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UNITED STATES
SECURITIES AND EXCHANGE COMMISSION
Washington, D.C. 20549
_______________________________
FORM 10-Q
_______________________________
(Mark One)
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☒ |
QUARTERLY REPORT PURSUANT TO SECTION 13 OR 15(d) OF THE SECURITIES EXCHANGE ACT OF 1934 |
For the quarterly period ended June 30, 2019
or
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TRANSITION REPORT PURSUANT TO SECTION 13 OR 15(d) OF THE SECURITIES EXCHANGE ACT OF 1934 |
For transition period from to .
Commission File Number: 001-37841
Kadmon Holdings, Inc.
(Exact name of registrant as specified in its charter)
_______________________________
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Delaware
(State or other jurisdiction of
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27 ‑3576929
(I.R.S. Employer
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450 East 29th Street, New York, NY (Address of principal executive offices) |
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10016 (Zip Code) |
(212) 308 ‑6000
(Registrant’s telephone number, including area code)
_______________________________
Indicate by check mark whether the registrant: (1) has filed all reports required to be filed by Section 13 or 15(d) of the Securities Exchange Act of 1934 during the preceding 12 months (or for such shorter period that the registrant was required to file such reports), and (2) has been subject to such filing requirements for the past 90 days. Yes ☒ No ☐
Indicate by check mark whether the registrant has submitted electronically every Interactive Data File required to be submitted pursuant to Rule 405 of Regulation S-T (§232.405 of this chapter) during the preceding 12 months (or for such shorter period that the registrant was required to submit such files). Yes ☒ No ☐
Indicate by check mark whether the registrant is a large accelerated filer, an accelerated filer, a non-accelerated filer, a smaller reporting company, or an emerging growth company. See the definitions of “large accelerated filer,” “accelerated filer,” “smaller reporting company,” and “emerging growth company” in Rule 12b-2 of the Exchange Act.:
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Large accelerated filer ☐ |
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Accelerated filer ☒ |
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Non-accelerated filer ☐ |
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Smaller reporting company ☒ |
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Emerging growth company ☒ |
If an emerging growth company, indicate by check mark if the registrant has elected not to use the extended transition period for complying with any new or revised financial accounting standards provided pursuant to Section 13(a) of the Exchange Act. ☒
Securities registered pursuant to Section 12(b) of the Act:
Title of each class |
Trading Symbol(s) |
Name of each exchange on which registered |
Common stock, par value $0.001 per share |
KDMN |
The New York Stock Exchange |
Indicate by check mark whether the registrant is a shell company (as defined in Rule 12b-2 of the Exchange Act). Yes ☐ No ☒
The number of shares of the registrant’s common stock outstanding as of July 29, 2019 was 129,634,540 .
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2
Form 10-Q
Table of Contents
3
FORWARD- LOOKING STATEMENTS
T his Quarterly Report on Form 10-Q contains forward- looking statements. All statements other than statements of historical facts contained in this Quarterly Rep ort on Form 10-Q may be forwar d - looking statements. Statements regarding our future results of operations and financial position, business strategy and plans and objectives of management for future operations, including, among others, statements regarding future capital expenditures and debt s ervice obligations, are forward- looking statements. In some cases, you can identify forward- looking statements by terms such as “may,” “will,” “should,” “expects,” “plans,” “anticipates,” “could,” “intends,” “targets,” “projects,” “contemplates,” “believes,” “estimates,” “predicts,” “potential” or “continue” or the negative of these terms or other similar expressions.
