Preferred Stock issuable upon conversion of a GreenLight Convertible Note having an aggregate principal amount of $1,662,130 and accrued but unpaid interest of $140,819 as of December 31, 2021, in each case held by Baird Venture Partners V Limited Partnership (together with BVP V Affiliates Fund Limited Partnership and BVP V Special Affiliates Limited Partnership, “
Baird
”). Mr. Michael Liang, a director of GreenLight, is the Director of Baird and has the power to vote, or to direct the voting of, the shares of GreenLight Stock held by Baird. By virtue of the foregoing, Mr. Liang may be deemed to indirectly beneficially own (as that term is defined in Rule
13d-3
of the Exchange Act) the shares of GreenLight Stock held by Baird. Mr. Liang disclaims beneficial ownership of these shares of GreenLight Stock except to the extent of any pecuniary interest therein. The business address of Baird and Mr. Liang is 277 W. Monroe St., Suite 1900, Chicago, IL 60606.
|
(8) |
Unless otherwise noted, the business address of each of the directors and named executive officers of GreenLight is 200 Boston Avenue, Suite 3100, Medford, MA 02155.
|
(9) |
Mr. Jason Dinges, an investment professional and intellectual property counsel at Morningside Technology Advisory LLC, disclaims beneficial ownership of shares held by Morningside as described in footnote 3.
|
(10) |
Includes (a) 1,223,651 shares of GreenLight Common Stock, (b) 3,747,548 shares of GreenLight Common Stock subject to GreenLight Options exercisable within 60 days of the Ownership Date and (c) 122,591 shares of GreenLight Common Stock issuable upon conversion of 122,591 shares of GreenLight Series B Preferred Stock.
|
(11) |
Includes 1,959,231 shares of GreenLight Common Stock subject to GreenLight Options exercisable within 60 days of the Ownership Date.
|
(12) |
Includes 609,376 shares of GreenLight Common Stock subject to GreenLight Options exercisable within 60 days of the Ownership Date.
|
• |
each person who is known to be the beneficial owner of more than 5% of ENVI Class A Common Stock and is expected to be the beneficial owner of more than 5% of shares of New GreenLight Common Stock post-Business Combination;
|
• |
each of ENVI’s current executive officers and directors;
|
• |
each person who will become an executive officer or director of New GreenLight post-Business Combination; and
|
• |
all executive officers and directors of ENVI as a group pre-Business Combination, and all executive officers and directors of New GreenLight post-Business Combination.
|
• |
a “No Redemption” scenario where (i) no holders of ENVI Class A Common Stock exercise their redemption rights in connection with the Business Combination and (ii) 103,470,217 shares of New GreenLight Common Stock are issued to equityholders of GreenLight in connection with the Merger; and
|
• |
a “Maximum Redemption” scenario where 20,375,179 shares of ENVI Class A Common Stock are redeemed in connection with the Business Combination for an aggregate payment of approximately $203.8 million (based on the estimated per share redemption price of approximately $10.00 per share) from the Trust Account, which represents the estimated maximum number of redemptions that could occur without a failure to satisfy the Aggregate Transaction Proceeds Condition.
|
Pre-Business Combination and PIPE Financing
|
Post-Business Combination and PIPE
Financing
|
|||||||||||||||||||||||||||||||
Maximum
|
||||||||||||||||||||||||||||||||
No Redemptions
|
Redemptions
|
|||||||||||||||||||||||||||||||
Name and Address of
Beneficial Owner |
# of
Shares of
ENVI Class A Common Stock |
% of ENVI
Class A Common Stock |
# of
Shares of
ENVI Class B Common Stock |
% of
ENVI Class B Common Stock |
# of
Shares of
New GreenLight Common Stock |
% of New
GreenLight Common Stock |
# of
Shares of
New
GreenLight
Common Stock |
% of New
GreenLight Common Stock |
||||||||||||||||||||||||
5% or Greater Holders of ENVI
|
||||||||||||||||||||||||||||||||
Canaccord Genuity Group Inc.
(1)
|
— | — | 1,552,500 | 30.0 | % | 1,552,500 | 1.1 | % | 1,552,500 | 1.3 | % | |||||||||||||||||||||
HB Strategies LLC
(2)
|
1,000,000 | 4.8 | % | 3,105,000 | 60.0 | % | 4,105,000 | 2.9 | % | 3,105,000 | 2.6 | % | ||||||||||||||||||||
Highbridge Funds
(3)
|
1,792,381 | 8.7 | % | — | — | 1,792,381 | * | — | — | |||||||||||||||||||||||
Directors and Officers of ENVI
(4)
|
||||||||||||||||||||||||||||||||
Daniel Coyne
|
— | — | — | — | — | — | — | — | ||||||||||||||||||||||||
Marc Marano
|
— | — | — | — | — | — | — | — |
Pre-Business Combination and PIPE
Financing |
Post-Business Combination and PIPE
Financing
|
|||||||||||||||||||||||||||||||
Maximum
|
||||||||||||||||||||||||||||||||
No Redemptions
|
Redemptions
|
|||||||||||||||||||||||||||||||
Name and Address of Beneficial
Owner |
# of
Shares
of ENVI Class A Common Stock |
% of ENVI
Class A Common Stock |
# of
Shares of
ENVI Class B Common Stock |
% of
ENVI Class B Common Stock |
# of
Shares of
New GreenLight Common Stock |
% of New
GreenLight Common Stock |
# of
Shares of
New
GreenLight
Common Stock |
% of New
GreenLight Common Stock |
||||||||||||||||||||||||
Andrew Viles
|
— | — | — | — | — | — | — | — | ||||||||||||||||||||||||
Jennifer Pardi
|
— | — | — | — | — | — | — | — | ||||||||||||||||||||||||
Deval Patrick
|
— | — | 172,500 | 3.3 | % | 172,500 | * | 172,500 | * | |||||||||||||||||||||||
David Brewster
|
— | — | 172,500 | 3.3 | % | 172,500 | * | 172,500 | * | |||||||||||||||||||||||
Dean Seavers
|
— | — | 172,500 | 3.3 | % | 172,500 | * | 172,500 | * | |||||||||||||||||||||||
All directors and executive officers as a
group (seven individuals)
|
— | — | 517,500 | 10.0 | % | 517,500 | * | 517,500 | * | |||||||||||||||||||||||
5% or Greater Holders of New
GreenLight
|
||||||||||||||||||||||||||||||||
S2G Ventures
(5)
|
— | — | — | — | 15,776,001 | 11.2 | % | 15,776,001 | 13.1 | % | ||||||||||||||||||||||
Morningside Venture Investments Limited
(6)
|
— | — | — | — | 13,802,359 | 9.8 | % | 13,802,359 | 11.4 | % | ||||||||||||||||||||||
Kodiak Venture Partners
(7)
|
— | — | — | — | 9,767,496 | 6.9 | % | 9,767,496 | 8.1 | % | ||||||||||||||||||||||
Fall Line Endurance Fund, LP
(8)
|
— | — | — | — | 8,863,014 | 6.3 | % | 8,863,014 | 7.3 | % | ||||||||||||||||||||||
Directors and Officers of New
GreenLight
(9)
|
— | — | — | — | ||||||||||||||||||||||||||||
Matthew Walker
(5)
|
— | — | — | — | 15,776,001 | 11.2 | % | 15,776,001 | 13.1 | % | ||||||||||||||||||||||
Eric O’Brien
(8)
|
— | — | — | — | 8,863,014 | 6.3 | % | 8,863,014 | 7.3 | % | ||||||||||||||||||||||
Ganesh Kishore
(10)
|
— | — | — | — | 5,793,752 | 4.1 | % | 5,793,752 | 4.8 | % | ||||||||||||||||||||||
Dr. Andrey Zarur
(11)
|
— | — | — | — | 3,375,773 | 2.3 | % | 3,375,773 | 2.7 | % | ||||||||||||||||||||||
Carole Cobb
(12)
|
— | — | — | — | 1,298,428 | * | 1,298,428 | 1.1 | % | |||||||||||||||||||||||
Charles Cooney
|
— | — | — | — | 303,994 | * | 303,994 | * | ||||||||||||||||||||||||
Susan E. Keefe
(13)
|
— | — | — | — | 403,848 | * | 403,848 | * | ||||||||||||||||||||||||
All directors and executive officers as a group
(9 individuals)
|
— | — | — | — |
* |
Less than 1%.
|
(1) |
Held directly by CG Investments Inc. VI, our sponsor and excludes 600,000 Insider Warrants owned by the Sponsor. Canaccord Genuity Group Inc. is the sole shareholder of our sponsor CGGI and an affiliate of Canaccord. Canaccord Genuity Group Inc. CGGI disclaims beneficial ownership over any securities directly held by our sponsor other than to the extent of any pecuniary interest it may have therein, directly or indirectly. The business address for Canaccord Genuity Group Inc. is 535 Madison Avenue, New York, New York 10022.
|
(2) |
Excludes 2,000,000 private placement warrants, 500,000 public warrants and 600,000 shares of ENVI Class A Common Stock to be purchased by Tech Opportunities LLC, an affiliate of Hudson Bay Capital Management, LP (“
Hudson Bay
”) in connection with the PIPE Financing. Hudson Bay is the investment manager of HB Strategies LLC and has voting and investment power over these securities. Sander Gerber is the managing member of Hudson Bay Capital GP LLC, which is the general partner of Hudson Bay. Each of HB Strategies LLC and Mr. Gerber disclaims beneficial ownership over these securities. The business address for HB Strategies LLC is c/o Hudson Bay Capital Management LP, 28 Havemeyer Place, 2nd Floor Greenwich CT 06830.
|
(3) |
Based on publicly available information and the Schedule 13G filed by Highbridge Capital Management, LLC, as the trading manager of Highbridge Tactical Credit Master Fund, L.P. and Highbridge SPAC Oportunity Fund, L.P. (collectively, the “
Highbridge Funds
”). The business address of Highbridge Capital Management, LLC is 277 Park Avenue, 23rd Floor, New York, New York 10172 and the business address of the Highbridge Funds is c/o Maples Corporate Services Limited, PO Box 309, Ugland House, South Church Street, George Town, Grand Cayman KY1-1104, Cayman Islands.
|
(4) |
Unless otherwise noted, the business address of each of the following entities or individuals is c/o Environmental Impact Acquisition Corp., 535 Madison Avenue, New York, New York 10022.
|
(5) |
Includes (a) 2,078,023 shares held by S2G Ventures Fund I, L.P., (b) 8,540,162 shares held by S2G Ventures Fund II, L.P.; (c) 3,657,816 shares held by S2G Ventures Fund III, L.P.; and (d) 1,500,000 shares held by S2G Builders Food & Agriculture Fund I, L.P. The General Partner of S2G Ventures Fund I, L.P. is S2G Ventures, LLC. The General Partner of S2G Ventures Fund II, L.P. is S2G Ventures II, LLC. The General Partner of S2G Ventures Fund III, L.P. is S2G Ventures III, LLC. The General Partner of S2G Builders Food & Agriculture III, L.P. is Builders Vision, LLC. Mr. Matthew Walker, a director of GreenLight and a
director-nominee
of New GreenLight, is a Managing Director at S2G Ventures. Each of S2G Ventures, LLC, S2G Ventures II, LLC, S2G Ventures III, LLC and Builders Vision, LLC has the power to vote or direct the voting of the shares of GreenLight Stock held by the respective S2G Ventures fund managed. By virtue of the foregoing, each of S2G Ventures LLC, S2G Ventures II, LLC, S2G Ventures III, LLC and Builders Vision, LLC may be deemed to indirectly beneficially own (as that term is defined in Rule 13d-3 of the Exchange Act) the shares of GreenLight Stock held by the respective S2G Ventures fund managed. Mr. Walker disclaims beneficial ownership of these shares of GreenLight Stock except to the extent of any pecuniary interest therein. The business address for S2G Ventures (other than S2G Builders Food & Agriculture Fund III, L.P.) is PO Box 1860, Bentonville, AR 72712. The address for S2G Builders Food & Agriculture Fund III, L.P. is 9218 Metcalf Ave. #238, Overland Park, KS 66212.
|
(6) |
Represents shares held by Morningside Venture Investments Limited (“
Morningside
”). Frances Anne Elizabeth Richard, Jill Marie Franklin, Peter Stuart Allenby Edwards and Cheung Ka Ho are the directors of Morningside and have shared voting power over the securities held by Morningside. Each of these individuals disclaims beneficial ownership of the shares owned by Morningside. The address of Morningside is c/o THC Management Services S.A.M., 2nd Floor, Le Prince de Galles, 3-5 Avenue des Citronniers, MC 98000, Monaco.
|
(7) |
Includes (a) 235,715 shares held by Kodiak Venture Partners III, L.P., and (b) 9,531,781 shares held by Kodiak III Entrepreneurs Fund, L.P. (together with Kodiak Venture Partners III, L.P. “
Kodiak
”). Kodiak Ventures Management III, L.P. (“
Kodiak Ventures
”) is the General Partner for Kodiak, Kodiak Venture Management (GP), LLC is the General Partner for Kodiak Ventures and Kodiak Ventures Management Company, Inc. is the Member of Kodiak Ventures Management (GP), LLC. Mr. David Furneaux is the Chief Executive Officer of Kodiak Ventures Management Company, Inc. Each therefore has the power to vote, or direct the voting of, the shares of GreenLight Stock held by Kodiak. By virtue of the foregoing, each of Kodiak Venture Partners and Mr. Furneaux may be deemed to indirectly beneficially own (as that term is defined in Rule 13d-3 of the Exchange Act) the shares of GreenLight Stock held by Kodiak. Mr. Furneaux disclaims beneficial ownership of these shares of GreenLight Stock except to the extent of any pecuniary interest therein. The business address for Kodiak and Mr. Furneaux is P.O. Box 550225, Waltham, MA 02455.
|
(8) |
Represents shares held by Fall Line Endurance Fund, LP (“
Fall Line
”). Mr. Eric O’Brien, a director of GreenLight, is the co-founder and Managing Director of Fall Line and has the power to vote, or to direct the voting of, the shares of GreenLight Stock held by Fall Line. By virtue of the foregoing, Mr. O’Brien may be deemed to indirectly beneficially own (as that term is defined in Rule 13d-3 of the Exchange Act) the shares of GreenLight Stock held by Fall Line. Mr. O’Brien disclaims beneficial ownership of these shares of GreenLight Stock except to the extent of any pecuniary interest therein. The business address of Fall Line and Mr. O’Brien is 119 South B Street, Suite B, San Mateo, CA 94401.
|
(9) |
Unless otherwise noted, the business address of each of the directors and named executive officers of GreenLight is 200 Boston Avenue, Suite 3100, Medford, MA 02155.
|
(10) |
Represents shares held by MLS. Mr. Kishore, a director of GreenLight, is the Manager of MLS and has the power to vote, or to direct the voting of, the shares held by MLS. By virtue of the foregoing, Mr. Kishore
|
may be deemed to indirectly beneficially own (as that term is defined in Rule 13d-3 of the Exchange Act) the shares held by MLS. Mr. Kishore disclaims beneficial ownership of these shares except to the extent of any pecuniary interest therein. The business address of MLS and Mr. Kishore is 100 Montgomery Street, Suite 2190, San Francisco, CA 94104. |
(11) |
Includes (a) 892,186 shares and (b) 2,483,587 shares subject to New GreenLight Options exercisable within 60 days of the Ownership Date.
|
(12) |
Represents shares subject to New GreenLight Options exercisable within 60 days of the Ownership Date.
|
(13) |
Represents shares subject to New GreenLight Options exercisable within 60 days of the Ownership Date.
|
• |
the amounts involved exceeded or will exceed the lesser of $120,000 or 1% of the average of ENVI or GreenLight’s total assets, as applicable, at
year-end
for the last two completed fiscal years; and
|
• |
a director, executive officer, holder of more than 5% of the outstanding capital stock of ENVI or GreenLight, or any member of such person’s immediate family had or will have a direct or indirect material interest.
|
Name
|
GreenLight
Convertible Note Principal Amount |
Total Purchase
Price |
||||||
S2G Ventures Fund II, L.P.
(1)
|
$ | 3,000,000 | $ | 3,000,000 | ||||
Fall Line Endurance Fund, LP
(2)
|
$ | 2,000,000 | $ | 2,000,000 | ||||
Baird Venture Partners V Limited Partnership
(3)
|
$ | 1,662,130 | $ | 1,662,130 | ||||
BVP V Affiliates Fund Limited Partnership
(3)
|
$ | 174,006 | $ | 174,006 | ||||
BVP Special Affiliates Limited Partnership
(3)
|
$ | 163,864 | $ | 163,864 |
(1) |
Matthew Walker was a member of the GreenLight board of directors at the time of the issuance of the GreenLight Convertible Notes and has continuously served on the GreenLight board of directors since that
|
time. S2G Ventures Fund II, L.P. (“
S2G II
”) and its affiliated funds, S2G Ventures Fund I, L.P. and S2G Builders Food & Agriculture Fund III, L.P., held more than 5% of GreenLight’s outstanding capital stock at the time of issuance of the GreenLight Convertible Notes to S2G II and has continuously held more than 5% of GreenLight’s outstanding capital stock at all times since the issuance of the GreenLight Convertible Notes. It is expected that Mr. Walker will serve on the New GreenLight Board.
|
(2) |
Eric O’Brien was a member of the GreenLight board of directors at the time of the issuance of the GreenLight Convertible Notes and has continuously served on the GreenLight board of directors since that time. During this period, he has been an affiliate of Fall Line Endurance Fund L.P. (“
Fall Line
”). Fall Line held more than 5% of GreenLight’s outstanding capital stock at the time of issuance of the GreenLight Convertible Notes to Fall Line and has continuously held more than 5% of GreenLight’s outstanding capital stock at all times since the issuance of the GreenLight Convertible Notes. It is expected that Mr. O’Brien will serve on the New GreenLight Board.
|
(3) |
Michael Liang was a member of the GreenLight board of directors at the time of the issuance of the GreenLight Convertible Notes and has continuously served on the GreenLight board of directors since that time. During this period, he has been an affiliate of each of Baird Venture Partners V Limited Partnership, BVP V Affiliates Fund Limited Partnership and BVP Special Affiliates Limited Partnership (all such funds collectively, “
Baird
”). Baird held less than 5% of GreenLight’s outstanding capital stock at the time of GreenLight Convertible Note Financing.
|
Name
|
Number
of Shares
|
Total
Purchase Price
|
||||||
Morningside Venture Investments Limited
(1)
|
19,317,805 | $ | 34,999,999 | |||||
S2G Builders Food & Agriculture Fund III, L.P.
(2)
|
5,519,372 | $ | 9,999,998 | |||||
S2G Ventures Fund II, L.P.
(2)
|
3,863,561 | $ | 7,000,000 | |||||
Fall Line Endurance Fund, LP
(3)
|
3,311,623 | $ | 5,999,999 | |||||
Baird Venture Partners V Limited Partnership
(4)
|
2,064,131 | $ | 3,739,793 | |||||
BVP Special Affiliates Limited Partnership
(4)
|
216,090 | $ | 391,512 | |||||
BVP V Affiliates Fund Limited Partnership
(4)
|
203,495 | $ | 368,692 | |||||
Series Greenlight 2, A Separate Series of BlueIO Growth LLC
(5)
|
1,421,238 | $ | 2,574,999 | |||||
MLS Capital Fund II, L.P.
(6)
|
1,103,874 | $ | 1,999,999 |
(1) |
Jason Dinges is a member of the GreenLight board of directors. Mr. Dinges joined the GreenLight board of directors at the time of the closing of the GreenLight Series D Preferred Stock Financing and has continuously served on the GreenLight board of directors since that time. Morningside acquired more than 5% of GreenLight’s outstanding capital stock in the GreenLight Series D Preferred Stock Financing.
|
(2) |
Matthew Walker was a member of the GreenLight board of directors at the time of the GreenLight Series D Preferred Stock Financing and has continuously served on the GreenLight board of directors since that time. S2G Ventures held more than 5% of GreenLight’s outstanding capital stock at the time of the GreenLight Series D Preferred Stock Financing and has continuously held more than 5% of GreenLight’s outstanding capital stock at all times since the GreenLight Series D Preferred Stock Financing. It is expected that Mr. Walker will serve on the New GreenLight Board.
|
(3) |
Eric O’Brien was a member of the GreenLight board of directors at the time of the GreenLight Series D Preferred Stock Financing and has continuously served on the GreenLight board of directors since that time. During this period, he has been an affiliate of Fall Line. Fall Line held more than 5% of GreenLight’s outstanding capital stock at the time of the GreenLight Series D Preferred Stock Financing and has continuously held more than 5% of GreenLight’s outstanding capital stock at all times since the GreenLight Series D Preferred Stock Financing. It is expected that Mr. O’Brien will serve on the New GreenLight Board.
|
(4) |
Michael Liang was a member of the GreenLight board of directors at the time of the GreenLight Series D Preferred Stock Financing and has continuously served on the GreenLight board of directors since that time. During this period, he has been an affiliate of Baird. Baird held less than 5% of GreenLight’s outstanding capital stock at the time of GreenLight Series D Preferred Stock Financing.
|
(5) |
David Furneaux was a member of the GreenLight board of directors at the time of the GreenLight Series D Preferred Stock Financing. Mr. Furneaux joined the board of directors in July 2013 and served on the GreenLight board of directors until the initial closing of the GreenLight Series D Preferred Stock Financing. During this period, he was an affiliate of Series Greenlight 2, A Separate Series of BlueIO Growth LLC (“
Series Greenlight 2
”). Series Greenlight 2 held less than 5% of GreenLight’s outstanding capital stock at the time of GreenLight’s Series D Preferred Stock Financing.
|
(6) |
Ganesh Kishore was a member of the GreenLight board of directors at the time of the GreenLight Series D Preferred Stock Financing and has continuously served on the GreenLight board of directors since that time. During this period, he has been an affiliate of MLS Capital Fund II, L.P. (“
MLS
”). MLS held more than 5% of GreenLight’s outstanding capital stock at the time of the GreenLight Series D Preferred Stock Financing and has continuously held more than 5% of GreenLight’s outstanding capital stock at all times since the GreenLight Series D Preferred Stock Financing. It is expected that Mr. Kishore will serve on the New GreenLight Board.
|
Name
|
Number
of Shares
|
Total
Purchase Price
|
||||||
S2G Ventures Fund I, L.P.
(1)
|
3,135,582 | $ | 4,985,575 | |||||
S2G Ventures Fund II, L.P.
(1)
|
3,135,583 | $ | 4,985,576 | |||||
Baird Venture Partners V Limited Partnership
(2)
|
3,762,699 | $ | 5,982,691 | |||||
Fall Line Endurance Fund, LP
(3)
|
3,135,583 | $ | 4,985,576 | |||||
Kodiak Venture Partners III, L.P.
(4)
|
2,753,920 | $ | 4,378,733 | |||||
Kodiak III Entrepreneurs Fund, L.P.
(4)
|
68,104 | $ | 108,285 | |||||
Series Greenlight, a Separate Series of BlueIO Growth LLC
(4)
|
1,301,266 | $ | 2,074,999 | |||||
Furneaux Capital Holdco, LLC (dba BlueIO)
(4)
|
188,134 | $ | 299,998 | |||||
MLS Capital Fund II, L.P.
(5)
|
1,881,350 | $ | 2,991,357 |
(1) |
Matthew Walker is a member of the GreenLight board of directors. Mr. Walker joined the board of directors at the time of the closing of the GreenLight Series C Preferred Stock Financing and has continuously served on the GreenLight board of directors since that time. S2G Ventures acquired more than 5% of GreenLight’s outstanding capital stock in the GreenLight Series C Preferred Stock Financing. It is expected that Mr. Walker will serve on the New GreenLight Board.
|
(2) |
Michael Liang is a member of the GreenLight board of directors. Mr. Liang joined the board of directors at the time of the closing of the GreenLight Series C Preferred Stock Financing and has continuously served on the GreenLight board of directors since that time. During this period, he has been an affiliate of Baird. Baird acquired more than 5% of GreenLight’s outstanding capital stock in the GreenLight Series C Preferred Stock Financing.
|
(3) |
Eric O’Brien was a member of the GreenLight board of directors at the time of the GreenLight Series C Preferred Stock Financing and has continuously served on the GreenLight board of directors since that time. During this period, he has been an affiliate of Fall Line. Fall Line held more than 5% of GreenLight’s outstanding capital stock at the time of the GreenLight Series C Preferred Stock Financing and has continuously held more than 5% of GreenLight’s outstanding capital stock at all times since the GreenLight Series C Preferred Stock Financing. It is expected that Mr. O’Brien will serve on the New GreenLight Board.
|
(4) |
David Furneaux was a member of the GreenLight board of directors at the time of the GreenLight Series C Preferred Stock Financing. Mr. Furneaux joined the board of directors in June 2013 and served on the GreenLight board of directors until the initial closing of the GreenLight Series D Preferred Stock Financing. During this period, he was an affiliate of (i) Kodiak Venture Partners III, L.P. and Kodiak III Entrepreneurs Fund, L.P. (collectively, “
Kodiak
”), (ii) Series Greenlight 2 and Series Greenlight, a Separate Series of BlueIO Growth LLC “(collectively, “
Series Greenlight
”) and (iii) Furneaux Capital Holdco, LLC (dba BlueIO) (“
Furneaux Capital
” and, together with Series Greenlight, “
BlueIO
”). Kodiak acquired more than 5% of GreenLight’s outstanding capital stock in the GreenLight Series C Preferred Stock Financing. BlueIO held less than 5% of GreenLight’s outstanding capital stock at the time of GreenLight Series C Preferred Stock Financing.
|
(5) |
Ganesh Kishore was a member of the GreenLight board of directors at the time of the GreenLight Series C Preferred Stock Financing and has continuously served on the GreenLight board of directors since that time. During this period, he has been an affiliate of MLS. MLS held more than 5% of GreenLight’s outstanding capital stock at the time of the GreenLight Series C Preferred Stock Financing and has continuously held more than 5% of GreenLight’s outstanding capital stock at all times since the GreenLight Series C Preferred Stock Financing. It is expected that Mr. Kishore will serve on the New GreenLight Board.
|
• |
the Subscription Agreements, which were executed and delivered by the following holders of more than 5% of GreenLight’s outstanding capital stock, as follows:
|
Name
|
Number
of Shares
|
Subscription
Amount |
||||||
S2G Builders Food & Agriculture Fund III, L.P.
(1)
|
1,500,000 | $ | 15,000,000 | |||||
Morningside Venture Investments Limited
|
1,000,000 | $ | 10,000,000 | |||||
Fall Line Endurance Fund, LP
|
700,000 | $ | 7,000,000 | |||||
MLS Capital Fund II, L.P.
|
75,000 | $ | 750,000 |
(1) |
S2G Builders Food & Agriculture Fund III, L.P. is affiliated with S2G Ventures.
|
• |
the Transaction Support Agreements, which were executed and delivered by the following holders of more than 5% of GreenLight’s outstanding capital stock: Fall Line, Khosla, Kodiak, MLS, Morningside, and S2G Ventures; and
|
• |
the Investor Rights Agreement, which was executed and delivered by the following holders of more than 5% of GreenLight’s outstanding capital stock: Fall Line, Khosla, Kodiak, MLS, Morningside, and S2G Ventures.
|
• |
any person who is, or at any time during the applicable period was, one of New GreenLight’s directors or executive officers;
|
• |
any person who is known by New GreenLight to be the beneficial owner of more than 5% of its voting stock;
|
• |
any immediate family member of any of the foregoing persons, which means any child, stepchild, parent, stepparent, spouse, sibling,
mother-in-law,
father-in-law,
son-in-law,
daughter-in-law,
brother-in-law
sister-in-law
|
• |
any firm, corporation or other entity in which any of the foregoing persons is a partner or principal, or in a similar position, or in which such person has a 10% or greater beneficial ownership interest.
|
GreenLight
|
New GreenLight
|
|
Authorized Capital Stock
|
||
GreenLight Common Stock
GreenLight Preferred Stock
A-1
Preferred Stock, 7,018,203 of which are designated as Series
A-2
Preferred Stock, 8,647,679 of which are designated as Series
A-3
Preferred Stock, 21,245,353 of which are designated as Series B Preferred Stock, 35,152,184 of which are designated as Series C Preferred Stock and 71,019,827 of which are designated as Series D Preferred Stock. As of August 31, 2021, there were outstanding 2,807,571 shares of GreenLight Series
A-1
Preferred Stock, 6,993,693 shares of GreenLight Series
A-2
Preferred Stock, 8,629,505 shares of GreenLight Series
A-3
Preferred Stock, 21,245,353 shares of GreenLight Series B Preferred Stock, 35,092,183 shares of GreenLight Series C Preferred Stock and 60,184,332 shares of GreenLight Series D Preferred Stock.
|
New GreenLight Common Stock
New GreenLight Preferred Stock
Change in Authorized Shares
|
|
Undesignated Preferred Stock
|
||
GreenLight is not currently authorized to issue any undesignated series of preferred stock. | The New GreenLight Board is authorized to provide for, out of the unissued shares of New GreenLight Preferred Stock, one or more series of preferred stock and to establish from time to time the number of shares to be included in each such series and to fix the voting rights, if any, designations, powers, preferences and relative, participating, optional, special and other rights, if any, of such series and any qualifications, limitations and restrictions thereof, as shall be stated in the resolution or resolutions adopted by the New GreenLight Board providing for the issuance of such series. |
GreenLight
|
New GreenLight
|
|
Each director will hold continue to office until the election and qualification of his or her successor, or until his or her earlier death, resignation, disqualification or removal. | ||
Election of Directors
|
||
The holders of record of the shares of each of the GreenLight Series A Preferred Stock, GreenLight Series B Preferred Stock, GreenLight Series C Preferred Stock and GreenLight Series D Preferred Stock, each voting exclusively and as a separate class, are entitled to elect one director of GreenLight, or a total of four directors in the aggregate (the “
Preferred Directors
Common Director
If the holders of GreenLight shares of any class or series of stock fail to elect a sufficient number of directors to fill all directorships for which they are entitled to elect directors, voting exclusively and as a separate class, then any directorship not so filled will remain vacant until the holders of such series or class of stock elect a person to fill such directorship by vote or written consent. No such directorship may be filled by stockholders of GreenLight other than by the stockholders of GreenLight that are entitled to elect a person to fill such directorship, voting exclusively and as a separate class.
At all meetings of stockholders for the election of directors at which a quorum is present, a plurality of the votes cast shall be sufficient to elect a director.
|
Following the Business Combination, subject to the rights of the holders of any New GreenLight Preferred Stock that may be issued in the future, holders of shares of New GreenLight Common Stock will have the exclusive right to vote for the election of directors, at any annual or special meeting of the stockholders of New GreenLight.
At any meeting of New GreenLight stockholders, the election of directors will be determined by a plurality of the votes cast by the stockholders present in person or represented by proxy at the meeting and entitled to vote thereon.
|
GreenLight
|
New GreenLight
|
|
Vacancies on the Board of Directors
|
||
Vacancies on the GreenLight board of directors and any newly created directorships resulting from an increase in the number of directors may be filled by vote of the stockholders at a meeting called for such purpose, or by a majority of the directors then in office, although less than a quorum, or by a sole remaining director. When one or more directors shall resign from the board effective at a future date, a majority of the directors then in office, including those who have resigned, will have power to fill such vacancy or vacancies, the vote or action in writing thereon to take effect when such resignation or resignations become effective; provided however, that any vacancy in any directorship filled by the holders of a specific class or series, may be filled only by the affirmative vote or written consent of the holders of such class or series. | Subject to the special rights of the holders of any series of New GreenLight Preferred Stock to elect directors, newly created directorships resulting from an increase in the number of directors and any vacancies on the New GreenLight Board resulting from death, resignation, retirement, disqualification, removal or other cause may be filled solely and exclusively by a majority vote of the remaining directors then in office, even if less than a quorum, or by a sole remaining director, and not by stockholders. Any director so chosen will hold office for the remainder of the full term of the class of directors to which the new directorship was added or in which the vacancy occurred and until his or her successor has been duly elected and qualified, subject, however, to such director’s earlier death, resignation, retirement, disqualification or removal. | |
Removal of Directors
|
||
The Preferred Directors and the Common Director may be removed without cause by, and only by, the affirmative vote of the holders of the shares of the class or series of stock entitled to elect such director or directors. The Preferred Directors and the Common Director may be removed with cause by the holders of a majority of the stock issued and outstanding and entitled to vote at an election of directors.
Any director of the GreenLight Board who is not a Preferred Director or the Common Director may be removed, with or without cause, by the holders of a majority of the stock issued and outstanding and entitled to vote at an election of directors. No director removed shall have any right to receive compensation as such director for any period following removal unless the body acting in the removal, in its discretion, provides for compensation.
|
Subject to the rights of holders of any New GreenLight Preferred Stock to elect and remove any directors whom such holders have the right to elect, any director may be removed at any time, but only for cause and only by the affirmative vote of at least a majority of the voting power of all then-outstanding shares of capital stock of New GreenLight entitled to vote generally in the election of directors, voting together as a single class. | |
Voting
|
||
Each GreenLight Common Share is entitled to one vote at all meetings of stockholders and written actions in lieu of meetings.
On any matter presented to the GreenLight stockholders, the holders of GreenLight Preferred Stock will be entitled to cast the number of votes equal to the number of whole shares of GreenLight Common Stock into which the shares of Preferred Stock are convertible as of the record date for determining stockholders entitled to vote on such matter.
|
Each share of New GreenLight Common Stock is entitled to one vote on each matter submitted to a vote of stockholders. |
GreenLight
|
New GreenLight
|
|
Preferred Stock Protective Provisions
|
||
At any time when at least 2,000,000 shares of Preferred Stock are outstanding, neither GreenLight nor any subsidiary of GreenLight may, either directly or indirectly by amendment, merger, consolidation or otherwise, do any of the following without (in addition to any other vote required by law or the Certificate of Incorporation) the written consent or affirmative vote of the holders of a majority of the outstanding shares of Preferred Stock, voting together as a single class on an
as-converted
basis:
liquidate, dissolve or
wind-up
the business and affairs of GreenLight, effect any Deemed Liquidation Event (as defined in the GreenLight Certificate of Incorporation), or effect a reorganization or recapitalization, or enter into a merger, acquisition, sale or other disposition of substantially all the assets of GreenLight in which the stockholders of GreenLight immediately prior to such transaction do not own at least
two-thirds
of the capital stock of the surviving or resulting corporation, or consent to any of the foregoing (any of the foregoing, a “
Liquidation Event
A-3
Original Issue Price (as defined in the GreenLight Certificate of Incorporation), only the written consent or affirmative vote of the holders of a majority of the outstanding shares of Series B Preferred Stock and Series C Preferred Stock, voting together as a single class on an
as-converted
basis, shall be required for this purpose;
amend, alter or repeal any provision of the Certificate of Incorporation or Bylaws of GreenLight;
create, authorize, issue or obligate itself to issue shares of any additional class or series of capital stock unless it ranks junior to each series of the Preferred Stock with respect to the distribution of assets on liquidation, dissolution or winding up, the payment of dividends, and rights of redemption;
change the authorized number of shares of Common Stock or Preferred Stock;
|
Not applicable. |
GreenLight
|
New GreenLight
|
|
reclassify, alter or amend any existing security of GreenLight that is pari passu with any series of the Preferred Stock in respect of the distribution of assets on liquidation, dissolution or winding up, the payment of dividends or rights of redemption, if doing so would render such other security senior to such series of Preferred Stock in respect of any such right, preference or privilege;
reclassify, alter or amend any existing security of GreenLight that is junior to any series of Preferred Stock in respect of the distribution of assets on liquidation, dissolution or winding up, the payment of dividends or rights of redemption, if such action would render such other security senior to or pari passu with such series of Preferred Stock in respect of any such right, preference or privilege;
purchase or redeem, or pay or declare any dividend or make any distribution on, any shares of capital stock of GreenLight, subject to specified exceptions;
create, authorize, issue or authorize the issuance of any debt security, other than equipment leases or bank lines of credit, unless such debt security has received the prior approval of the Board, including the approval of a majority of the Preferred Directors then serving on the Board;
change the number of directors constituting the Board; or
change the principal line of business of GreenLight.
In addition, neither GreenLight nor any subsidiary of GreenLight may, either directly or indirectly by amendment, merger, consolidation or otherwise, do any of the following without (in addition to any other vote required by law or the Certificate of Incorporation) the written consent or affirmative vote of the holders of a
majority of the outstanding shares of Series C Preferred Stock, voting together as a separate class, and the holders of a majority of the outstanding shares of Series D Preferred Stock, voting together as a separate class:
effect a Liquidation Event;
|
GreenLight
|
New GreenLight
|
|
Amendment to Certificate of Incorporation
|
||
Under Delaware law, an amendment to a certificate of incorporation generally requires the affirmative vote of a majority of the outstanding shares of stock entitled to vote thereon and a majority of the outstanding shares of stock of each class entitled to vote thereon as a class. See “
Preferred Stock Protective Provisions
|
Subject to the rights of the holders of any New GreenLight Preferred Stock that may be issued in the future, in addition to any vote required by applicable law or the certificate of incorporation or bylaws of New GreenLight, the affirmative vote of the holders of at least 75% of the voting power of all then-outstanding shares of capital stock of New GreenLight entitled to vote generally in the election of directors, voting together as a single class, is required to reduce the authorized number of shares of New GreenLight Preferred Stock or to amend, alter, change or repeal, or adopt any provision inconsistent with, the following provisions of the Proposed Charter:
Section 4.2, which relates to the authorization and designation of New GreenLight Preferred Stock;
Article V, which relates to the number, powers and term of the New GreenLight Board, the filling of vacancies in the New GreenLight Board and the removal of directors;
Article VI, which relates to the amendment, alteration, repeal or adoption of bylaws;
Article VII, which relates to the calling of meetings of stockholders, notice requirements for stockholder proposals and director nominations and the prohibition of actions by written consent of stockholders;
Article IX, which relates to the amendment, alteration, change or repeal of any provision of the Proposed Charter; and
Article X, which relates to exclusive forum provisions for certain lawsuits.