Forward- looking statements involve known and unknown risks, uncertainties and other important factors that may cause our actual results, performance or achievements to be materially different from any future results, performance or achievements expr essed or implied by the forward- looking statements. We believe that these factors include, but are not limited to, the following:
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the initiation, timing, progress and results of our preclinical studies and clinical trials, and our research and development programs; |
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our ability to advance product candidates into, and successfully complete, clinical trials; |
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our reliance on the success of our product candidates; |
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the timing or likelihood of regulatory filings and approvals; |
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our ability to expand our sales and marketing capabilities; |
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the commercialization , pricing and reimbursement of our product candidates, if approved; |
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the implementation of our business model, strategic plans for our business, product candidates and technology; |
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the scope of protection we are able to establish and maintain for intellectual property rights covering our product candidates and technology; |
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our ability to operate our business without infringing, misappropriating or otherwise violating the intellectual property rights and proprietary technology of third parties; |
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cost associated with defending or enforcing, if any, intellectual property infringement, misappropriation or other intellectual property violation, product liability and other claims; |
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regulatory and governmental policy developments in the United States, Europe and other jurisdictions; |
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estimates of our expenses, future revenues, capital requirements and our needs for additional financing; |
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the potential benefits of strategic collaboration agreements and our ability to enter into strategic arrangements; |
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our ability to maintain and establish collaborations or obtain additional grant funding; |
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the rate and degree of market acceptance, if any, of our product candidates, if approved; |
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developments relating to our competitors and our industry, including competing therapies; |
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our ability to effectively manage our anticipated growth; |
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our ability to attract and retain qualified employees and key personnel; |
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our ability to achieve cost savings and benefits from our efforts to streamline our operations and to not harm our business with such efforts; |
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our expectations regarding the period during which we qualify as an emerging growth company under the Jumpstart Our Business S tartups Act ; |
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statements regarding future revenue, hiring plans, expenses, capital expenditures, capital requirements and share performance ; |
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litigation, including costs associated with prosecuting or defending pending or threatened claims and any adverse outcomes or settlements not covered by insurance; |
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our expected use of cash and cash equivalents and other sources of liquidity; |
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our ability to repay, amend or refinance our credit agreement with Perceptive Credit Opportunities Fund, L.P., as amended, due July 1, 2020 (“the 2015 Credit Agreement”); |
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the future trading price of shares of our common stock and impact of securities analysts’ reports on these prices; |
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the future trading price of our investments and our potential inability to sell those securities; |
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our ability to apply unused federal and state net operating loss carryforwards against future taxable income; and |
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other risks and uncertainties, including those listed in this report and in our most recent Annual Report on Form 10-K. |
The forward- looking statements in this Quarterly Report on Form 10-Q are only predictions, and we may not actually achieve the plans, intentions or expec tations included in our forward- looking statements. We have based thes e forward- looking statements largely on our current expectations and projections about future events and financial trends that we believe may affect our business, financial condition and results of operations. Because forward- looking statements are inherently subject to risks and uncertainties, some of which cannot be predicted or quantified, you s hould not rely on these forward- looking statements as predictions of future events. The events and circums tances reflected in our forward- looking statements may not be achieved or occur and actual results could differ materially from those projected in the forward- looking statements.
4
Consolidated balance sheets
(in thousands, except share amounts)
See accompanying notes to consolidated financial statements (unaudited)
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Consolidated statements of operations (unaudited)
(in thousands, except share and per share amounts )
See accompanying notes to consolidated financial statements (unaudited)
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Consolidated statements of stockholders’ equity (unaudited)
(in thousands, except share amounts )
See accompanying notes to consolidated financial statements (unaudited)
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Consolidated statements of cash flows (unaudited)
(in thousands)
See accompanying notes to consolidated financial statements (unaudited)
8
Notes to consolidated financial statements (unaudited)
1. Organization
Nature of Business
Kadmon Holdings, Inc. (together with its subsidiaries, “Kadmon” or “Company”) is a fully integrated biopharmaceutical company engaged in the discovery, development and commercialization of small molecules and biologics to address disease areas of significant unmet medical needs, with a near-term clinical focus on inflammatory and fibrotic diseases as well as immun o -oncology . The Company leverages its multi- disciplinary research and clinical development team members to identify and pursue a diverse portfolio of novel product candidates, both through in-licensing products and employing its small molecule and biologics platforms. By retaining global commercial rights to its lead product candidates, the Company believes that it has the ability to develop these candidates while maintaining flexibility for commercial and licensing arrangements. The Company expects to continue to progress its clinical candidates and have further clinical trial events in the second half of 201 9 and in 2020 .
Liquidity
The Company maintained cash and cash equivalents of $86.2 million at June 30, 2019 . The Company had an accumulated deficit of $257.9 million and working capital of $58.9 million at June 30, 2019 . The Company entered into a Sales A greement with Cantor Fitzgerald & Co. in August 2017 under which the Company may sell up to $40.0 million in shares of its common stock in one or more placements at prevailing market prices for its common stock (the “ATM Offering”). Any such sales would be effected pursuant to the Company’s registration statement on Form S-3 (File No. 333-222364), declared effective by the Securities Exchange Commission (“ SEC ”) on January 10, 2018. As of December 31, 2018, the Company had not sold any shares of common stock through the ATM Offering. In January 2019, the Company sold 13,778,705 shares of common stock at a weighted average price of $2.17 per share through the ATM Offering and received total gross proceeds of $29.9 million ( $29.0 million net of $0.9 million of comm issions payable by the Company) . I n April 2019, the Company sold 2, 538,1 00 shares of common stock at a price of $2. 7 0 per share through the ATM Offering and received total gross proceeds of $6. 9 million ( $6. 7 million net of $0.2 million of commissions payable by the Company ) . The Company’s existing cash and cash equivalents are expected to enable it to advance its Phase 2 clinical studies of KD025 and advance certain of its other pipeline product candidates and provide for other working capital purposes.
Management’s plans include continuing to finance operations through the issuance of additional equity securities , monetization of assets and expanding the Company’s commercial portfolio through the development of its current pipeline or through strategic collaborations. Any transactions that occur may contain covenants that restrict the ability of management to operate the business or may have rights, preferences or privileges senior to the Company’s common stock and may dilute current stockholders of the Company.
Going Concern
The accompanying financial statements have been prepared in conformity with accounting principles generally accepted in the United States of America (“GAAP”) , which contemplate continuation of the Company as a going concern. The Company has not established a source of revenues sufficient to cover its operating costs, and as such, ha s been dependent on funding operations through the issuance of debt and sale of equity securities. Since inception, the Company has experienced significant loses and incurred negative cash flows from operations. The Company expects to incur further losses over the next several years as it develops its business. The Company has spent, and expects to continue to spend, a substantial amount of funds in connection with implementing its business strategy, including its planned product development efforts, preparation for its planned clinical trials, performance of clinical trials and its research and discovery efforts.
The Company’s cash and cash equivalents are not expected to be sufficient to enable the Company to meet its long-term expected plans, including commercialization of clinical pipeline products, if approved, or initiation or completion of future registrational studies. The Company has no current commitments for additional financing and may not be successful in its efforts to raise additional funds or achieve profitable operations , and there can be no assurance that additional financing will be available to the Company on commercially acceptable terms or at all . Any amounts raised will be used for further development of the Company’s product candidates, for marketing and promotion, to secure additional prope rty and equipment and for other working capital purposes.
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If the Company is unable to obtain additional capital, its long-term business plan may not be accomplished and the Company may be forced to curtail or cease operations. Further, the 2015 Credit Agreement contains certain developmental milestones, as well as a minimum liquidity covenant. The Company’s failure to achieve these milestones as anticipated by December 31, 2019 or its violation of its minimum liquidity covenant would constitute an event of default under the 2015 Credit Agreement. Upon an event of default, the Lender may terminate the commitments under the 2015 Credit Agreement and declare the loans then outstanding under the 2015 Credit Agreement to be due and payable in whole or in part, together with any applicable fees and accrued interest thereon. The Company considers some of these developmental milestones to be outside of its control. As a result, if an event of default arises under the Credit Agreement, the Company may need to use cash and cash equivalents on hand to fund certain repayment commitments under the 2015 Credit Agreement.