For an amendment of any other provision of the Proposed Charter, the Proposed Charter applies Delaware law, which allows an amendment to a certificate of incorporation generally with the affirmative vote of a majority of the outstanding shares of stock entitled to vote thereon.
|
GreenLight
|
New GreenLight
|
|
Special Stockholder Meetings
|
||
A special meeting of GreenLight’s stockholders may be called at any time by the President and must be called by the President or the Secretary at the request in writing of a majority of the board of directors, or at the request in writing of the holders of at least ten percent of all capital stock of GreenLight issued and outstanding and entitled to vote at such meeting for the purposes prescribed in the notice and at a place, date and time fixed by the board of directors. Business transacted at any special meeting of stockholders shall be confined to the purposes stated in the notice. | The Proposed Bylaws provides that special meetings of stockholders for any purpose or purposes may be called only by the New GreenLight Board acting pursuant to a resolution approved by the affirmative vote of a majority of the directors then in office. Nominations of persons for election to the New GreenLight Board and stockholder proposals of other business may not be brought before a special meeting of stockholders to be considered by the stockholders, unless the special meeting is held in lieu of an annual meeting, in which case such special meeting will be deemed an annual meeting of the stockholders. | |
Notice of Stockholder Meetings
|
||
Written notice stating the place, if any, date and hour of the meeting, the means of remote communications, if any, by which stockholders and proxy holders may be deemed to be present in person and vote at such meeting, the record date for determining the stockholders entitled to vote at the meeting (if such date is different from the record date for stockholders entitled to notice of the meeting) and, in case of a special meeting, the purpose or purposes for which the meeting is called, must be given not less than ten nor more than 60 days before the date of the meeting to each stockholder entitled to vote at such meeting as of the record date for determining the stockholders entitled to notice of the meeting. | Written notice stating the place, if any, date and time of each meeting, the means of remote communications, if any, by which stockholders and proxy holders may be deemed to be present in person and vote at such meeting, the record date for determining the stockholders entitled to vote at the meeting (if such date is different from the record date for stockholders entitled to notice of the meeting) and, in case of a special meeting, the purpose or purposes for which the meeting is called, must be mailed to or transmitted electronically not less than ten nor more than 60 days before the date of the meeting to each stockholder entitled to vote thereat as of the record date for determining the stockholders entitled to notice of the meeting. | |
Stockholder Proposals (Other than Nomination of Persons for Election as Directors)
|
||
Any proper business, including the election of directors, may be transacted at the annual meeting of stockholders. Business transacted at any special meeting of stockholders is limited to the purposes stated in the notice. |
No business may be transacted at an annual meeting of stockholders, other than business that is either (i) specified in New GreenLight’s notice of meeting (or any supplement thereto) given by or at the direction of the New GreenLight Board, (ii) properly brought before the annual meeting by or at the direction of the New GreenLight Board or (iii) otherwise properly brought before the annual meeting by any stockholder of New GreenLight who is entitled to vote at the meeting, who complies with the requisite notice procedures and who is a stockholder of record both at the time such notice is delivered to the Secretary of New GreenLight and on the record date for the determination of stockholders entitled to vote at such annual meeting.
|
GreenLight
|
New GreenLight
|
|
Indemnification of Directors, Officers, Employees and Agents
|
||
GreenLight will indemnify and hold harmless, to the fullest extent permitted by the DGCL, any person for any proceeding by reason of the fact that such person is or was a director, officer or agent of GreenLight or, while a director or officer, is or was serving at the request of GreenLight as a director, officer, employee or agent of another corporation, partnership, joint venture, trust or other enterprise,
The right to indemnification covers all expenses, liability and loss reasonably incurred or suffered by such person in connection with any such proceeding, but an advancement of expenses will be made only upon delivery to GreenLight of an undertaking by or on behalf of the indemnitee to repay all amounts so advanced if it should be determined that the indemnitee is not entitled to be indemnified for the expenses.
Notwithstanding the foregoing, GreenLight will not be required to indemnify or advance expenses to any person in connection with any action, suit, proceeding, claim or counterclaim initiated by or on behalf of such person.
Any amendment, repeal or modification of the indemnification provisions in the GreenLight Certificate of Incorporation will not adversely affect any right or protection of a director, officer or other agent of GreenLight existing at the time of such amendment, repeal or modification.
|
New GreenLight will indemnify and hold harmless, to the fullest extent permitted by the DGCL, any person for any proceeding by reason of the fact that such person is or was a director or officer of New GreenLight or, while a director or officer, is or was serving at the request of New GreenLight as a director, officer, employee or agent of another corporation, partnership, joint venture, trust or other enterprise, whether the basis of such proceeding is alleged action in an official capacity as a director, officer, employee or agent, or in any other capacity while serving as a director, officer, employee or agent.
The right to indemnification covers all liability and loss suffered and expenses (including, without limitation, attorneys’ fees, judgments, fines, penalties, excise taxes under the Employee Retirement Income Security Act of 1974, as amended from time to time, and amounts paid in settlement) incurred by such person in connection with any such proceeding.
An indemnitee will also have the right to be reimbursed for the expenses (including attorneys’ fees) reasonably incurred in defending or otherwise participating in a proceeding in advance of its final disposition, provided, however, that if required by law any such reimbursement will be made only upon receipt of an undertaking by the indemnitee to repay all amounts advanced if it should be determined that the indemnitee is not entitled to be indemnified for the expenses.
Except for proceedings to enforce rights to indemnification, New GreenLight will indemnify an indemnitee in connection with a proceeding (or part thereof) initiated by such indemnitee only if such proceeding (or part thereof) was authorized by the New GreenLight Board.
New GreenLight has the power to indemnify and hold harmless, to the fullest extent permitted by applicable law, any employee or agent of New GreenLight who was or is made a party or is otherwise involved in a proceeding by reason of the fact that he or she is or was an employee or agent of New GreenLight or is or was serving at the request of New GreenLight as a director, officer, employee or agent of another corporation or of a partnership, joint venture, trust or other enterprise against all liability and loss suffered and expenses reasonably incurred by such person in connection with any such proceeding.
|
• |
in whole and not in part;
|
• |
at a price of $0.01 per warrant;
|
• |
upon not less than 30 days’ prior written notice of redemption (the “
30-day
redemption period
|
• |
if, and only if, the reported last sale price of New GreenLight Common Stock equals or exceeds $18.00 per share (as adjusted for stock splits, stock dividends, reorganizations, recapitalizations and the like) for any 20 trading days within a
30-trading
day period ending three business days before we send the notice of redemption to the warrantholders.
|
• |
transfers to New GreenLight or in connection with its liquidation or dissolution;
|
• |
transfers pursuant to a bona fide business combination or other transaction or series of related transactions involving a change in control of New GreenLight;
|
• |
the establishment of a Rule
10b5-1
plan, as long as the plan does not provide for the transfer of any
Lock-up
Securities during the
Lock-up
Period;
|
• |
transfers pursuant to a qualified domestic relations order or court order or in connection with a divorce settlement; or
|
• |
transfers to generate cash to pay the exercise price of, and/or satisfy tax withholding obligations in connection with, the exercise of options expiring within the
Lock-up
Period (including a “broker-assisted cashless exercise” involving a market sale).
|
• |
transfers as a bona fide gift or charitable contribution;
|
• |
transfers to a trust, family limited partnership or other entity formed primarily for estate planning purposes for the primary benefit of specified family members;
|
• |
transfers by will or intestate succession upon the death of the holder;
|
• |
if the holder is a corporation, partnership, limited liability company, trust or other business entity, (i) transfers to another entity that controls, is controlled by or is under common control or management with the holder, or (ii) dividends, distributions or other dispositions to the equity holders of the holder;
|
• |
if the holder is a trust, transfers to a trustor or beneficiary of such trust or to the estate of a beneficiary of such trust;
|
• |
transfers to New GreenLight’s officers, directors or their affiliates;
|
• |
transfers to any other holder subject to the
Lock-up,
any affiliates of any such holder or any related partnerships, funds or investment vehicles controlled or managed by such persons or entities;
|
• |
Certain pledges or postings of
Lock-up
Securities as security or collateral in connection with any borrowing or the incurrence of any indebtedness by any holder; and
|
• |
transfers to a nominee or custodian of a permitted transferee.
|
• |
Section 4.2 of the Proposed Charter, which relates to the authorization and designation of New GreenLight Preferred Stock;
|
• |
Article V of the Proposed Charter, which relates to the number, powers and term of the New GreenLight Board, the filling of vacancies in the New GreenLight Board and the removal of directors;
|
• |
Article VI of the Proposed Charter, which relates to the amendment, alteration, repeal or adoption of bylaws;
|
• |
Article VII of the Proposed Charter, which relates to the calling of meetings of stockholders, notice requirements for stockholder proposals and director nominations and the prohibition of actions by written consent of stockholders;
|
• |
Article IX of the Proposed Charter, which relates to the amendment, alteration, change or repeal of any provision of the Proposed Charter; and
|
• |
Article X of the Proposed Charter, which relates to exclusive forum provisions for certain lawsuits.
|
• |
before the person becomes an interested stockholder, the board of directors approves the business combination or the transaction that results in the person becoming an interested stockholder;
|
• |
the interested stockholder owns at least 85% of the outstanding voting stock of the corporation at the time the business combination commences (excluding voting stock owned by directors who are also officers and certain employee stock plans); or
|
• |
the business combination is approved by the board of directors and the affirmative vote, at a meeting and not by written consent, of
two-thirds
of the outstanding voting stock which is not owned by the interested stockholder.
|
• |
1% of the total number of securities then outstanding; or
|
• |
the average weekly reported trading volume of the securities during the four calendar weeks preceding the filing of a notice on Form 144 with respect to the sale.
|
• |
the issuer of the securities that was formerly a shell company has ceased to be a shell company;
|
• |
the issuer of the securities is subject to the reporting requirements of Section 13 or 15(d) of the Exchange Act;
|
• |
the issuer of the securities has filed all Exchange Act reports and material required to be filed, as applicable, during the preceding twelve months (or such shorter period that the issuer was required to file such reports and materials), other than Form
8-K
reports; and
|
• |
at least one year has elapsed from the time that the issuer filed current Form 10 information with the SEC reflecting its status as an entity that is not a shell company.
|
• |
not later than the 120th day; and
|
• |
not earlier than the 150th day before the
one-year
anniversary of the preceding year’s annual meeting;
provided, however
|
Page
|
||||
F-2 | ||||
F-3 | ||||
F-4 | ||||
F-5 | ||||
F-6 | ||||
F-27 | ||||
F-28 | ||||
F-29 | ||||
F-30 | ||||
F-31 | ||||
F-32 |
Page
|
||||
F-42 | ||||
F-43 | ||||
F-44 | ||||
F-45 | ||||
F-47 | ||||
F-49 | ||||
F-78
|
||||
F-79 | ||||
F-80 | ||||
F-81 | ||||
F-82 |
September 30,
2021 |
December 31,
2020 |
|||||||
(Unaudited,
restated) |
||||||||
ASSETS
|
||||||||
Current assets
|
||||||||
Cash
|
$ | 158,337 | $ | 156,848 | ||||
Prepaid expenses
|
698,309 | — | ||||||
|
|
|
|
|||||
Total Current Assets
|
856,646 | 156,848 | ||||||
Deferred offering costs
|
— | 168,152 | ||||||
Investments held in Trust Account
|
207,008,746 | — | ||||||
|
|
|
|
|||||
TOTAL ASSETS
|
$ | 207,865,392 | $ | 325,000 | ||||
|
|
|
|
|||||
LIABILITIES AND STOCKHOLDERS’ (DEFICIT) EQUITY
|
||||||||
Current liabilities
|
||||||||
Accounts payable and accrued expenses
|
$ | 3,017,789 | $ | 2,528 | ||||
Accrued offering costs
|
118,569 | — | ||||||
Promissory note — related party
|
500,000 | 300,000 | ||||||
|
|
|
|
|||||
Total Current Liabilities
|
3,636,358 | 302,528 | ||||||
Warrant liabilities
|
13,341,000 | — | ||||||
Deferred underwriting fee payable
|
— | — | ||||||
|
|
|
|
|||||
Total Liabilities
|
16,977,358 | 302,528 | ||||||
|
|
|
|
|||||
Commitments and Contingencies
|
||||||||
Class A common stock subject to possible redemption 20,700,000 and no shares at redemption value as of September 30, 2021 and December 31, 2020, respectively
|
207,000,000 | — | ||||||
Stockholders’ (Deficit) Equity
|
||||||||
Preferred stock, $0.0001 par value; 1,000,000 shares authorized; none issued or outstanding
|
— | — | ||||||
Class A common stock, $0.0001 par value; 100,000,000 shares authorized
|
— | — | ||||||
Class B common stock, $0.0001 par value; 20,000,000 shares authorized; 5,175,000 shares issued and outstanding as of September 30, 2021 and December 31, 2020
|
518 | 518 | ||||||
Additional
paid-in
capital
|
— | 24,482 | ||||||
Accumulated deficit
|
(16,112,484 | ) | (2,528 | ) | ||||
|
|
|
|
|||||
Total Stockholders’ (Deficit) Equity
|
(16,111,966 | ) | 22,472 | |||||
|
|
|
|
|||||
TOTAL LIABILITIES AND STOCKHOLDERS’ (DEFICIT) EQUITY
|
$ | 207,865,392 | $ | 325,000 | ||||
|
|
|
|
Three Months
Ended September 30, 2021 |
Nine Months
Ended September 30, 2021 |
For the
Period from July 2, 2020 (Inception) Through September 30, 2020 |
||||||||||
General and administrative expenses
|
$ | 2,556,742 | $ | 4,084,445 | $ | 878 | ||||||
|
|
|
|
|
|
|||||||
Loss from operations
|
|
(2,556,742
|
)
|
|
(4,084,445
|
)
|
|
(878
|
)
|
|||
|
|
|
|
|
|
|||||||
Other income (expense):
|
||||||||||||
Interest earned on marketable securities held in Trust Account
|
3,180 | 8,746 | — | |||||||||
Loss in initial issuance of Private Placement Warrants
|
— | (1,272,500 | ) | — | ||||||||
Change in fair value of warrant liabilities
|
1,027,000 | 1,840,000 | — | |||||||||
|
|
|
|
|
|
|||||||
Other income, net
|
1,030,180 | 576,246 | — | |||||||||
|
|
|
|
|
|
|||||||
Net loss
|
$
|
(1,526,562
|
)
|
$
|
(3,508,199
|
)
|
$
|
(878
|
)
|
|||
|
|
|
|
|
|
|||||||
Weighted average shares outstanding, Class A common stock (restated)
|
20,700,000 | 19,335,165 | — | |||||||||
|
|
|
|
|
|
|||||||
Basic and diluted net loss per share, Class A common stock (restated)
|
$ | (0.06 | ) | $ | (0.14 | ) | $ | — | ||||
|
|
|
|
|
|
|||||||
Weighted average shares outstanding, Class B common stock (restated)
|
5,175,000 | 5,130,495 | 4,500,000 | |||||||||
|
|
|
|
|
|
|||||||
Basic and diluted net loss per share, Class B common stock (restated)
|
$
|
(0.06
|
)
|
$
|
(0.14
|
)
|
$
|
(0.00
|
)
|
|||
|
|
|
|
|
|
|
|
Class B
Common Stock
|
|
|
Additional
Paid-in
Capital
|
|
|
Accumulated
Deficit
|
|
|
Total
Stockholders’
Equity
(Deficit)
|
|
||||||||
|
|
Shares
|
|
|
Amount
|
|
||||||||||||||
Balance — January 1, 2021
|
|
5,175,000
|
|
$
|
518
|
|
$
|
24,482
|
|
$
|
(2,528
|
)
|
$
|
22,472
|
|
|||||
Accretion of Class A common stock subject to possible redemption
|
— | — | (24,482 | ) | (12,601,757 | ) | (12,626,239 | ) | ||||||||||||
Net income
|
— | — | — | 1,042,799 | 1,042,799 | |||||||||||||||
Balance — March 31, 2021 (restated)
|
|
|
5,175,000
|
|
|
$
|
518
|
|
|
$
|
—
|
|
|
$
|
11,561,486
|
|
|
$
|
(11,560,968
|
)
|
Net loss
|
|
|
—
|
|
|
|
—
|
|
|
|
—
|
|
|
|
(3,024,436
|
)
|
|
|
(3,024,436
|
)
|
|
|
|
|
|
|
|
|
|
|
|||||||||||
Balance — June 30, 2021 (restated)
|
|
5,175,000
|
|
$
|
518
|
|
$ | — |
$
|
(14,585,922
|
)
|
$
|
(14,585,404
|
)
|
||||||
Net loss
|
— | — | — | (1,526,562 | ) | (1,526,562 | ) | |||||||||||||
|
|
|
|
|
|
|
|
|
|
|||||||||||
Balance — September 30, 2021
|
|
5,175,000
|
|
$
|
518
|
|
$ | — |
$
|
(16,112,484
|
)
|
$
|
(16,111,966
|
)
|
||||||
|
|
|
|
|
|
|
|
|
|
Class A
Common Stock
|
Class B
Common Stock
|
Additional
Paid-in
Capital
|
Accumulated
Deficit
|
Total
Stockholders’
Equity
|
||||||||||||||||||||||||
Shares
|
Amount
|
Shares
|
Amount
|
|||||||||||||||||||||||||
Balance — July 2, 2020 (inception)
|
|
—
|
|
$
|
—
|
|
|
—
|
|
$
|
—
|
|
$
|
—
|
|
$
|
—
|
|
$
|
—
|
|
|||||||
Issuance of Class B common stock to Sponsor
|
— | — | 5,175,000 | 518 | 24,482 | — | 25,000 | |||||||||||||||||||||
Net loss
|
— | — | — | — | — | (878 | ) | (878 | ) | |||||||||||||||||||
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|||||||||||||||
Balance — September 30, 2020
|
|
—
|
|
$
|
—
|
|
$
|
5,175,000
|
|
$
|
518
|
|
$
|
24,482
|
|
$
|
(878
|
)
|
$
|
24,122
|
|
|||||||
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Nine Months
Ended September 30, 2021 |
For the Period
from July 2, 2020 (Inception) through September 30, 2020 |
|||||||
Cash Flows from Operating Activities:
|
||||||||
Net loss
|
$ | (3,508,199 | ) | $ | (878 | ) | ||
Adjustments to reconcile net loss to net cash used in operating activities:
|
||||||||
Loss on issuance of Private Placement Warrants
|
1,272,500 | — | ||||||
Change in fair value of warrant liabilities
|
(1,840,000 | ) | — | |||||
Transaction costs incurred in connection with warrants
|
50,179 | — | ||||||
Interest earned on marketable securities held in Trust Account
|
(8,746 | ) | — | |||||
Changes in operating assets and liabilities:
|
||||||||
Prepaid expenses
|
(698,309 | ) | — | |||||
Accounts payable and accrued expenses
|
3,015,261 | 878 | ||||||
|
|
|
|
|||||
Net cash used in operating activities
|
|
(1,717,314
|
)
|
— | ||||
|
|
|
|
|||||
Cash Flows from Investing Activities:
|
||||||||
Investment of cash into Trust Account
|
(207,000,000 | ) | — | |||||
|
|
|
|
|||||
Net cash used in investing activities
|
|
(207,000,000
|
)
|
— | ||||
|
|
|
|
|||||
Cash Flows from Financing Activities:
|
||||||||
Proceeds from issuance of Class B common stock to Sponsor
|
— | 25,000 | ||||||
Proceeds from sale of Units, net of underwriting discounts paid
|
206,750,000 | — | ||||||
Proceeds from sale of Private Placement Warrants
|
2,000,000 | — | ||||||
Proceeds from sale of Unit Purchase Option
|
6,000 | — | ||||||
Proceeds from promissory note — related party
|
500,000 | 27,450 | ||||||
Repayment of promissory note — related party
|
(300,000 | ) | — | |||||
Payment of offering costs
|
(237,197 | ) | (27,450 | ) | ||||
|
|
|
|
|||||
Net cash provided by financing activities
|
|
208,718,803
|
|
25,000 | ||||
|
|
|
|
|||||
Net Change in Cash
|
|
1,489
|
|
|
25,000
|
|
||
Cash — Beginning
|
156,848 | — | ||||||
|
|
|
|
|||||
Cash — Ending
|
$
|
158,337
|
|
$
|
25,000
|
|
||
|
|
|
|
|||||
Non-cash
investing and financing activities:
|
||||||||
Offering costs included in accrued offering costs
|
$ | 118,569 | $ | 38,243 | ||||
|
|
|
|
|||||
Offering costs paid through promissory note
|
$ | — | $ | 81,125 | ||||
|
|
|
|
|||||
Initial classification of warrant liabilities
|
$ | 15,181,000 | $ | — | ||||
|
|
|
|
Balance Sheet as of January 19, 2021 (audited)
|
As Previously
Reported |
Adjustment
|
As Restated
|
|||||||||
Class A common stock subject to possible redemption
|
$ | 188,080,750 | $ | 18,919,250 | $ | 207,000,000 | ||||||
Class A common stock
|
$ | 189 | $ | (189 | ) | $ | — | |||||
Additional
paid-in
capital
|
$ | 6,323,303 | $ | (6,323,303 | ) | $ | — | |||||
Accumulated deficit
|
$ | (51,506 | ) | $ | (12,595,758 | ) | $ | (12,647,264 | ) | |||
Total Stockholders’ Equity (Deficit)
|
$ | 6,272,504 | $ | (18,919,250 | ) | $ | (12,646,746 | ) | ||||
Balance Sheet as of March 31, 2021 (unaudited)
|
||||||||||||
Class A common stock subject to possible redemption
|
$ | 190,439,030 | $ | 16,560,970 | $ | 207,000,000 | ||||||
Class A common stock
|
$ | 166 | $ | (166 | ) | $ | — | |||||
Additional
paid-in
capital
|
$ | 3,959,047 | $ | (3,959,047 | ) | $ | — | |||||
Accumulated deficit
|
$ | 1,040,271 | $ | (12,601,757 | ) | $ | (11,561,486 | ) | ||||
Total Stockholders’ Equity (Deficit)
|
$ | 5,000,002 | $ | (16,560,970 | ) | $ | (11,560,968 | ) | ||||
Balance Sheet as of June 30, 2021 (unaudited)
|
||||||||||||
Class A common stock subject to possible redemption
|
$ | 187,414,590 | $ | 19,585,410 | $ | 207,000,000 | ||||||
Class A common stock
|
$ | 196 | $ | (196 | ) | $ | — | |||||
Additional
paid-in
capital
|
$ | 6,983,457 | $ | (6,983,457 | ) | $ | — | |||||
Accumulated deficit
|
$ | (1,984,165 | ) | $ | (12,601,757 | ) | $ | (14,585,922 | ) | |||
Total Stockholders’ Equity (Deficit)
|
$ | 5,000,006 | $ | (19,585,410 | ) | $ | (14,585,404 | ) |
Statement of Cash Flows for the Three Months Ended
March 31, 2021 (unaudited) |
As Previously
Reported |
Adjustment
|
As Restated
|
|||||||||
Initial classification of Class A ordinary shares subject to possible redemption
|
$ | 190,439,030 | $ | 16,560,970 | $ | 207,000,000 | ||||||
Change in value of Class A ordinary shares subject to possible redemption
|
(12,816,720 | ) | 12,816,720 | — | ||||||||
Statement of Cash Flows for the Six Months Ended June 30, 2021 (unaudited)
|
||||||||||||
Initial classification of Class A ordinary shares subject to possible redemption
|
$ | 187,414,590 | $ | 19,585,410 | $ | 207,000,000 | ||||||
Change in value of Class A ordinary shares subject to possible redemption
|
(3,024,440 | ) | 3,204,440 | — | ||||||||
Statement of Changes in Stockholders’ Equity (Deficit)
March 31, 2021 |
As Previously
Reported |
Adjustment
|
As Restated
|
|||||||||
Sale of 20,700,000 Class A shares, net of underwriting discounts
|
$ | 194,373,761 | $ | (194,373,761 | ) | $ | — | |||||
Accretion for Class A common stock to redemption amount
|
— | (12,626,239 | ) | (12,626,239 | ) | |||||||
Change in value of Class A common stock subject to redemption
|
(190,439,030 | ) | 190,439,030 | — | ||||||||
Total stockholders’ equity (deficit)
|
5,000,002 | (16,560,970 | ) | (11,560,968 | ) | |||||||
Statement of Changes in Stockholders’ Equity (Deficit) June 30, 2021
|
||||||||||||
Change in value of Class A common stock subject to redemption
|
$ | 3,024,440 | $ | (3,024,440 | ) | $ | — | |||||
Total stockholders’ equity (deficit)
|
5,000,006 | (19,585,410 | ) | (14,585,404 | ) |
As Previously
Reported For the Three Months Ended March 31, 2021 |
As Restated
For the Three Months Ended March 31, 2021 |
As Previously
Reported For the Three Months Ended June 30, 2021 |
As Restated
For the Three Months Ended June 30, 2021 |
As
Previously Reported For the Six Months Ended June 30, 2021 |
As Restated
For the Six Months Ended June 30, 2021 |
|||||||||||||||||||
Basic and diluted weighted average shares outstanding, Class A common stock
|
20,700,000 | 16,560,000 | 20,700,000 | 20,700,000 | 20,700,000 | 18,641,436 | ||||||||||||||||||
Basic and diluted net loss per share, Class A common stock
|
$ | — | $ | 0.05 | $ | — | $ | (0.12 | ) | $ | — | $ | (0.08 | ) | ||||||||||
Basic and diluted weighted average shares outstanding, Class B common stock
|
5,032,500 | 5,040,000 | 5,175,000 | 5,175,000 | 5,107,873 | 5,107,873 | ||||||||||||||||||
Basic and diluted net loss per share, Class B common stock
|
$ | 0.21 | $ | 0.05 | $ | (0.58 | ) | $ | (0.12 | ) | $ | (0.39 | ) | $ | (0.08 | ) |
Gross proceeds
|
$ | 207,000,000 | ||
Less:
|
||||
Proceeds allocated to Public Warrants
|
(11,902,500 | ) | ||
Class A common stock issuance costs
|
(723,739 | ) | ||
Plus:
|
||||
Accretion of carrying value to redemption value
|
12,626,239 | |||
|
|
|||
Class A common stock subject to possible redemption
|
$
|
207,000,000
|
|
|
|
|
Three Months Ended
September 30, 2021 |
Nine Months Ended
September 30, 2021 |
For the Period
from July 2, 2020 (Inception) Through September 30, 2020 |
||||||||||||||||||||||
Class A
|
Class B
|
Class A
|
Class B
|
Class A
|
Class B
|
|||||||||||||||||||
Basic and diluted net loss per common share
|
||||||||||||||||||||||||
Numerator:
|
||||||||||||||||||||||||
Allocation of net loss, as adjusted
|
$ | (1,221,250 | ) | $ | (305,312 | ) | $ | (2,765,190 | ) | $ | (743,009 | ) | $ | — | $ | (878 | ) | |||||||
Denominator:
|
||||||||||||||||||||||||
Basic and diluted weighted average shares outstanding
|
20,700,000 | 5,175,000 | 19,335,165 | 5,130,495 | — | 4,500,000 | ||||||||||||||||||
|
|
|
|
|
|
|
|
|
|
|
|
|||||||||||||
Basic and diluted net loss per common share
|
$ | (0.06 | ) | $ | (0.06 | ) | $ | (0.14 | ) | $ | (0.14 | ) | $ | — | $ | (0.00 | ) |
• |
The stockholders of GreenLight that have agreed to participate in the transaction will exchange (the “
Exchange
ENVI Class
A Common Stock
|
• |
ENVI Merger Sub will merge with and into GreenLight (the “
Merger
Surviving Company
|
• |
In connection with the Merger, each issued and outstanding share of capital stock of GreenLight (other than treasury stock and any dissenting shares) (a “
Greenlight Share
Exchange Ratio
|
• |
Each option to purchase shares of capital stock of GreenLight (“
GreenLight Option
Rollover Option
|
• |
Shares of ENVI Class A Common Stock issued in respect of shares of Greenlight common stock that are subject to vesting or forfeiture (“
Greenlight Restricted Shares
|
• |
Each warrant of GreenLight (“
GreenLight Warrant
|
Stock equal to the product (rounded down to the nearest whole number) of (x) the number of common shares of GreenLight (on an as converted basis) subject to such GreenLight Warrant immediately prior to the effective time of the Merger, multiplied by (y) the Exchange Ratio, at an exercise price per share (rounded up to the nearest whole cent) equal to the quotient of (i) the exercise price per share of such GreenLight Warrant immediately prior to the effective time of the Merger, divided by (ii) the Exchange Ratio. |
• |
in whole and not in part;
|
• |
at a price of $0.01 per Public Warrant;
|
• |
upon not less than 30 days’ prior written notice of redemption to each warrant holder; and
|
• |
if, and only if, the reported last sale price of the Class A common stock equals or exceeds $18.00 per share (as adjusted for stock splits, stock dividends, reorganizations, recapitalizations and the like) for any 20 trading days within a
30-trading
day period ending three business trading days before sending the notice of redemption to warrant holders.
|
Level 1: | Quoted prices in active markets for identical assets or liabilities. An active market for an asset or liability is a market in which transactions for the asset or liability occur with sufficient frequency and volume to provide pricing information on an ongoing basis. | |
Level 2: | Observable inputs other than Level 1 inputs. Examples of Level 2 inputs include quoted prices in active markets for similar assets or liabilities and quoted prices for identical assets or liabilities in markets that are not active. | |
Level 3: | Unobservable inputs based on our assessment of the assumptions that market participants would use in pricing the asset or liability. |
Level
|
Fair Value
|
|||||||
Assets:
|
||||||||
Investments held in Trust Account — Money market funds
|
1 | $ | 207,007,744 | |||||
Liabilities: | ||||||||
Warrant Liability — Public Warrants
|
1 | 10,453,500 | ||||||
Warrant Liability — Private Placement Warrants
|
3 | 2,100,000 | ||||||
Warrant Liability — Sponsor and Directors
|
3 | 787,500 |
Input
|
January 13,
2021 |
September 30,
2021 |
||||||
Risk-free interest rate
|
0.74 | % | 1.07 | % | ||||
Expected term (years)
|
5.00 | 5.00 | ||||||
Expected volatility
|
21 | % | 16.3 | % | ||||
Exercise price
|
$ | 11.50 | $ | 11.50 | ||||
Fair value of Units
|
$ | 9.43 | $ | 9.89 |
Private
Placement |
Public
|
Warrant
Liabilities |
||||||||||
Fair value as of January 1, 2021
|
$ | — | $ | — | $ | — | ||||||
Initial measurement on January 19, 2021
|
3,272,500 | 11,902,500 | 15,175,000 | |||||||||
Change in valuation inputs or other assumptions
|
(385,000 | ) | (2,898,000 | ) | (3,283,000 | ) | ||||||
Transfers to Level 1
|
— | (9,004,500 | ) | (9,004,500 | ) | |||||||
|
|
|
|
|
|
|||||||
Fair value as of September 30, 2021
|
$ | 2,887,500 | $ | — | $ | 2,887,500 | ||||||
|
|
|
|
|
|
ASSETS
|
||||
Current asset — cash
|
$ | 156,848 | ||
Deferred offering costs
|
181,027 | |||
|
|
|||
TOTAL ASSETS
|
$
|
337,875
|
|
|
|
|
|||
LIABILITIES AND STOCKHOLDERS’ EQUITY
|
||||
Liabilities
|
||||
Current liabilities
|
||||
Accrued expenses
|
$ | 2,528 | ||
Accrued offering costs
|
12,875 | |||
Promissory note — related party
|
300,000 | |||
|
|
|||
Total Current Liabilities
|
|
315,403
|
|
|
|
|
|||
Commitments and Contingencies
|
||||
Stockholders’ Equity
|
||||
Preferred stock, $0.0001 par value; 1,000,000 shares authorized; no shares issued and outstanding
|
— | |||
Class A common stock, $0.0001 par value; 100,000,000 shares authorized; no shares issued and outstanding
|
— | |||
Class B common stock, $0.0001 par value; 20,000,000 shares authorized; 5,175,000 shares issued and outstanding
(1)
|
518 | |||
Additional
paid-in
capital
|
24,482 | |||
Accumulated deficit
|
(2,528 | ) | ||
|
|
|||
Total Stockholders’ Equity
|
|
22,472
|
|
|
|
|
|||
TOTAL LIABILITIES AND STOCKHOLDERS’ EQUITY
|
$
|
337,875
|
|
|
|
|
(1) |
Included up to 675,000 shares of Class B common stock that were subject to forfeiture depending on the extent to which the underwriters’ over-allotment option was exercised. In December 2020, the Company cancelled an aggregate of 3,306,250 shares of Class B common stock and issued an aggregate of 431,250 shares of Class B common stock to its independent director nominees, resulting in an aggregate of 4,312,500 shares of Class B common stock outstanding. In January 2021, the Company effected a stock dividend of 1.2 shares for each share of common stock outstanding, resulting in the Company’s Initial Stockholders holding an aggregate of 5,175,000 Founder Shares. All share and
per-share
amounts have been retroactively restated to reflect the stock dividend (see Note 5).
|
Formation and operating costs
|
$ | 2,528 | ||
|
|
|||
Net Loss
|
$
|
(2,528
|
)
|
|
|
|
|||
Weighted average shares outstanding, basic and diluted
(1)
|
4,500,000 | |||
|
|
|||
Basic and diluted net loss per common share
|
$
|
(0.00
|
)
|
|
|
|
(1) |
Excluded up to 675,000 shares of Class B common stock that were subject to forfeiture depending on the extent to which the underwriters’ over-allotment option was exercised. In December 2020, the Company cancelled an aggregate of 3,306,250 shares of Class B common stock and issued an aggregate of 431,250 shares of Class B common stock to its independent director nominees, resulting in an aggregate of 4,312,500 shares of Class B common stock outstanding. In January 2021, the Company effected a stock dividend of 1.2 shares for each share of common stock outstanding, resulting in the Company’s Initial Stockholders holding an aggregate of 5,175,000 Founder Shares. All share and
per-share
amounts have been retroactively restated to reflect the stock dividend (see Note 5).
|
Class B
Common Stock |
Additional
Paid-in
Capital
|
Accumulated
Deficit
|
Total
Stockholders’
Equity
|
|||||||||||||||||
Shares
|
Amount
|
|||||||||||||||||||
Balance — July 2, 2020 (inception)
|
|
—
|
|
$
|
—
|
|
$
|
—
|
|
$
|
—
|
|
$
|
—
|
|
|||||
Issuance of Class B common stock to Initial Stockholders
(1)
|
5,175,000 | 518 | 24,482 | — | 25,000 | |||||||||||||||
Net loss
|
— | — | — | (2,528 | ) | (2,528 | ) | |||||||||||||
|
|
|
|
|
|
|
|
|
|
|||||||||||
Balance — December 31, 2020
|
|
5,175,000
|
|
$
|
518
|
|
$
|
24,482
|
|
$
|
(2,528
|
)
|
$
|
22,472
|
|
|||||
|
|
|
|
|
|
|
|
|
|
(1) |
Included up to 675,000 shares of Class B common stock that were subject to forfeiture depending on the extent to which the underwriters’ over-allotment option was exercised. In December 2020, the Company cancelled an aggregate of 3,306,250 shares of Class B common stock and issued an aggregate of 431,250 shares of Class B common stock to its independent director nominees, resulting in an aggregate of 4,312,500 shares of common stock outstanding. In January 2021, the Company effected a stock dividend of 1.2 shares for each share of common stock outstanding, resulting in the Company’s Initial Stockholders holding an aggregate of 5,175,000 Founder Shares. All share and
per-share
amounts have been retroactively restated to reflect the stock dividend (see Note 5).
|
Cash Flows from Operating Activities:
|
||||
Net loss
|
$ | (2,528 | ) | |
Adjustments to reconcile net loss to net cash used in operating activities:
|
||||
Changes in operating assets and liabilities:
|
||||
Accrued expenses
|
2,528 | |||
|
|
|||
Net cash used in operating activities
|
— | |||
|
|
|||
Cash Flows from Financing Activities:
|
||||
Proceeds from issuance of Class B common stock to the Initial Stockholders
|
25,000 | |||
Proceeds from promissory note — related party
|
180,632 | |||
Payment of offering costs
|
(48,784 | ) | ||
|
|
|||
Net cash provided by financing activities
|
156,848 | |||
|
|
|||
Net Change in Cash
|
156,848 | |||
Cash — Beginning
|
— | |||
|
|
|||
Cash — Ending
|
$ | 156,848 | ||
|
|
|||
Non-cash
Investing and Financing Activities:
|
||||
Deferred offering costs included in accrued offering costs
|
$ | 12,875 | ||
|
|
|||
Deferred offering costs paid through promissory note — related party
|
$ | 119,368 | ||
|
|
• |
in whole and not in part;
|
• |
at a price of $0.01 per Public Warrant;
|
• |
upon not less than 30 days’ prior written notice of redemption to each warrant holder; and
|
• |
if, and only if, the reported last sale price of the Class A common stock equals or exceeds $18.00 per share (as adjusted for stock splits, stock dividends, reorganizations, recapitalizations and the like) for any 20 trading days within a
30-trading
day period ending three business trading days before sending the notice of redemption to warrant holders.