These factors individually and collectively continue to raise substantial doubt about the Company’s ability to continue as a going concern. The accompanying financial statements do not include any adjustments or classifications that may result from the possible inability of the Company to continue as a going concern.
2 . Summary of Significant Accounting Policies
Basis of Presentation
The Company operates in one segment considering the nature of the Company’s products and services, class of customers , methods used to distribute its products and the regulatory environment in which the Company operates.
Principles of Consolidation
The accompanying consolidated financial statements have been prepared in conformity with GAAP . The consolidated financial statements include the accounts of Kadmon Holdings, Inc. and its domestic and international subsidiaries, all of which are wholly owned by Kadmon Holdings, Inc.
Interim Financial Statements
The accompanying financial statements have been prepared in accordance with GAAP for interim financial information and with the instructions to Form 10-Q and Article 10 of Regulation S-X. Accordingly, they do not include all of the information and footnotes required by GAAP for complete financial statements. In the Company’s opinion , the financial statements include all adjustments (consisting of normal recurring accruals) necessary in order to make the financial statements not misleading. Operating results for the three and six months ended June 30, 2019 are not necessarily indicative of the final results that ma y be expected for the year ending December 31, 201 9 . These unaudited financial statements should be read in conjunction with the audited financial statements included in Item 8 of the Company’s Annual Report on Form 10-K for the year ended December 31, 201 8 .
Use of Estimates
The preparation of financial statements in conformity with GAAP requires management to make estimates and assumptions that affect the reported amounts of assets and liabilities and disclosure of contingent assets and liabilities at the date of the consolidated financial statements. Actual results could differ from those estimates.
Critical A ccounting P olicies
The Company’s significant accounting policies are disclosed in the audited financial statements included in Item 8 of the Company’s Annual Report on Form 10-K for the year ended December 31, 201 8 . Since the date of such financial statements, there have been no changes to the Company’s significant accounting policies, other than those described below.
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Accounting for Leases
In February 2016, the Financial Accounting Standards Board (“FASB”) issued Accounting Standards Update (“ASU”) No. 2016 02, “Leases” ( “ ASC 842 ” ) to enhance the transparency and comparability of financial reporting related to leasing arrangements. Under this new lease standard, most leases are required to be recognized on the balance sheet as right-of-use (“ROU”) assets and lease liabilities. Disclosure requirements have been enhanced with the objective of enabling financial statement use rs to assess the amount, timing and uncertainty of cash flows arising from leases. Prior to January 1, 2019, GAAP did not require lessees to recognize assets and liabilities related to operating leases on the balance sheet. The new standard establishes a ROU model that requires a lessee to recognize a ROU asset and corresponding lease liability on the balance sheet for all leases with a term longer than 12 months. Leases will be classified as finance or operating, with classification affecting the pattern and classification of expense recognition in the statement of operations as well as the reduction of the right of use asset . The Company has adopted the standard effective January 1, 2019 and has chosen to use the effective date as our date of initial application. Consequently, financial information will not be updated and the disclosures required under the new standard will not be provided for dates and periods prior to January 1, 2019. The new standard provides a number of optional practical expedients in transition. The Company has elected to apply the ‘package of prac tical expedients’ , which allow it to not reassess ( i) whether existing or expired arrangements contain a lease, ( ii) the lease classification of existing or expired leases, or ( iii) whether previous initial direct costs would qualify for capitalization under the new lease standard. The Company has also elected to apply ( i) the practical expedient , which allows it to not separate lease and non-lease components, for new leases entered into after adoption and ( ii ) the short-term lease exemption for all leases with an original term of less than 12 months, for purposes of applying the recognition and measurements requirements in the new standard. In preparation for adoption of the standard, the Company implemented internal controls to enable the preparation of financial information including the assessment of the impact of the standard. For the impact to the Company’s consolidated financial statement upon adoption of the new leasing standard, see Note 8 to the unaudited consolidated financial statements included elsewhere in this Quarterly Report on Form 10-Q.