|
YEAR ENDED
DECEMBER 31, |
||||||||
2019
|
2020
|
|||||||
REVENUE:
|
||||||||
Collaboration Revenue
|
$ | 3,001 | $ | 962 | ||||
Grant Revenue
|
— | 785 | ||||||
|
|
|
|
|||||
Total revenue
|
3,001 | 1,747 | ||||||
OPERATING EXPENSES:
|
||||||||
Research and development
|
23,489 | 42,866 | ||||||
General and administrative
|
8,714 | 11,165 | ||||||
|
|
|
|
|||||
Total operating expenses
|
32,203 | 54,031 | ||||||
|
|
|
|
|||||
LOSS FROM OPERATIONS
|
(29,202 | ) | (52,284 | ) | ||||
OTHER INCOME (EXPENSE), NET:
|
||||||||
Interest income
|
865 | 83 | ||||||
Interest expense
|
(317 | ) | (1,028 | ) | ||||
Change in fair value of warrant liability
|
5 | (22 | ) | |||||
|
|
|
|
|||||
Total other income (expense), net
|
553 | (967 | ) | |||||
|
|
|
|
|||||
Net loss
|
$ | (28,649 | ) | $ | (53,251 | ) | ||
|
|
|
|
|||||
Preferred Stock Dividends
|
(8,505 | ) | (13,445 | ) | ||||
|
|
|
|
|||||
Net loss attributable to common stockholders — basic and diluted (Note 15)
|
$ | (37,154 | ) | $ | (66,696 | ) | ||
|
|
|
|
|||||
Net loss per share attributable to common stockholders — basic and diluted
|
$ | (10.81 | ) | $ | (20.76 | ) | ||
|
|
|
|
|||||
Weighted-average common stock outstanding — basic and diluted
|
3,437,367 | 3,211,968 | ||||||
|
|
|
|
REDEEMABLE CONVERTIBLE PREFERRED STOCK
|
||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
$0.001 PAR VALUE
SERIES A |
$0.001 PAR VALUE
SERIES B |
$0.001 PAR VALUE
SERIES C |
$0.001 PAR VALUE
SERIES D |
COMMON STOCK
$0.001 PAR VALUE |
TREASURY STOCK
$0.001 PAR VALUE |
ADDITIONAL
PAID-IN
CAPITAL
|
ACCUMULATED
DEFICIT
|
TOTAL
STOCKHOLDERS’
DEFICIT
|
||||||||||||||||||||||||||||||||||||||||||||||||||||
SHARES
|
AMOUNT
|
SHARES
|
AMOUNT
|
SHARES
|
AMOUNT
|
SHARES
|
AMOUNT
|
SHARES
|
AMOUNT
|
SHARES
|
AMOUNT
|
|||||||||||||||||||||||||||||||||||||||||||||||||
BALANCE, January 1, 2019
|
18,430,769 | $ | 35,766 | 21,245,353 | $ | 18,671 | 26,182,114 | $ | 41,673 | — |
$
|
—
|
|
3,498,898 | $ | 3 | 1,200,000 | $ | (128 | ) | $ | 933 | $ | (59,359 | ) | (58,551 | ) | |||||||||||||||||||||||||||||||||
Issuance of series C redeemable convertible preferred stock, net of issuance costs of $30
|
— | — | — | — | 8,889,375 | 14,145 | — | — | — | — | ||||||||||||||||||||||||||||||||||||||||||||||||||
Vesting of restricted stock
|
— | — | — | — | — | — | — | — | 12,850 | — | — | |||||||||||||||||||||||||||||||||||||||||||||||||
Retirement of 1,200,000 shares of common stock held in treasury
|
(1,200,000 | ) | (1 | ) | (1,200,000 | ) | 128 | (127 | ) | — | ||||||||||||||||||||||||||||||||||||||||||||||||||
Stock-based compensation
|
— | — | — | — | 20,694 | 33 | — | — | 260,257 | 397 | — | 397 | ||||||||||||||||||||||||||||||||||||||||||||||||
Stocks issued for prior periods board fees
|
— | — | — | — | — | — | — | — | 520,243 | 1 | 172 | — | 173 | |||||||||||||||||||||||||||||||||||||||||||||||
Exercise of common stock options
|
— | — | — | — | — | — | — | — | 29,266 | — | — | 6 | — | 6 | ||||||||||||||||||||||||||||||||||||||||||||||
Net loss
|
— | — | — | — | — | — | — | — | — | — | — | — | — | (28,649 | ) | (28,649 | ) | |||||||||||||||||||||||||||||||||||||||||||
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|||||||||||||||||||||||||||||||
BALANCE, January 1, 2020
|
18,430,769 | $ | 35,766 | 21,245,353 | $ | 18,671 | 35,092,183 | $ | 55,851 | — |
$
|
—
|
|
3,121,514 | $ | 3 | — | $ | — | $ | 1,381 | $ | (88,008 | ) | $ | (86,624 | ) | |||||||||||||||||||||||||||||||||
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
REDEEMABLE CONVERTIBLE PREFERRED STOCK
|
||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
$0.001 PAR VALUE
SERIES A |
$0.001 PAR VALUE
SERIES B |
$0.001 PAR VALUE
SERIES C |
$0.001 PAR VALUE
SERIES D |
COMMON STOCK
$0.001 PAR VALUE |
TREASURY
STOCK $0.001 PAR VALUE |
ADDITIONAL
PAID-IN
CAPITAL
|
ACCUMULATED
DEFICIT
|
TOTAL
STOCKHOLDERS’
DEFICIT
|
||||||||||||||||||||||||||||||||||||||||||||||||||||
SHARES
|
AMOUNT
|
SHARES
|
AMOUNT
|
SHARES
|
AMOUNT
|
SHARES
|
AMOUNT
|
SHARES
|
AMOUNT
|
SHARES
|
AMOUNT
|
|||||||||||||||||||||||||||||||||||||||||||||||||
Issuance of series D redeemable convertible preferred stock, net of issuance costs of $543
|
— | — | — | — | — | — | 60,184,332 | 108,499 | 357 | — | 357 | |||||||||||||||||||||||||||||||||||||||||||||||||
Vesting of restricted stock
|
31,086 | — | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Stock-based compensation
|
— | — | — | — | — | — | — | — | 659 | — | 659 | |||||||||||||||||||||||||||||||||||||||||||||||||
Exercise of common stock options
|
— | — | — | — | — | — | — | — | 100,036 | — | — | 37 | — | 37 | ||||||||||||||||||||||||||||||||||||||||||||||
Net loss
|
— | — | — | — | — | — | — | — | — | — | — | — | — | (53,251 | ) | (53,251 | ) | |||||||||||||||||||||||||||||||||||||||||||
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|||||||||||||||||||||||||||||||
BALANCE, December 31, 2020
|
18,430,769 | $ | 35,766 | 21,245,353 | $ | 18,671 | 35,092,183 | $ | 55,851 | 60,184,332 |
$
|
108,499 |
|
3,252,636 | $ | 3 | — |
$
|
—
|
|
$ | 2,434 | $ | (141,259 | ) | $ | (138,822 | ) | ||||||||||||||||||||||||||||||||
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
YEAR ENDED DECEMBER 31,
|
||||||||
2019
|
2020
|
|||||||
Reconciliation of cash, cash equivalents and restricted cash:
|
||||||||
Cash and cash equivalents
|
$ | 25,916 | $ | 95,068 | ||||
Restricted cash
|
30 | 80 | ||||||
|
|
|
|
|||||
Total cash, cash equivalents and restricted cash
|
$ | 25,946 | $ | 95,148 | ||||
|
|
|
|
1.
|
NATURE OF BUSINESS AND BASIS OF PRESENTATION
|
2.
|
SUMMARY OF SIGNIFICANT ACCOUNTING POLICIES
|
• |
Level 1 inputs are quoted prices (unadjusted) in active markets for identical assets or liabilities.
|
• |
Level 2 inputs are inputs other than quoted prices included within Level 1 that are observable for a similar asset or liability, either directly or indirectly.
|
• |
Level 3 inputs are unobservable inputs that reflect the Company’s own assumptions about the inputs that market participants would use in pricing the asset or liability.
|
ESTIMATED USEFUL LIFE
|
||
Laboratory equipment
|
5 years | |
Computer equipment and software
|
3 years | |
Leasehold improvements
|
Shorter of useful life or lease term |
• |
Identify the contract with a customer
|
• |
Identify the performance obligations in the contract
|
• |
Determine the transaction price
|
• |
Allocate the transaction price to the performance obligations in the contract
|
• |
Recognize revenue when or as performance obligations are satisfied
|
3.
|
BAYER ASSET ACQUISITION
|
4.
|
FAIR VALUE MEASUREMENTS
|
DESCRIPTION
|
DECEMBER 31,
2019 |
QUOTED PRICES
IN ACTIVE MARKETS FOR IDENTICAL ASSETS
(LEVEL 1)
|
SIGNIFICANT
OBSERVABLE INPUTS
(LEVEL 2)
|
UNOBSERVABLE
SIGNIFICANT INPUTS
(LEVEL 3)
|
||||||||||||
Asset
|
||||||||||||||||
Money market funds
|
$ | 26,032 | $ | 26,032 | $ | — | $ | — | ||||||||
|
|
|
|
|
|
|
|
|||||||||
Total financial assets
|
$ | 26,032 | $ | 26,032 | $ | — | $ | — | ||||||||
|
|
|
|
|
|
|
|
|||||||||
Liabilitiy
|
||||||||||||||||
Warrant Liability
|
$ | 103 | $ | — | $ | — | $ | 103 | ||||||||
|
|
|
|
|
|
|
|
|||||||||
$ | 103 | $ | — | $ | — | $ | 103 | |||||||||
|
|
|
|
|
|
|
|
DESCRIPTION
|
DECEMBER 31,
2020 |
QUOTED PRICES
IN ACTIVE MARKETS FOR IDENTICAL ASSETS
(LEVEL 1)
|
SIGNIFICANT
OBSERVABLE INPUTS (LEVEL 2) |
SIGNIFICANT
UNOBSERVABLE INPUTS
(LEVEL 3)
|
||||||||||||
Asset
|
||||||||||||||||
Money market funds
|
||||||||||||||||
Total financial assets
|
$ | 55,747 | $ | 55,747 | $ | — | $ | — | ||||||||
|
|
|
|
|
|
|
|
|||||||||
$ | 55,747 | $ | 55,747 | $ | — | $ | — | |||||||||
|
|
|
|
|
|
|
|
|||||||||
Liability
|
||||||||||||||||
Warrant Liability
|
$ | 125 | $ | — | $ | — | $ | 125 | ||||||||
|
|
|
|
|
|
|
|
|||||||||
$ | 125 | $ | — | $ | — | $ | 125 | |||||||||
|
|
|
|
|
|
|
|
WARRANT
LIABILITY |
||||
Balance - January 1, 2019
|
$ | 108 | ||
Change in fair value
|
(5 | ) | ||
|
|
|||
Balance - December 31, 2019
|
103 | |||
Change in fair value
|
22 | |||
|
|
|||
Balance - December 31, 2020
|
$ | 125 | ||
|
|
5.
|
COLLABORATION ARRANGEMENT
|
6.
|
GRANT REVENUE
|
7.
|
PROPERTY AND EQUIPMENT, NET
|
DECEMBER 31,
|
||||||||
2019
|
2020
|
|||||||
Computer hardware and software
|
$ | 12 | $ | 533 | ||||
Laboratory equipment
|
4,320 | 8,040 | ||||||
Leasehold improvements
|
228 | 4,545 | ||||||
Construction in progress
|
1,181 | 6,847 | ||||||
|
|
|
|
|||||
Total
|
5,741 | 19,965 | ||||||
Less: Accumulated depreciation and amortization
|
(1,992 | ) | (3,686 | ) | ||||
|
|
|
|
|||||
Property and equipment, net
|
$ | 3,749 | $ | 16,279 | ||||
|
|
|
|
8.
|
ACCRUED EXPENSES
|
DECEMBER 31,
|
||||||||
2019
|
2020
|
|||||||
Accrued Employee compensation and benefits
|
$ | 2,752 | $ | 4,024 | ||||
Accrued Research and development
|
405 | 612 | ||||||
Accrued Professional fees
|
242 | 568 | ||||||
Accrued Other
|
119 | 1,622 | ||||||
|
|
|
|
|||||
Total accrued expenses
|
$ | 3,518 | $ | 6,826 | ||||
|
|
|
|
9.
|
DEBT
|
a) |
From the date of the initial closing of the then-next equity financing of the Company (the “Series D Financing”) until maturity, conversion at the option of the holder into Series D Preferred Stock (based upon the original issue price of the Series D Preferred Stock) or the right to receive certain royalty payments over a
15-year
period, commencing on the conversion date (such royalty payment being equal to the net sales of specified GLPRI products multiplied by the adjusted royalty rate, such royalty payment not to exceed the net profit in any quarter).
|
b) |
Upon the occurrence of certain contingent events after the Company’s Series D Financing and before maturity, automatic conversion into Series D Preferred Stock (based upon on the original issue price of the Series D Preferred Stock).
|
c) |
Automatic redemption upon an event of default, as defined in the 2020 Notes. Upon the occurrence of an event of default, the 2020 Notes will either automatically become due and payable or can become due and payable at the holder’s option (based on the nature of the event of default). Upon such acceleration, all outstanding principal (with no penalty) and unpaid accrued interest will become payable.
|
10.
|
WARRANTS
|
Warrant Class
|
Shares
|
Issuance Date
|
Exercise Price
|
Expiration Date
|
||||||||||
Series D
|
874,130 | July 24, 2020 | $ | 1.8118 |
The earlier of July 24, 2025 or the
date of a qualifying acquisition or IPO |
|||||||||
|
|
|||||||||||||
Total
|
874,130 | |||||||||||||
|
|
Warrant Class
|
Shares
|
Issuance Date
|
Exercise Price
|
Expiration Date
|
||||||||||
Common stock warrant
|
40,000 | June 14, 2016 | $ | 0.22 |
The earlier of June 13, 2026, or the
date of a qualifying acquisition |
|||||||||
|
|
|||||||||||||
Total
|
40,000 | |||||||||||||
|
|
11.
|
REDEEMABLE CONVERTIBLE PREFERRED STOCK
|
AS OF DECEMBER 31, 2019
|
||||||||||||||||||||
PREFERRED
STOCK AUTHORIZED |
PREFERRED
STOCK ISSUED AND OUTSTANDING |
CARRYING
VALUE |
LIQUIDATION
VALUE |
COMMON
STOCK ISSUABLE UPON CONVERSION |
||||||||||||||||
Series
A-1
|
2,865,698 | 2,807,571 | $ | 4,411 | $ | 5,858 | 3,550,068 | |||||||||||||
Series
A-2
|
7,018,203 | 6,993,693 | 11,438 | 17,302 | 9,058,757 | |||||||||||||||
Series
A-3
|
8,647,679 | 8,629,505 | 19,917 | 27,347 | 12,274,540 | |||||||||||||||
Series B
|
21,245,353 | 21,245,353 | 18,671 | 21,108 | 21,245,353 | |||||||||||||||
Series C
|
35,152,184 | 35,092,183 | 55,851 | 60,470 | 35,092,183 | |||||||||||||||
|
|
|
|
|
|
|
|
|
|
|||||||||||
74,929,117 | 74,768,305 | $ | 110,288 | $ | 132,085 | 81,220,901 | ||||||||||||||
|
|
|
|
|
|
|
|
|
|
AS OF DECEMBER 31, 2020
|
||||||||||||||||||||
PREFERRED
STOCK AUTHORIZED |
PREFERRED
STOCK ISSUED AND OUTSTANDING |
CARRYING
VALUE |
LIQUIDATION
VALUE |
COMMON
STOCK ISSUABLE UPON CONVERSION |
||||||||||||||||
Series
A-1
|
2,865,698 | 2,807,571 | $ | 4,411 | $ | 6,079 | 3,550,068 | |||||||||||||
Series
A-2
|
7,018,203 | 6,993,693 | 11,438 | 18,224 | 9,058,757 | |||||||||||||||
Series
A-3
|
8,647,679 | 8,629,505 | 19,917 | 28,952 | 12,274,540 | |||||||||||||||
Series B
|
21,245,353 | 21,245,353 | 18,671 | 22,567 | 21,245,353 | |||||||||||||||
Series C
|
35,152,184 | 35,092,183 | 55,851 | 65,014 | 35,092,183 | |||||||||||||||
Series D
|
71,019,827 | 60,184,332 | 108,499 | 113,736 | 60,184,332 | |||||||||||||||
|
|
|
|
|
|
|
|
|
|
|||||||||||
145,948,944 | 134,952,637 | $ | 218,787 | $ | 254,572 | 141,405,233 | ||||||||||||||
|
|
|
|
|
|
|
|
|
|
12.
|
COMMON STOCK
|
DECEMBER 31
|
||||||||
2019
|
2020
|
|||||||
Redeemable convertible preferred stock
|
81,220,901 | 141,405,233 | ||||||
Convertible debt with accrued interest
|
— | 9,583,023 | ||||||
Unvested restricted stock
|
27,842 | 37,465 | ||||||
Options to purchase common stock
|
19,701,693 | 22,538,570 | ||||||
Common stock warrants
|
40,000 | 40,000 | ||||||
|
|
|
|
|||||
100,990,436 | 173,604,291 | |||||||
|
|
|
|
13.
|
TREASURY STOCK
|
14.
|
STOCK-BASED COMPENSATION
|
YEAR ENDED DECEMBER 31
|
||||
2019
|
2020
|
|||
Fair value of underlying common stock
|
$0.33 | $0.46—$0.65 | ||
Weighted average risk-free interest rate
|
1.62%—2.56% | 0.27%—1.55% | ||
Expected term (in years)
|
5.0—6.4 | 5.0—6.0 | ||
Expected volatility
|
70.0%—74.4% | 69.5%—70.4% | ||
Expected dividend yield
|
0 | 0 |
SHARES
|
WEIGHTED-
AVERAGE EXERCISE PRICE |
WEIGHTED-AVERAGE
REMAINING CONTRACTUAL TERM (in years) |
AGGREGATE
INTRINSIC VALUE |
|||||||||||||
Outstanding at December 31, 2019
|
19,701,693 | $ | 0.29 | 9.0 | $ | 3,404 | ||||||||||
Granted
|
8,354,564 | 0.65 | ||||||||||||||
Exercised
|
(140,745 | ) | 0.26 | $ | 79 | |||||||||||
Cancelled or forfeited
|
(5,376,942 | ) | 0.32 | |||||||||||||
|
|
|
|
|||||||||||||
Outstanding at December 31, 2020
|
22,538,570 | $ | 0.41 | 8.5 | $ | 9,170 | ||||||||||
|
|
|
|
|||||||||||||
Vested and expected to vest at December 31, 2019
|
19,701,693 | $ | 0.29 | 9.0 | $ | 3,404 | ||||||||||
Vested and expected to vest at December 31, 2020
|
22,538,570 | $ | 0.41 | 8.5 | $ | 9,170 | ||||||||||
Exercisable at December 31, 2019
|
4,354,321 | $ | 0.21 | 6.6 | $ | 1,083 | ||||||||||
Exercisable at December 31, 2020
|
6,947,529 | $ | 0.25 | 7.0 | $ | 3,957 |
SHARES
|
WEIGHTED-
AVERAGE
GRANT-DATE
FAIR VALUE |
|||||||
Unvested shares as of December 31, 2018
|
40,692 | $ | 0.23 | |||||
Vested
|
(12,850 | ) | 0.23 | |||||
|
|
|
|
|||||
Unvested shares as of December 31, 2019
|
27,842 | $ | 0.23 | |||||
|
|
|
|
|||||
Granted
|
40,709 | 0.46 | ||||||
Vested
|
(31,086 | ) | 0.36 | |||||
|
|
|
|
|||||
Unvested shares as of December 31, 2020
|
37,465 | $ | 0.37 | |||||
|
|
|
|
YEAR ENDED DECEMBER 31
|
||||||||
2019
|
2020
|
|||||||
Research and development
|
$ | 166 | $ | 306 | ||||
General and administrative
|
264 | 353 | ||||||
|
|
|
|
|||||
$ | 430 | $ | 659 | |||||
|
|
|
|
15.
|
NET LOSS PER SHARE
|
YEAR ENDED DECEMBER 31,
|
||||||||
2019
|
2020
|
|||||||
Numerator:
|
||||||||
Net loss
|
$ | (28,649 | ) | $ | (53,251 | ) | ||
Less: Accruals of dividends of preferred stock
|
(8,505 | ) | (13,445 | ) | ||||
|
|
|
|
|||||
Net loss attributable to common stockholders
|
$ | (37,154 | ) | $ | (66,696 | ) | ||
|
|
|
|
|||||
Denominator:
|
||||||||
Weighted-average common stock outstanding
|
3,437,367 | 3,211,968 | ||||||
|
|
|
|
|||||
Net loss per share, basic and diluted
|
$ | (10.81 | ) | $ | (20.76 | ) | ||
|
|
|
|
YEAR ENDED DECEMBER 31,
|
||||||||
2019
|
2020
|
|||||||
Preferred stock
|
81,220,901 | 141,405,233 | ||||||
Convertible debt with accrued interest
|
— | 9,583,023 | ||||||
Unvested restricted stock
|
27,842 | 37,465 | ||||||
Options to purchase common stock
|
19,701,693 | 22,538,570 | ||||||
Warrants
|
171,096 | 1,045,226 | ||||||
|
|
|
|
|||||
101,121,532 | 174,609,517 | |||||||
|
|
|
|
16.
|
INCOME TAXES
|
YEAR ENDED DECEMBER 31,
|
||||||||
2019
|
2020
|
|||||||
Federal income tax (benefit)/expense at statutory rate
|
21.0 | % | 21.0 | % | ||||
State income tax benefit
|
6.0 | % | 5.4 | % | ||||
Permanent items
|
-0.3 | % | -0.2 | % | ||||
Change in Valuation Allowance
|
-29.7 | % | -29.3 | % | ||||
Federal R&D Tax Credits
|
3.1 | % | 3.1 | % | ||||
Other
|
-0.1 | % | 0.0 | % | ||||
|
|
|
|
|||||
Effective income tax rate
|
0.0 | % | 0.0 | % | ||||
|
|
|
|
YEAR ENDED DECEMBER 31,
|
||||||||
2019
|
2020
|
|||||||
Deferred tax assets
|
||||||||
Federal net operating loss carryforwards
|
$ | 13,626 | $ | 26,464 | ||||
State net operating loss carryforwards
|
3,807 | 6,542 | ||||||
Tax credits
|
1,759 | 4,059 | ||||||
Stock based compensation
|
17 | 89 | ||||||
Capitalized research and development expenses
|
5,157 | 4,398 | ||||||
Accruals and other
|
517 | 763 | ||||||
|
|
|
|
|||||
Total deferred tax assets
|
24,883 | 42,315 | ||||||
Valuation allowance
|
(24,340 | ) | (39,965 | ) | ||||
|
|
|
|
|||||
Total net deferred tax assets
|
$ | 543 | $ | 2,350 | ||||
|
|
|
|
|||||
Deferred tax liabilities
|
||||||||
Depreciation and amortization
|
$ | (543 | ) | $ | (2,350 | ) | ||
|
|
|
|
|||||
Total deferred tax liabilities
|
$ | (543 | ) | $ | (2,350 | ) | ||
|
|
|
|
|||||
Total deferred tax assets (liability)
|
$ | — | $ | — | ||||
|
|
|
|
17.
|
COMMITMENTS AND CONTINGENCIES
|
FOR THE YEAR ENDED DECEMBER 31,
|
||||
2021
|
$ | 3,436 | ||
2022
|
6,108 | |||
2023
|
4,879 | |||
2024
|
655 | |||
2025
|
405 | |||
Thereafter
|
402 | |||
|
|
|||
$ | 15,885 | |||
|
|
18.
|
LICENSE AGREEMENT
|
19.
|
SUBSEQUENT EVENTS
|
NINE MONTHS ENDED
SEPTEMBER 30, |
||||||||
2020
|
2021
|
|||||||
REVENUE:
|
||||||||
Collaboration Revenue
|
$ | 962 | $ | — | ||||
Grant Revenue
|
513 | 1,180 | ||||||
|
|
|
|
|||||
Total Revenue
|
1,475 | 1,180 | ||||||
OPERATING EXPENSES:
|
||||||||
Research and development
|
28,901 | 62,081 | ||||||
General and administrative
|
7,699 | 13,943 | ||||||
|
|
|
|
|||||
Total operating expenses
|
36,600 | 76,024 | ||||||
|
|
|
|
|||||
LOSS FROM OPERATIONS
|
(35,125 | ) | (74,844 | ) | ||||
OTHER INCOME (EXPENSE), NET:
|
||||||||
Interest income
|
74 | 20 | ||||||
Interest expense
|
(704 | ) | (1,471 | ) | ||||
Change in fair value of warrant liability
|
(8 | ) | (1,343 | ) | ||||
|
|
|
|
|||||
Total other income (expense), net
|
(638 | ) | (2,794 | ) | ||||
|
|
|
|
|||||
Net loss
|
$ | (35,763 | ) | $ | (77,638 | ) | ||
|
|
|
|
|||||
Preferred Stock Dividends
|
(9,101 | ) | (13,033 | ) | ||||
|
|
|
|
|||||
Net Loss available to common stockholders
|
$ | (44,864 | ) | $ | (90,671 | ) | ||
|
|
|
|
|||||
Net loss per share available to common stockholders — basic and diluted
|
$ | (14.01 | ) | $ | (27.27 | ) | ||
|
|
|
|
|||||
Weighted-average common stock outstanding — basic and diluted
|
3,201,202 | 3,324,547 | ||||||
|
|
|
|
$0.001 PAR VALUE
CONVERTIBLE PREFERRED STOCK |
COMMON STOCK
$0.001 PAR VALUE |
ADDITIONAL
PAID-IN
CAPITAL
|
ACCUMULATED
DEFICIT
|
TOTAL
STOCKHOLDERS’
DEFICIT
|
||||||||||||||||||||||||
SHARES
|
AMOUNT
|
SHARES
|
AMOUNT
|
|||||||||||||||||||||||||
BALANCE, January 1, 2020
|
74,768,305 | $ | 110,288 | 3,121,514 | $ | 3 | $ | 1,381 | $ | (88,008 | ) | $ | (86,624 | ) | ||||||||||||||
Issuance of series D redeemable convertible preferred stock at $1.8118 per share, net of issuance costs of $543
|
60,184,332 | $ | 108,499 | 357 | 357 | |||||||||||||||||||||||
Vesting of restricted stock
|
23,814 | — | — | — | ||||||||||||||||||||||||
Stock-based compensation
|
442 | — | 442 | |||||||||||||||||||||||||
Exercise of common stock options
|
92,004 | — | 34 | — | 34 | |||||||||||||||||||||||
Net loss
|
— | — | — | (35,763 | ) | (35,763 | ) | |||||||||||||||||||||
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|||||||||||||||
BALANCE, September 30, 2020
|
134,952,637 | $ | 218,787 | 3,237,332 | $ | 3 | $ | 2,214 | $ | (123,771 | ) | $ | (121,554 | ) | ||||||||||||||
|
|
|
|
|
|
|
|
|
|
|
|
|
|
$0.001 PAR VALUE
CONVERTIBLE PREFERRED STOCK |
COMMON STOCK
$0.001 PAR VALUE |
ADDITIONAL
PAID-IN
CAPITAL
|
ACCUMULATED
DEFICIT
|
TOTAL
STOCKHOLDERS’
DEFICIT
|
||||||||||||||||||||||||
SHARES
|
AMOUNT
|
SHARES
|
AMOUNT
|
|||||||||||||||||||||||||
BALANCE, January 1, 2021
|
134,952,637 | $ | 218,787 | 3,252,636 | $ | 3 | $ | 2,434 | $ | (141,259 | ) | $ | (138,822 | ) | ||||||||||||||
Vesting of restricted stock
|
39,876 | — | — | — | ||||||||||||||||||||||||
Warrants issued in connection with Debt
|
231 | 231 | ||||||||||||||||||||||||||
Stock-based compensation
|
1,292 | — | 1,292 | |||||||||||||||||||||||||
Exercise of common stock options
|
180,218 | — | 105 | — | 105 | |||||||||||||||||||||||
Net loss
|
— | — | — | (77,638 | ) | (77,638 | ) | |||||||||||||||||||||
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|||||||||||||||
BALANCE, September 30, 2021
|
134,952,637 | $ | 218,787 | 3,472,730 | $ | 3 | $ | 4,062 | $ | (218,897 | ) | $ | (214,832 | ) | ||||||||||||||
|
|
|
|
|
|
|
|
|
|
|
|
|
|
1.
|
NATURE OF BUSINESS AND BASIS OF PRESENTATION
|
2.
|
SUMMARY OF SIGNIFICANT ACCOUNTING POLICIES
|
3.
|
BAYER ASSET ACQUISITION
|
4.
|
LICENSE AGREEMENT
|
5.
|
FAIR VALUE MEASUREMENTS
|
DESCRIPTION
|
DECEMBER 31,
2020 |
QUOTED PRICES
IN ACTIVE MARKETS FOR IDENTICAL ASSETS (LEVEL 1) |
SIGNIFICANT
OBSERVABLE INPUTS (LEVEL 2) |
SIGNIFICANT
UNOBSERVABLE INPUTS (LEVEL 3) |
||||||||||||
Asset
|
||||||||||||||||
Money market funds
|
$ | 55,747 | $ | 55,747 | $ | — | $ | — | ||||||||
|
|
|
|
|
|
|
|
|||||||||
Total financial assets
|
$ | 55,747 | $ | 55,747 | $ | — | $ | — | ||||||||
|
|
|
|
|
|
|
|
|||||||||
Liabilitiy
|
||||||||||||||||
Warrant Liability
|
$ | 125 | $ | — | $ | — | $ | 125 | ||||||||
|
|
|
|
|
|
|
|
|||||||||
$ | 125 | $ | — | $ | — | $ | 125 | |||||||||
|
|
|
|
|
|
|
|
DESCRIPTION
|
SEPtEMBER 30,
2021 |
QUOTED PRICES
IN ACTIVE MARKETS FOR IDENTICAL ASSETS (LEVEL 1) |
SIGNIFICANT
OBSERVABLE INPUTS (LEVEL 2) |
SIGNIFICANT
UNOBSERVABLE INPUTS (LEVEL 3) |
||||||||||||
Asset
|
||||||||||||||||
Money market funds
|
$ | 33,714 | $ | 33,714 | $ | — | $ | — | ||||||||
|
|
|
|
|
|
|
|
|||||||||
Total financial assets
|
$ | 33,714 | $ | 33,714 | $ | — | $ | — | ||||||||
|
|
|
|
|
|
|
|
|||||||||
Liabilitiy
|
||||||||||||||||
Warrant Liability
|
$ | 1,606 | $ | — | $ | — | $ | 1,606 | ||||||||
|
|
|
|
|
|
|
|
|||||||||
$ | 1,606 | $ | — | $ | — | $ | 1,606 | |||||||||
|
|
|
|
|
|
|
|
WARRANT
LIABILITY |
||||
Balance - January 1, 2020
|
$ | 103 | ||
Change in fair value
|
8 | |||
|
|
|||
Balance - September 30, 2020
|
$ | 111 | ||
|
|
WARRANT
LIABILITY |
||||
Balance - January 1, 2021
|
$ | 125 | ||
Issuance of warrant
|
138 | |||
Change in fair value
|
1,343 | |||
|
|
|||
Balance - September 30, 2021
|
$ | 1,606 | ||
|
|
6.
|
COLLABORATION ARRANGEMENT
|
7.
|
GRANT REVENUE
|
8.
|
PROPERTY AND EQUIPMENT, NET
|
DECEMBER 31,
2020 |
SEPTEMBER 30,
2021 |
|||||||
Computer hardware and software
|
$ | 533 | $ | 701 | ||||
Laboratory equipment
|
8,040 | 15,816 | ||||||
Leasehold improvements
|
4,545 | 9,832 | ||||||
Construction in progress
|
6,847 | 2,695 | ||||||
|
|
|
|
|||||
Total
|
19,965 | 29,044 | ||||||
Less: Accumulated depreciation and amortization
|
(3,686 | ) | (7,300 | ) | ||||
|
|
|
|
|||||
Property and equipment, net
|
$ | 16,279 | $ | 21,744 | ||||
|
|
|
|
9.
|
ACCRUED EXPENSES
|
DECEMBER 31,
2020 |
SEPTEMBER 30,
2021 |
|||||||
Accrued employee compensation and benefits
|
$ | 4,024 | $ | 5,332 | ||||
Accrued research and development
|
612 | 1,659 | ||||||
Accrued professional fees
|
568 | 933 | ||||||
Accured other
|
1,622 | 1,427 | ||||||
|
|
|
|
|||||
Total accrued expenses
|
$ | 6,826 | $ | 9,351 | ||||
|
|
|
|
10.
|
DEBT
|
11.
|
WARRANTS
|
AS OF DECEMBER 31, 2020
|
||||||||||||||||||||
Warrant Class
|
Shares
|
Fair Value
|
Issuance Date
|
Exercise Price
|
Expiration Date
|
|||||||||||||||
Series A-1
|
58,127 | $ | 75 | December 31, 2011 | $ | 0.15 |
|
The earlier of January 17, 2022, or a
deemed liquidation or IPO |
|
|||||||||||
Series A-2
|
24,510 | 21 | August 26, 2014 | $ | 1.53 |
|
The earlier of August 25, 2024 or the
date of a qualifying acquisition |
|
||||||||||||
Series A-3
|
18,174 | 29 | December 18, 2015 | $ | 0.23 |
|
The earlier of December 18, 2025 or
a deemed liquidation or IPO |
|
||||||||||||
|
|
|
|
|||||||||||||||||
Total
|
100,811 | $ | 125 | |||||||||||||||||
|
|
|
|
As of December 31, 2020
|
||||||||||||
Valuation Assumptions
|
Series A-1
|
Series A-2
|
Series A-3
|
|||||||||
Fair value of underlying series of preferred stock
|
$ | 1.45 | $ | 1.54 | $ | 1.76 | ||||||
Risk free interest rate
|
0.10 | % | 0.27 | % | 0.36 | % | ||||||
Expected volatility
|
88.4 | % | 78.5 | % | 82.4 | % | ||||||
Estimated time (in years)
|
1.05 | 3.65 | 4.97 |
As of September 30, 2021
|
||||||||||||
Valuation Assumptions
|
Series A-1
|
Series A-2
|
Series A-3
|
|||||||||
Fair value of underlying series of preferred stock
|
$ | 5.55 | $ | 5.58 | $ | 5.64 | ||||||
Risk free interest rate
|
0.04 | % | 0.53 | % | 0.76 | % | ||||||
Expected volatility
|
72.7 | % | 89.8 | % | 83.2 | % | ||||||
Estimated time (in years)
|
0.30 | 2.90 | 4.22 |
Warrant Class
|
Shares
|
Issuance Date
|
Exercise Price
|
Expiration Date
|
||||||||||||
Series D
|
874,130 | July 24, 2020 | $ | 1.8118 |
|
The earlier of July 24, 2025
or the date of a qualifying acquisition or IPO |
|
|||||||||
|
|
|||||||||||||||
Total
|
874,130 | |||||||||||||||
|
|
Warrant Class
|
Shares
|
Fair
Value |
Issuance Date
|
Exercise
Price |
Expiration Date
|
|||||||||||||
Common stock
|
219,839 | $ | 1,084 | March 29, 2021 | $ | 0.82 |
The earlier of March 29, 2031
or the date of a qualifying acquisition |
Valuation Assumptions
|
At Issuance (as of
March 29, 2021) |
As of September 30,
2021
|
||||||
Fair value of common stock
|
$ | 0.82 | $ | 5.26 | ||||
Risk free interest rate
|
1.73 | % | 1.52 | % | ||||
Expected volatility
|
72.10 | % | 82.50 | % | ||||
Expected term (in years)
|
10.00 | 9.5 |
As of September 30, 2021
|
||||||||||||||
Warrant Class
|
Shares
|
Issuance Date
|
Price per Share
|
Expiration Date
|
||||||||||
Common stock warrant
|
40,000 | June 14, 2016 | $ | 0.22 | The earlier of June 13, 2026 or the date of a qualifying acquisition | |||||||||
Common stock warrant
|
51,724 | September 22, 2021 | $ | 1.74 | The earlier of September 21, 2031 or the date of a qualifying acquisition | |||||||||
|
|
|||||||||||||
Total
|
91,724 | |||||||||||||
|
|
12.
|
REDEEMABLE CONVERTIBLE PREFERRED STOCK
|
Redeemable Convertible Preferred Stock Classes
|
December 31,
2020 |
September 30,
2021 |
||||||
Series A-1 redeemable convertible preferred stock, $0.001 par value, 2,865,698 shares authorized, 2,807,571 shares issued and outstanding as of December 31, 2020 and September 30, 2021 Liquidation preference of $6,079 and $6,247 at December 31, 2020 and September 30, 2021 respectively
|
$ | 4,411 | $ | 4,411 | ||||
Series A-2 redeemable convertible preferred stock, $0.001 par value, 7,018,203 shares authorized, 6,993,693 shares issued and outstanding as of December 31, 2020 and September 30, 2021 Liquidation preference of $18,224 and $18,913 at December 31, 2020 and September 30, 2021 respectively
|
11,438 | 11,438 | ||||||
Series A-3 redeemable convertible preferred stock, $0.001 par value, 8,647,679 shares authorized 8,629,505 shares issued and outstanding as of December 31, 2020 and September 30, 2021 Liquidation preference of $28,952 and $30,149 at December 31, 2020 and September 30, 2021 respectively
|
19,917 | 19,917 | ||||||
Series B redeemable convertible preferred stock, $0.001 par value, 21,245,353 shares authorized, issued and outstanding as of December 31, 2020 and September 30, 2021 Liquidation preference of $22,567 and $23,656 at December 31, 2020 and September 30, 2021 respectively
|
18,671 | 18,671 | ||||||
Series C redeemable convertible preferred stock, $0.001 par value, 35,152,184 shares authorized, 35,092,183 shares issued and outstanding as of December 31, 2020 and September 30, 2021 Liquidation preference of $65,014 and $68,379 at December 31, 2020 and September 30, 2021 respectively
|
55,851 | 55,851 | ||||||
Series D redeemable convertible preferred stock, $0.001 par value, 71,019,827 shares authorized, 60,184,332 shares issued and outstanding and as of December 31, 2020 and September 30, 2021 Liquidation preference of $113,736 and $120,261 at December 31, 2020 and September 30, 2021 respectively
|
108,499 | 108,499 | ||||||
|
|
|
|
|||||
Total
|
$ | 218,787 | $ | 218,787 | ||||
|
|
|
|
13.
|
COMMON STOCK
|
DECEMBER 31,
2020 |
SEPTEMBER 30,
2021 |
|||||||
Redeemable convertible preferred stock
|
141,405,233 | 141,405,233 | ||||||
Convertible debt with accrued interest
|
9,583,023 | 9,934,084 | ||||||
Unvested restricted stock
|
37,465 | 61,839 | ||||||
Options to purchase common stock
|
22,538,570 | 26,490,587 | ||||||
Warrants
|
1,045,226 | 1,299,548 | ||||||
|
|
|
|
|||||
174,609,517 | 179,191,290 | |||||||
|
|
|
|
14.