At the inception of an arrangement, the Company determines whether the arrangement is or contains a lease based on specific facts and circumstances, the existence of an identified asset(s), if any, and the Company’s control over the use of the identified asset(s), if applicable. Operating lease liabilities and their corresponding ROU assets are recorded based on the present value of future lease payments over the expected lease term. The interest rate implicit in lease contracts is typically not readily determinable. As such, the Company will utilize the incremental borrowing rate, which is the rate incurred to borrow on a collateralized basis over a similar term an amount equal to the lease payments in a similar economic environment. As of the ASC 842 effective date, the Company’s incremental borrowing rate range d from approximately 4.0% - 5.6% based on the remaining lease term of the applicable leases.
The Company has elected to combine lease and non-lease components as a single component. Operating leases are recognized on the balance sheet as ROU lease assets, lease liabilities current and lease liabilities non-current. Fixed rents are included in the calculation of the lease balances while variable costs paid for certain operating and pass-through costs are excluded. Lease expense is recognized over the expected term on a straight-line basis.
Revenue Recognition
The Company adopted FASB ASC 606, Revenue from Contracts with Customers ( “ ASC 606 ” ), on January 1, 2018 using the modified retrospective method for all contracts not completed as of the date of adoption– i.e. by recognizing the cumulative effect of initially applying ASC 606 as an adjustment to the opening balance of stockholder s ’ equity at January 1, 2018. The Company recognizes revenue in accordance with ASC 606, the core principle of which is that an entity should recognize revenue to depict the transfer of promised goods or services to customers in an amount that reflects the consideration to which the entity expects to be entitled to receive in exchange for those goods or services. To achieve this core principle, five basic criteria must be met before revenue can be recognized: (1) identify the contract with a customer; (2) identify the performance obligations in the contract; (3) determine the transaction price; (4) allocate the transaction price to performance obligations in the contract; and (5) recognize revenue when or as the Company satisfies a performance obligation.
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Disaggregation of Revenue
The following table summarizes revenue from contracts with customers for the three and six months ended June 30, 2019 and 2018 :
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Three Months Ended |
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Six Months Ended |
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June 30, |
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June 30, |
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2019 |
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2018 |
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2019 |
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2018 |
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Product sales |
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$ |
47 |
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$ |
161 |
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$ |
114 |
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$ |
435 |
Other revenue |
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179 |
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198 |
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353 |
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357 |
Total revenue |
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$ |
226 |
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$ |
359 |
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$ |
467 |
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$ |
792 |
Product Sales
The Company markets and distributes a portfolio of products, including ribavirin and tetrabenazine . These contracts typically include a single promise to deliver a fixed amount of product to the customer with payment due within 30 days of shipment. Revenues are recognized when control of the promised goods is transferred to the customer, in an amount that reflects the consideration the Company expects to be entitled to in exchange for those goods.
As is typical in the pharmaceutical industry, gross product sales are subject to a variety of deductions, primarily representin g rebates, chargebacks, returns and discounts to g overnment agencies, wholesalers and managed care organizations. These deductions represent management’s best estimates of the related reserves and, as such, judgment is required when estimating the impact of these sales deductions on gross sales for a reporting period. If estimates are not representative of the actual future settlement, results could be materially affected.
Other Revenue
O ther revenue generated by the Company is primarily related to a transition services agreement and sublease agreement with MeiraGTx Holdings plc (“MeiraGTx”) (Note 1 1 ). The Company performed various professional services under a transition services agreement ( the “TSA”) that support ed MeiraGTx until the expiration of the TSA in April 2018 . The Company continues to provide office space to MeiraGTx under a sublease agreement. The Company recognizes revenue related to transition services and sublease agreements as they are performed.
Contract Balances
The timing of revenue recognition may differ from the timing of invoicing to customers. Accounts receivable are recorded at the invoiced amount, net of an allowance for doubtful accounts. A receivable is recognized in the period the Company deliver s goods or provide s services or when its right to consideration is unconditional. The Company has not recognized any assets for costs to obtain or fulfill a contract with a customer as of June 30, 2019 .
Transaction Price Allocated to Future Performance Obligations
ASC 606 requires that the Company disclose the aggregate amount of a transaction price that is allocated to performance obligations that have not yet been satisfied as of June 30, 2019 . The guidance provides certain practical expedients that limit this requirement. The Company has various contracts that meet the following practical expedients provided by ASC 606:
1. The performance obligation is part of a contract that has an original expected duration of one year or less.
2. Revenue is recognized from the satisfaction of the performance obligations in the amount billable to the customer.
3. The variable consideration is allocated entirely to a wholly unsatisfied performance obligation or to a wholly unsatisfied promise to transfer a distinct good or service that forms part of a single performance obligation.
The Company does no t have any performance obligations that have not yet been satisfied as of June 30, 2019 and therefore there is no transaction price allocated to future performance obligations under ASC 606.
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Recent Accounting Pronouncements
In November 2018, the FASB issue d ASU No. 2018-18, “Collaborative Arrangements (Topic 808): Clarifying the Interaction Between Topic 808 and Topic 606”, which requires transactions in collaborative arrangements to be accounted for under ASC 606 if the counterparty is a customer for a good or service (or bundle of goods and services) that is a distinct unit of account. The ASU also preclude s entities from presenting consideration from transactions with a collaborator that is not a customer together with revenue recognized from contracts with customers. The ASU is effective for annual or interim periods beginning after December 15, 2019. Early adoption is permitted for entities that have adopted ASC 606. The Company is evaluating the impact of adopting this standard.
In August 2018, the FASB issued ASU No. 2018-15, “Intangibles—Goodwill and Other—Internal-Use Software (Subtopic 350-40): Customer’s Accounting for Implementation Costs Incurred in a Cloud Computing Arrangement That Is a Service Contract (a consensus of the FASB Emerging Issues Task Force)”, which requires customers in a cloud computing arrangement that is a service contract to follow the internal-use software guidance in Accounting Standards Codification 350-40 to determine which implementation costs to capitalize as assets. This ASU is effective for annual or any interim periods beginning after December 15, 2019. The Company does not expect the standard to have a significant impact on its consolidated financial statements, as the Company’s cloud computing contracts are not material.
In June 2018, the FASB issued ASU No. 2018-07, “Compensation – Stock Compensation”, which expands the scope of Topic 718 to include share-based payment transactions for acquiring goods and services from non - employees, subject to specific exceptions. This ASU is effective for annual or any interim periods beginning after December 15, 2018. The Company adopted this standard on January 1, 2019 , which did not have a significant impact on its consolidated financial statements as the fair value of the Company’s awards to non - employees is not material.
In January 2017, the FASB issued ASU No. 2017-04, “Intangibles – Goodwill and Other”, which simplifies the subsequent measurement of goodwill by eliminating “Step 2” from the goodwill impairment test. Instead of performing Step 2 to determine the amount of an impairment charge, the fair value of a reporting unit will be compared with its carrying amount and an impairment charge will be recognized for the value by which the carrying amount exceeds the reporting unit’s fair value. ASU 2017-04 is effective for annual or any interim goodwill impairment tests in fiscal years beginning after December 15, 2019. Early adoption is permitted for interim or annual goodwill impairment tests performed on testing dates after January 1, 2017. The Company does not expect the standard to have a significant impact on its consolidated financial statements.