|
STOCK-BASED COMPENSATION
|
NINE MONTHS ENDED SEPTEMBER 30,
|
||||
2020
|
2021
|
|||
Fair value of underlying common stock
|
$0.46 - $0.65
|
$0.82 - $5.26
|
||
Weighted average risk-free interest rate
|
0.27% -1.55%
|
0.48% -1.29%
|
||
Expected term (in years)
|
5 - 6 | 5 - 6 | ||
Expected volatility
|
69.53% -70.36%
|
67.27% - 68.80%
|
||
Expected dividend yield
|
0.00% | 0.00% |
SHARES
|
WEIGHTED-
AVERAGE EXERCISE PRICE |
WEIGHTED-
AVERAGE REMAINING CONTRACTUAL TERM (in years) |
AGGREGATE
INTRINSIC VALUE (in thousands) |
|||||||||||||
Outstanding at December 31, 2020
|
22,538,570 | $ | 0.41 | 8.5 | $ | 9,170 | ||||||||||
Granted
|
4,594,102 | 1.33 | ||||||||||||||
Cancelled or Forfeited
|
(397,617 | ) | 0.39 | |||||||||||||
Exercised
|
(244,468 | ) | 0.43 | $ | 1,181 | |||||||||||
|
|
|
|
|||||||||||||
Outstanding at September 30, 2021
|
26,490,587 | $ | 0.57 | 8.1 | $ | 124,331 | ||||||||||
|
|
|
|
|||||||||||||
Vested and expected to vest at December 31, 2020
|
22,538,570 | $ | 0.41 | 8.5 | $ | 9,170 | ||||||||||
Vested and expected to vest at September 30, 2021
|
26,490,587 | $ | 0.57 | 8.1 | $ | 124,331 | ||||||||||
Exercisable at December 31, 2020
|
6,947,529 | $ | 0.25 | 7.0 | $ | 3,957 | ||||||||||
Exercisable at September 30, 2021
|
9,203,021 | $ | 0.28 | 6.6 | $ | 45,789 |
SHARES
|
WEIGHTED
AVERAGE GRANT DATE FAIR VALUE |
|||||||
Unvested shares as of December 31, 2020
|
37,465 | $ | 0.37 | |||||
Granted
|
64,250 | 0.82 | ||||||
Vested
|
(39,876 | ) | 0.55 | |||||
|
|
|
|
|||||
Unvested at September 30, 2021
|
61,839 | $ | 0.72 | |||||
|
|
|
|
NINE MONTHS ENDED
SEPTEMBER 30, |
||||||||
2020
|
2021
|
|||||||
Research and development
|
$ | 201 | $ | 580 | ||||
General and administrative
|
241 | 712 | ||||||
|
|
|
|
|||||
Total stock-based compensation expense
|
$ | 442 | $ | 1,292 | ||||
|
|
|
|
15.
|
NET LOSS PER SHARE
|
NINE MONTHS ENDED
SEPTEMBER 30, |
||||||||
2020
|
2021
|
|||||||
Numerator:
|
||||||||
Net loss
|
$ | (35,763 | ) | $ | (77,638 | ) | ||
Less: Accruals of dividends of preferred stock
|
(9,101 | ) | (13,033 | ) | ||||
|
|
|
|
|||||
Net loss available to common stockholders
|
$ | (44,864 | ) | $ | (90,671 | ) | ||
|
|
|
|
|||||
Denominator:
|
||||||||
Weighted-average common stock outstanding
|
3,201,202 | 3,324,547 | ||||||
|
|
|
|
|||||
Net loss per share, basic and diluted
|
$ | (14.01 | ) | $ | (27.27 | ) | ||
|
|
|
|
NINE MONTHS ENDED
SEPTEMBER 30, |
||||||||
2020
|
2021
|
|||||||
Preferred stock
|
141,405,233 | 141,405,233 | ||||||
Convertible debt with accrued interest
|
9,464,717 | 9,934,084 | ||||||
Unvested restricted stock
|
44,737 | 61,839 | ||||||
Options to purchase common stock
|
19,477,614 | 26,490,587 | ||||||
Warrants
|
1,045,226 | 1,299,548 | ||||||
|
|
|
|
|||||
171,437,527 | 179,191,290 | |||||||
|
|
|
|
16.
|
COMMITMENTS AND CONTINGENCIES
|
FOR THE YEARS ENDED DECEMBER 31,
|
||||
2021 (remaining 3 months)
|
$ | 1,899 | ||
2022
|
7,646 | |||
2023
|
6,418 | |||
2024
|
1,687 | |||
2025
|
565 | |||
Thereafter
|
402 | |||
|
|
|||
Total minimum lease payments
|
$ | 18,617 | ||
|
|
FOR THE YEARS ENDED DECEMBER 31,
|
||||
2021 (remaining 3 months)
|
$ | 198 | ||
2022
|
779 | |||
2023
|
330 | |||
Thereafter
|
— | |||
|
|
|||
Total minimum lease payments
|
$ | 1,307 | ||
Less: amount representing interest
|
160 | |||
|
|
|||
Present value of obligations under capital leases
|
1,147 | |||
|
|
17.
|
SUBSEQUENT EVENTS
|
PAGE | ||||||
Article 1 CERTAIN DEFINITIONS
|
A-3 | |||||
Section 1.1
|
Definitions | A-3 | ||||
Article 2 MERGER
|
A-21 | |||||
Section 2.1
|
The Merger | A-21 | ||||
Section 2.2
|
Closing of the Transactions Contemplated by this Agreement | A-23 | ||||
Section 2.3
|
Allocation Schedule; Aggregate Transaction Proceeds Schedule | A-23 | ||||
Section 2.4
|
Treatment of Company Options and Company Warrants | A-24 | ||||
Section 2.5
|
Company Shareholder Deliverables | A-25 | ||||
Section 2.6
|
Withholding | A-26 | ||||
Section 2.7
|
Company Dissenting Shares | A-26 | ||||
Section 2.8
|
Further Assurances | A-27 | ||||
Article 3 REPRESENTATIONS AND WARRANTIES RELATING TO THE GROUP COMPANIES
|
A-27 | |||||
Section 3.1
|
Organization and Qualification | A-27 | ||||
Section 3.2
|
Capitalization of the Group Companies | A-28 | ||||
Section 3.3
|
Authority | A-29 | ||||
Section 3.4
|
Financial Statements; Undisclosed Liabilities | A-30 | ||||
Section 3.5
|
Consents and Requisite Governmental Approvals; No Violations | A-31 | ||||
Section 3.6
|
Permits; Schedule of Permits | A-31 | ||||
Section 3.7
|
Material Contracts | A-31 | ||||
Section 3.8
|
Absence of Changes | A-33 | ||||
Section 3.9
|
Litigation | A-33 | ||||
Section 3.10
|
Compliance with Applicable Law | A-33 | ||||
Section 3.11
|
Employee Plans | A-34 | ||||
Section 3.12
|
Environmental Matters | A-35 | ||||
Section 3.13
|
Intellectual Property | A-36 | ||||
Section 3.14
|
Labor Matters | A-38 | ||||
Section 3.15
|
Insurance | A-39 | ||||
Section 3.16
|
Tax Matters | A-39 | ||||
Section 3.17
|
Brokers | A-41 | ||||
Section 3.18
|
Real and Personal Property | A-41 | ||||
Section 3.19
|
Transactions with Affiliates | A-42 | ||||
Section 3.20
|
Data Privacy and Security | A-42 | ||||
Section 3.21
|
Compliance with International Trade & Anti-Corruption Laws | A-43 | ||||
Section 3.22
|
Information Supplied | A-43 | ||||
Section 3.23
|
Regulatory Compliance | A-44 | ||||
Section 3.24
|
Suppliers | A-44 | ||||
Section 3.25
|
Investigation; No Other Representations | A-44 | ||||
Section 3.26
|
EXCLUSIVITY OF REPRESENTATIONS AND WARRANTIES | A-45 | ||||
Article 4 REPRESENTATIONS AND WARRANTIES RELATING TO THE ENVI PARTIES
|
A-45 | |||||
Section 4.1
|
Organization and Qualification | A-45 | ||||
Section 4.2
|
Authority | A-46 | ||||
Section 4.3
|
Consents and Requisite Governmental Approvals; No Violations | A-46 | ||||
Section 4.4
|
Brokers | A-47 | ||||
Section 4.5
|
Information Supplied | A-47 | ||||
Section 4.6
|
Capitalization of the ENVI Parties | A-47 | ||||
Section 4.7
|
SEC Filings | A-49 | ||||
Section 4.8
|
Absence of Changes | A-49 |
Section 4.9
|
Contracts; No Defaults | A-49 | ||||
Section 4.10
|
Investment Company Act | A-50 | ||||
Section 4.11
|
Trust Account; Financial Ability | A-50 | ||||
Section 4.12
|
Transactions with Affiliates | A-50 | ||||
Section 4.13
|
Litigation | A-51 | ||||
Section 4.14
|
Compliance with Applicable Law | A-51 | ||||
Section 4.15
|
ENVI Party Activities | A-51 | ||||
Section 4.16
|
Internal Controls: Listing: Financial Statements | A-51 | ||||
Section 4.17
|
No Undisclosed Liabilities | A-52 | ||||
Section 4.18
|
Employees | A-53 | ||||
Section 4.19
|
Tax Matters | A-53 | ||||
Section 4.20
|
CFIUS Foreign Person Status | A-55 | ||||
Section 4.21
|
Compliance with International Trade & Anti-Corruption Laws | A-55 | ||||
Section 4.22
|
Change of Control Payments | A-55 | ||||
Section 4.23
|
PIPE Financing | A-55 | ||||
Section 4.24
|
Investigation; No Other Representations | A-56 | ||||
Section 4.25
|
EXCLUSIVITY OF REPRESENTATIONS AND WARRANTIES | A-56 | ||||
Article 5 COVENANTS
|
A-57 | |||||
Section 5.1
|
Conduct of Business of the Company | A-57 | ||||
Section 5.2
|
Efforts to Consummate; Transaction Litigation | A-60 | ||||
Section 5.3
|
Confidentiality and Access to Information | A-61 | ||||
Section 5.4
|
Public Announcements | A-62 | ||||
Section 5.5
|
Tax Matters | A-63 | ||||
Section 5.6
|
Company Exclusive Dealing | A-65 | ||||
Section 5.7
|
ENVI Exclusive Dealing | A-65 | ||||
Section 5.8
|
Preparation of Registration Statement / Proxy Statement | A-66 | ||||
Section 5.9
|
ENVI Shareholder Approval | A-67 | ||||
Section 5.10
|
Merger Sub Shareholder Approval | A-68 | ||||
Section 5.11
|
Conduct of Business of ENVI | A-68 | ||||
Section 5.12
|
Nasdaq Listing; ENVI Public Filings | A-70 | ||||
Section 5.13
|
Trust Account | A-70 | ||||
Section 5.14
|
Company Shareholder Approval | A-70 | ||||
Section 5.15
|
Financing | A-71 | ||||
Section 5.16
|
ENVI Indemnification; Directors’ and Officers’ Insurance | A-72 | ||||
Section 5.17
|
Company Indemnification; Directors’ and Officers’ Insurance | A-73 | ||||
Section 5.18
|
Post-Closing Directors and Officers | A-74 | ||||
Section 5.19
|
PCAOB Financials | A-75 | ||||
Section 5.20
|
ENVI Incentive Equity Plan; ENVI Employee Stock Purchase Plan | A-76 | ||||
Section 5.21
|
FIRPTA Certificates | A-76 | ||||
Section 5.22
|
Section 16 Matters | A-76 | ||||
Section 5.23
|
Post-Closing Cooperation; Further Assurances | A-76 | ||||
Section 5.24
|
Affiliate Agreements | A-76 | ||||
Section 5.25
|
Pre-Closing
Actions
|
A-76 | ||||
Article 6 CONDITIONS TO CONSUMMATION OF THE TRANSACTIONS CONTEMPLATED BY THIS AGREEMENT
|
A-77 | |||||
Section 6.1
|
Conditions to the Obligations of the Parties | A-77 | ||||
Section 6.2
|
Other Conditions to the Obligations of the ENVI Parties | A-77 | ||||
Section 6.3
|
Other Conditions to the Obligations of the Company | A-78 | ||||
Section 6.4
|
Frustration of Closing Conditions | A-79 |
Article 7 TERMINATION
|
A-79 | |||||
Section 7.1
|
Termination | A-79 | ||||
Section 7.2
|
Effect of Termination | A-80 | ||||
Article 8 MISCELLANEOUS
|
A-81 | |||||
Section 8.1
|
Non-Survival
|
A-81 | ||||
Section 8.2
|
Entire Agreement; Assignment | A-81 | ||||
Section 8.3
|
Amendment | A-81 | ||||
Section 8.4
|
Notices | A-81 | ||||
Section 8.5
|
Governing Law | A-82 | ||||
Section 8.6
|
Fees and Expenses | A-82 | ||||
Section 8.7
|
Construction; Interpretation | A-82 | ||||
Section 8.8
|
Exhibits and Schedules | A-83 | ||||
Section 8.9
|
Parties in Interest | A-83 | ||||
Section 8.10
|
Severability | A-83 | ||||
Section 8.11
|
Counterparts; Electronic Signatures | A-84 | ||||
Section 8.12
|
Knowledge of Company; Knowledge of ENVI | A-84 | ||||
Section 8.13
|
No Recourse | A-84 | ||||
Section 8.14
|
Extension; Waiver | A-84 | ||||
Section 8.15
|
Waiver of Jury Trial | A-85 | ||||
Section 8.16
|
Submission to Jurisdiction | A-85 | ||||
Section 8.17
|
Remedies | A-86 | ||||
Section 8.18
|
Trust Account Waiver | A-86 |
Annex A
|
PIPE Investors | |
Annex B
|
Supporting Company Shareholders | |
Exhibit A
|
Form of Sponsor Letter Agreement | |
Exhibit B
|
Form of PIPE Subscription Agreement | |
Exhibit C
|
Form of Investor Rights Agreement | |
Exhibit D
|
Form of Transaction Support Agreement | |
Exhibit E
|
Form of Letter of Transmittal | |
Exhibit F
|
Form of Amended and Restated Certificate of Incorporation of ENVI | |
Exhibit G
|
Form of Amended and Restated Bylaws of ENVI | |
Exhibit H
|
Form of Company Shareholder Written Consent | |
Exhibit I
|
Form of ENVI Incentive Equity Plan | |
Exhibit J
|
Form of ENVI Employee Stock Purchase Plan |
ENVIRONMENTAL IMPACT ACQUISITION CORP.
|
||
By: | /s/ Daniel Coyne | |
Name: Daniel Coyne
|
||
Title: Chief Executive Officer
|
||
HONEY BEE MERGER SUB, INC.
|
||
By: | /s/ Daniel Coyne | |
Name: Daniel Coyne
|
||
Title: Chief Executive Officer
|
||
GREENLIGHT BIOSCIENCES, INC.
|
||
By: | /s/ Andrey Zarur | |
Name: Andrey Zarur, Ph.D.
|
||
Title: Chief Executive Officer
|
(a) |
Voting
|
ENVIRONMENTAL IMPACT ACQUISITION CORP.
|
By: |
|
Name:
|
||
Title:
|
ENVIRONMENTAL IMPACT ACQUISITION CORP.
|
||
By: | /s/ Daniel Coyne | |
Name: | Daniel Coyne | |
Title: | Chief Executive Officer and Director |
GREENLIGHT BIOSCIENCES, INC.
|
||
By: | /s/ Andrey Zarur | |
Name: | Andrey Zarur | |
Title: | Chief Executive Officer |
CG INVESTMENTS INC. VI
|
||
By: | /s/ Jeffrey Barlow | |
Name: Jeffrey Barlow | ||
Title: Director |
HB STRATEGIES LLC
|
||
By: | /s/ George Antonopoulos | |
Name: George Antonopoulos | ||
Title: Authorized Signatory |
/s/ David Brewster |
David Brewster |
/s/ Dean Seavers
|
Dean Seavers |
/s/ Deval L. Patrick |
Deval L. Patrick |
(i) |
no suspension of the qualification of the Shares for offering or sale or trading in any jurisdiction, or initiation or threatening of any proceedings for any of such purposes, shall have occurred and be continuing;
|
(ii) |
no governmental authority of competent jurisdiction shall have rendered, issued, promulgated, enforced, enacted or entered any judgment, order, law, rule or regulation (whether temporary, preliminary or permanent) which is then in effect and which then makes the consummation of the transactions contemplated hereby illegal or then restrains or prohibits the consummation of the transactions contemplated hereby; and
|
(iii) |
all conditions precedent to the Transaction Closing set forth in the Transaction Agreement, including all necessary approvals of the Company’s stockholders and regulatory approvals, if any, shall have been satisfied or waived (other than those conditions which, by their nature, are to be satisfied at the Transaction Closing).
|
(i) |
all representations and warranties of the Subscriber contained in this Subscription Agreement shall be true and correct in all material respects (other than representations and warranties that are qualified as to materiality, which representations and warranties shall be true and correct in all respects) at and as of the Closing Date (except for representations and warranties made as of a specific date, which shall be true and correct in all material respects (other than representations and warranties that are qualified as to materiality, which representations and warranties shall be true and correct in all respects) as of such date); and
|
(ii) |
the Subscriber shall have performed, satisfied and complied in all material respects with all covenants, agreements and conditions required by this Subscription Agreement to be performed, satisfied or complied with by it at or prior to the Closing except where the failure of such performance or compliance would not delay, or materially impair, the ability of the Subscriber to consummate the Closing.
|
(i) |
all representations and warranties of the Company contained in this Subscription Agreement shall be true and correct in all material respects (other than representations and warranties that are qualified as to materiality or Material Adverse Effect (as defined herein), which representations and warranties shall be true and correct in all respects) at and as of the Closing Date (except for representations and warranties made as of a specific date, which shall be true and correct in all material respects (other than representations and warranties that are qualified as to materiality or Material Adverse Effect, which representations and warranties shall be true and correct in all respects) as of such date);
|
(ii) |
the Company shall have performed, satisfied and complied in all material respects with all covenants, agreements and conditions required by this Subscription Agreement to be performed, satisfied or complied with by it at or prior to the Closing;
|
(iii) |
the terms of the Transaction Agreement (as in effect on the date hereof, including the conditions thereto), shall not have been amended or waived in a manner that would reasonably be expected to be materially adverse to the economic benefits of the Common Stock to be received under this Subscription Agreement;
|
(iv) |
There shall have been no amendment, waiver or modification to any Other Subscription Agreement that materially benefits one or more Other Subscribers unless the Subscriber shall have been offered the same benefits; and
|
(v) |
The Company shall have filed with the Nasdaq Stock Market, Inc. (“
NASDAQ
”) an application or supplemental listing application for listing of the Shares and the Shares shall have been approved for listing on NASDAQ, subject to official notice of issuance.
|
(i) |
except for such times as the Company is permitted hereunder to suspend the use of the prospectus forming part of a Registration Statement, use its commercially reasonable efforts to keep such registration, and any qualification, exemption or compliance under state securities laws which the Company determines to obtain, continuously effective with respect to the Subscriber, and to keep the applicable Registration Statement or any subsequent shelf registration statement free of any material misstatements or omissions;
|
(ii) |
advise the Subscriber within two (2) business days:
|
(1) |
when a Registration Statement or any post-effective amendment thereto has become effective;
|
(2) |
of any request by the SEC for amendments or supplements to any Registration Statement or the prospectus included therein or for additional information;
|
(3) |
of the issuance by the SEC of any stop order suspending the effectiveness of any Registration Statement or the initiation of any proceedings for such purpose;
|
(4) |
of the receipt by the Company of any notification with respect to the suspension of the qualification of the Shares included therein for sale in any jurisdiction or the initiation or threatening of any proceeding for such purpose; and
|
(5) |
subject to the provisions in this Subscription Agreement, of the occurrence of any event that requires the making of any changes in any Registration Statement or prospectus included therein so that, as of such date, the statements therein are not misleading and do not omit to state a material fact required to be stated therein or necessary to make the statements therein (in the case of a prospectus, in the light of the circumstances under which they were made) not misleading.
|
(iii) |
use its commercially reasonable efforts to obtain the withdrawal of any order suspending the effectiveness of any Registration Statement as soon as reasonably practicable;
|
(iv) |
upon the occurrence of any event contemplated above, except for such times as the Company is permitted hereunder to suspend, and has suspended, the use of a prospectus forming part of a Registration Statement, the Company shall use its commercially reasonable efforts to as soon as reasonably practicable prepare a post-effective amendment to such Registration Statement or a supplement to the related prospectus, or file any other required document so that, as thereafter delivered to purchasers of the Shares included therein, such prospectus will not include any untrue statement of a material fact or omit to state any material fact necessary to make the statements therein, in the light of the circumstances under which they were made, not misleading;
|
(v) |
use its commercially reasonable efforts to cause all Shares to be listed on each securities exchange or market, if any, on which the Common Stock is then listed;
|
(vi) |
use its commercially reasonable efforts (A) to take all other steps necessary to effect and maintain the registration of the Shares contemplated hereby and (B) until the Effectiveness Expiration, to timely file all reports and other materials required to be filed by the Exchange Act so long as the Company remains subject to such requirements and the filing of such reports and other materials is required for the applicable provisions of Rule 144 to enable the Subscriber to sell the Shares under Rule 144; and
|
(vii) |
upon request of the Subscriber, use commercially reasonable efforts to promptly cause the removal of any restrictive legends on the Shares and issue a certificate or a book entry record without any such legends to the holder of the Shares if (A) such Shares are registered for resale pursuant to an effective registration statement under the Securities Act, upon the sale thereof, (B) the Shares are sold pursuant to Rule 144, or (C) the Shares can be sold, assigned or transferred without restriction or current public information requirements pursuant to Rule 144, including without limitation, any volume and manner of sale restrictions which may be applicable to affiliates under Rule 144 and any requirement for the Company to be in compliance with the current public information required under Rule 144(c) or Rule 144(i), as applicable, and in each case, the holder provides the Company with an undertaking to effect any sales or other transfers in accordance with the Securities Act.
|
If to the Company, to:
Environmental Impact Acquisition Corp.
535 Madison Avenue
New York, NY 10022
Attention: Legal Department
E-mail:
lteipner@cgf.com
Telephone No.: (212)
389-8109
|
with copies (which shall not constitute notice) to:
Latham & Watkins LLP
10250 Constellation Blvd., Suite 1100
Los Angeles, CA 90067
Attention: Steven B. Stokdyk
E-mail:
steven.stokdyk@lw.com
Telephone No.: (213)
891-7421
|
Environmental Impact Acquisition Corp.
|
||
By: | /s/ Daniel Coyne | |
Name: Daniel Coyne | ||
Title: Chief Executive Officer and Director |
SUBSCRIBER
|
||
Name(s) of Subscriber: | ||
Signature of Authorized Signatory of Subscriber:
|
|
||
Name of Authorized Signatory: | ||
Title of Authorized Signatory: | ||
Address for Notice to Subscriber: |
Attention:
|
||
Email:
|
||
Facsimile No.: | ||
Telephone No.: | ||
Address for Delivery of Shares to Subscriber (if not same as address for notice): |
Subscription Amount:
|
$ | |||
|
|
|||
Number of Shares:
|
||||
|
|
|||
EIN:
|
||||
|
|
_______ | A bank as defined in Section 3(a)(2) of the Securities Act, or any savings and loan association or other institution as defined in Section 3(a)(5)(A) of the Securities Act, whether acting in its individual or fiduciary capacity; | |
_______ |
A broker or dealer registered pursuant to Section 15 of the Securities Exchange Act of 1934, as amended (the “
Exchange Act
”);
|
|
_______ |
An investment adviser registered pursuant to Section 203 of the Investment Advisers Act of 1940, as amended (the “
Investment Advisers Act
”), or registered pursuant to the laws of a state, or an investment adviser relying on the exemption from registering with the SEC under Section 203(l) or (m) of the Investment Advisers Act;
|
|
_______ | An insurance company as defined in Section 2(a)(13) of the Securities Act; | |
_______ | An investment company registered under the Investment Company Act of 1940, as amended, or a business development company as defined in Section 2(a)(48) of that act; | |
_______ | A Small Business Investment Company licensed by the U.S. Small Business Administration under Section 301(c) or (d) of the Small Business Investment Act of 1958; | |
_______ | A Rural Business Investment Company as defined in section 384A of the Consolidated Farm and Rural Development Act; | |
_______ | A plan established and maintained by a state, its political subdivisions, or any agency or instrumentality of a state or its political subdivisions for the benefit of its employees, if such plan has total assets in excess of $5,000,000; | |
_______ | An employee benefit plan within the meaning of ERISA, if the investment decision is made by a plan fiduciary, as defined in Section 3(21) of such act, which is either a bank, savings and loan association, insurance company, or registered investment adviser, or if the employee benefit plan has total assets in excess of $5,000,000 or, if a self-directed plan, with investment decisions made solely by persons that are accredited investors; | |
_______ | A private business development company as defined in Section 202(a)(22) of the Investment Advisers Act of 1940; | |
_______ | An organization described in Section 501(c)(3) of the Internal Revenue Code, or a corporation, Massachusetts or similar business trust, partnership, or limited liability company, not formed for the specific purpose of acquiring the Shares, with total assets in excess of $5,000,000; | |
_______ | A trust, with total assets in excess of $5,000,000, not formed for the specific purpose of acquiring the Shares, whose purchase is directed by a sophisticated person who has such knowledge and experience in financial and business matters that such person is capable of evaluating the merits and risks of investing in the Company; |
_______ |
An entity in which
all
of the equity owners qualify as an accredited investor under any of the above subparagraphs.
|
|
_______ | The Subscriber does not qualify under any of the investor categories set forth above. |
☐ | Corporation | ☐ | Limited Partnership | |||||
☐ | Limited Liability Company | ☐ | General Partnership | |||||
☐ | Revocable Trust | |||||||
☐ | Other Type of Trust (indicate type): |
|
||||||
☐ | Other (indicate form of organization): |
|
|
True | |
|
False |
SUBSCRIBER
|
||
Name(s) of Subscriber: |
|
|
Signature of Authorized Signatory of Subscriber:
|
|
||
Name of Authorized Signatory: | ||
Title of Authorized Signatory: | ||
Address for Notice to Subscriber: |
Attention:
|
||
Email:
|
||
Facsimile No.: | ||
Telephone No.: |
☐ |
The Subscriber is not and will not be, and is not acting on behalf of or using the assets of, an entity or any other person that is or will be a Benefit Plan Investor (as defined below).
|
☐ |
The Subscriber is, or is acting on behalf of or using the assets of, a Benefit Plan Investor.
|
☐ |
The Subscriber is, or is acting on behalf of or using the assets of, an employee benefit plan that is not subject to ERISA or Section 4975 of the Code but is subject to any Similar Law.
|
☐ |
an “employee benefit plan” (as defined in Section 3(3) of ERISA) that is subject to the provisions of Part 4 of Subtitle B of Title I of ERISA.
|
☐ |
a plan, account or arrangement to which Section 4975 of the Code applies.
|
☐ |
an entity (other than an insurance company general account) the assets of which are treated as “plan assets” for purposes of ERISA or Section 4975 of the Code; and
|
☐ |
an insurance company general account, some or all of the assets of which are considered “plan assets” for purposes of ERISA or Section 4975 of the Code; and
|
SUBSCRIBER
|
||
Name(s) of Subscriber: |
|
|
Signature of Authorized Signatory of Subscriber:
|
|
||
Name of Authorized Signatory: | ||
Title of Authorized Signatory: | ||
Address for Notice to Subscriber: |
Attention:
|
||
Email:
|
||
Facsimile No.: | ||
Telephone No.: |
COMPANY:
|
||
Environmental Impact Acquisition Corp.
|
||
By: | /s/ Daniel Coyne | |
Name: | Daniel Coyne | |
Title: | Chief Executive Officer and Director |
Holder:
|
||
Name of Holder
|
||
By: |
|
|
Name:
|
||
Title:
|
||
Address for Notice: | ||
|
||
|
||
|
||
Telephone No.:
|
||
Facsimile No.:
|
||
Email Address:
|
||
|
ENVIRONMENTAL IMPACT
ACQUISITION CORP.
|
||
By: |
/s/ Daniel Coyne
|
|
Name: | Daniel Coyne | |
Title: | Chief Executive Officer and Director |
Name of Stockholder | ||
By: |
|
|
Name:
|
|
|
Title: |
|
|
Email: |
|
Owned Shares
|
||
Class/Series Securities
|
Number of Shares
|
|
Company Series A Preferred Shares
1
|
||
Company Series B Preferred Shares | ||
Company Series C Preferred Shares | ||
Company Series D Preferred Shares | ||
Company Common Shares | ||
Other Equity Securities of the Company
|
||
Company Options | ||
Company Warrants | ||
Convertible Notes |
1
|
To list all shares of Series
A-1
Preferred Stock, Series
A-2
Preferred Stock, and/or Series
A-3
Preferred Stock (each, as defined in the Company’s Certificate of Incorporation) held by the Shareholder.
|
ENVIRONMENTAL IMPACT ACQUISITION CORP.
|
By: |
|
Name:
|
||
Title:
|
Confidential
|
August 9, 2021 |
1. |
Reviewed the following documents:
|
a. |
ENVI’s audited balance sheet as of January 19, 2021 included in ENVI’s Form 8-K filed with the Securities and Exchange Commission (“
SEC”
) on January 25, 2021, ENVI’s audited balance sheet as of December 31, 2020 and the related statements of operations, changes in stockholder’s equity and cash flows for the period from July 2, 2020 (Inception) through December 31, 2020 included in ENVI’s Form 10-K filed with the SEC on March 26, 2021, and ENVI’s unaudited interim financial statements as of and for the three months ended March 31, 2021 included in ENVI’s Form 10-Q filed with the SEC on May 24, 2021;
|
b. |
Audited financial statements of GreenLight as of and for the year ended December 31, 2019, unaudited financial information of GreenLight as of and for the year ended December 31, 2020 and for the three months ended March 31, 2021 and the six months ended June 30, 2021, which GreenLight’s management identified as being the most current financial statements available;
|
c. |
Other internal documents relating to the history, current operations, and probable future outlook of GreenLight, including financial projections of Greenlight for the years ended December 31, 2021 through December 31, 2025, prepared by GreenLight and provided to us by the management of ENVI (the “
Financial Projections
”);
|
d. |
A letter dated August 9, 2021 from the management of ENVI and GreenLight which made certain representations as to historical financial statements, the Financial Projections and the assumptions underlying the Financial Projections, for ENVI and GreenLight, respectively;
|
e. |
Industry reports that Duff & Phelps deemed relevant;
|
f. |
The GreenLight PIPE Investor Deck, dated August 9, 2021; and
|
g. |
A draft of the Business Combination Agreement, by and among Environmental Impact Acquisition Corp., Honey Bee Merger Sub, Inc., and GreenLight Biosciences, Inc., dated August 8, 2021;
|
2. |
Discussed the information referred to above and the background and other elements of the Initial Business Combination with the management of ENVI and with the management of GreenLight;
|
3. |
Discussed with ENVI management and GreenLight management the plans and intentions with respect to the management and operation of ENVI following the completion of the Initial Business Combination;
|
4. |
Reviewed the historical trading price and trading volume of ENVI’s common stock and the publicly traded securities of certain other companies that Duff & Phelps deemed relevant;
|
5. |
Performed certain valuation and comparative analyses using generally accepted valuation and analytical techniques, including a discounted cash flow analysis, an analysis of selected public companies that Duff & Phelps deemed relevant and an analysis of selected transactions that Duff & Phelps deemed relevant; and
|
6. |
Conducted such other analyses and considered such other factors as Duff & Phelps deemed appropriate.
|
1. |
Relied upon the accuracy, completeness, and fair presentation of all information, data, advice, opinions and representations obtained from public sources or provided to it from private sources, including ENVI management, and did not independently verify such information;
|
2. |
Relied upon the fact that the Board of Directors and ENVI have been advised by counsel as to all legal matters with respect to the Initial Business Combination, including whether all procedures required by law to be taken in connection with the Initial Business Combination have been duly, validly and timely taken;
|
3. |
Assumed that any estimates, evaluations, forecasts and projections, including the Financial Projections, furnished to Duff & Phelps were reasonably prepared and based upon the best currently available information and good faith judgment of the person furnishing the same, and Duff & Phelps expresses no opinion with respect to such estimates, evaluations, forecasts and projections or the underlying assumptions;
|
4. |
Assumed that information supplied by and representations made by ENVI management are substantially accurate regarding ENVI, GreenLight and the Initial Business Combination;
|
5. |
Assumed that the representations and warranties made in the Business Combination Agreement are substantially accurate;
|
6. |
Assumed that the final versions of all documents reviewed by Duff & Phelps in draft form conform in all material respects to the drafts reviewed;
|
7. |
Assumed that there has been no material change in the assets, liabilities, financial condition, results of operations, business, or prospects of ENVI or GreenLight since the date of the most recent financial statements and other information made available to Duff & Phelps, and that there is no information or facts that would make the information reviewed by Duff & Phelps incomplete or misleading;
|
8. |
Assumed that all of the conditions required to implement the Initial Business Combination will be satisfied and that the Initial Business Combination will be completed in accordance with the
|
Business Combination Agreement without any material amendments thereto or any material waivers of any terms or conditions thereof; and |
9. |
Assumed that all governmental, regulatory or other consents and approvals necessary for the consummation of the Initial Business Combination will be obtained without any adverse effect on ENVI, GreenLight, or the contemplated benefits expected to be derived in the Initial Business Combination.
|
Exhibit
Number |
Description
|
|
101.PRE | Inline XBRL Definition Linkbase Document | |
101.DEF | Inline XBRL Definition Linkbase Document | |
104 | Cover Page Interactive Data File (formatted as Inline XBRL and contained in Exhibit 101) |
* |
Previously filed
|
** |
To be filed by amendment.
|
+ |
Indicates management contract or compensatory plan.
|
† |
Certain confidential portions (indicated by brackets and asterisks) have been omitted from this exhibit.
|
†† |
Schedules and exhibits to this Exhibit omitted pursuant to Regulation
S-K
Item 601(b)(2). The Registrant agrees to furnish supplementally a copy of any omitted schedule of exhibit to the SEC upon request.
|
11. |
The undersigned Registrant hereby undertakes:
|
(a) |
To file, during any period in which offers or sales are being made, a post-effective amendment to this Registration Statement:
|
(i) |
To include any prospectus required by section 10(a)(3) of the Securities Act of 1933;
|
(ii) |
To reflect in the prospectus any facts or events arising after the effective date of this Registration Statement (or the most recent post-effective amendment thereof) which, individually or in the aggregate, represent a fundamental change in the information set forth in this Registration Statement. Notwithstanding the foregoing, any increase or decrease in volume of securities offered (if the total dollar value of securities offered would not exceed that which was registered) and any deviation from the low or high end of the estimated maximum offering range may be reflected in the form of prospectus filed with the Commission pursuant to Rule 424(b) if, in the aggregate, the changes in volume and price represent no more than 20% change in the maximum aggregate offering price set forth in the “Calculation of Registration Fee” table in the effective registration statement; and
|
(iii) |
To include any material information with respect to the plan of distribution not previously disclosed in this Registration Statement or any material change to such information in this Registration Statement.
|
(b) |
That, for the purpose of determining any liability under the Securities Act of 1933, each such post-effective amendment that contains a form of prospectus shall be deemed to be a new registration statement relating to the securities offered therein, and the offering of such securities at that time shall be deemed to be the initial bona fide offering thereof.
|
(c) |
To remove from registration by means of a post-effective amendment any of the securities being registered which remain unsold at the termination of the offering.
|
(d) |
That, for the purpose of determining liability under the Securities Act of 1933 to any purchaser, each prospectus filed pursuant to Rule 424(b) as part of a registration statement relating to an offering, other than registration statements relying on Rule 430B or other than prospectuses filed in reliance on Rule 430A, shall be deemed to be part of and included in the registration statement as of the date it is first used after effectiveness. Provided, however, that no statement made in a registration statement or prospectus that is part of the registration statement or made in a document incorporated or deemed incorporated by reference into the registration statement or prospectus that is part of the registration statement will, as to a purchaser with a time of contract of sale prior to such first use, supersede or modify any statement that was made in the registration statement or prospectus that was part of the registration statement or made in any such document immediately prior to such date of first use.
|
(e) |
That, for the purpose of determining liability of the registrant under the Securities Act of 1933 to any purchaser in the initial distribution of the securities, the undersigned registrant undertakes that in a primary offering of securities of the undersigned registrant pursuant to this registration statement, regardless of the underwriting method used to sell the securities to the purchaser, if the securities are offered or sold to such purchaser by means of any of the following communications, the undersigned registrant will be a seller to the purchaser and will be considered to offer or sell such securities to such purchaser:
|
(i) |
Any preliminary prospectus or prospectus of the undersigned registrant relating to the offering required to be filed pursuant to Rule 424;
|
(ii) |
Any free writing prospectus relating to the offering prepared by or on behalf of the undersigned registrant or used or referred to by the undersigned registrant;
|
(iii) |
The portion of any other free writing prospectus relating to the offering containing material information about the undersigned registrant or its securities provided by or on behalf of the undersigned registrant; and
|
(iv) |
Any other communication that is an offer in the offering made by the undersigned registrant to the purchaser.
|
12. |
Insofar as indemnification for liabilities arising under the Securities Act of 1933 may be permitted to directors, officers and controlling persons of the Registrant pursuant to the foregoing provisions, or otherwise, the Registrant has been advised that in the opinion of the SEC such indemnification is against public policy as expressed in the Securities Act of 1933 and is, therefore, unenforceable. In the event that a claim for indemnification against such liabilities (other than the payment by the Registrant of expenses incurred or paid by a director, officer or controlling person of the Registrant in the successful defense of any action, suit or proceeding) is asserted by such director, officer or controlling person in connection with the securities being registered, the Registrant will, unless in the opinion of its counsel the matter has been settled by controlling precedent, submit to a court of appropriate jurisdiction the question whether such indemnification by them is against public policy as expressed in the Securities Act of 1933 and will be governed by the final adjudication of such issue.
|
13. |
The undersigned registrant hereby undertakes as follows: that prior to any public reoffering of the securities registered hereunder through use of a prospectus which is a part of this registration statement, by any person or party who is deemed to be an underwriter within the meaning of Rule 145(c), the issuer undertakes that such reoffering prospectus will contain the information called for by the applicable registration form with respect to reofferings by persons who may be deemed underwriters, in addition to the information called for by the other items of the applicable form.
|
14. |
The registrant undertakes that every prospectus: (1) that is filed pursuant to the immediately preceding paragraph, or (2) that purports to meet the requirements of Section 10(a)(3) of the Act and is used in connection with an offering of securities subject to Rule 415, will be filed as a part of an amendment to the registration statement and will not be used until such amendment is effective, and that, for purposes of determining any liability under the Securities Act of 1933, each such post-effective amendment shall be deemed to be a new registration statement relating to the securities offered therein, and the offering of such securities at that time shall be deemed to be the initial bona fide offering thereof.
|
15. |
The undersigned Registrant hereby undertakes to respond to requests for information that is incorporated by reference into the prospectus pursuant to Items 4, 10(b), 11, or 13 of this Form
S-4,
within one business day of receipt of such request, and to send the incorporated documents by first class mail or other equally prompt means. This includes information contained in documents filed subsequent to the effective date of the Registration Statement through the date of responding to the request.
|
16. |
The undersigned Registrant hereby undertakes to supply by means of a post-effective amendment all information concerning a transaction, and the company being acquired involved therein, that was not the subject of and included in the Registration Statement when it became effective.
|
ENVIRONMENTAL IMPACT ACQUISITION CORP.
|
||
By: | /s/ Daniel Coyne | |
Name: Daniel Coyne | ||
Title: Chief Executive Officer |
NAME
|
POSITION
|
DATE
|
||
/s/ Daniel Coyne
Daniel Coyne
|
Chief Executive Officer, President and Director
(Principal Executive Officer)
|
December 6, 2021
|
||
/s/ Marc Marano
Marc Marano
|
Chief Financial Officer and Treasurer
(Principal Financial and Accounting Officer)
|
December 6, 2021
|
||
*
Jennifer Pardi
|
Director
|
December 6, 2021
|
||
*
Deval Patrick
|
Director
|
December 6, 2021
|
||
*
David Brewster
|
Director
|
December 6, 2021
|
||
*
Dean Seavers
|
Director
|
December 6, 2021
|
*By: |
/s/ Daniel Coyne
|
|
Daniel Coyne | ||
attorney-in-fact |
Exhibit 10.30
Certain identified information has been omitted from this exhibit because it is not material and of the type that the registrant treats as private or confidential. [***] indicates that information has been omitted.
LICENSE AND SPONSORED
RESEARCH AGREEMENT
THIS LICENSE AND SPONSORED RESEARCH AGREEMENT (this Agreement), effective as of April ___, 2010 is made and entered into by and between YISSUM RESEARCH DEVELOPMENT COMPANY OF THE HEBREW UNIVERSITY OF JERUSALEM LTD., of Hi Tech Park, Edmond J Safra Campus, Givat Ram, Jerusalem 91390, Israel (Yissum), and BEEOLOGICS, INC., a corporation organized and existing under the laws of the British Virgin Islands, having its principal place of business at 11800 SW 77 Ave, Miami, Fl. 3315, U.S (the Company). (Yissum and the Company may be sometimes referred to herein individually as, a Party and collectively as, the Parties.)
R E C I T A L S
A. The rights and title to all inventions and research results of scientists of the University (as defined below) vest solely with Yissum.
B. The Company has represented to Yissum that the Company has the knowledge and experience necessary to conduct research and develop products based on the inventions and research that are the subject of this Agreement; and that, either by itself or through third Parties, it has or will have the financial capacity and the strategic commitment to facilitate the research, development, production, marketing and distribution of products.
C. Yissum wishes to collaborate with the Company for research, development and commercial exploitation of certain inventions and research; and for that purpose has requested the Company to participate m the research and development activities pertaining to same.
D In order to implement said collaboration the Parties executed a memorandum of understanding on February 17, 2008 (the MOU), with this Agreement substituting and repealing such MOU for all intents and purposes.
E. The Parties agree to continue said collaboration upon the terms and conditions set forth herein.
NOW THEREFORE, in consideration of the foregoing and the obligations, undertakings and promises contained herein, and for good and valuable consideration the sufficiency of which is hereby acknowledged, the Parties agree as follows.
A G R E E M E N T
1. |
DEFINITIONS |
1.1 As used herein, the following terms shall have the following meaning:
(a) Assigned Technology has the meaning given to it in Section 4,2 hereof.
(b) Affiliate means any person, organization or other legal entity which controls, or is controlled by, or is under common control with, the Company or Yissum, as applicable. Control shall mean the holding of more than fifty percent (50%) or more of (i) the voting rights of a given entity, and (ii) the right to elect or appoint directors of such entity.
(c) Combination Product has the meaning given to it in Section 7 1(a) hereof.
(d) Committee has the meaning given to it in Section 5 2 hereof.
(e) Company has the meaning given to it in the preamble hereof.
(f) Company Cessation Event has the meaning given to it in Section 14.2 hereof.
(g) Company Shareholders Option has the meaning given to it in Section 14 2 hereof.
(h) Development Plan has the meaning given to it in Section 5.1 hereof,
(i) Development Reports has the meaning given to it in Section 5.2 hereof.
(j) Development Results has the meaning given to it in Section 3 3 hereof.
(k) Expense Deposit has the meaning given to it in Section 9.2 hereof.
(l) HAY Technology [***].
(m) IP means any and all intellectual property rights, including, but not limited to, any and all, Patents, copyrights, trademarks, trade names, service marks, design marks, trade secrets and other proprietary rights of any kind or nature, all whether or not pending, perfected, registered, registrable or patentable, and including, further, any and all rights, interests or titles in and to any Know-How; Company IP means any and all IP owned by the Company, including, but not limited to, the Companys relative ownership in the Joint IP, and will include IP licensed, obtained or received from third parties. The Company IP as of the date hereof is depicted on Appendix Al hereof; Yissum IP means the IP owned by Yissum, including, but not limited to, Yissums relative ownership in the Joint IP. Yissum IP as of the date hereof is described in Appendix A2 hereof; and Joint IP means any and all IP jointly owned by the Company and Yissum with respect to the Licensed Technology, including any and all IP deriving from Research Results in accordance with Section 3.2 hereof. The Joint IP as of the date hereof, is depicted on Appendix A3 hereof.
2
(n) Joint Patents means such Patents that are included in the Joint IP.
(o) Know-How means any information, ancillary materials, processes, results, devices and/or know-how developed and owned by either or both Parties, (as applicable), whether patentable or not, provided that the said information is not public knowledge or in the public domain Notwithstanding the aforesaid, the Know-How shall not be regarded as public domain or public knowledge if, the particulars, the application or utilization of a general principal or a certain idea (that are regarded as public knowledge), are not themselves public knowledge or in the public domain.
(p) Indemnitees has the meaning given to it in Section 13.3 hereof.
(q) License has the meaning given to it in Section 4.1 hereof.
(r) License Maintenance Fee has the meaning given to it in Section 7 1 hereof.
(s) Licensed Technology has the meaning given to it is Section 4.1 hereof.
(t) MOU has the meaning given to it in the preamble hereof.
(u) Net Sales means (x) the gross sales price invoiced for sales, leases or other transfers of Products by the Company, an Affiliate or Sublicensee to a third Party who will be an end user of the Products, or (y) the market value of non-monetary consideration actually received in connection with such sales, leases or transfers; after deduction of (i) all commercially reasonable discounts, rebates and return credits, provided that such deductions shall be directly related to the sale of Products that were awarded within the regular running of the business of the Company, Affiliate or Sublicensee; and (ii) VAT; and (iii) Third Parties Royalties, actually paid in connection with the applicable Products as appearing on the books of the Company, the Affiliate or the Sublicensee, as applicable, provided that the Company shall disclose all the details of the requirement to pay such Third Party Royalties, including, but not limited to, any written agreements pursuant to which the payment of such Third Party Royalties is required. In the event of sales made through a distributor or marketing agent, the sales made by such distributors or marketing agent shall be deemed gross sales of the Company for the purposes of this Agreement and amounts paid by the Company to such distributor or marketing agent as commissions or marketing fees for such sales shall be deducted from such gross sales, provided that such deductions shall not exceed fifteen percent (15%) of the gross sales price of the Products, unless the Company can demonstrate through a written agreement negotiated at arms-length and disclosed to Yissum that a greater percentage is required. In the event of sales or deductions not made at arms length, then for the purpose of calculation of Royalties to Yissum, Net Sales shall be calculated in accordance with arms length prices for sale of Products to end users and arms length deductions, to be determined by the current market conditions, of in the absence of such conditions, according to the assessment of an independent appraiser to be selected by the Parties,
3
the costs of whom to be paid by the Party whose claim was rejected by the independent appraiser. For the sake of clarity, sales to end users for the purpose of the conduct of clinical trials required for the regulatory approval of a Product shall not be considered sales pursuant to this Section 1, provided that the Company, the Affiliate or Sublicensee shall provide Yissum, within reasonable time after its written request, with documentation demonstrating the nature of such sale upon request.
(v) OCS means the Office of the Chief Scientist of the Israeli Ministry of Industry and Trade.
(w) Ongoing Patent Costs has the meaning given to it in Section 9.1 hereof.
(x) Party has the meaning given to it in the preamble hereof.
(y) Pass-Through Right has the meaning given to it m Section 14 2 hereof.
(z) Patent means all patent applications or registered patents, any patent application that claims priority therefrom; all divisions, continuations, continuations-in-part, re-examinations, reissues, substitutions, or extensions, including European Supplementary Protection Certificates (SPCs), and any and all patents issuing from, and inventions, methods, processes, and other patentable subject matter disclosed or claimed m same.
(aa) Product means any product that is either (x) [***]; or (y) [***], and any product or composition comprising said inserts, but excluding products designated to control other pests.
(bb) Representatives has the meaning given to it in Section 5.2 hereof.
(cc) Research means the sponsored research to be conducted by or under the supervision of the Researcher in connection with controlling the varroa mite by silencing varroa genes via RNAi constructs provided to the bees and transferred to the varroa. For the sake of clarity, any research, development or other activity relating to horizontal transfer of RNAi molecules other than transfer from bees to varroa is expressly excluded from the scope of this Agreement, and each party will be free to perform any such activity as it deems fit separately without any accountability to the other party.
(dd) Research Debt has the meaning given to it in Section 2.5 hereof.
(ee) Research Fee has the meaning given to it in Section 2,4 hereof. Researcher means Prof. Ilan Sela, or such other person as determined and appointed from time to time by Yissum in accordance with Section 2.2 hereof, to supervise and to perform the Research, if applicable.
(ff) Research Period has the meaning given to it in Section 2.3 hereof.
4
(gg) Research Program means the program as shall be approved by the Company from tune to time under which the Research shall be carried out and conducted by or under the supervision of the Researcher and/or any Company Researchers. The current Research Program is annexed hereto as Appendix B.
(hh) Research Report has the meaning given to it in Section 2.5 hereof.
(ii) Research Results means the results of the Research m accordance with the Research Program, including any Patents and Know-How directly resulting therefrom. For the avoidance of doubt, the HAV Technology is not part of the Research Results.
(jj) Royalties has the meaning given to it in Section 7.1 hereof.
(kk) Sublicense means any grant by the Company or its Affiliates to third parties of the right to develop the Licensed Technology, which right may include the rights to manufacture, market and distribute the Products.
(ll) Sublicense Considerations means any proceeds or consideration or benefit of any kind whatsoever, other than royalties on Net Sales, which the Company or an Affiliate may receive from a Sublicensee as a direct or indirect consideration of the grant of a Sublicense or an option to obtain such Sublicense.
(mm) Sublicense Fees has the meaning given to it in Section 7 1 hereof.
(nn) Sublicensee means any third party to whom the Company or an Affiliate shall grant a Sublicense or option to obtain such Sublicense. For the sake of clarity, Sublicensee shall include any other third party to whom such rights shall be transferred, assigned, or who may assume control thereof by operation of law or otherwise.
(oo) Territory means worldwide.
(pp) Third Parties Royalties means royalties calculated on any amount invoiced by the Company or an Affiliate thereof in connection with the sale of a Product and actually paid by the Company to any third party for the right to use Patents or other IP, without which right of use the Company would not be entitled to perform research, develop, manufacture or sell such Product, provided that the duty to pay such royalty to such third party has been established in good faith, arises under applicable law or statute or is set out m a written agreement.
(qq) University means the Hebrew University of Jerusalem and each of its branches.
(rr) VAT means value added taxes, sales taxes or any other similar taxes, all at the rate prescribed by the applicable laws.
(ss) Yissum has the meaning given to it in the preamble hereof.
5
(tt) Yissum Auditors has the meaning given to it in Section 8.7 hereof.
1.2 Unless the context otherwise requires, as used in this Agreement, the singular number includes the plural and the plural number may include the singular. The use of any gender shall be applicable to all genders. The terms hereof, herein, hereunder, hereby and hereto as well as words of similar import when used in this Agreement shall refer to this Agreement as a whole and not to any particular provision, unless otherwise is expressly specified.
2. |
SPONSORED RESEARCH |
2.1 The Company hereby undertakes to finance performance of the Research in accordance with the Research Program or any mutually agreed upon amendment thereof.
2.2 The Research shall be conducted by and under the supervision of the Researcher and the Company Researchers. Should the Researcher be unable to complete the Research for any reason or if the Researcher does not meet his obligations and undertakings hereunder m a complete and timely manner, the Company shall have the right to terminate Research and perform it by itself, provided that (a) no monies paid to Yissum on account of the Research Fee will be refundable, and (b) the Company shall be responsible for the payment of any accrued fees and expenses due to Yissum based on work duly performed up to the date of termination and those irrevocable commitments entered into by Yissum in accordance with the Research Program prior to having received the Companys written notice of termination.
2.3 The Research shall be conducted during the period set forth in the Research Program (the Research Period). Any further Research shall be conducted in accordance with future agreements between the Company and Yissum.
2.4 As sole and full compensation to Yissum for the Research and subject to any earlier termination of the Research pursuant to Section 2,2 hereof, the Company shall pay Yissum the amount set forth in the Research Program (the Research Fee) plus VAT, if any (inclusive of Yissum or University overhead), for each Research Period, to be paid monthly in advance until the Company has closed its next round of investment in an amount of not less than [***], The Company agrees that any late payment of the Research Fee pursuant to this Section 2.4, shall bear interest at an annual rate of ten percent (10%).
2.5 [***].
2.6 For the avoidance of doubt, nothing herein shall prevent Yissum or the University or the Researcher from obtaining further finance or grants from other entities for research regarding the Licensed Technology, provided that such entities shall not be granted rights in the Research or Research Results prejudicial to the rights granted to the Company in this Agreement.
2.7 [***].
6
2.8 Nothing contained in this Agreement shall be construed as a warranty on the part of Yissum that any results or inventions will be achieved by the Research, or that the Research Results, if any, are or will be commercially exploitable Yissum makes no warranties whatsoever as to the commercial or scientific value of the Research Results. Notwithstanding the foregoing, the Researcher shall ensure that the reports required by Section 2.7 hereof, contain complete results of the Research.
2.9 The following provisions will apply in Company choose to retain the services of the Researcher or any other employee of the University, as a consultant in connection with the Research:
(a) Should the Company choose to (i) retain the services of the Researcher or any other employee of the University as a consultant in connection with the Research, or (ii) grant any benefit, including but not limited to, cash payments or securities of any kind, to the Researcher or any other employee of the University in connection with the Research, it shall do so only through a written agreement executed between the Company and Yissum.
(b) [***].
(c) [***].
(d) [***].
3. |
INTELLECTUAL PROPERTY RIGHTS |
3.1 Other than as expressly set forth herein and subject to any assignment or transfer of any IP made in accordance herewith or pursuant hereto, Yissum retains full and sole title to Yissum IP and the Company retains full and sole title to the Company IP. Any IP of either Party which does not pertain to the Licensed Technology or the Assigned Technology is expressly excluded from the scope of this Agreement.
3.2 Any IP deriving from the Research Results will be jointly owned by the Parties and will become, from inception, part of the Joint IP, in the proportions to be mutually agreed upon by the Parties and the absence of such agreement, to be determined by the arbitrator referred to Section 16 hereof, which IP to be added to Appendix A3. For the sake of clarity, Yissums rights in any Joint IP thus created shall be deemed and considered from inception as part of the Licensed Technology and the terms and conditions of this Agreement shall govern the use thereof by the Company.
3.3 Any results of activities carried out by the Company or by third Parties (including, but not limited to, any work made for hire) at the direction of the Company (other than Research conducted by the Researcher, or under his supervision) pursuant to the Development Plan, including any Patents and Know-How resulting therefrom, including any regulatory filing filed, or approval obtained, by the Company, an Affiliate or Sublicensee in respect of the Products (Development Results) will he with the Company and will become and be deemed from inception an integral part of the Company IP.
7
3.4 It is hereby specifically agreed that Yissum shall not transfer its interest in any Joint IP to any third party without the advanced written consent of the Company.
4. |
LICENSES; ASSIGNMENT |
4.1 Yissum hereby grants the Company an exclusive license to make commercial use of Yissum IP (the Licensed Technology), m order to develop, manufacture, market, distribute or sell a Product, all within the Territory only and subject to and in accordance with the terms and conditions of this Agreement (the License).
4.2 [***].
4.3 The provisions of Section 4.1 hereof notwithstanding, Yissum, on behalf of the University, shall retain the right, provided, always, that the exercise of such right shall not result in competition to the Company, the Licensed Technology, the Assigned Technology or the Products, (a) to make, use and practice the Licensed Technology for the Universitys own internal research and educational purposes; (b) to license or otherwise convey to other academic and not-for-profit research organizations for no charge other than shipping fees the Licensed Technology for use in non-commercial research; all provided, always, that such license does not directly or indirectly harm the Companys commercial interests in the Company IP, the Licensed Technology or the Assigned Technology, and provided further that any transfer of materials shall not be made without first giving notice to the Company. Said right of Yissum is further conditional upon, and subject to, Yissum ensuring that each recipient of Licensed Technology hereunder has properly executed an undertaking (or is otherwise bound by law) to maintain confidentiality in such degree that will not fall below that which is contemplated in Section 11 hereof and that it has given a written notice to the Company of its intention to exercise such right at least thirty (30) days in advance.
4.4 The License shall end, on a country-by-country basis, upon the later of, (x) the date of expiration of the last valid Patent included in the Licensed Technology; (y) the end of any exclusivity on the Product granted by a regulatory or government body, or (z) the end of a period of twenty (20) years from the date of the First Commercial Sale Should the periods referred to in paragraphs (i) or (ii) expire prior to twenty (20) years from the date of the First Commercial Sale in a particular country or countries, the license in that country or those countries shall be deemed a license to the Know-How.
4.5 Otherwise than as set forth in Section 4 5 hereof, the License may terminate only upon termination of this Agreement.
5. |
DEVELOPMENT AND COMMERCIALIZATION |
5.1 The Company undertakes, at its own expense, to use its best efforts to carry out the development, regulatory, manufacturing and marketing work necessary to develop and commercialize Products in accordance with a written plan and timetable for the development and the commercialization of Products or subsequent results of any commercial development (the Development Plan), a copy of which is annexed to this Agreement as Appendix C. The Development Plan may be modified from time to time by the Company as reasonably required in order to achieve the commercialization goals set forth above, upon Yissums approval, which shall not be unreasonably withheld, conditioned or delayed. All terms and conditions of the License and this Agreement shall apply to the modified Development Plan and subsequent Development Results.
8
5.2 The Parties shall establish a steering committee (the Committee) to oversee the exercise of the License. Each Party shall be entitled to designate two (2) representatives to the Committee (the Representatives), who shall meet at least twice per calendar year unless the Parties agree otherwise, The Representatives shall be bound by the confidentiality arrangements set out in this Agreement, The Company shall consult with Yissum, via Yissums Representatives, in respect of significant decisions related to the exercise of the License. For the avoidance of doubt, the Committee shall be a forum for the exchange of information between the Parties with respect to the foregoing matters, shall act only in an advisory capacity and shall not have decision-making powers. It is agreed that any and all expenses incurred in by Yissums Representatives as a result of their participation in the Committee shall be borne and paid by the Company. The Parties further agree that the Company shall be entitled to convene Committee meetings by telephone or video conference. Notwithstanding anything to the contrary, including any reports regarding the Research, the Company shall (a) provide Yissum via Yissums Representatives with periodic written reports in the OCS format (Development Reports) not less than once per every twelve (12) months concerning all material activities undertaken in respect of the exercise of the License, (b) keep Yissum informed via Yissums Representatives substantially on a timely basis concerning all material activities and changes to the Development Plan undertaken in respect of the exercise of the License, and (c) at Yissums request, from time to time, provide Yissum with further information relating to the Companys activities in exercise of the License. The Development Reports shall include a summary of the Development Results and any other elated work effected by the Company or by any Affiliate or Sub-Licensee during the six (6) month period prior to the report. Development Reports shall also set forth a general assessment regarding the achievement of any milestones; the projected or actual completion date of the development of a Product and the marketing thereof; sales forecasts, if any have been made in the regular course of the Companys business; a description of any corporate transaction involving the Products or the Licensed Technology, and shall detail all proposed changes to the Development Plan, including the reasons therefor.
5.3 Upon completion of the development of any Product as defined in Section 1.1(aa)(y), the Company undertakes to perform commercially reasonable actions necessary to maximize Net Sales of such Product on a regular and consistent basis.
5.4 If the Company shall not commercialize the Products, as defined m Section 1 1(aa)(y), within a reasonable time frame, unless such delay is caused by (a) the requirements of a regulatory authority; (b) force majeure; (c) lack of commercial viability caused by factors external to the Company, provided that the Company shall make commercially reasonable efforts to remove such factors; or (d) unless the Company and Yissum have agreed in writing to amend the Development Plan, Yissum shall notify the Company in writing of the Companys failure to meet its obligations of diligence and shall allow the Company ninety (90) days to cure its failure of diligence. The Companys failure to clue within such ninety (90) day period to Yissums reasonable satisfaction shall give Yissum the right to terminate this Agreement as its sole remedy in such event.
9
6. |
SUBLICENSES |
6.1 The Company shall be entitled to grant a Sublicense only after obtaining Yissums written approval regarding the identity of the Sublicensee and all material terms and conditions of the Sublicense, which approval shall not be unreasonably withheld, conditioned or delayed, Failure by Yissum to respond within thirty (30) days of receiving the Companys request to that effect, will be deemed approval for purposes hereof. For the avoidance of doubt, an agreement with either (x) a subcontractor or IP collaborator in which the Company must grant the subcontractor or collaborator the right to make use of the Licensed Technology or Assigned Technology on behalf of the Company, and for which use the Company is required to pay or otherwise compensate the subcontractor; or (y) a distributor, reseller or sales agent that is responsible for selling finished Products to end users shall not be considered a Sublicense for purposes of this section 6.1.
6.2 Upon submission of its request to obtain the written consent of Yissum to a Sublicense, the Company shall fully disclose and submit to Yissum all relevant material documentation relating to the Sublicense, adequately disclose to Yissum any other business connection which it now has or is in the process of forming with the Sublicensee which may reasonably effect the decision of the Company regarding terms and conditions of the Sublicense; and shall notify Yissum in writing, whether a proposed Sublicensee is an Affiliate or is otherwise related to the Company In addition, the Company shall provide Yissum with an executed copy of the Sublicense within ten (10) working days of its execution.
6.3 If the Company is unable or unwilling to serve or develop a potential market or market territory for which there is another third party willing to be a sublicensee, the Company will, at Yissums request, negotiate in good faith a sublicense with such third party, unless such third party is a competitor of the Company or its Affiliates or, otherwise, contracting with such third party is reasonably likely to be detrimental to the Companys or its Affiliates business.
6.4 Any Sublicense shall be dependent on the validity of the License and shall terminate upon termination of the License.
6.5 The Company shall ensure that any Sublicense shall include material terms that bind the Sublicensee to observe the terms of this Agreement, including, but not limited to, Section 13 hereof, the breach of which terms shall be a material breach resulting in the prompt termination of the Sublicense In such an event, the Company undertakes to take all reasonable steps to enforce such terms upon the Sublicensee, including the termination of the Sublicense. In all cases, the Company shall immediately notify Yissum of any breach of the material terms of a Sublicense, shortly after it becomes aware of any such circumstance and shall copy Yissum on all material and relevant correspondence with regard such breach.
6.6 The Company shall require any Sublicensee to provide it with royalty reports that include at least the detail that the Company is required to produce pursuant to Section 8 2 hereof Upon request, the Company shall produce such reports to Yissum.
6.7 Any breach of a Sublicense Agreement by a Sublicensee which would have constituted a breach of this Agreement by the Company had it been an act or omission of the Company, and which the Company has not terminated the Sublicense m the absence of the Sublicensee curing such breach, shall constitute a breach of this Agreement by the Company.
10
6.8 Under no circumstance whatsoever shall a Sublicensee be entitled to grant the Sublicense or any part thereof to any third party.
7. |
CONSIDERATIONS |
7.1 In consideration for the grant of the License, and in addition to the Research Fee, the Company shall pay Yissum the following considerations during the term of the License.
(a) Royalties at a rate [***] of the Net Sales of Products, as defined in Section 1 1(aa)(y) hereof, and Royalties at a rate [***] of Net Sales of Products as defined in Section 1.1(aa)(x) hereof, (as applicable, the Royalties). Notwithstanding anything to the contrary set forth herein, in the event a Product is sold by the Company, an Affiliate or a Sublicensee in the form of a combination product, that is, a product which is based on IP other than Yissum IP, Joint Patents or the HAV Technology, (a Combination Product), Net Sales from such Combination Product, for purposes of determining royalty payments, [***], In such event, the parties shall negotiate in good faith to arrive at a determination of the respective fair market values of the Product and all other ingredients included in the Combination Product.
(b) Commencing seven (7) years from the date the MOU was signed, and each year thereafter, the Company shall pay Yissum an annual maintenance fee [***] for maintaining the License (the License Maintenance Fee) The License Maintenance Fee is non-refundable and shall be credited each year against Royalties payable on account of Net Sales and Sublicense Fees made during that year.
(c) Sublicense fees at a rate of [***] of Sublicense Consideration (Sublicense Fees). For the sake of clarity, under no circumstances may sales and marketing agents, distributors or resellers of the Products or similar functionaries be deemed or considered as Sublicensees.
7.2 [Omitted].
8. |
REPORTS AND ACCOUNTING |
8.1 The Company shall give Yissum written notice of any Sublicense Consideration received or First Commercial Sale made within thirty (30) days of such event.
8.2 [***].
8.3 On the date prescribed for the submission of each Periodic Report, the Company shall pay the Royalties and Sublicense Fees due to Yissum for the reported period. All payments under this Agreement shall be computed and paid in US dollars, using the appropriate foreign exchange rate reported in the Wall Street Journal on the last working day of the calendar quarter Payment of Value Added Tax or of any analogous foreign tax, charge or levy (if charged), applicable to the sale of Products shall be added to each payment in accordance with the statutory rate in force at such time Payments may be made by check or by wire transfer to the following account:
[***]
11
8.4 The Company shall keep, and shall require its Affiliates and Sublicensees to keep, full and correct books of account in accordance with Generally Accepted Accounting Principles as required by international accounting standards enabling the Royalties and Sublicense Fees to be calculated accurately. Starting from the first calendar year after the First Commercial Sale, or the first grant of a Sublicense, whichever occurs first, an annual report, authorized by a certified public accountant, shall be submitted to Yissum within ninety (90) days of the end of each calendar year, detailing Net Sales and Sublicense Considerations, Royalties and Sublicense Fees, both due and paid. Said annual reports shall also include the Companys sales and royalty forecasts for the following calendar year, if available. This Section 8.4 will mutatis mutandis apply to Yissum in case it will be obligated to pay to the Company any royalties or other payment hereunder.
8.5 Yissum and the Company shall (and the Company shall require and cause its Affiliates and Sublicensees to) retain such books of account for five (5) years after the end of each calendar year during the period of this Agreement, and, if this Agreement is terminated for any reason whatsoever, for five (5) years after the end of the calendar year in which such termination becomes effective.
8.6 [***].
8.7 Yissum shall be entitled to appoint not more than two (2) representatives who must be independent certified public accountants or such other professionals as appropriate (Yissum Auditors) to inspect during normal business hours the Companys and Affiliates books of account, records and other relevant documentation to the extent relevant or necessary for the sole purpose of verifying the performance of the Companys payment obligations under this Agreement, the calculation of amounts due to Yissum under this Agreement and of all financial information provided in the Periodic Reports, provided that Yissum shall coordinate such inspection with the Company or Affiliate (as the case may be) in advance. In addition, Yissum may require that the Company, through Yissum Auditors, inspect during normal business hours the books of account, records and other relevant documentation of any Sublicensees, to the extent relevant or necessary for the sole purpose of verifying the performance of the Companys payment obligations under this Agreement, the calculation of amounts due to Yissum under this Agreement and of all financial information provided in the Periodic Reports, and the Company shall cause such inspection to be performed. The Parties shall reconcile any underpayment or overpayment within thirty (30) days after the Representatives deliver the results of the audit. Any underpayment shall be subject to interest in accordance with the terms of Section 8.8 hereof In the event that any inspection as aforesaid reveals any underpayment by the Company to Yissum in respect of any year of the Agreement in an amount exceeding five percent (5%) of the amount actually paid by the Company to Yissum in respect of such year, then the Company shall pay the cost of such inspection.
12
8.8 Any sum of money due to either Party which is not duly paid on time shall bear interest from the due date of payment until the actual date of payment [***].
8.9 Should any payment required to be made to Yissum in accordance with the provisions of this Agreement be subject to withholding of any taxes assessable upon Yissum, the Company shall inform Yissum of such withholding requirement sufficiently in advance of such withholding to allow Yissum to obtain and provide the Company with an appropriate certificate of exemption, if available. The Company shall fully cooperate with Yissum, at Yissums expense, in its efforts to obtain such exemption (or in obtaining any refund if applicable). No withholding shall be made if an exemption is obtained All payments made shall be free and clear of any other withholding of any kind.
9. |
PATENT REGISTRATION |
9.1 Yissum, in consultation with the Company, shall be responsible for the filing, prosecution and maintenance of the Joint Patents, if any, in the Territory, at the Companys expense (the Ongoing Patent Costs) Each application and every patent registration of the Joint Patents shall be made and registered jointly in the name of Yissum and the Company. The Parties shall jointly choose patent counsel who will prosecute and maintain the Joint Patents, The Company agrees to such patent counsel directly bill the Company for such expenses and shall directly pay such bills in accordance with patent counsels directions.
9.2 For the avoidance of doubt, the Company will be solely responsible for the filing, prosecution and maintenance of any Patents which cover only Development Results that are not jointly owned with Yissum.
9.3 Notwithstanding the forgoing in Section 9.1 above, upon or immediately after the filing of the first Joint Patent, the Company shall deposit with Yissum the amount [***] to secure the payment of the Ongoing Patent Costs (the Expense Deposit). Should the Company fail to pay any amounts due in connection with the Ongoing Patent Expenses within thirty (30) days following receipt of Yissums written request accompanied by a detailed account, Yissum shall be entitled to pay the unpaid expenses from the Expense Deposit. In the event that Yissum utilizes some or all of the Expense Deposit as set forth in this section, it shall so notify the Company in writing The Company shall be obligated to deposit with Yissum [***]. The obligation of the Company under this Section 9 2 shall expire in the event that all Joint Patents have been refused, canceled or revoked.
9.4 Subject to the above, the Parties shall consult and make every effort to reach agreement in all respects relating to the manner of making applications and registering the Patents, including the time of making the applications, the countries where applications will be made and all other particulars relating to the registration and maintenance of the Joint Patents Notwithstanding the foregoing, Yissum reserves the sole right, to be exercised reasonably and in good faith, to make all final decisions with respect to the preparation, filing, prosecution and maintenance of such patent applications and patents.
9.5 The Parties shall assist each other in all respects relating to the preparation of documents for the registration of any patent or any patent-related right upon the request of the other Party, Both Parties shall take all appropriate action in order to assist the other to extend the duration of a Joint Patent or obtain any other extension obtainable under law, to maximize the scope of the protection afforded by the Joint Patents.
13
9.6 The Company shall give Yissum immediate notice of any approach made to it by a patent examiner or attorney in connection with any matter that is the subject matter of this Agreement. The Company shall only reply to such approaches after consultation with Yissum and subject to its consent.
9.7 The Company, its Affiliates and Sublicensees shall mark all Products covered by one or more of the Joint Patents with patent numbers (or the legend patent pending) in accordance with the statutory requirements in the country or countries of manufacture, use and sale. The Company shall require its Sublicensee complies with the provisions of this section.
9.8 [***].
9.9 The foregoing does not constitute an obligation or warranty on the part of Yissum that any Patent will indeed be made or registered or be registrable in respect of the Licensed Technology or any part thereof, nor shall it constitute an obligation, warranty, or declaration on the part of Yissum that a registered patent will afford due protection. For the avoidance of doubt, the provisions of this Agreement do not constitute a representation or warranty on the part of Yissum regarding the validity of or the protection afforded by any of the Patents, and Yissum hereby expresses that it has made no examination as to the validity of the Joint Patents.
10. |
PATENT RIGHTS PROTECTION |
10.1 The Company and Yissum shall each inform the other promptly in writing of any alleged infringements by a third party of the Joint Patents in the Territory, together with any available written evidence of such alleged infringement.
10.2 The Company, its Affiliate or Sublicensee shall have the right, but not the obligation, to prosecute m its own name and at its own expense any infringement of such Joint Patents. Before the Company, its Affiliate or its Sublicensee commences an action with respect to any infringement, the Company shall give careful consideration to the views of Yissum in making its decision whether or not to sue and, if relevant, make these views known to its Affiliate or Sublicensee The Company (or its Affiliate or Sublicensee, where relevant) shall keep Yissum reasonably apprised of all developments in the action and shall seek Yissums input and approval on any substantive submissions or positions taken in the litigation regarding the scope, validity or enforceability of the Joint Patents.
10.3 If the Company, its Affiliate or its Sublicensee elects to commence an action as described above and Yissum is a legally indispensable party to such action, Yissum, at the Companys expense, may be joined as a co-plaintiff. Regardless of whether Yissum is a legally indispensable party, Yissum, to the extent permitted by law, and at its own cost, may elect to join the action as a co-plaintiff and shall jointly control the action with the Company, its Affiliate or its Sublicensee. Irrespective of whether Yissum joins the action, it shall provide reasonable cooperation to the Company, its Affiliate or its Sublicensee, The Company shall reimburse Yissum for any costs it incurs as part of an action brought pursuant to this section where Yissum has not elected to join the action as a co-plaintiff.
14
10.4 [***].
10.5 [***].
10.6 [***].
10.7 If either Party commences an action and then decides to abandon it, such Party will give timely notice to the other Party. The other Party may continue the prosecution of the suit, after both Parties agree on the sharing of expenses.
10.8 [***].
11. |
CONFIDENTIALITY; [***] |
11.1 The Parties warrant and undertake that during the term of this Agreement and subsequent thereto, they shall maintain full and absolute confidentiality, and shall also be liable for their officers or employees or representatives maintaining absolute confidentiality, concerning all information, details and data which is in or comes to their knowledge or that of their officers, employees, representatives or any person acting on their behalf directly or indirectly relating to the Research, the Licensed Technology, Yissum, the University, the Researchers and their employees or the Company, its officers, employees, representatives or any person acting on its behalf directly or indirectly, The Parties undertake not to convey or disclose anything in connection with the foregoing to any entity without the prior written permission of the disclosing Party.
11.2 The obligation contained in this Section 11 shall not apply to information which is in the public domain as of the date of this Agreement or hereafter comes into the public domain through no fault of the receiving Party, its officers, employees, representatives or persons acting on its behalf.
11.3 Notwithstanding the above, a Party may disclose details and information to its officers, employees, representatives or persons acting on its behalf, Affiliates and Sublicensees, as necessary for the performance of its obligations pursuant to this Agreement, provided that it procures that such Parties execute a confidentiality agreement substantially similar in content to this Section 11.
11.4 Yissum shall procure that the Researchers and any other person connected with it with regard to the License execute a confidentiality agreement substantially similar in content to this Section 11.
11.5 As a precondition to any Sublicense, the Company shall require its Sublicensees to procure that the Sublicensees officers, employees, representatives or persons acting on the Sublicensees behalf are bound by a written confidentiality agreement substantially similar in content to this Section 11.
15
11.6 The provisions of this Section 11 shall be subject to permitted publications pursuant to section 13, below.
11.7 The above provisions of this Section 11 notwithstanding, the Company shall be entitled to disclose the information set forth below to any potential investors, sublicensee, IP providers, strategic or other business partners, provided that they have executed a confidential disclosure agreement substantially similar to this Section 11, Such permitted disclosure will refer to any materials or data as may be required in a due diligence process.
11.8 [***].
12. |
PUBLICATIONS |
12.1 Yissum shall ensure that no publications in writing, in scientific journals or orally at scientific conventions relating to the Licensed Technology, the Research Results, the Development Plan, the Development Results or any Product, are published by it or its Researchers, without first seeking the consent of the Company.
12.2 The Company undertakes to reply to any such request for publication by Yissum within thirty (30) days of its receipt of a request in connection with the publication of articles in scientific journals, and within thirty (30) days of its receipt of a request in connection with article abstracts. The Company may only decline such an application upon reasonable grounds, which shall be fully detailed in writing.
12.3 Should the Company decide to object to publication as provided in Section 12,2, publication shall be postponed for a period of not more than sixty (60) days from the date the publication was sent to the Company to enable the filing of patent applications or the removal of the Companys confidential information. The Company may withhold publication for an additional period of eleven (11) months at its discretion, subject to written notification to Yissum, thereafter the publication will be automatically permitted.
12.4 The provisions of this Section 12 shall not prejudice any other right, which Yissum has pursuant to this Agreement or at law.
12.5 For the avoidance of doubt, the provisions of this section in connection with the prohibition against publication shall not apply to internal publication made in the University for the Researchers and University employees provided that such persons are subject to written obligations of confidentiality substantially similar to those set forth in Section 11 hereof.
12.6 The Parties will ensure that any agreements with third parties concerning the Licensed Technology, the Research Results, the Development Plan, the Development Results or the Products include provisions substantially similar to this Section 12.