3. Stockholders’ Equity
5% Convertible Preferred Stock
The Company had 28,708 shares of 5% convertible preferred stock outstanding at June 30, 2019, which shares convert into shares of the Company’s common stock at a 20% discount to the initial public offering price per share of common stock in the Company’s initial public offering ( the “IPO”) of $12.00 per share. In May 2019, the holder of 1,292 shares of 5% convertible preferred stock exercised its right to convert such shares into 154,645 share s of the Company’s common stock . T he Company accrued dividends on the 5% convertible preferred stock of $0.4 million and $0.8 million during the three and six months ended June 30, 2019 and 2018 , respectively. T he Company calculated a deemed dividend of $0.1 million on the $0.4 million of accrued dividends during each of the three months ended June 30, 2019 and 2018, and $0.2 million on the $0.8 million of accrued dividends during each of the six months ended June 30, 2019 and 2018 , which is a beneficial conversion feature. The stated liquidation preference amount on the 5% convertible preferred stock totaled $33.1 million at June 30, 2019.
Common Stock
The Company’s restated certificate of incorporation authorizes the issuance of up to 400,000,000 shares of the Company’s common stock, par value $0.001 per share.
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4. Net Income per Share Attributable to Common Stockholders
Basic net income attributable to common stockholders per share is computed by dividing the net income attributable to common stockholders by the wei ghted average number of common shares outstanding for the period. Shares issued during the period are weighted for the portion of the period during which they were outstanding. Diluted net income per share is calculated in a manner consistent with basic net income per share while giving effect to all potentially dilutive common shares that were outstanding during the period. The following table summarizes the computation of basic and diluted net income per share attributable to common stockholders of the Company (in thousands, except share and per share amounts):
The amounts in the table below were excluded from the calculation of diluted net income per share, due to their anti-dilutive effect:
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5 . Debt
The Company is a party to one credit agreement (the 2015 Credit Agreement) with outstanding indebtedness in the following amount (in thousands):
Secured Term Debt
August 2015 Secured Term Debt
In August 2015, the Company entered into a secured term loan in the amount of $35.0 million with two lenders ( the “2015 Credit Agreement”). The interest rate on the loan is LIBOR plus 9.375% with a 1% floor. As of June 30, 2019 , there were five amendments to the 2015 Credit Agreement, which, among other things, have extended the maturity date and due date of principal payments under the 2015 Credit Agreement , repaid all amounts due to one of the lenders, revised terms of certain warrants issued in connection with the 2015 Credit Agreement (Note 6) , and amended certain covenants , including certain non-financial developmental milestone s that must be met by December 31, 2019 . As amended, t he key terms of the loan require mo nthly payments of interest only through December 31, 2019 , with principal payments in the amount of $750,000 payable monthly beginning on January 31, 2020. Any outstanding balance of the loan and accrued interest is required to be repaid on July 1, 2020 , the maturity date . The secured term loan is collateralized by a first priority perfected security interest in all the tangible and intangible property of the Company.
The Company entered into a sixth waiver agreement to the 2015 Credit Agreement in March 2019 under which the lenders under the 2015 Credit Agreement agreed to refrain from exercising certain rights under the 2015 Credit Agreement, including the declaration of a default and to forbear from acceleration of any repayment rights with respect to existing covenants. The report and opinion of our independent registered public accounting firm, BDO USA, LLP, for the year ended December 31, 2018 contains an explanatory paragraph regarding our ability to continue as a going concern, which is an event of default under the 2015 Credit Agreement.
The 2015 Credit Agreement contains certain developmental milestones, as well as a minimum liquidity covenant. The Company’s failure to achieve these milestones as anticipated by December 31, 2019 or its violation of its minimum liquidity covenant would constitute an event of default under the 2015 Credit Agreement. Upon an event of default, the Lender may terminate the commitments under the 2015 Credit Agreement and declare the loans then outstanding under the 2015 Credit Agreement to be due and payable in whole or in part, together with any applicable fees and accrued interest thereon. The Company considers some of these developmental milestones to be outside of its control. As a result, if an event of default arises under the Credit Agreement, the Company may need to use cash and cash equivalents on hand to fund certain repayment commitments under the 2015 Credit Agreement.