16
13. |
LIABILITY AND INDEMNITY |
13.1 YISSUM MAKES NO WARRANTIES OF ANY KIND WITH RESPECT TO THE LICENSED TECHNOLOGY. IN PARTICULAR, YISSUM MAKES NO EXPRESS OR IMPLIED WARRANTIES OF MERCHANTABILITY OR FITNESS FOR A PARTICULAR PURPOSE, OR THAT THE USE OF THE LICENSED TECHNOLOGY WILL NOT INFRINGE ANY PATENT, COPYRIGHT, TRADEMARK OR OTHER RIGHTS OF ANY THIRD PARTY. IN ADDITION, NOTHING IN THIS AGREEMENT MAY BE DEEMED A REPRESENTATION OR WARRANTY BY YISSUM AS TO THE VALIDITY OF ANY OF THE PATENTS OR THEIR REGISTRABILITY OR OF THE ACCURACY, SAFETY, EFFICACY, OR USEFULNESS, FOR ANY PURPOSE, OF THE LICENSED TECHNOLOGY. YISSUM HAS NO OBLIGATION, EXPRESS OR IMPLIED, TO SUPERVISE, MONITOR, REVIEW OR OTHERWISE ASSUME RESPONSIBILITY FOR THE PRODUCTION, MANUFACTURE, TESTING, MARKETING OR SALE OF ANY PRODUCT OR SERVICE [***].
13.2 [***].
13.3 [***].
13.4 The Company shall procure and maintain, at its sole cost and expense, to the extent that it is commercially reasonable to do so, policies of comprehensive general liability insurance in amounts not less than is customary in its industry. Such policy shall name the Indemnitees as additional insureds. Such comprehensive general liability insurance shall provide (a) product liability coverage and (b) broad form contractual liability coverage for the Companys indemnification obligations under this Section 13. The insurance coverage required above shall not be construed to create a limit of the Companys liability with respect to its indemnification obligations under this Section 13.
13.5 The Company shall provide Yissum with written evidence of such insurance upon request. The Company shall provide Yissum with written notice at least sixty (60) days prim to the cancellation, non-renewal or material change in such insurance If the Company does not obtain replacement insurance providing comparable coverage within such fifteen (15) day period, Yissum shall have the right to terminate this Agreement effective at the end of such fifteen (15) day period without notice or any additional waiting periods.
13.6 The Company shall maintain, at its own expense, liability insurance as set forth in Section 13 4 hereof, beyond the expiration or termination of this Agreement as long as a Product relating to or developed pursuant to this Agreement is being commercially distributed or sold by the Company, an Affiliate or a Sublicensee.
14. |
TERMINATION OF THE AGREEMENT |
14.1 Notwithstanding any provisions to the contrary by law, this Agreement may be terminated only upon the circumstances set forth in this Section 14.1 below (without prejudice to the Parties right to pursue remedies available by law other than termination).
(a) By either Party giving written notice to the other, in which case termination will become effective immediately upon receipt by the other Party of such written notice, if (w) the other Party passes a resolution for voluntary winding up or a winding up application is made against it and not set aside within ninety (90) days, or (x) a receiver or liquidator is appointed for the other Party unless the order or decision effectuating such
17
appointment is set aside within ninety (90) days of the date such order or decision; or (y) the other Party enters into winding up or insolvency or bankruptcy proceedings and such proceedings are not set aside within ninety (90) days, or (z) an attachment is made over all or substantially all of the other Partys assets or if execution proceedings are taken against the other Party and the same are not set aside within ninety (90) days of the date the attachment is made or the execution proceedings are taken Each of the Parties undertakes to notify the other within seven (7) days if any of the abovementioned events occur; or
(b) By Yissum giving written notice to the Company in the following circumstances, if the pertinent circumstance is not cured within ninety (90) of receipt of Yissums notice requiring the Company to do so.
(i) In the circumstances set out in Section 5.4 hereof.
(ii) Uncured lapse of insurance coverage (if insurance policies are to be obtained and maintained in accordance with Section 13.4 hereof) under Section 13 5 hereof unless such lapse was covered (retroactively if necessary); or
(iii) Commercially unreasonable failure to respond to third party claims as required under Section 10 hereof.
14.2 Upon the occurrence of any of the events set forth in Section 14.1(a) hereof or in the event that the Company is insolvent, declared bankrupt, is voluntarily or involuntarily dissolved, or otherwise ceases operations, excluding, however, dissolution or cessation of operations which result from an M&A transaction or the sale of all or substantially all of the assets of the Company, (each, a Company Cessation Event), the following provisions will apply.
(a) Some or all of the Companys shareholders, but acting as a single group, shall be entitled, but not obligated, to assume the Companys rights and obligations pursuant to this Agreement, either directly or through a new corporate entity (Company Shareholders Option), in which case the Companys interest in the Joint IP shall be transferred to them or to such new corporate entity, as appropriate.
(b) Should the Company Shareholders Option not be exercised, ownership of the Companys interest in the Joint IP shall be transferred and assigned to Yissum in accordance with the letter of assignment m the form annexed hereto as Appendix E, which shall then be free to license the Joint IP to others as it sees fit.
(c) [***].
14.3 Upon termination of the Agreement for any other reason than those referenced in Section 14 2 hereof; the License will terminate and the Licensed Technology and all rights included therein shall revert to Yissum. In addition, the Company, or its successors or assigns, shall grant Yissum an exclusive, perpetual, irrevocable, royalty-free license to its interest in the Joint IP and Yissum shall thereafter be free to enter into agreements with any other third parties for the granting of a license or to deal in any other manner with the Licensed Technology and the Joint IP as it shall see fit with no further obligation to the Company, or its successors or assigns.
18
14.4 If this Agreement is duly terminated, and the Company Shareholders Option is not exercised (if termination is made for Company Cessation Event), then upon termination of the Agreement, the Company shall return or transfer to Yissum, within thirty (30) days of termination of the Agreement, all material, in soft or hard copy, relating to the Licensed Technology, and it may not make any further use thereof. In case of termination as set forth herein, the Company will not be entitled to any reimbursement of any amount paid to Yissum under this Agreement with respect to such terminated portion of the License. Yissum shall be entitled to conduct an audit in order to ascertain compliance with this provision and the Company agrees to allow reasonable access to Yissum or its representatives for this purpose.
14.5 Sections 3, 4.2, 7, 8, 9, 10, 11, 13, 14, 15 and 16 hereof shall survive the termination of this Agreement to the extent required to effectuate the intent of the Parties as reflected in this Agreement.
15. |
LAW |
The provisions of this Agreement and everything concerning the relationship between the Parties in accordance with this Agreement shall be governed by Israeli law and jurisdiction shall be granted only to the appropriate court in Tel Aviv. The Company undertakes not to object to the enforcement against it of writs and decisions issued by any other jurisdiction outside the State of Israel under such circumstances. The Company hereby waives any immunity it may have against enforcement of any judgment obtained against it by Yissum.
16. |
ARBITRATION |
16.1 Notwithstanding and in addition to the provisions of Section 15 hereof, all differences of opinion and disputes arising between the Parties in connection with the Agreement or its interpretation or its performance or breach, shall be referred for the decision of a single arbitrator, whose identity shall be determined by mutual consent of the Parties.
16.2 Should the Parties not reach agreement as to the identity of the arbitrator within fourteen (14) days of request by either Party for the appointment of an arbitrator, the arbitrator shall be appointed by the Chairman of the Israel Bar Association on the application of either of the Parties. In any event, in any disputes concerning issues of intellectual property rights the arbitrator will be a patent attorney.
16.3 The arbitration shall be held in Israel. The proceedings before and all documents submitted to such arbitrator shall be in the English language. The arbitrator shall not be bound by the civil procedure regulations and laws of evidence but shall base his/her decision on the substantive law of Israel and shall give grounds for his/her decision. The arbitrator shall be empowered to grant temporary injunctions and orders, which shall be enforceable in foreign jurisdictions, in accordance with Section 15 hereof.
19
16.4 The decision of the arbitrator shall be final and binding upon the Parties, and shall be enforceable in foreign jurisdictions.
16.5 The execution of this Agreement shall constitute the execution of an Arbitration Agreement.
17. |
MISCELLANEOUS |
17.1 Relationship of the Parties. It is hereby agreed and declared between the Parties that they shall act in all respects relating to this Agreement as independent contractors and there neither is nor shall there be any employer-employee or principal-agent relationship or partnership relationship between the Company (or any of its employees) and Yissum. Each Party will be responsible for payment of all salaries and taxes and social welfare benefits and any other payments of any kind in respect of its employees and officers, regardless of the location of the performance of their duties, or the source of the directions for the performance thereof.
17.2 Assignment. The Parties may not transfer or assign or endorse their rights or duties or any of them pursuant to this Agreement to another, without the prior written consent of the Party, which consent shall not be unreasonably denied, conditioned or delayed.
17.3 No Waiver. The failure or delay of a Party to the Agreement to claim the performance of an obligation of the other Party shall not be deemed a waiver of the performance of such obligation or of any future obligations of a similar nature.
17.4 Representation by Legal Counsel. Each Party represents that it has been represented by legal counsel in connection with this Agreement and acknowledges that it has participated in drafting tins Agreement. In interpreting and applying the terms and provisions of this Agreement, the Parties agree that no presumption shall exist of be implied against the Party which drafted such terms and provisions.
17.5 Legal Costs. Each Party shall bear its own legal expenses involved in the making of this Agreement.
17.6 Taxes. Monetary amounts mentioned in this agreement do not include VAT. All taxes and duties to be paid in connection with this Agreement by the Company, including any VAT, shall be borne by the Company. Any duties or taxes payable by Yissum in connection with this Agreement shall be paid by Yissum.
17.7 Force Majeure. Neither Party shall be held liable or responsible to the other Party nor be deemed to have defaulted under or breached the Agreement for failure or delay in fulfilling or performing any term of this Agreement to the extent, and for so long as, such failure or delay is caused by or results from causes beyond the reasonable control of the affected Party including but not limited to fires, earthquakes, floods, embargoes, wars, acts of war (whether war is declared or not), insurrections, riots, civil commotions, strikes, lockouts or other labor disturbances, acts of God or acts, omissions or delays in acting by any governmental authority or other Party provided that the nonperforming Party uses commercially reasonable efforts to avoid or remove such causes of nonperformance and continues performance under this Agreement with reasonable dispatch whenever such causes are removed. The Party affected by such circumstances shall promptly notify the other Party in writing when such circumstances cause a delay or failure in performance and when they cease to do so.
20
17.8 Counterparts. This Agreement may be executed in two or more counterparts, each of which shall be deemed an original.
17.9 Binding Effect. This Agreement shall be binding upon the Parties once executed by both Parties and shall enter into force and become effective as of the later of the signature dates.
17.10 Entire Agreement. This Agreement constitutes the full and complete agreement between the Parties and supersedes any and all agreements or understandings, whether written or oral, concerning the subject matter of this Agreement (including, but not limited to, the MOU), and may only be amended by a document signed by both Parties.
17.11 Notices. All notices and communications pursuant to this Agreement shall be made in writing and sent by facsimile or by registered mail or served personally at the following addresses:
Yissum
Yissum Research Development Company
of the Hebrew University of Jerusalem,
P.O. Box 39135,
Jerusalem 91390
Israel
BEEOLOGICS, INC.
11800 SW 77th Avenue, Miami Florida 33156, USA
Att: Eyal Ben-Chanoch
21
or such other address furnished in writing by one Party to the other. Any notice served personally shall be deemed to have been received on the day of service, any notice sent by registered mail as aforesaid shall be deemed to have been received seven days after being posted by prepaid registered mail. Any notice sent by facsimile shall be deemed to have been received by the next business day after receipt of confirmation of transmission.
IN WITNESS THE HANDS OF THE PARTIES
YISSUM | THE COMPANY | |||||||
By: |
/s/ Ziv Shomroni |
By: |
/s/ Eyal Ben-Chanoch |
|||||
Name: | Ziv Shomroni | Name: | Eyal Ben-Chanoch | |||||
Title: | VP Licensing Agricultural & Natural Science | Title: | President & CEO | |||||
Date: |
|
Date: |
|
I the undersigned, Prof Ilan Sela, have reviewed, am familiar with and agree to all of the above terms and conditions including, but not limited to the non-compete provisions set forth in Section 11.8, above. I hereby undertake to cooperate fully with Yissum in order to ensure its ability to fulfill its obligations hereunder, as set forth herein.
/s/ Ilan Sela |
October 22, 2010 |
|||
Prof. Ilan Sela | Date signed |
22
or such other address furnished in writing by one Party to the other. Any notice served personally shall be deemed to have been received on the day of service, any notice sent by registered mail as aforesaid shall be deemed to have been received seven days after being posted by prepaid registered mail. Any notice sent by facsimile shall be deemed to have been received by the next business day after receipt of confirmation of transmission.
IN WITNESS THE HANDS OF THE PARTIES
YISSUM | THE COMPANY | |||||||
By: |
|
By: |
/s/ Eyal Ben-Chanoch |
|||||
Name: |
|
Name: | Eyal Ben-Chanoch | |||||
Title: |
|
Title: | President & CEO | |||||
Date: |
|
Date: |
|
I the undersigned, Prof Ilan Sela, have reviewed, am familiar with and agree to all of the above terms and conditions including, but not limited to the non-compete provisions set forth in Section 11.8, above. I hereby undertake to cooperate fully with Yissum in order to ensure its ability to fulfill its obligations hereunder, as set forth herein.
/s/ Ilan Sela |
October 22, 2010 |
|||
Prof. Ilan Sela | Date signed |
23
[***]
A-1 Company IP
1. |
[***] |
2 |
Relative portion in Joint IP. |
A-2 Yissum IP
Relative portion in Joint IP
A-3 Joint IP
1 |
Provisional patent application: No. 61/251,339 : By: HUJI (Eyal Maori, Ilan SELA, Nitzan Paldi, Ethan Glick, Eyal Ben-Chanoch and Gal Yarden); Title: COMPOSITIONS FOR CONTROLLING VARROA MITES IN BEES. The patent resulting from said patent application will be jointly owned by Yissum and the Company [***]. |
2. |
Other Research Results, including Know-How. |
YISSUM | THE COMPANY | |||||||
By: |
/s/ Yaacov Michlin |
By: |
/s/ Eyal Ben-Chanoch |
|||||
Name: | President & CEO | Name: | Eyal Ben-Chanoch | |||||
Title: |
|
Title: | President & CEO | |||||
Date: |
|
Date: |
|
I the undersigned, Prof Ilan Sela, have reviewed, am familiar with and agree to all of the above terms and conditions. I hereby undertake to cooperate fully with Yissum in order to ensure its ability to fulfill its obligations hereunder, as set forth herein.
/s/ Ilan Sela |
|
|||
Prof. Ilan Sela | Date signed |
24
EXHIBIT A INTELLECTUAL PROPERTY
A-1 Company IP
1. |
[***] |
2 |
Relative portion in Joint IP. |
A-2 Yissum IP
Relative portion in Joint IP
A-3 Joint IP
1 |
Provisional patent application: No. 61/251,339 : By: HUJI (Eyal Maori, Ilan SELA, Nitzan Paldi, Ethan Glick, Eyal Ben-Chanoch and Gal Yarden); Title: COMPOSITIONS FOR CONTROLLING VARROA MITES IN BEES. The patent resulting from said patent application will be jointly owned by Yissum and the Company in proportions of 50%Yissum and 50%the Company and an assignment with respect thereto will be executed m favor of both Yissum and the Company. |
2. |
Other Research Results, including Know-How. |
YISSUM |
THE COMPANY |
|||||||
By: |
|
By: [***] |
||||||
Name: |
|
Name: [***] |
||||||
Title: |
|
Title: [***] |
||||||
Date: |
|
Date: [***] |
[***]
[***]
25
Exhibit 10.31
Certain identified information has been omitted from this exhibit because it is
not material and of the type that the registrant treats as private or confidential.
[***] indicates that information has been omitted.
ASSIGNMENT AGREEMENT
THIS ASSIGNMENT AGREEMENT, effective as of December 10, 2020 (the Assignment), is made by and between BEEOLOGICS, INC., having its principal business offices at 800 North Lindbergh Boulevard, St. Louis, Missouri 63167 (Assignor), and GREENLIGHT BIOSCIENCES, INC., having its principal business offices at 200 Boston Ave. Suite 1000, Medford, MA 02155 (Assignee).
WHEREAS, Assignor entered into a License and Sponsored Research Agreement dated April 2010 (the Bee Health License) with Yissum Research Development Company of the Hebrew University of Jerusalem LTD. (Yissum);
WHEREAS, Assignor and Assignee are parties to an Assignment and License Agreement dated as of December 10, 2020 (the Agreement), pursuant to which, among other things, Assignor has agreed to assign and deliver to Assignee, and Assignee has agreed to accept, all of Assignors right, title, interest, and obligations in and to the Bee Health License; and
WHEREAS, Yissum has consented to the assignment of the Bee Health License to Assignee, such consent attached as Exhibit A.
NOW THEREFORE, for good and valuable consideration acknowledged by Assignor to have been received in full from Assignee and pursuant to the terms of the Agreement, Assignor and Assignee hereby agrees as follows:
1. Assignor hereby conveys, transfers, assigns, and delivers unto Assignee, absolutely and forever, all of Assignors right, title, interest, obligations, responsibilities, and duties in and to the Bee Health License.
2. Assignee hereby accepts the assignment of all of Assignors obligations, responsibilities, and duties under the Bee Health License and all of Assignors right, title, and interest in and to the Bee Health License. All terms and conditions of the Bee Health License shall remain in full force and effect.
3. Notwithstanding any other provisions of this Assignment to the contrary, nothing contained in this Assignment shall in any way supersede, modify, replace, amend, change, rescind, waive, exceed, expand, enlarge, or in any way affect the provisions, including warranties, covenants, agreements, conditions, representations, or in general any of the rights and remedies, or any of the obligations and indemnifications of Assignor or Assignee set forth in the Agreement. This Agreement is intended only to effect the transfer of certain property transferred pursuant to the Agreement and shall be governed entirely in accordance with the terms and conditions of the Agreement.
4. This Assignment shall be binding on, and shall inure to the benefit of, Assignor, Assignee, and their respective successors and/or assigns, and all others acting by, through, with, or under their direction, and all those in privity therewith.
IN WITNESS WHEREOF, Assignee has caused this Assignment to be executed by its duly authorized representatives effective this 17 day of December, 2020.
BEEOLOGICS, INC. | ||
By: |
/s/ Deryck Jeremy Williams |
|
Name: | Deryck Jeremy Williams | |
Title: | Director of Beelogics, Inc. |
[Signature Page to Assignment]
IN WITNESS WHEREOF, Assignee has caused this Assignment to be executed by its duly authorized representatives effective this day of , 2020.
GREENLIGHT BIOSCIENCES, INC. |
||
By: |
/s/Andrey Zarur |
|
Name: | Andrey Zarur | |
Title: | President & CEO |
[Signature Page to Assignment]
Exhibit 10.31
EXHIBIT A
Sent Via Fax: fax no. [***]
Yissum Research and Development Company of the Hebrew
University of Jerusalem (hereinafter Yissum)
Hi-Tech Park, Edmond J Safra Campus Givat-Ram, Jerusalem
Jerusalem 91390
Israel
SUBJECT: NOTICE OF ASSIGNMENT
Dear Yissum:
We refer to the License and Sponsored Research Agreement (as extended, renewed, amended or restated from time to time, the Agreement), dated March 15, 2013 between Beeologics, Inc. (a wholly owned subsidiary of Monsanto Company (hereinafter Monsanto), which is a wholly owned subsidiary of Bayer AG) and Yissum. Pursuant to Section 17.2 of the Agreement, we hereby give you notice of that Monsanto desires to assign the Agreement and all rights and interests thereto to GreenLight Bioscience, Inc. (hereinafter GreenLight). GreenLight agrees to assume such rights and obligations, such assignment and assumption to be effective on December 7, 2020. We therefore request Yissums express written consent of such assignment, which, pursuant to Section 17.2, such consent shall not be unreasonably denied, conditioned or delayed.
In order to ensure that the Agreement can be continued without interruption, we would like to ask you to duly sign below and return this letter to Bayer Crop Science LLP, 800 North Lindbergh Boulevard, St. Louis, MO, USA, Attn: Amanda Carmany-Rampey, Associate General Counsel Intellectual Property & Licensing with a copy emailed to [***] at your earliest convenience. Your
signature will serve as your consent to the assignment and assumption of the Agreement, acknowledgement that this letter constitutes sufficient notice of the assignment and assumption of the Agreement and irrevocable waiver of any termination rights you may have according to the Agreement as a result of the assignment and assumption.
Sincerely,
Amanda Carmany-Rampey
Assistant General Counsel
Intellectual Property & Licensing
Bayer Crop Science
Agreed to and accepted this day of , 2020. | ||
Yissum Research and Development Company of the Hebrew University of Jerusalem | ||
By: |
|
|
Title: |
|
Exhibit 10.33
Certain identified information has been omitted from this exhibit because it is
not material and of the type that the registrant treats as private or confidential.
[***] indicates that information has been omitted.
MASTER SERVICES AGREEMENT
between
SAMSUNG BIOLOGICS CO., LTD.
And
GREENLIGHT BIOSCIENCES, INC.
1
Table of Contents
SECTION 1 |
DEFINITIONS | 3 | ||||
SECTION 2 |
RELATED AGREEMENTS AND EXHIBITS | 11 | ||||
SECTION 3 |
MANAGEMENT OF SERVICE | 11 | ||||
SECTION 4 |
SERVICE DESCRIPTIONS | 13 | ||||
SECTION 5 |
CHANGES TO THE SPECIFICATIONS, ANALYTICAL METHODS, MANUFACTURING PROCESS, FACILITY OR EQUIPMENT | 19 | ||||
SECTION 6 |
REGULATORY APPROVALS AND INSPECTIONS | 20 | ||||
SECTION 7 |
QUALITY COMPLIANCE | 21 | ||||
SECTION 8 |
CONSIDERATION AND PAYMENT TERMS | 21 | ||||
SECTION 9 |
CONFIDENTIALITY | 23 | ||||
SECTION 10 |
OWNERSHIP OF MATERIALS AND INTELLECTUAL PROPERTY | 25 | ||||
SECTION 11 |
WARRANTIES. | 25 | ||||
SECTION 12 |
INDEMNIFICATION | 26 | ||||
SECTION 13 |
DISCLAIMER OF CONSEQUENTIAL DAMAGES; LIMITATION OF LIABILITY | 27 | ||||
SECTION 14 |
TERM AND TERMINATION OF AGREEMENT | 28 | ||||
SECTION 15 |
ARBITRATION | 31 | ||||
SECTION 16 |
MISCELLANEOUS | 31 |
2
Certain identified information has been omitted from this exhibit because it is
not material and of the type that the registrant treats as private or confidential.
[***] indicates that information has been omitted.
MASTER SERVICES AGREEMENT
This Master Services Agreement (this MSA) is made and entered into as of the date of last signature below (the Effective Date) by and between Greenlight Biosciences, Inc., a Delaware corporation having its principal place of business at 200 Boston Avenue, Suite 1000, Medford, MA 02155 (Client), and Samsung Biologics Co., Ltd., a Korean corporation having its principal place of business at 300, Songdo bio-daero, Yeonsu-gu, Incheon, 21987, Republic of Korea (SBL). Client and SBL are sometimes referred to herein individually as a Party and collectively as the Parties.
WHEREAS, Client and SBL wish to enter into a business relationship whereby SBL will provide Client with certain services related to pharmaceutical development and/or manufacturing;
NOW, THEREFORE, in consideration of the mutual promises, covenants and agreements hereinafter set forth and for other valuable consideration, the Parties agree as follows:
SECTION 1 DEFINITIONS
Each of the following capitalized terms as used in this MSA, whether in the singular or plural, shall have the respective meanings set forth below.
1.1 |
Acceptance Procedure means the review of the Batch Related Documents and any reasonably necessary test(s) of a Batch of Product which are performed to verify that the Product meets the Specifications and complies with Regulatory Authority requirements, which are conducted by Client before or after SBLs release of a Batch of Product in accordance with the applicable PSA and QAG. |
1.2 |
Affected Party means the Party affected by Force Majeure under Section 16.3. |
1.3 |
Affiliate means any corporation, company, partnership or other entity which directly or indirectly, controls, is controlled by or is under common control with either Party hereto. A corporation or other entity shall be regarded as controlling another corporation or other entity if it owns or directly or indirectly controls more than fifty percent (50%) of the voting stock or other ownership interest of the corporation or other entity, or if possesses, directly or indirectly, the power to direct or cause the direction of the management and policies of the corporation or other entity or the power to elect or appoint more than fifty percent (50%) of the members of the governing body of the corporation or other entity. |
1.4 |
Annual Service Fees means the total Service Fees paid or payable by Client to SBL in a given calendar year (excluding costs of Raw Materials, SBL handling fees, and other expense or cost reimbursements) pursuant to a particular Product Specific Agreement. |
1.5 |
Applicable Laws means any and all laws, rules, or regulations of any jurisdiction which are applicable to the Parties in carrying out activities described in this MSA or any PSAs that may be in effect from time to time. |
3
1.6 |
Assignment, Assigning, or to Assign means a merger, change of control, sale of stock, inheritance of stock, transfer of all or substantially all of the assets, or transfer of all or substantially all rights to any Product. |
1.7 |
Background IP means any Intellectual Property related to a Product and/or its use, or the Manufacture of such Product, in each case, which is owned and/or controlled by such Party prior to the Effective Date. |
1.8 |
Batch means one lot of Bulk Drug Product. |
1.9 |
Batch Failure means that all of a Batch is Non-Conforming Product as reasonably determined by the Core Team during Manufacture of a Batch and prior to SBLs Batch release. |
1.10 |
Batch Record, if not defined in the applicable QAG, means the document, proposed by SBL and approved by Client in writing, which defines the manufacturing methods, test methods, and other procedures, direction, and controls associated with the manufacture and testing of a Batch. |
1.11 |
Batch Related Documents means Manufacturing Documentation in support of SBLs release of a Product. |
1.12 |
Bulk Drug Product means formulated Drug Substance, which is Drug Substance encapsulated in a delivery medium such as liquid nano particles. |
1.13 |
Certificate of Analysis, if not defined in the applicable QAG, means a document prepared by SBL listing tests performed by SBL or an External Laboratory certifying that a particular Batch of Product meets the applicable Specifications, and the results of such tests. |
1.14 |
Certificate of Compliance means a document prepared by SBL with respect to a particular Batch that verifies completion of all operations in accordance with the Batch Record and cGMP, if applicable and was processed in accordance with the QAG and Applicable Laws. |
1.15 |
Change means any modification, alteration, adjustment, or correction to the Manufacturing Process, Services, or Specifications. |
1.16 |
Client is defined in the preamble. |
1.17 |
Client Invention means any Invention that is conceived and first reduced to practice by either Party which is derived from, or arises out of Client Technology, Client Background IP or Clients Confidential Information or any other proprietary right of Client. |
1.18 |
Client Materials means Client reagents and other materials supplied by Client or its third party supplier as set forth in the applicable PSA to be used in the Service hereunder. |
4
1.19 |
Client Technology means means (A) Client Materials and any intermediates, components, or derivatives of Client Materials; (B) Products and any works-in-progress, components, or derivatives of Product; (C) Specifications; (D) test methods provided by Client for use in the Services; (E) the Technology of Client, and all know-how, technology, research and other information of Client including and relating to the Services, Manufacturing Process, analytical methods, quality control analysis, specifications, transportation and storage requirements provided by Client to SBL in connection with this MSA and applicable PSA. |
1.20 |
Clinical Product means Product which is Manufactured by SBL pursuant to a PSA and which is to be used by Client in a research study or studies that prospectively assigns human participants or groups of humans to one or more health-related interventions to evaluate the effects on health outcomes. |
1.21 |
Commercial Product means Product which is Manufactured by SBL which is intended for commercial sale and use by humans and for importation or exportation into countries or regions designated in each PSA. Notwithstanding the foregoing, any Batches manufactured prior to PAI and including PAI Batches (if applicable) shall not be considered Commercial Product until such PAI even if such Batches are intended for commercial sale and human use. |
1.22 |
Commercially Reasonable Efforts means with respect to an activity to be carried out by a Party pursuant to this MSA, the carrying out of such activity in a diligent manner, and using efforts and resources comparable to the efforts and resources commonly used in the contract manufacturing of pharmaceutical products (in the case of SBL) or in the biopharmaceutical industry (in the case of Client) by companies with resources and expertise similar to those of such Party. Commercially Reasonable Efforts requires prompt assignment of responsibility for such task or activity to specific qualified employee(s) and allocation of resources designed to advance progress with respect to such task or activity but does not require the taking of actions (a) which would require or is likely to require a material adverse change in such Partys business strategy, existence or solvency, or significant assets, (b) disproportionate to the benefits received under this MSA, or (c) would require either Party to violate Applicable Laws or break any existing contractual commitments with third parties which were entered into by prior to the Effective Date. |
1.23 |
Confidential Information means any and all scientific, business, financial, contractual, marketing and technical information of or about a party or a Product which has been or may be disclosed, or to which access is provided, by such party (Disclosing Party) or any of its representatives to the other Party (Receiving Party) or any of its representatives, which (a) if in writing, is marked confidential, proprietary or other similar marking at the time of disclosure, or (b) if provided orally or visually, is identified as confidential at the time of disclosure and confirmed in writing to Receiving Party within fifteen (15) days of such disclosure, or (c) Receiving Party knows or has reason to know is confidential, trade secret or proprietary information of the Disclosing Party at the time of disclosure. For clarity, the existence and terms of this MSA shall be deemed to be the Confidential Information of both Parties. |
1.24 |
Core Team means a committee composed of an equal number of representatives from each of SBL and Client to oversee, review, and coordinate the day-to-day performance of the Services and/or Manufacture with the goal of ensuring effective communication between the Parties. |
5
1.25 |
Critical Raw Material means any Raw Materials with significant financial value and importance, as reasonably agreed between the Parties. Critical Raw Materials shall be specified in the applicable PSA. |
1.26 |
Current Good Manufacturing Practices or cGMP means current good manufacturing practices and regulations applicable to the Manufacture of Product that are promulgated by any Regulatory Authority, including as promulgated under and in accordance with (i) the U.S. Federal Food, Drug and Cosmetic Act, Title 21 of the U.S. Code of Federal Regulations, Parts 210, 211, 600, 601 and 610, (ii) relevant EU legislation, including European Directive 2003/94/EC or national implementations of that Directive, (iii) relevant guidelines, including the EU Guidelines for Good Manufacturing Practices for Medicinal Products (Eudralex Vol. 4 and Annexes thereto), (iv) International Conference on Harmonisation Good Manufacturing Practice Guide for Active Pharmaceuticals Ingredients and (v) and any analogous set of regulations, guidelines or standards as defined, from time to time, by any relevant Regulatory Authority having jurisdiction over the development, manufacture or commercialization of the Product, as applicable, in each case as in effect as of the date such manufacturing for the Product are or were conducted. |
1.27 |
Customized or Dedicated Raw Materials means any Raw Materials that (a) require customization or specific testing and/or (b) are dedicated just for Client and not intended to be used across multiple product or customers. |
1.28 |
Damages means any direct damages, costs, expenses, fines, penalties (including reasonable attorneys fees and costs), losses and liabilities. |
1.29 |
Decision Memo means a binding memorandum summarizing and memorializing the Parties discussion, understanding, and agreement as to any aspect of the Manufacture that are not directly and/or specifically elaborated in the MSA, PSA, or any previous Decision Memo. |
1.30 |
Fill/Finish Product means a finished or intermediate dosage form such as vial or pre-filled syringe that contains a Bulk Drug Product, generally, but not necessarily, in association with one or more other ingredients. |
1.31 |
Drug Substance means an mRNA-based active ingredient that is intended to furnish pharmacological activity or other direct effect in the diagnosis, cure, mitigation, treatment, or prevention of disease or to affect the structure or any function of the human body. |
1.32 |
Effective Date is defined in the preamble. |
1.33 |
EMA means the European Medicines Agency, or any successor agency. |
1.34 |
Engineering Batch means a Batch manufactured prior to Commercial Products with the purpose of confirming successful transfer and/or implementation of the Manufacturing Process to the Facility. |
6
1.35 |
External Laboratory means a third party laboratory instructed by SBL, with Clients prior consent, to conduct activities required to complete certain Services as discussed and agreed upon by the Parties. |
1.36 |
Facility means one or more of the facilities of SBL where the Services shall be performed, as further specified in each PSA. |
1.37 |
FDA means the United States Food and Drug Administration or any successor agency thereto. |
1.38 |
Firm Period means the portion of the Forecast that is binding on both Parties. |
1.39 |
Forecast means a projection of Clients requirements for delivery of Product. |
1.40 |
Force Majeure Event means any event or occurrence which is beyond the non-performing Partys reasonable control, including fire, explosion, flood, landslide, epidemics, or other acts of God; acts, regulations, export and/or import restrictions, embargos (including but not limited to those promulgated by any U.S. Regulatory Authority), or laws of any government; terrorism, war; failure of public utilities; acts of decisions of duly constituted municipal, state, national or supra-national governmental authorities or of courts of law; or impossibility to obtain Raw Materials, equipment, supplies, fuel or other required materials or the occurrence of other supply or manufacture interruptions (at its and/or third-party facilities), in spite of having acted with Commercially Reasonable Efforts. |
1.41 |
Implementation Plan and Budget means an estimated plan and budget of the reasonable and necessary costs that would be incurred by SBL as a result of the implementation of any such Change(s), including, but not limited to (i) process and analytical development; (ii) equipment and/or the Facility modifications, qualification, validation, maintenance, and decommissioning/disposal; (iii) process and analytical validation; (iv) document revisions or changes, the Facility, equipment, and system modifications or changes; (v) additional stability testing; and (vi) preparing submissions to Regulatory Authorities. |
1.42 |
Indemnified Party means the Party claiming indemnification under Sections 12.3 and 13.2. |
1.43 |
Indemnifying Party means the Party subject to an indemnification claim from the other Party. |
1.44 |
Intellectual Property means: (i) patents, trade secrets, copyrights, trademarks, trade names and domain names, rights in designs, rights in computer software, database rights, know-how, and any other intellectual property rights, in each case whether registered or unregistered; (ii) all applications (or rights to apply) for, and renewals or extensions of, any of the rights described in the foregoing sub-clause (i); and (iii) all rights and applications that are similar or equivalent to the rights and applications described in the foregoing sub-clauses (i) and (ii), which exist now, or which come to exist in the future, in any part of the world. |
1.45 |
Invention means any Intellectual Property created by either Party which arises out of or results from the Services under the MSA. |
7
1.46 |
Joint Steering Committee or JSC means a committee composed of an equal number of representatives from each of SBL and Client, generally at least Director-level or equivalent to provide guidance to the Core Team and resolve any issues or disputes which in good-faith are not able to be resolved by the Core Team. |
1.47 |
Manufacturing or to Manufacture means the manufacturing of a Batch of Product, and any services relating to such manufacturing, including, but not limited to, testing, quality control, documentations, archiving, and packaging, and up to release of the Batch of Product, to be performed by SBL under the MSA and any applicable PSA. |
1.48 |
Manufacturing Documentation means with respect to a given Batch of Product, the data acquired and generated, documents and records describing or otherwise related to the Manufacturing Process. |
1.49 |
Manufacturing Process means the mutually agreed production process for the Manufacturing of a Batch the Product. |
1.50 |
Non-Affected Party means the Party other than the Affected Party under Section 16.3. |
1.51 |
Non-Conforming Product means a Batch of Product that fails to conform to the Specifications, or other mutually agreed upon written express requirements for SBL to follow, resulting in a materially adverse impact on the quality of Product as reasonably determined by the relevant document, record, or data. |
1.52 |
Other Raw Material means any Raw Material other than Critical Raw Material and Customized or Dedicated Raw Material. |
1.53 |
Party and Parties is defined in the preamble. |
1.54 |
Pre-Approval Inspection or PAI means an on-site inspection of the Facility by the Regulatory Authority prior to granting the Regulatory Approval for Commercial Product as required by various Regulatory Authorities to ensure that the Manufacturing Process and the Facility meet the appropriate requirements and comply with cGMP. |
1.55 |
Process Validation Batch means a Batch of Product produced by SBL hereunder to (i) demonstrate and document the consistency and reproducibility of the Manufacturing Process at the Facility, and (ii) support the Regulatory Approval of both the Product Manufactured and the Manufacturing Process at the Facility. |
1.56 |
Product means Clinical Product or Commercial Product to be Manufactured by SBL pursuant to this MSA and any applicable PSA. |
1.57 |
Product-in-process means any unfinished Product under the Manufacturing Process. |
8
1.58 |
Product Purchase Commitment means the minimum number of Batches that Client shall be obligated to purchase in any given calendar year. |
1.59 |
Product Specific Agreement or PSA means a separate agreement specific to each Product and/or Services entered into and mutually agreed from time to time by duly authorized representatives of the Parties. Each PSA shall be governed by and be integrated into this MSA and may include, without limitation, details such as (i) a scope of work of the Services to be performed under such PSA which describes key activities and assumptions, (ii) the Product for which Samsung will perform such Services for Client, (iii) fees to be paid to SBL by Client for the Services, and (iv) any other deliverables. |
1.60 |
PSA Effective Date means the effective date of any PSA entered into between the Parties. |
1.61 |
Purchase Order is a commercial document issued by Client to SBL indicating, among other things, the quantity to be manufactured, the agreed prices for Product or Service, and the estimated delivery date to be later confirmed and fixed in accordance with Section 4.12.2(b). |
1.62 |
Quality Agreement or QAG means the quality agreement entered into by the Parties that governs the responsibilities related to quality systems and quality requirements for the Product(s) Manufactured hereunder, including quality control, testing and release of such Product(s) at the Facility entered into by the Parties. |
1.63 |
Quarter means each period of three (3) consecutive calendar months beginning on January 1, April 1, July 1, or October 1. |
1.64 |
Raw Materials means those materials procured by SBL that are used in the Services. Raw Materials exclude the Client Materials. |
1.65 |
Regulatory Approval means all approvals, licenses, registrations or authorizations thereof of any national, regional, state or local regulatory agency, department, bureau or other governmental entity in any jurisdiction where the Product is marketed or intended to be marketed, necessary for the manufacture and sale of the Product manufactured by SBL at the Facility. |
1.66 |
Regulatory Authority means any national (e.g., the FDA), supra-national (e.g., the EMA), regional, state or local regulatory agency, department, bureau, commission, council or other governmental entity, in any jurisdiction responsible for granting the Regulatory Approval. |
1.67 |
Reserved Capacity means the capacity for Manufacturing the Product within SBLs Facility reserved and dedicated to Client, the costs of which shall be calculated based on the Service Fees for Batches that were scheduled to be Manufactured using the Reserved Capacity. |
1.68 |
SBL Assignable Error means: [***]. |
9
1.69 |
SBL Invention means any Invention which is not a Client Invention . |
1.70 |
Scope of Work means the document generally forming part of a PSA, specifying in detail the scope and schedule of the Services and the Service Fees as mutually agreed upon by the Parties. |
1.71 |
Service or Services means any service related to development and/or manufacturing for Client as specified in PSA and in accordane with the terms and conditions of this MSA. |
1.72 |
Service Fee is the fee due and payable to SBL in consideration for SBLs performance of Services and other obligations, but excluding the costs of Raw Materials, SBL handling fees, and other expense or cost reimbursements. |
1.73 |
Specification(s) means for a given Product, the tests, references to any analytical procedures and acceptance criteria which are numerical limits, ranges or other criteria for tests described in order to establish a set of criteria for the Products, Client Materials, or Raw Materials, as the case may be, and which details are provided in documentation as reviewed and approved in writing by the Parties. |
1.74 |
Standard Operating Procedure(s) or SOP(s) means the standard operating procedures established by and mutually agreed upon by both Parties regarding the Manufacturing Process. |
1.75 |
Tax means all taxes, charges, customs duties, fees, levies, imposts, or withholding of whatever nature imposed by any law or regulations in any country in respect of the Services, importation or exportation of Raw Materials, Client Materials, Batches, and Product. |
1.76 |
Technology Transfer means the activities by the Parties necessary for SBL to perform the Services as further described in the applicable PSA which may include, among other things: (i) transfer of the Background IP and Client Material from Client to SBL; (ii) implementation of the Manufacturing Process at the Facility; (iii) Manufacturing Process fit activities, and (iv) tests and studies. |
1.77 |
Term means the duration for which this MSA stays in effect, which shall begin as of the Effective Date and will be in effect for as long as any PSA is in effect. |
1.78 |
Territory means the United States, Europe, Africa, and Middle East and any other country set forth in the applicable PSA, or as that the parties otherwise agree in writing to add to this definition of Territory in an amendment to this MSA, but excluding any countries that are targeted by the comprehensive sanctions, restrictions or embargoes administered by the United Nations, European Union, United Kingdom, or the United States. |
1.79 |
Warehouse means SBLs warehouse for storage of the Product located at 300, Songdo bio-daero, Yeonsu-gu, Incheon, 21987, Republic of Korea. |
10
SECTION 2 RELATED AGREEMENTS AND EXHIBITS
2.1 |
Product Specific Agreements. SBL will perform Services for Client as specified in PSAs and in accordance with the terms and conditions of this MSA. In the event of a conflict between any provision of this MSA and the PSA, this MSA shall control, except where the PSA specifically states otherwise and references this Section 2.1. |
2.2 |
Quality Agreement (QAG). As required and within sixty (60) days of execution of this MSA, the Parties shall agree upon a Quality Agreement applying to such Services, and such Quality Agreement shall be incorporated into this MSA. |
SECTION 3 MANAGEMENT OF SERVICE
3.1 |
General. SBL shall adequately staff the Facility with personnel with necessary expertise to perform its obligations under the MSA. Each Party will be responsible for its internal decision making process and for reasonably informing the other Party of decisions affecting the performance of the Service by SBL in a regular and timely manner. SBL shall complete the Services in accordance with the estimated timelines set forth in the applicable PSA. Client shall supply to SBL all information or materials that are reasonably required for SBL to perform the Services, and SBL shall not be responsible for any delays arising out of Clients failure to do so. Client shall be responsible for additional costs and expenses arising out of such delay including, if applicable, the costs of Reserved Capacity. |
3.2 |
Core Team and Joint Steering Committee. |
3.2.1 |
Core Team and Joint Steering Committee. The Parties shall establish the Core Team, which shall resolve any issues arising from the Services including but not limited to those relating to changes to the project assumptions and timelines, development activities, Specifications, or Manufacturing Process. The Parties shall also establish a Joint Steering Committee providing guidance to the Core Team and resolving any issues or disputes which in good-faith are not able to be resolved by the Core Team. |
3.2.2 |
Meetings and Decision Making. The Core Team and JSC shall meet on schedules and in manners that are acceptable to their respective members. Each Party may appoint temporary or permanent substitutes for any of such Partys members on the Core Team or JSC and each Party may, in its reasonable discretion, invite non-member representatives of such Party to attend Core Team or JSC meetings. Each Party shall be responsible for its own expenses of traveling to and participating in any Core Team or JSC meeting. All decisions of the JSC and Core Team shall be made by the unanimous agreement of all of their members or their designated representatives, and shall be reflected in written meeting reports. Written reports of the JSC and Core Team shall be subject to approval by the authorized representatives of the Parties; provided, however, that the JSC and Core Team may not amend or waive any provision of the MSA or applicable PSA except by the terms of this MSA. |
3.2.3 |
Disputes. In the event that the Core Team, is unable, despite the good faith efforts of the members, to resolve a disputed issue that is within the purview of the Core Team for a period of ten (10) days, one Party shall formally request referral of the issue to the JSC. If the dispute still cannot be resolved within an additional thirty (30) days after referral to the JSC, the matter may be handled in accordance with Section 15. |
11
3.3 |
Person in Plant. Client may request up to three (3) of its personnel to be on-site at the Facility to observe and consult with SBL during the performance of certain Services under this MSA including but not limited to Technology Transfer and process development activities, and such additional personnel in such numbers as deemed necessary shall be accommodated upon mutual agreement. Expenses associated with such on-site Client personnel shall be passed through to Client by SBL. While at the Facility, all such Client personnel shall have reasonable access to all areas as are relevant to SBLs performance of the Service hereunder, provided that SBL may reasonably restrict Client personnels access to the Facility as it deems necessary, and all such Client personnel shall agree to and comply with confidentiality obligations to third parties, SBL policies and procedures related to safety, confidentiality, and cGMP, and all instructions of SBL employees at the Facility. Client shall remain responsible at all times for the compliance with the terms of this MSA and PSA by its employees and personnels. |
3.4 |
Subcontract. SBL may subcontract any portion of the Services with prior approval from the Client. In the event SBL subcontracts any portion of the Services, SBL shall be primarily obligated to Client for ensuring that suchsubcontracted services are carried out as intended; provided however that, SBL shall not be responsible for any delay or breach caused by third parties or External Laboratories despite SBLs exercise of reasonable care and efforts commonly used and customary in the industry. All costs associated with activities outsourced to third parties or External Laboratories will be passed through to Client with an additional ten percent (10%) handling fee. |
3.5 |
Development and Manufacturing Site. Unless otherwise agreed by Client, all Services shall be performed by SBL at the Facility. |
3.6 |
Manufacturing Documentation. SBL shall maintain Manufacturing Documentation to be true and accurate, and shall keep in strict confidence and shall not use for purposes other than providing or performing the Service or other obligations hereunder. SBL shall maintain all such Manufacturing Documentation for at least that period specified in the applicable QAG. Upon written request of Client and at mutually agreeable times, Client shall have the right to review Manufacturing Documentation at the Facility as further defined in the applicable QAG. Client may also request scanned or printed copies of such Manufacturing Documentation, but shall be responsible for reasonable costs associated therewith. SBL shall record and maintain such records, data, documentation and other information in the language as so required in the applicable QAG or as so required by a Regulatory Authority and in compliance with Applicable Law. SBL shall not provide Manufacturing Documentation provided pursuant to this MSA or any applicable PSA to any third party and shall protect such as the confidential information of Client. To the extent necessary, SBL may redact or withhold Manufacturing Documentation provided pursuant to this MSA or any applicable PSA to protect the confidential information of its other clients or third parties. The form and style of Batch documents, including, but not limited to, Batch production records, lot packaging records, equipment set up control, operating parameters, and data printouts, raw material data, and laboratory notebooks are the exclusive property of SBL. Notwithstanding anything to the contrary, SBLs SOPs not specific to the Clients Products may be provided to Client for on-site review if deemed necessary by both SBL and Client. Such SOPs cannot be removed from the SBL premises, copied, photographed or otherwise replicated. |
12
SECTION 4 SERVICE DESCRIPTIONS
4.1 |
Technology Transfer. Client shall transfer to and grant SBL the license set forth below in Section 10 in respect of the Client Technology and Client Materials to SBL in accordance with the plan, timelines and quantities agreed upon by the Parties. In the event that Client agrees to utilize SBLs data sharing portal for Technology Transfer, Client agrees that (a) in the event of any relevant change that affects a Client users authorization to use such portal, Client shall immediately notify SBL so that SBL may disable their usernames and remove / change passwords in order to secure the SBL Portal and (b) Client shall ensure that all of Client users have up-to-date antivirus software installed on the computer devices used to access such portal. |
4.2 |
Engineering Batch. SBL makes no warranty that Engineering Batches will meet the Specifications or be successful. In the event there is a failure of an Engineering Batch, the parties will agree on whether another Engineering Batch is necessary or whether the next run should be a Process Validation Batch. If the parties do not agree, the matter will be escalated to the Joint Steering Committee. |
4.3 |
Process Validation Batch. Prior to commencement of Process Validation Batches, SBL and Client shall agree to a validation plan identifying the validation requirements of the Manufacturing Process. The costs of process validation activities are excluded from the price of Process Validation Batches and shall be paid for by Client at the price set forth in the applicable PSA, subject to the Clients prior approval on the scope and nature of such validation activities. |
4.4 |
Facility Modification and Equipment. Client and SBL will agree on what equipment in the Facility is necessary to perform the Services, and if Client reasonably deems it necessary to procure additional equipment beyond that which is in the Facility as of the applicable PSA Effective Date, SBL shall procure such equipment at Clients expense in accordance with Section 8.2.4 and be responsible during the Term for validation, installation, maintenance, commissioning, and decommissioning at SBLs expense, unless otherwise agreed in writing by the Parties. Thereafter, if any additional equipment is necessary, such costs shall be dealt with by Section 5 of this MSA. Notwithstanding anything to the contrary in this MSA, the ownership of any and all such equipment shall remain at all times with SBL unless otherwise agreed in writing by both Parties. |
4.5 |
Additional Work. Should the Parties mutually agree to any additional work to be added to the Scope of Work, the Service Fees for such additional work shall be based on SBLs standard pricing at the time of adding such additional work, and depending on the nature of such additional work, the Parties shall execute a Decision Memo or an amendment to the PSA accordingly. In the event of changes to the Services based on Clients request, Client shall bear all additional costs and expenses associated therewith. |
13
4.6 |
Raw Materials. |
4.6.1 |
Management. SBL shall procure and maintain a reasonable quantity of Raw Materials, required for the Services in accordance with the MSA and any applicable PSA. On a per-Product basis, SBL shall prepare the categorization of the Raw Materials into (i) Critical Raw Materials, (ii) Customized or Dedicated Raw Materials, and (iii) Other Raw Materials, and send the categorization to Client for approval as soon as practicable after the Effective Date. Client shall approve the categorization in accordance with this MSA and any applicable PSA no later than one (1) month after the receipt of such a categorization from SBL. SBL shall not be liable for any delay soley resulting from Clients failure to approve the categorization in a timely manner. The list of Raw Materials may be amended from time to time, subject to the Parties mutual agreement; provided however that, Client shall at all times be solely responsible for the costs of Raw Materials including those used in small scale runs during Technology Transfer, which is not included in the Service Fees. During Technology Transfer, the Core Team shall agree on estimates for Raw Materials anticipated to be consumed in the Manufacture of each Batch. Although SBL will make Commercially Reasonable Efforts to use no more than those amounts, SBL will not be responsible for Raw Materials used in excess of the agreed-upon estimate; provided, however, that SBL shall be responsible for any excess use, loss, spoilage, or waste of such Raw Materials to the extent caused by an SBL Assignable Error. Client and SBL shall mutually agree to strategies regarding Raw Material safety stock and sourcing from qualified vendors. |
4.6.2 |
Raw Material Specifications. Client and SBL shall agree on the Specifications of Raw Materials, including without limitation analytical methods, supplier information including supplier site information, and other information concerning the stability, storage, and safety thereof that are required for the Manufacturing hereunder, as further described in the applicable QAG. |
4.6.3 |
Testing and Evaluation. SBL or vendors qualified by SBL shall perform all testing and evaluation of Raw Materials as required by the Specifications for the Raw Materials and the cGMPs, as further described in the applicable QAG, if applicable. |
4.6.4 |
Storage. SBL shall secure sufficient and suitable storage for the Raw Materials; provided that such storage requirements shall be customary within SBLs industry. SBL shall exercise reasonable care to preserve and protect Raw Materials from loss after receipt by SBL and prior to Manufacture and except for loss due to SBL Assignable Error, Client shall be responsible for the risk of loss of Raw Materials. At the end of each calendar year of the relevant PSA, Client shall be responsible for the loss of Raw Material to the extent purchased in reliance on a Purchase Order or Firm Period, and such Raw Material expires or becomes obsolete because Client fails to honor such a Purchase Order or Firm Period, and SBL cannot reasonably otherwise utilize such Raw Material. |
4.6.5 |
Handling Fee Related to Raw Material. Raw Materials will be charged on a pass-through basis to Client in accordance with Sections 8.1(ii) and 8.2.2, subject to any changes as agreed between the Parties. |
14
4.7 |
Client Materials. |
4.7.1 |
Management. Client shall provide, either by itself or through its third party supplier, to SBL free of charge, Client Materials in amounts reasonably necessary to carry out the Services as agreed by the Parties. SBL shall make Commercially Reasonable Efforts to import the Client Materials to the Republic of Korea in a timely manner, and Client shall provide reasonable assistance necessary for such a timely importation. Delivery conditions for the Client Materials shall be DDP Facility (INCOTERMS 2010) provided that the title and risk of loss to such Client Materials shall remain at all times with the Client and shall not transfer to SBL. During Technology Transfer, the Core Team shall agree on estimates for Client Material anticipated to be consumed in the Manufacture of each Batch. Although SBL will make Commercially Reasonable Efforts to use no more than those amounts, SBL will not be responsible for Client Materials used in excess of the agreed-upon estimate; provided, however, that SBL shall be responsible for any excessive use, loss, spoilage, or waste of such Client Materials to the extent caused by an SBL Assignable Error. Client and SBL shall mutually agree to strategies regarding Client Material safety stock and sourcing from qualified vendors. |
4.7.2 |
Client Material Specifications. Client shall provide SBL with the Specifications of the Client Materials, including without limitation analytical methods, supplier information, and other information concerning the stability, storage, and safety thereof that are required for the Manufacturing hereunder, as may be further described in the applicable QAG. |
4.7.3 |
Testing and Evaluation. SBL shall perform testing of the Client Materials in accordance with the applicable QAG and/or Clients instruction prior to the performance of the Manufacturing hereunder, in order to determine whether such Client Materials meet the Specification described in the applicable QAG (if applicable). SBL shall inform Client of (a) any damage to the Client Materials received that is visually obvious (e.g., damaged or punctured containers and temperature monitoring results outside of predetermined Specifications) within ten (10) days after SBLs receipt of the Client Materials and (b) any non-conformance of the Client Materials to Specification either: (i) within ninety (90) days after SBLs receipt of the Client Materials or (ii) if release testing of Client Materials is not performed until it is needed for Manufacture, within ninety (90) days after such release testing is performed; or (iii) as other wise agreed between the Parties. If, prior to performing any Service on the Client Materials, SBL determines that such Client Materials are defective or damaged, SBL shall not perform the Service on such Client Materials and shall follow Clients written instructions regarding disposal or return of such Client materials to Client, such disposal or return to be at Clients discretion and cost. |
4.7.4 |
Storage. SBL shall secure sufficient and suitable storage for the Client Materials; provided that such storage requirements shall be customary within SBLs industry. SBL shall exercise reasonable care to preserve and protect the Client Materials from loss after receipt by SBL and prior to Manufacture. |
4.7.5 |
Handling Fee Related to Client Material. Handling fees relating to the Client Material will be charged to Client in accordance with Sections 8.1(iii) and 8.2.3. |
15
4.8 |
Forecasts. For each Commercial Product, the Parties shall determine a mutually agreeable mechanism for forecasting of each Product, which shall be detailed in writing in each relevant PSA. For Clinical Product, the Parties shall agree upon the number and schedule of Batches to be Manufactured by SBL in the applicable PSA. |
4.9 |
Purchase Orders. For each Clinical Product or Commercial Product, Client shall notify SBL in a binding form and procedure to be agreed upon in the applicable PSA requesting a specific amount of Product to be Manufactured in the Purchase Order. The Parties acknowledge that, with or without a Purchase Orders issued in advance, an invoice may be issued in accordance with this MSA, PSA, or applicable Decision Memo for Services, Raw Materials, handling fees and Equipment, and such invoices shall be processed and paid in accordance with Section 8.3. |
4.10 |
Product Purchase Commitment. As further set forth in a PSA, during the Term, the Parties may agree that Client will purchase a minimum quantity of Batches of a certain Product in a given year (a Product Purchase Commitment). |
4.11 |
Batch Failure during Manufacture |
4.11.1 |
If, during Manufacture of a Batch and prior to SBLs batch release, the Core Team determines that all of a Batch is Non-Conforming Product (a Batch Failure), SBL shall take promptly re-Manufacture and deliver to Client a replacement Batch on a date to be mutually agreed by the Parties, which Service Fees and associated costs/fees (as set forth in Section 8.1 below) shall be invoiced and paid for by the Client. Client shall ensure that SBL has adequate Client Materials to Manufacture such Batches. The remedies contained in Section 4.11 of this MSA shall be the sole and exclusive remedies of Client regarding a Batch Failure and a Batch Failure shall not constitute a material breach of this MSA or a PSA unless SBL fails to provide the remedies contained in this Section 4.11. |
4.11.2 |
The Parties shall conduct a root cause analysis of the Batch Failure, which shall be done through SBLs deviation process and which result will be reviewed and confirmed by the JSC. If either the Core Team does not agree on the Batch Failure root cause, or the JSC does not agree on the results of the Core Teams Batch Failure root cause analysis, the Parties shall refer to an independent mutually agreed-on laboratory or firm with international repute, acting as a neutral arbiter, to conduct a root cause analysis of the Batch Failure. The costs of the independent laboratory will be shared by the Parties equally; provided, however, that the Party that is determined to be incorrect as to the Batch Failure will be responsible for those reasonable costs and must reimburse the correct Party for its share of the reasonable costs incurred. The decision of the independent laboratory must be in writing and will be binding on the Parties. |
4.11.3 |
In the event of Batch Failure due solely to SBL Assignable Error (other than due to gross negligence, fraud, or willful misconduct of SBL), SBL shall be responsible for the following costs: [***] |
16
[***]. In the case of Batch Failure due solely to SBL Assignable Error due to gross negligence, fraud, or willful misconduct of SBL, in addition to the costs described in (1) (4) above, SBL shall additionally be responsible for [***]. In the event of Batch Failure due to a reason not solely SBL Assignable Error, Client shall be responsible for the full costs described in (1) (4) in the preceding sentence. Any such cost responsibility shall be refunded to Client or, at Clients option, issued as a credit against future invoices by SBL. |
4.11.4 |
In the event that any of the foregoing procedures result in a Batch being delivered in a different year than the year in which the original Batch was ordered for delivery by Client, the Service Fee for such re-Manufactured Batch shall be the Service Fee set forth in the PSA. |
4.12 |
Storage, Packaging and Delivery. |
4.12.1 |
Service Deliverables other than Products.Storage, packaging and delivery of the Service deliverables other than Products Manufactured and the Products Manufactured hereunder shall be made in accordance with the terms of this MSA, applicable PSA, applicable QAG and the Applicable Laws. |
4.12.2 |
Products. |
(a) |
Release by SBL and Acceptance by Client. |
(i) |
SBL shall perform all testing in accordance with the Specifications of the Product and release the Product in accordance with the terms of the applicable QAG. Upon such release, SBL shall deliver to Client the Batch Related Documents, including a Certificate of Analysis and Certificate of Compliance, in accordance with the applicable QAG; |
(ii) |
Acceptance of Product. Client will complete the Acceptance Procedure and determine the acceptability of such Product in accordance with the applicable QAG and notify SBL of the result within thirty (30) days of Clients receipt of the Batch Related Documents. Upon Clients acceptance, SBL will have no liability for such Product. If Client does not reject such Product within the thirty (30) day period or within a shorter period as agreed by the Parties, the Product will be deemed to have been irrevocably accepted by Client and SBL will have no liability for such Product. |
(iii) |
Non-Conforming. If, during the Acceptance Procedure, any Product is determined by Client as Non-Conforming Product, and SBL confirms such non-conformity, such non-conformity shall be treated as a Batch Failure, and the remedy set forth in Section 4.11 above shall apply to the Non-Conforming Product mutatis mutandis. Notwithstanding anything to the contrary, Client agrees to waive any and all rights to reject the Product after delivery in the event the Product has been altered, changed, or modified in any way for conjugation or otherwise. The remedies contained in this Section 4.12.2 shall be the sole and exclusive remedy of client in the event of Non-Conforming Product. |
17
(b) |
Delivery. Shipping conditions for the Product Manufactured hereunder shall be FCA Facility (INCOTERMS 2010), unless otherwise agreed to in the applicable PSA. The title to Product hereunder shall be transferred from SBL to Client when the Product is made available at the point of delivery consistent with FCA or the Incoterm set forth in the PSA. The Parties further agree as follows: |
(i) |
After SBLs release of the Product and prior to each pick-up by Client or Clients designated carrier, SBL shall propose to Client a delivery schedule of the Product, in order for the Parties to agree on it in advance for each pick-up. SBL shall schedule Delivery with the carrier selected and paid for by Client; |
(ii) |
SBL shall not deliver the Product until it has been instructed to by Client in accordance with the applicable QAG. Client shall confirm specific delivery instructions with SBL prior to SBLs release. Upon SBLs release of Product, SBL shall store the Manufactured Product as described in Section 4.12.2(c) and Client shall compensate SBL for storage costs for the Manufactured Product as set forth in the applicable PSA; |
(iii) |
SBL shall provide Client with invoice, packing lists, supporting export documents as specified by Client by separate delivery and shipment documentation instructions, together with each shipment of the Product (or such other deliverables); and |
(iv) |
In cooperation with Client and subject to the delivery schedule agreed by the Parties, SBL shall adhere to the first-expire-first-out (FEFO) principle in shipping all released Product. |
(c) |
Storage, Packaging and Shipping Container. |
(i) |
Pursuant to the terms of this MSA and any applicable PSA, SBL shall store the Products Manufactured hereunder. |
(ii) |
SBL shall store, package, label and prepare shipment according to the Specifications for the Product Manufactured hereunder, the applicable QAG and the SOPs, and using storage and/or shipping containers determined in the applicable PSA. |
18
(iii) |
If Client does not direct SBL to prepare Manufactured Product to be picked up by Client or Clients designated carrier with a pick-up date within thirty (30) days of Clients receipt of the Batch Related Documents, SBL shall store the Product at the Warehouse, subject to the availability of space and storage conditions, and Client shall pay storage fees to SBL as set forth in Section 8.1 for the period of storage at the Warehouse until the actual delivery date; provided however that under no circumstances shall the period of storage in the Warehouse exceed sixty (60) days. SBL shall be responsible for risk of loss and damage to Manufactured Product in the event of SBL Assignable Error. |
SECTION 5 CHANGES TO THE SPECIFICATIONS, ANALYTICAL METHODS, MANUFACTURING PROCESS, FACILITY OR EQUIPMENT
5.1 |
Approval for Change. Change shall be implemented only with mutual agreement between the Parties acting reasonably and in good faith and in accordance with the applicable QAG. |
5.2 |
Changes Required by cGMP, Regulatory Authorities or Requested by Client. Except as otherwise expressly set forth to the contrary in the applicable QAG, in the event that cGMP, a Regulatory Authority, Applicable Law, or any other regulatory or legal authority requires, or Client requests, a Change, SBL shall accommodate such requirements or requests, subject to the following: |
(a) |
Client shall promptly notify SBL in writing of the required and/or requested Change(s), and provide information necessary for SBL to evaluate the effect of such Change(s), and SBL shall promptly advise Client as to any (i) additional equipment required, modifications to the Facility or equipment, and/or additional equipment and the Facility qualification and validation requirements; (ii) Manufacturing Process development, transfer, scale-up, testing, qualification, or validation requirements; (iii) regulatory requirements pursuant to such Changes; (iv) changes to the Manufacturing scheduling and/or Product delivery schedule; and (v) other impacts on the Facility or SBLs ability to manufacture products (including the Products) in the Facility, if any, which may result from such Change(s). The notification and formal approval procedure of such Changes shall be in accordance with the applicable QAG (i.e., change control procedures) (if applicable). The Parties shall meet in a timely manner to identify and discuss such Changes as appropriate; |
(b) |
Prior to implementation of any such Change(s), SBL shall provide Client with an Implementation Plan and Budget. Following review and approval by Client of such Implementation Plan and Budget, subject to the Core Teams approval and agreement followed by the Parties written agreement pursuant to Section 16.9 (if applicable), SBL shall commence implementation of such Change(s); |
(c) |
During any such implementation, SBL shall provide Client with regular updates on the progress of implementation. Subject to any timeframe imposed by Applicable Law, SBL shall exercise Commercially Reasonable Efforts to implement the Change according to the Implementation Plan and Budgets target completion date. SBL shall provide written notice to Client if SBL becomes aware of any cause which may create delay with the implementation of Changes. Following any such notice, both Parties shall discuss an amendment of Implementation Plan and Budget; and |
19
(d) |
Upon the approval of the Implementation Plan and Budget for Change(s), both Parties shall negotiate in good faith to determine the allocation of the costs incurred by SBL for the implementation of any such Change(s) between the Parties, in accordance with the following principles: |
(i) |
the costs for the general Facility Changes required by cGMP, any Regulatory Authority, or any Applicable Laws related to the maintaining the Manufacturing Facility by SBL as set forth in Section 6.2, shall be borne by SBL, provided that where the Change relates exclusively or partially to the Manufacture of Product in which case the costs shall be borne by Client fully or proportionally, respectively; |
(ii) |
the costs for the Changes other than (i) above, and requested by Client and required uniquely to the Manufacture of the Product and beneficial solely to Client shall be borne by Client; and |
(iii) |
the costs for the Changes other than (i) and (ii) above shall be discussed in good faith by the Parties to achieve equitable allocation of costs. |
SECTION 6 REGULATORY APPROVALS AND INSPECTIONS.
6.1 |
Regulatory Approvals. To the extent applicable, SBL shall provide reasonable assistance and cooperation in order for Client to obtain and maintain the Regulatory Approvals. The costs and fees associated with such assistance and cooperation, to the extent not detailed in the MSA or PSA shall be borne by Client. As specified in the applicable PSA, the Parties shall discuss and agree on which Regulatory Approvals are to be obtained. |
6.2 |
Regulatory Approvals for the Facility. To the extent applicable, SBL shall obtain and maintain all approvals, licenses, registrations or authorizations of any federal, state or local regulatory agency, department, bureau or other governmental entity (other than the Regulatory Approvals, which will be obtained or maintained by Client) that are required to Manufacture the Product at the Facility and perform the Services. |
6.3 |
Regulatory Support Activities. Any regulatory support activities (including Pre-Approval Inspections) required and agreed to by Client to support Regulatory Approval of the Product from the Facility shall be performed and supported by SBL as reasonably requested by Client. All such regulatory support activities are excluded from the price of Process Validation Batches, shall be approved by the Client in advance, and shall be paid for by the Client at the price set out in the applicable PSA. SBL shall notify Client according to the applicable QAG provisions of any contacts or inquiries by the Regulatory Authorities, including inspections, Pre-Approval Inspections, sample requests, and written correspondence and its result, related to the Product. |
20
SECTION 7 QUALITY COMPLIANCE
7.1 |
Quality Agreement. Both Parties shall adhere to the provisions of the applicable QAG and the Parties agree that all elements of quality assurance, quality control and the like shall be governed by the terms and conditions of the applicable QAG. In the event of a conflict between a Quality Agreement and either any provision of this MSA or any PSA, the MSA or PSA shall control except with respect to matters directly and specifically related to Product quality or regulatory requirements, in which case, the Quality Agreement will control. |
7.2 |
Records & Audit. |
7.2.1 |
Audit by Client. Upon Clients request, but no more than once per year, SBL shall accept a formal audit of the Facility and, if necessary, the Warehouse, by Client and allow Client to inspect the Facility and, if necessary, the Warehouse, and Manufacture of the Product during provision of the Services solely to ascertain compliance by SBL with the terms of this MSA or any applicable PSA; provided, however that in the event Client uses a designee, SBL must provide prior written consent. SBL shall be reimbursed for its reasonable costs for additional audits, other than for-cause audits, beyond the audit described in the first sentence of this Section 7.2.1. SBL will make Commercially Reasonable Efforts to require vendors or subcontractor to accept an audit of their facilities by Client upon similar notice as described in Section 7.2.2 below. |
7.2.2 |
Audit Notice. Client shall provide SBL with a written notice at least two (2) months prior to the initiation of the audit of the Facility and, if necessary the Warehouse, set forth in Section 7.2.1, which shall be conducted on a mutually agreeable date and time, and with a mutually agreed duration, agenda, and visitor list. Notwithstanding the foregoing, if the audit is required for cause (i) due to safety reasons that necessitate immediate audit of or visit to the Facility or (ii) Client asserts that a substantial violation of the Quality Agreement has occurred which cannot be resolved through the normal Core Team / JSC process, the foregoing sentence shall not apply and Client may conduct such audit or visit by providing SBL with a prior notice by email. Access to SBLs facilities shall be coordinated with SBL so as to minimize disruption to SBLs ability to perform services for its other clients. Client representatives must comply with all of SBLs cGMP, confidentiality and security procedures and protocols during such observations, consultations, and inspections. SBL shall at all times cooperate and provide all the necessary documents reasonably required by Client during such audit; provided that, to the extent necessary, SBL may redact or withhold documents to protect the confidential information of its other clients. Client shall be solely responsible for any costs and liability caused by Clients or its representatives failure to comply with SBLs security, safety or confidentiality procedures. |
SECTION 8 CONSIDERATION AND PAYMENT TERMS
8.1 |
Consideration. In consideration for SBLs performance of the Service and other obligations undertaken by SBL pursuant to a PSA, Client shall pay SBL (i) the Service Fees as set forth in the applicable PSA; (ii) a handling surcharge of a certain percentage or certain amount to be set forth in the applicable PSA of the costs of Raw Materials paid by SBL (including but not limited to applicable Taxes); (iii) a handling surcharge of a certain percentage or certain amount to be set forth in the applicable PSA related to the Client Materials (which shall be based on the actual costs of such materials as supported by reasonable documentary evidence as opposed to the market value thereof and which include Taxes); and (iv) storage fees as set forth in the relevant PSA. |
21
8.2 |
Invoices. |
8.2.1 |
Service Fee of the Project Stages and Batches. The Service Fees for any Batches shall be invoiced upon SBLs release of a Batch of Product. All other Service Fees shall be invoiced after the completion of each applicable project stage in accordance with the PSA. SBLs invoices pursuant to this MSA shall be electronic, unless otherwise agreed by the Parties. |
8.2.2 |
Raw Materials. With respect to the Raw Materials, SBL shall submit invoices to Client for the applicable Raw Materials cost (including any safety stock) as set forth according to Section 8.1 as follows. SBL shall submit an invoice to Client (i) for the cost of Critital Raw Materials, and Customized or Dedicated Raw Materials upon receipt of the invoice from vendors/suppliers; and (ii) for the cost of Other Raw Materials used upon SBLs completion of such project stage or upon SBLs release of a Batch of Product as applicable. In each case, for all Raw Materials, SBL shall prepare a billing summary detailing the Raw Materials used and send the same to Client in accordance with Section 8.2.5. Within 2 weeks of receiving the billing summary for Raw Materials from SBL, Client shall either (1) accept and issue a purchase order for the Raw Material in accordance with the billing summary or (2) reject the billing summary based on reasonable grounds, in which case SBL shall promptly re-issue the billing summary. Clients failure to accept or reject a billing summary within the two (2) week period shall be deemed an acceptance of the billing summary, and SBL will issue the corresponding invoice with or without a previously issued purchase order from Client. |
8.2.3 |
Client Materials. With respect to the Client Materials, which shall be supplied by Client to SBL at no cost during SBLs performance of the Service, SBL shall submit an invoice to Client for reasonable and mutual agreed handling fees as set forth in the PSA upon SBLs completion of such project stage of the Service or SBLs release of a Batch of Product, as applicable. |
8.2.4 |
Equipment. With respect to Equipment, SBL shall submit an invoice to Client subject to Section 4.4 upon receipt of the relevant invoice from equipment vendor/supplier. |
8.2.5 |
Diclosure of Original Invoices. For any Raw Materials or Equipment purchased from third party vendors, Client agrees and acknowledges that SBL shall be under no obligation to disclose the original invoice or any confidential information therein from the vendors due to its confidentiality obligation with such vendors, and that not furnishing such documents shall not constitute a valid ground for rejecting SBLs billing summary or invoice. Client may, however, request a third party audit at Clients expense upon presenting reasonably objective and reliable market date or price quotation justifying such an audit, and confirm through the auditor the sole issue of whether there is any discrepancy or inaccuracy between the vendors invoices and SBLs billing summary or invoice (without the auditor disclosing any confidential information of the vendor to Client). Should a discrepancy or inaccuracy be found through such an audit, SBL shall be responsible for the costs of such an audit and promptly re-issue the invoice with the correct amount and/or reimburse the amount paid in excess of the correct amount. |
22
8.3 |
Payment. |
8.3.1 |
Mode of Payment; Foreign Exchange. All payments to SBL due under the MSA or any applicable PSA shall be made in US$ within [***] days from the receipt of SBLs invoice in US$ by means of telegraphic transfer to the account with the bank designated by SBL in the applicable invoice without any deduction, deferment, set-off or lien. For the purpose of computing payment amounts incurred by SBL in a currency other than US$, such currency shall be converted into US$ using the Standard Rate published by the Bank of Korea at the opening of business on such invoice date. |
8.3.2 |
Taxes. All prices and charges are exclusive of any Taxes, which shall be paid by Client. For the avoidance of doubt, the foregoing shall not include any taxes imposed on the income or profit of SBL levied on any payment to be made by Client to SBL, each of which shall be solely borne by SBL. Client shall pay or reimburse SBL for all Taxes in connection with the purchase, sale, storage, importation or exportation of any Raw Materials, Client Materials, Batches, or Product or the provision of Services, except to the extent such Taxes are recoverable by or refundable to SBL. SBL agrees to use Commercially Reasonable Efforts to assist Client in claiming exemption under double taxation or similar agreement or treaty from time to time in force to obtain a refund of any customs duties, value added taxes, and other taxes payable by SBL. |
8.3.3 |
Price Adjustments. The Service Fees as set forth in the applicable PSA, shall be adjusted annually on January 1 of each year during the Term, effective immediately, by the percentage change in the consumer price index as published by the Bank of Korea for the immediately preceding twelve (12) months, provided that any given years adjustment shall be no more than [***]. The relevant date for price adjustment under this Section shall be the issue date of SBLs invoice. |
8.3.4 |
Default Interest. Any amount that is not paid by a Party to the other when due under the MSA or any PSA shall bear default interest at the rate of [***] per annum on a pro rata basis from the day following the due date until paid in full. In the event there is an amount which is invoiced by SBL but not paid by Client for more than six (6) months after the due date, such event shall be considered a material breach of the relevant PSA. |
SECTION 9 CONFIDENTIALITY
9.1 |
Confidential Information. Both Parties agree not to use the other Partys Confidential Information except in accordance with the terms of this MSA, the QA and the applicable PSA and to maintain the Disclosing Partys Confidential Information in confidence and not to disclose the Disclosing Partys Confidential Information, in whole or in part, to any third party, and not use the Disclosing Partys Confidential Information for any purpose other than performing the obligations under the MSA or applicable PSA. The Receiving Party recognizes the proprietary nature of the Disclosing Partys Confidential Information and agrees that no right, title, ownership, license, or |
23
interest of any character in the Disclosing Partys Confidential Information other than as specifically granted herein, is conveyed or transferred to the Receiving Party. Each Party shall guard such Confidential Information, including any trade secret information, using the same degree of care as it normally uses to guard its own confidential, proprietary or trade secret information of like importance, but in any event no less than reasonable care. The Receiving Party shall limit disclosure of the Disclosing Partys Confidential Information to its and its Affiliates directors, officers, employees, consultants and agents (Representatives) only on a need-to-know basis, provided that, the Receiving Party shall undertake procedures such that each of its Representatives to whom the Disclosing Partys Confidential Information is disclosed understands (i) the confidential nature of the Disclosing Partys Confidential Information and (ii) that he or she is under obligations at least as protective of Clients Confidential Information as those contained herein, including to not use or disclose the Disclosing Partys Confidential Information. SBL shall maintain accurate records of each of SBLs Representatives who have accessed Clients Confidential Information contained within SBLs cGMP document management systems, provided that such systems are capable of maintaining such records, and such records will be provided to Client upon request, including as part of an audit scheduled pursuant to Section 7.2 above. To SBLs knowledge, its current cGMP document management systems are capable of maintaining such records. |
9.2 |
Exceptions. Notwithstanding Section 9.1 above, Confidential Information shall not include the portion of information, which as evidenced by written records: (a) was at the time of disclosure by the Disclosing Party hereunder publicly known or available; (b) after disclosure by the Disclosing Party hereunder, became publicly known or available by publication or otherwise, other than by an unauthorized act or omission by the Receiving Party; (c) was in the possession of the Receiving Party without confidentiality restriction at the time of the disclosure by the Disclosing Party hereunder; (d) was lawfully received from any third party having the lawful right to make such disclosure, without obligation of confidentiality; or (e) was independently developed by the Receiving Partys directors, officers or employees without reference to the Confidential Information, as demonstrated by records contemporaneous with such development. |
9.3 |
Authorized Disclosures. Disclosure is permitted in the event that (a) the Disclosing Partys Confidential Information is reasonably required to obtain or maintain any Regulatory Approvals for the Products in any or all jurisdictions or (b) the Disclosing Party needs to disclose such Confidential Information to comply with Applicable Law; provided that such Receiving Party shall limit disclosure of the Disclosing Partys Confidential Information to that which is necessary for compliance and to otherwise maintain the confidentiality of the Confidential Information. |
9.4 |
Survival of confidential obligations. The confidential obligations of the Receiving Party shall survive for a period of ten (10) years from the expiration or termination of this MSA except with respect to Confidential Information which consititutes trade secrets, for which the obligations will continue for so long as such information remains a trade secret under Applicable Law. |
9.5 |
Return of the Confidential Information. All written, printed or other tangible Confidential Information of the Disclosing Party disclosed under the MSA, and all copies thereof shall be returned to the Disclosing Party (or destroyed at the Disclosing Partys request) by the Receiving Party within thirty (30) days from the written request by the Disclosing Party. All Confidential Information disclosed electronically shall be completely deleted and destroyed by the Receiving Party within |
24
thirty (30) days from the written request by the Disclosing Party. Notwithstanding the foregoing, digital backup files automatically generated by the Receiving Partys customary electronic data processing system may be retained and properly stored as confidential files for the sole purpose of backup and will be deleted in accordance with the Receiving Partys retention policy. |
SECTION 10 OWNERSHIP OF MATERIALS AND INTELLECTUAL PROPERTY
10.1 |
Background Intellectual Property. It is acknowledged that each Party owns or controls Background IP and nothing in this MSA shall affect such rights in Background IP. Client hereby grants SBL a non-transferrable, royalty-free, irrevocable, sublicensable (to the extent necessary to conduct the Services) and fully-paid-up right and license to use Clients Confidential Information and Intellectual Property during the Term for the sole purposes of performing the Services in accordance with the MSA. Except as otherwise provided herein, the Parties shall not acquire any right, title, or interest in any Background IP of the other Party. |
10.2 |
Inventions. |
10.2.1 |
Client Invention. SBL shall notify Client of any Client Invention(s) immediately after such conception and reduction to practice, and shall take all reasonable measures so that Client would have the sole and exclusive ownership of any and all Client Invention. Client may use any Client Invention for any purpose, including filing patent application and SBL shall provide reasonable cooperation to Client at the expense of Client as to all reasonable out-of pocket expenses incurred by SBL. |
10.2.2 |
SBL Invention. SBL Invention shall be the property of SBL and shall not be deemed to be Client Invention or joint invention for the purposes of the MSA: provided, however, that SBL grants to Client a geographically unrestricted, irrevocable, non-transferable, non-sublicensable, royalty-free and fully-paid-up right and license under such SBL Invention to make, use, sell, offer to sell, export and import and otherwise exploit the Product, without an obligation of accounting to SBL, to the extent such SBL Invention is incorporated into the Product or its manufacture. |
SECTION 11 WARRANTIES.
11.1 |
The Parties General Warranties. Each Party warrants and represents that: (i) it has the corporate power and authority to enter into this MSA and has taken all necessary action on its part required to authorize the execution, delivery and performance of this Agreement; (ii) it is aware of no legal, contractual or other restriction, limitation or condition that might adversely affect its ability to enter into this MSA and perform its obligations hereunder; (iii) it is duly organized, validly existing and in good standing under the laws of the jurisdiction in which it is incorporated; (iv) this MSA (a) has been duly executed and delivered by a duly authorized representative of it, and (b) is the legal, valid and binding obligation of it, enforceable against it in accordance with its terms, except as enforceability may be limited by applicable bankruptcy, insolvency, reorganization, moratorium or other similar laws now or hereafter in effect relating to or affecting creditors rights generally; and (v) the execution, delivery and performance of this Agreement by it does not and will not (a) violate any Applicable Laws applicable to it, or (b) violate or conflict with any provision of its Articles of Incorporation or By-laws or other organizational documents. |
25
11.2 |
Clients Warranties. Client represents and warrants to SBL that as of the Effective Date of the MSA and during the Term: (a) the Product shall comply with all Applicable Laws and that, during the Term Client will comply with Applicable Law in relation to such Product and shall perform all obligations and take other necessary actions to be in compliance with such requirements, Applicable Laws, rules and regulations, including applicable cGMPs; (b) Client will comply with all Applicable Laws, and that it will keep SBL informed of any information known to Client which would affect SBLs provision of the Service hereunder; (c) all Client Technology, Client Materials provided to SBL by or on behalf of Client will be suitable for the Manufacture of the Product; and (d) to the best of its knowledge, SBLs use of the Client Materials, Manufacturing Process, and Client Technology related to the Service in accordance with the terms of this MSA will not infringe any third partys Intellectual Property rights. |
11.3 |
SBLs Warranties. SBL represents and warrants that: |
11.3.1 |
As of the Effective Date and during the Term, (i) SBL is the lawful owner, lessee, operator, or licensee of the Facility, equipment, machinery, as well as permissions required, to enable SBL to perform its obligations under this MSA, and (ii) to the best of SBLs knowledge, none of the SBL Inventions or SBL Background IP infringes any third party Intellectual Property Right. |
11.3.2 |
All Product Batches, at the time of delivery to Clients designated carrier, shall (a) be Manufactured, packaged, handled and stored in compliance with the requirements of cGMPs (except for Engineering Batches unless otherwise agreed) and all Applicable Laws; (b) comply with the Standard Operating Procedures; and (c) be transferred free and clear of any liens, claims or encumbrances of any kind. |
11.4 |
No Other Warranties. THE REPRESENTATIONS AND WARRANTIES CONTAINED IN THIS SECTION ARE EXPRESSLY IN LIEU OF AND EXCLUDE, AND THE PARTIES HEREBY EXPRESSLY DISCLAIM AND NEGATE, TO THE MAXIMUM EXTENT PERMITTED BY APPLICABLE LAWS, ALL OTHER REPRESENTATIONS AND WARRANTIES OF ANY KIND, EXPRESS OR IMPLIED (ARISING BY OPERATION OF LAW OR OTHERWISE), INCLUDING IMPLIED WARRANTIES OF MERCHANTABILITY AND FITNESS FOR A PARTICULAR PURPOSE, EVEN IF THAT PURPOSE IS KNOWN. |
SECTION 12 INDEMNIFICATION
12.1 |
Indemnification by SBL. SBL shall indemnify and hold harmless Client, its Affiliates, and their officers, directors, employees or agents from and against any Damages arising or resulting from any third party (which shall exclude Client Affiliates) claims to the extent such Damages are relating to, arising out of, in connection with, or resulting from claims, demands, or actions based upon SBL Assignable Error, except to the extent that such Damages are caused by the causes as set forth in Section 12.2 for which Client is obliged to indemnify. |
12.2 |
Indemnification by Client. Client shall indemnify and hold harmless SBL, its Affiliates, and their officers, directors, employees or agents from and against any Damages arising or resulting from any third party (which shall exclude SBL Affiliates) claims to the extent such Damages are relating to, arising out of, in connection with, or resulting from claims, demands or actions based upon (i) gross |
26
negligence or willful misconduct of Client or its officers, directors, employees or agents, (ii) any product liability claims related to manufacture, sale, or distribution of Products that have been accepted by Client under Section 4.12.2, or (iii) any claim that any SBL activity undertaken for the purposes of or in relation to the Services pursuant to the MSA or any PSA (including but not limited to use of the Client Materials, Manufacturing Process and Client Technology, as well as any tests, studies, experiments, or other activities undertaken at the request of, or with the consent of, Client) infringes any third partys Intellectual Property rights; in each case (i), (ii) and (iii) except to the extent that such Damages are caused by the causes as set forth in Section 12.1 for which SBL is obliged to indemnify. |
12.3 |
Indemnification Procedure. The foregoing indemnification by SBL or Client shall be conditioned, if and to the extent Damages are based on or related to a third party claim, upon a Party who intends to claim indemnification under Sections 12.1 and 12.2 (the Indemnified Party) (i) providing written notice to the other Party (Indemnifying Party) within twenty (20) days after the Indemnified Party have been given written notice of such third party claim, provided that absence or delay of such prior written notice will not relieve the Indemnifying Party of its obligation to indemnify except to the extent such absence or delay materially prejudices the Indemnifying Partys ability to defend the third party claim; (ii) permitting the Indemnifying Party, upon timely notice by the Indemnified Party, the opportunity to assume full responsibility (at the Indemnifying Partys cost and expense) for the investigation and defense of any such claim with counsel reasonably satisfactory to the Indemnified Party, provided, however, that the Indemnifying Party shall keep the Indemnified Party informed as to the progress of the defense of any claim and that the Indemnified Party shall cooperate in such defense and shall make available all records, materials and witness reasonably requested by the Indemnifying Party in connection therewith; and (iii) not settling or compromising any such claim without the Indemnifying Partys prior written consent, with such consent not to be unreasonably denied, withheld or conditioned. |
SECTION 13 DISCLAIMER OF CONSEQUENTIAL DAMAGES; LIMITATION OF LIABILITY
13.1 |
Disclaimer of Consequential Damages. EXCEPT WITH RESPECT TO (I) BREACHES OF SECTIONS 9 AND 10; (II) INSTANCES OF GROSS NEGLIGENCE OR WILLFUL MISCONDUCT; AND/OR (III) THIRD PARTY DEATH OR BODILY INJURY CAUSED BY SBL TO CLIENT EMPLOYEES OR CONTRACTORS WHO MAY VISIT SBL SITES, NEITHER PARTY WILL BE LIABLE UNDER THIS AGREEMENT FOR ANY SPECIAL, PUNITIVE, CONSEQUENTIAL, INCIDENTAL OR OTHER INDIRECT DAMAGES OF ANY TYPE OR NATURE, WHETHER BASED IN CONTRACT, TORT, STRICT LIABILITY, NEGLIGENCE OR OTHERWISE, INCLUDING LOSS OF PROFITS OR REVENUES. |
13.2 |
Limitation of Liability. Except with respect to Damages or allowable indirect damages arising under or in connection with a PSA arising out of (i) breaches of Sections 9 and 10; (ii) instances of gross negligence or willful misconduct (which shall not include Materials Claims, defined below); (iii) damage or destruction of Critical Raw Materials due to the gross negligence or willful misconduct of SBL (including pursuant to Section 4.11.3 above) (such claims arising under this 13.2(iii) shall be referred to herein as (Materials Claims); and/or (iv) third party death or bodily injury caused by SBL to Client employees or contractors who may visit SBL sites, Client agrees that |
27
SBLs aggregate total liability to Client in respect of any Damages or allowable indirect damages arising under or in connection with a PSA (whether in contract, tort, negligence, under indemnity or otherwise however arising) (collectively, Ordinary Claims) in a given calendar year shall be capped at an amount equal to [***] the amounts payable by Client to SBL in such calendar year under such PSA. Client agrees that SBLs aggregate total liability to Client in respect of any Materials Claims arising in a given calendar year shall be capped at an amount equal to [***] of the amounts payable by Client to SBL in such calendar year under such PSA. SBLs aggregate total liability to Client in any given calendar year for Materials Claims and Ordinary Claims combined shall not exceed [***] of the amounts payable by Client to SBL in such calendar year under such PSA. |
SECTION 14 TERM AND TERMINATION OF AGREEMENT
14.1 |
Term. This MSA will become effective as of the Effective Date and will be in effect for as long as a PSA is in effect; provided that if the only currently effective PSA has expired and such expiry causes an unintentional expiration of this MSA, the term of the MSA shall be extended upon mutual agreement of the Parties. Each PSA will have its own initial term as stated therein and shall renew upon mutual agreement. |
14.2 |
Termination. This MSA or a PSA may be earlier terminated as set forth in this Section 14.2. |
14.2.1 |
By Client. Client may terminate a PSA and/or this MSA without cause on thirty (30) days prior written notice to SBL. |
14.2.2 |
Material Breach. A Party may terminate any PSA for a material breach by the other Party; provided, however, that the non-breaching Party shall give the breaching Party written notice of such breach and if the breaching Party fails to commence Commercially Reasonable Efforts to cure that breach within thirty (30) days after receipt of such written notice, then the non-breaching Party may terminate this Agreement on thirty (30) days written notice after expiration of such thirty (30) day period. This MSA shall terminate if all effective PSAs are terminated. |
14.2.3 |
Insolvency. This MSA may be terminated by either Party upon written notice at any time during the MSA if the other Party: (a) files in any court pursuant to any statute a petition in bankruptcy or insolvency or for reorganization or for an arrangement or for the appointment of a receiver or trustee of such Party, or of its assets; (b) proposes a written agreement of composition for extension of its debts; (c) is served with an involuntary petition against it, filed in any insolvency proceeding which is admitted in the court; or (d) makes an assignment for the benefit of its creditors. The Party affected shall immediately notify the other Party in writing of the occurrence of any of the foregoing events. |
14.2.4 |
Force Majeure. Either Party may terminate a PSA if a Party is unable to perform its obligations pursuant to a PSA in the event of a Force Majeure Event in accordance with Section 16.3. |
28
14.2.5 |
Other Specified Events. The Parties may additionally terminate a PSA as set forth in the applicable PSA . |
14.3 |
Effect of Expiration or Termination. |
14.3.1 |
Payment of Amounts Due. Expiration or termination of the MSA or PSA for any reason shall not exempt either Party from paying to the other Party any amounts owing at the time of such expiration or termination. |
14.3.2 |
Survival. Any termination or expiration of this MSA shall not affect any outstanding obligations due hereunder prior to such termination or expiration, nor shall it prejudice any other remedies that the parties may have under this MSA. For greater certainty, except as otherwise expressly provided, termination or expiration of this MSA, irrespective of the cause, shall not affect any rights or obligations which, from the context thereof, are intended to survive termination or expiration of this MSA, including but not limited to Sections 8, 9, 10, 11, 12, 13, 14, 15, and 16. |
14.3.3 |
Effect of Termination. Upon termination of a PSA for any reason, SBL shall promptly cease and refrain from the Services described in any applicable PSA (including the Manufacturing and supplying the Product) for Client unless otherwise provided in this Section 14.3.3. SBL shall take all reasonable steps to mitigate the out-of-pocket expenses incurred in connection therewith. In particular, SBL shall use its best efforts to: (a) immediately cancel, to the greatest extent possible, any third party obligations; (b) promptly inform Client of any irrevocable commitments made in connection with any pending purchase order prior to termination; (c) promptly inform Client of the cost of any remaining unused, unreturnable Raw Materials ordered pursuant to any pending purchase order, and either deliver such materials to Client (or its designee) or properly dispose of them, as instructed by Client; and (d) perform only those services and activities mutually agreed upon by Client and SBL as being necessary or advisable in connection with the close-out of the PSA. Both Parties shall pursue decommissioning activities as set forth hereunder: |
(a) |
Settlement of Payment. SBL shall be compensated no later than sixty (60) days after a termination for: |
(i) |
all Service Fees incurred up to the date of termination including the Service Fees for completing the Manufacture of Product-in-process, subject however to Section 14.3.3(b) below; |
(ii) |
all costs incurred through the date of termination, including the costs of procuring Raw Materials used or purchased for use in connection with Services; and |
(iii) |
any unreimbursed procurement fee of additional equipment that SBL has purchased on behalf of Client pursuant to Section 4.4. |
(b) |
Delivery. Unless any major issue related to quality that reasonably would have a materially adverse impact on any Product Manufactured by SBL exists, upon consent of Client, SBL shall continue manufacturing Product-in-process as of the date of termination and deliver the fully manufactured Product to Client in accordance with |
29
the schedule then agreed upon by the Parties. As soon as practically possible after the termination and provided that Client has paid the invoice for such Raw Materials, SBL shall deliver to Client and Client shall accept (1) any Raw Material purchased for use in connection with Services, (2) any Client Material then in possession of SBL; provided however that the Parties may mutually agree instead to destroy or discard such Raw Material or Client Material, in which case SBL shall promptly destroy or dispose of the same without making any further use of such materials. Any costs incurred in connection with such a delivery or destruction, as the case may be, shall be borne by the Party responsible for termination in accordance with (c) and (d) below; provided that, for all other cases, the Parties shall negotiate in good faith the allocation of all such costs and expenses. |
(c) |
Termination by SBL pursuant to Clause 14.2.2. In the event of termination by SBL pursuant to Clauses 14.2.2, the outstanding binding obligations to purchase Product as of the date of termination shall survive termination of such PSA, including but not limited to a Firm Period, Binding Forecast, Purchase Order, and Product Purchase Commitment, and the Client shall be responsible for the costs incurred in connection with delivery or disposal of Raw Materials, Client Material, or equipment during decommissioning activities. |
(d) |
Termination by Client pursuant to Clause 14.1. In the event of termination of a PSA by Client pursuant to Clause 14.2.1, the Parties shall agree in such PSA what fee shall be due by Client to SBL. |
(e) |
Termination by Client pursuant to Clauses 14.2.2 or 14.2.3. In the event of termination by Client pursuant to Clauses 14.2.2 or Clause 14.2.3, Client shall be released from any outstanding binding obligations to purchase Product as of the date of termination including but not limited to any obligation pursuant to a Firm Period, Binding Forecast, Purchase Order, and Product Purchase Commitment, except the decommissioning activities set forth in this Section 14.3.3 of the MSA which shall be binding on both Parties. |
(f) |
Termination by either Party based on Clause 14.2.4. Both Parties shall negotiate in good faith and based on industry standards for the handling and delivery of the fully Manufactured Product, Product-in-process, Client Materials, and Raw Materials and the allocation of costs and expenses between the Parties. |
14.3.4 |
Effect of Expiration. Upon expiration of a PSA at the end of the Term or any renewed Term, SBL shall cease and refrain from the Services described in any applicable PSA (including the Manufacturing and supplying the Product), and Section 14.3.3 above shall apply mutatis mutandis, and both Parties shall negotiate in good faith the allocation of related costs and expenses for such decommissioning activities. |
30
SECTION 15 ARBITRATION
15.1 |
Informal Discussions. Except as otherwise provided herein, in the event of any controversy or claim arising out of or relating to this MSA, or the rights or obligations of the Parties hereunder, the Parties shall first try to settle their differences amicably between themselves through the Core Team and then JSC level. Thereafter, either Party may initiate informal dispute resolution on the Executive level by sending written notice of the dispute to the other Party, and within fifteen (15) days after such notice appropriate Executives of the Parties shall attempt resolution by good faith negotiations. If such representatives are unable to resolve promptly such disputed matter within the said fifteen (15) days, either Party may refer the matter by written notice to the Chief Executive Officer of the other Party, or his/her designee, and the Chief Executive Officer of such Party, for discussion and resolution. If such individuals or their designees are unable to resolve such dispute within thirty (30) days of such written notice, either Party may initiate arbitration proceedings in accordance with the provisions of this Article 15. |
15.2 |
Arbitration. If the Parties do not fully settle a dispute pursuant to Section 15.1, and a Party wishes to pursue the matter, each such dispute, controversy or claim shall be finally resolved by binding arbitration in accordance with the Commercial Arbitration Rules of the International Chamber of Commerce (ICC), and judgment on the arbitration award may be entered in any court having jurisdiction thereof to enforce the arbitration award. The arbitration shall be conducted by a panel of three persons experienced in the pharmaceutical business, and within thirty (30) days after initiation of arbitration, each Party shall select one person to act as arbitrator and the two Party-selected arbitrators shall select a third arbitrator within thirty (30) days of their appointment. If the arbitrators selected by the Parties are unable or fail to agree upon the third arbitrator, the third arbitrator shall be appointed by the ICC. The place of arbitration shall be New York, New York, United States and all proceedings and communications shall be in English. Either Party may apply to the arbitrators for interim injunctive relief until the arbitration award is rendered or the controversy is otherwise resolved. Either Party also may, without waiving any remedy under this Agreement, seek from any court having jurisdiction any injunctive or provisional relief necessary to protect the rights or property of that Party pending the arbitration award. The arbitrators shall have no authority to award punitive or any other type of damages not measured by a Partys direct compensatory damages, and in all cases, any decision or determination by the arbitrators shall comply with Article 14, as applicable. The Parties agree that, in the event of a good faith dispute over the nature or quality of performance under this Agreement, neither Party may terminate this Agreement until final resolution of the dispute through arbitration or other judicial determination. |
15.3 |
Costs and Fees. Each Party shall bear its own attorneys fees, costs, and disbursements arising out of the arbitration, and shall pay an equal share of the fees and costs of the arbitrators. Absent the filing of an application to correct or vacate the arbitration award as permitted by Applicable Law, each Party shall fully perform and satisfy the arbitration award within fifteen (15) days after the service of the award on such Party. |
SECTION 16 MISCELLANEOUS
16.1 |
Notices. Any notice required or permitted under the MSA shall be in writing with duly authorized signature and made to the following addresses: |
31
If to Client:
Greenlight Biosciences, Inc.
200 Boston Avenue, Suite 1000
Medford, MA 02155
Attention: Legal Affairs
If to SBL:
Samsung Biologics Co., Ltd.
300, Songdo bio-daero, Yeonsu-gu
Incheon 21987, South Korea
Attention: SBL Legal Team
Either Party may change its designated address by notice to the other Party in the manner provided in this Section 16.1.
Any notice shall be deemed to have been delivered on the date of delivery if delivered personally, or on the third day after being delivered by a national or internationally recognized overnight or two-day courier service, or on the fifth day of posting if sent by registered or certified mail with return receipt requested and postage prepaid.
16.2 |
Governing Law. This MSA shall be construed and interpreted in accordance with the laws of State of New York, United States and all rights and remedies shall be governed by such laws without regard to principles of conflicts of law. The United Nations Convention on Contracts for the International Sale of Goods shall not apply to the transactions contemplated by the MSA. |
16.3 |
Effect of Force Majeure Event. Except as set forth in this Section 16.3,the Affected Party shall be liable to the other Party for failure or delay to perform its obligation under the MSA or any applicable PSA when such failure or delay is due to Force Majeure Event. |
Each Party agrees to give the other Party prompt written notice of the occurrence of any Force Majeure Event, the nature thereof, and the extent to which the affected Party will be unable fully to perform its obligations under the MSA. If a condition constituting Force Majeure Event as defined herein exists for more than one hundred eighty (180) consecutive days, the Parties shall negotiate a mutually satisfactory solution to the problem, if practicable, including termination of this MSA upon thirty (30) days written notice from the failure of reaching a mutually satisfactory solution to the Force Majeure Event, or the use of a third party to fulfill the obligations hereunder of the party invoking Force Majeure Event, at the expense of the party invoking Force Majeure Event.
32
16.4 |
Assignment. |
16.4.1 |
This Agreement and all rights and obligations hereunder may not be Assigned or transferred by either Party, by operation of law or otherwise, without the express prior written consent of the other Party, which shall not be unreasonably withheld. Notwithstanding the foregoing, Client may, without SBLs consent, Assign this Agreement in its entirety (a) to an Affiliate or (b) to a successor entity in the event of a merger, consolidation or change of control or (c) in connection with the transfer or sale of all or substantially all of the business or assets of the assigning party to which this Agreement relates. For clarity, withholding consent in the event of the potential assignees refusal to agree in writing to assume all rights and obligations under this MSA or a PSA shall not be deemed unreasonable. Any attempted Assignment in violation of this Section shall be deemed null and void for all purposes. |
16.4.2 |
In the event of an Assignment, the Party Assigning this Agreement or all rights and obligations hereunder shall be responsible for any and all additional costs and expenses incurred as a result of such an Assignment, including but not limited to any additional Services that need to be performed by SBL. |
16.5 |
No Grant of License. Nothing in the MSA shall affect, or grant any right to, patents, know-how or other intellectual property owned by either Party prior to the commencement of the MSA unless otherwise expressly provided in the MSA. |
16.6 |
No Right to Use Names. Except as expressly provided herein, no right, expressed or implied, is granted by the MSA to use in any manner the name of either of the Parties or any other trade name, symbol, logo or trademark of the other Party in connection with the performance of the MSA, without the prior written consent of the other Party. |
16.7 |
Independent Contractors. The Parties hereto are independent contractors and nothing contained in the MSA shall be deemed or construed to create a partnership, joint venture, employment, franchise, agency or fiduciary relationship between the Parties. |
16.8 |
Integration. This MSA constitutes the entire agreement between the Parties relating to the subject matter of the MSA and supersedes all previous oral and written communications between the Parties with respect to the subject matter of the MSA. |
16.9 |
Decision Memo; Amendment; Waiver. A Decision Memo may be entered into by the Core Teams or JSCs with a binding effect, with it being understood that, in the event of a conflict between a Scope of Work, or Decision Memo and a later executed Decision Memo, the later executed Decision Memo shall prevail. Except as otherwise expressly provided herein, no alteration of or modification to the MSA shall be effective unless made in writing and executed by an authorized representative of both Parties. No course of dealing or failing of either Party to strictly enforce any term, right or condition of the MSA in any instance shall be construed as a general waiver or relinquishment of such term, right or condition. The observance of any provision of the MSA may be waived (either generally or any given instance and either retroactively or prospectively) only with the written consent of the Party granting such waiver. |
16.10 |
Severability. The Parties do not intend to violate any applicable law. However, if any sentence, paragraph, clause or combination of the MSA is in violation of any law or is found to be otherwise unenforceable, such sentence, paragraph, clause or combination of the same shall be deleted and the remainder of the MSA shall remain binding, provided that such deletion does not alter the basic purpose and structure of the MSA. |
33
16.11 |
Construction. The Parties mutually acknowledge that they have participated in the negotiation and preparation of the MSA. Ambiguities, if any, in the MSA shall not be construed against any Party, irrespective of which Party may be deemed to have drafted the MSA or authored the ambiguous provision. |
16.12 |
Interpretation. The captions and headings to the MSA are for convenience only, and are to be of no force or effect in construing or interpreting any of the provisions of the MSA. Unless context otherwise clearly requires, whenever used in the MSA: (a) the words include or including shall be construed as incorporating, also, but not limited to or without limitation; (b) the words hereof, herein, hereby and derivative or similar words refer to the MSA; (c) all references to the word will are interchangeable with the word shall and shall be understood to be imperative or mandatory in nature. All references to days, months, quarters or years are references to calendar days, calendar months, calendar quarters, or calendar years. Whenever any matter hereunder requires consent or approval, such consent or approval shall not be unreasonably withheld or delayed. |
16.13 |
Counterparts. This MSA may be executed in two or more counterparts, each of which will be deemed an original, but all of which together will constitute one and the same instrument. |
IN WITNESS WHEREOF, the Parties have executed the MSA as of the date first above written.
Greenlight Biosciences, Inc.
Signature: |
/s/ Andrey Zarur |
|
Name: | Andrey Zarur | |
Title: | CEO | |
Date: | 11/22/2021 |
SAMSUNG BIOLOGICS CO., LTD.
Signature: |
/s/ John Rim |
|
Name: | John Rim | |
Title: | CEO & President | |
Date: |
|
34
Exhibit 10.34
Certain identified information has been omitted from this exhibit because it is
not material and of the type that the registrant treats as private or confidential.
[***] indicates that information has been omitted.
SAMSUNG BIOLOGICS CO., LTD.
PRODUCT SPECIFIC AGREEMENT CLINICAL PRODUCT DRUG SUBSTANCE
This Product Specific Agreement (this PSA) is made effective as of the date of last signature below (the PSA Effective Date) by and between GreenLight Biosciences, Inc., a Delaware corporation having its principal place of business at 200 Boston Avenue, Suite 1000, Medford, MA 02155 (Client) and Samsung Co., Ltd., a Korean corporation having its principal place of business at 300, Songdo bio-daero, Yeonsu-gu, Incheon, 21987, Republic of Korea (SBL). Client and SBL are sometimes referred to herein individually as a Party and collectively as the Parties.
WHEREAS, Client and SBL entered into a Master Services Agreement effective November 24, 2021 (the MSA) and whereas pursuant to Section 2.1 of the MSA, the Parties wish to enter into this PSA whereby SBL will provide certain Services as detailed herein;
NOW, THEREFORE, the Parties agree as follows:
1. |
Relationship to the MSA. All capitalized terms not defined in this PSA will have the meanings given to them in the MSA. This PSA is hereby incorporated by reference into the MSA. |
2. |
Definitions |
a. |
Campaign shall mean a series of Batches of the Product that are produced in sequence using the same manufacturing equipment followed by validated cleaning of such equipment and for the purposes of counting the number of Product batches in a Campaigns in a given period, the start date of such Campaign shall be the determining factor. A Campaign will be deemed to end upon the completion of such cleaning. |
b. |
Product: GreenLight Biosciences mRNA COVID vaccine |
c. |
Product Purchase Commitment Shortfall means the number of Batches of Product falling short of the Product Purchase Commitment. |
d. |
Year means each one (1) year period that begins on January 1 and ends on December 31. |
3. |
General Information. |
a. |
Clinical Product Specification: The Product Specification will be mutually agreed upon and set forth in cGMP documentation. |
b. |
Manufacturing Facility: [***] scale mRNA facility in Plant #3, located at 300, Songdo bio-daero, Yeonsu-gu, Incheon 21987, Republic of Korea. |
1
4. |
Raw Materials. |
a. |
Client Materials. Client Materials to be supplied by Client to SBL free of charge by itself or a third party designee. |
i. |
List: See Exhibit A: Client Materials |
ii. |
Timing of provision of Client Materials to SBL: one month in advance of production unless otherwise agreed to by the Parties. If Process Validation runs require additional testing, the Parties will mutually agree on the timing. |
b. |
Raw Materials. As set forth in Section 4.6.1 of the MSA, the Parties shall finalize the categorization of Raw Materials to be used in performing the Services of this PSA into (i) Critical Raw Materials, (ii) Dedicated or Customized Raw Materials, and (iii) Other Raw Materials, which list shall form part of this PSA as Exhibit B. |
i. |
Handling Fee for Customized or Dedicated Raw Materials and Other Raw Materials to be procured by SBL at Clients expense: [***]. For a Batch, the Handling Fee shall be capped at [***]. |
ii. |
Handling Fee for Critical Raw Materials to be procured by SBL at Clients expense: [***]. For a Batch, the Handling Fee shall be capped at [***]. |
5. |
Technology Transfer, Manufacturing, and Supply Services. SBL shall perform the Services as set forth in this Section 5. |
a. |
Services. |
i. |
SBL shall provide the Services as set forth in Exhibit C in accordance with this PSA, Project Plan, or Scope of Work. |
ii. |
Fees and invoicing. |
1. |
Services shall be invoiced upon completion of activities by SBL, or as otherwise agreed by the Parties. |
2. |
Bulk Drug Product Batches shall be invoiced according to Section 8.2.1 of the MSA. |
b. |
Service Fees. In consideration for SBLs performance of the Services pursuant to this Section 5, Client shall pay the Service Fees as set forth in Exhibit C. Additional Service Fees and costs may be detailed in an amendment to this PSA or in accordance with the MSA. |
c. |
Product Purchase Commitment. |
i. |
If the Parties execute a subsequent PSA for commercial production of Bulk Drug Product of the Product, the Parties agree that such subsequent PSA shall contain the following Product Purchase Commitment: [***]. Such PSA shall also include a term such that if Client makes an improvement to the Product manufacturing process which reduces facility time, the Parties shall in good faith reevaluate the Batch price. |
2
ii. |
This PSAs Product Purchase Commitment is [***]. Upon execution of this PSA, Client shall issue a Purchase Order for the Product Purchase Commitment, and such Purchase Order shall be fully binding on a minimum take or pay basis. |
iii. |
Each Year, Client shall pay to SBL the price set forth in this PSA for each of the Product Purchase Commitment Shortfall, if any. For any Year for which a Product Purchase Commitment Shortfall payment is owed to SBL no later than December 31 of the Year when there is a Product Purchase Commitment Shortfall for such Year. |
6. |
2023 Capacity Right of First Refusal. [***]. For clarity after such right expires the Parties may nevertheless agree on the sale of such capacity to Client. |
7. |
Regulatory Approvals. The Regulatory Approvals covered by this PSA are the Food and Drug Administration (FDA), European Medicines Evaluation Agency (EMEA), and South African Health Products Regulatory Authority (SAHPRA) |
8. |
Storage. Pursuant to Section 4.12.2(a)(ii) of the MSA, if Client does not direct SBL to prepare Manufactured Commercial Product to be picked up by Client or Clients designated carrier with a pick-up date within thirty (30) days of Clients or Clients designees receipt of the Batch Related Documents, SBL shall store the Commercial Product at the Warehouse and Client shall pay storage fees to SBL for the period of storage at the Warehouse until the actual delivery date. Storage fees shall be as follows: [***] per month per 10L bag. |
9. |
Outbound Technology Transfer. Once during the term of this PSA or upon its termination, SBL shall provide support for outbound technology transfer to a Client facility or a Third Partys facility designated by the Client. The outbound technology transfer request must be made with at least six (6) months prior written notice. The scope of such outbound technology transfer will be mutually agreed upon scope of work but in no event shall SBL be obligated to provide more than two full time employee equivalent (FTE) months. |
10. |
Termination Fee for Termination without Cause. In the event Client terminates this PSA pursuant to MSA Section 14.2.1, the termination fee payable by Client shall be as follows: the value of the Product Purchase Commitment, to the extent not already paid prior to termination. |
11. |
Limitation of Liability. Notwithstanding Section 13.2 of the MSA, except with respect to Damages or allowable indirect damages arising under or in connection with this PSA arising out of (i) breaches of Sections 9 and 10 of the MSA; (ii) instances of gross negligence or willful misconduct (which shall not include Materials Claims); (iii) Materials Claims; and/or (iv) third party death or bodily injury caused by SBL to Client employees or contractors who may visit SBL sites, Client agrees that SBLs aggregate total liability to Client in respect of any Ordinary Claims arising out of this PSA shall be |
3
capped at an amount equal to [***] the amounts payable by Client to SBL pursuant to this PSA. Client agrees that SBLs aggregate total liability to Client in respect of any Materials Claims arising out of this PSA shall be capped at an amount equal to [***] of the amounts payable by Client to SBL under such PSA. SBLs aggregate total liability to Client pursuant to this PSA for Materials Claims and Ordinary Claims combined shall never exceed [***] of the amounts payable by Client to SBL under such PSA. |
12. |
Term. This PSA will commence as of the PSA Effective Date and will continue in full force and effect until [***] or unless earlier terminated in accordance with the termination provisions of this PSA and/or the MSA. |
The Parties have entered into this PSA as of the PSA Effective Date by their respective duly authorized representatives.
SAMSUNG BIOLOGICS CO., LTD. | GREENLIGHT BIOSCIENCES, INC. | |||||||
By: |
/s/ John Rim |
By: |
/s/ Andrey Zarur |
|||||
Name: | John Rim | Name: | Andrey Zarur | |||||
Title: | CEO & President | Title: | CEO |
4
Exhibit A: Client Materials
[***]
5
Exhibit B: Categorization of Raw Materials
[***]
6
Exhibit C: Services
Estimated Project Timeline
|
Actual activity start dates may adjusted subject to the dates which Parties mutually agree after the execution of this PSA |
[***]
mRNA Manufacturing Price
* |
Service fee for Stage 3, 4, 6, and 10 shall be updated based on further discussion with GreenLight Biosciences |
PRICING AND PAYMENT ASSUMPTIONS
Standard pricing and payment terms are listed below.
|
The price is based on information provided in the RFP regarding the product and manufacturing process [***]. Further communication between Samsung Biologics and GreenLight Biosciences regarding the specifics of the project may result in changes to the scope of work and associated price. Any change in scope or price will be documented via an amendment to this PSA. |
7
|
Tiered batch price is based on a single campaign per year and resets [***]. |
|
Commercial Run pricing is based on [***]. Further process details provided by GreenLight Biosciences may impact the pricing. |
|
The assays listed in Appendix A2: Analytical Methods for Covid-19 Vaccine DS will be transferred. |
|
Samsung Biologics will conduct Mycoplasma testing at Samsung Biologics QC (Quality Control) Laboratory, if requested. |
|
The proposed prices are based on regulatory requirements that complies with FDA, EMEA, Canada, SAHPRA, and PMDA. Prices may change depending on the additional requirements necessary to comply with other regulatory authorities. |
|
Unless otherwise noted, all batches are intended for human use and will be aseptically filled, 100% inspected, bulk packaged, shipped and released for further processing to the client. Client or Clients designee is responsible for final product release. |
|
Samsung Biologics will support shipping validation execution activities by following the Client packaging/preparation instructions; Client is accountable for shipping validation, strategy, execution and documentation. |
8
Exhibit D: Scope of Work
[***]
9
Exhibit 23.1
CONSENT OF INDEPENDENT REGISTERED PUBLIC ACCOUNTING FIRM
We hereby consent to the use in the Prospectus constituting a part of this Registration Statement on Amendment No. 2 to Form S-4, of our report dated March 26, 2021, relating to the financial statements of Environmental Impact Acquisition Corp. which is contained in the Prospectus. We also consent to the reference to us under the caption Experts in the Prospectus.
/s/ WithumSmith+Brown, PC
New York, New York
December 6, 2021
EXHIBIT 23.2
CONSENT OF THE INDEPENDENT REGISTERED PUBLIC ACCOUNTING FIRM
We consent to the use in this Registration Statement No. 333-259375 on Form S-4 of our report dated September 7, 2021, relating to the financial statements of GreenLight Biosciences, Inc. We also consent to the reference to us under the heading Experts in such Registration Statement.
/s/ Deloitte & Touche LLP
Boston, Massachusetts
December 6, 2021
Exhibit 99.2
CONSENT OF DUFF & PHELPS
Duff & Phelps, A Kroll Business operating as Kroll, LLC (Duff & Phelps) hereby consents to (i) the filing of our fairness opinion dated August 9, 2021 (the Opinion) to the Board of Directors of Environmental Impact Acquisition Corp. (ENVI) as Annex K to this Registration Statement on Form S-4, (ii) the references therein to Duff & Phelps and (iii) the inclusion therein of (a) the summaries of and excerpts from the Opinion, (b) the description of certain financial analyses underlying the Opinion and (c) certain terms of our engagement by the Board of Directors of ENVI. In giving such consent, we do not thereby admit that we are in the category of persons whose consent is required under Section 7 of the Securities Act of 1933.
Duff & Phelps, A Kroll Business |
||||||
/s/ Christopher L. Janssen |
||||||
By: |
Christopher L. Janssen |
|||||
Title: |
Managing Director |
|||||
Kroll, LLC
December 6, 2021 |