The minimum payments required on the outstanding balances of the 2015 Credit Agreement at June 30, 2019 are (in thousands):
15
The following table provides components of interest expense and other related financing costs (in thousands):
6 . Financial Instruments
Equity Issued P ursuant to Credit Agreements
In connection with the 2015 Credit Agreement (Note 5), as fees to the lenders thereunder, the Company issued warrants to purchase an aggregate of $6.3 million of the Company’s Class A units , which were exchanged for 617,651 warrants with a strike price of $10.20 per share to purchase the same number of shares of the Company’s common stock upon consummation of the Company’s IPO in August 2016 ( the “2015 Warrants”) .
As of June 30, 2019 , the exercise price of a portion of the 2015 Warrants to purchase an aggregate of 529,413 shares of the Company’s common stock wa s $3.30 per warrant share and the exercise price of the remaining 2015 Warrants to purchase an aggregate of 88,238 shares of the Company’s common stock wa s $4.50 per warrant share. Since these warrants are exercisable and are redeemable at the option of the holder upon the occurrence of, and during the continuance of, an event of default, the fair value of the warrants is recorded as a short-term liability of approximately $0.5 million at both June 30, 2019 and December 31, 2018 .
The Company used the Black-Scholes pricing model to value the warrant liability at June 30, 2019 with the following assumptions: risk-free interest rate of 1.7% , expected term of 3.2 years, expected volatility of 73.4% and a dividend rate of 0% . The change in fair value of the warrants was approximately $(0.3) million and $(0.1) million for three and six months ended June 30, 2019 , respectively , and approximately $ (0.2) million and $0.1 million for the three and six months ended June 30, 2018, respectively . None of these instruments have been exercised as of June 30, 2019 and December 31, 2018 .
Other Warrants
In connection with a sale of common stock by the Company in March 2017, warrants to purchase 2,707,138 shares of common stock were issued at an exercise price of $4.50 per share. During April 2018, warrants to purchase 119,047 shares of common stock were exercised for which the Company received proceeds of $0.5 million. The remaining 2,588,091 warrants expired in April 2018. These warrants included a cash settlement option requiring the Company to record a liability for the fair value of the warrants at the time of issuance and at each reporting period with any change in the fair value reported as other income or expense. The change in the fair value of these warrants was $(0.3) mil lion and $(0.7) million for the three and six months ended June 30, 2018, respectively. As these warrants expired in April 2018, no change in fair value was recorded for the se warrants i n 2019.
Fair Value of Long- term Debt
The Company maintained a long-term secured debt balan c e of $23.2 million and $27.5 million at June 30, 2019 and December 31, 2018 , respectively. As the secured debt becomes due on July 1, 2020 and monthly principal payments of $750,000 will become due starting January 31, 2020, it has been recorded as long-term secured debt at December 31, 2018 . At June 30, 2019 , $4 . 5 million of principal payments due in the first and second quarter of 2 020 have been recorded as short- term secured debt and the remaining balance is recorded as long-term secured debt . The underlying agreements for these balances were negotiated with third parties on an arms-length basis , at an interest rate which is considered to be i n line with overall market conditions. Based on these factors , management considers the carrying value of the debt to approximate fair value at June 30, 2019 .
16
Fair Value Classification
The Company held certain liabilities that are required to be measured at fair value on a recurring basis. Fair value guidance establishes a three-tier fair value hierarchy, which prioritizes the inputs used in measuring fair value. These
tiers include:
|
· |
|
Level 1—Quoted prices in active markets for identical assets or liabilities. |
|
· |
|
Level 2—Inputs other than Level 1 that are observable, either directly or indirectly, such as quoted prices for similar assets or liabilities; quoted prices in markets that are not active; or other inputs that are observable or can be corroborated by observable market data for substantially the full term of the assets or liabilities. |
|
· |
|
Level 3—Unobservable inputs that are supported by little or no market activity and that are significant to the fair value of the assets or liabilities. |
The table below represents the values of the Company’s financial instruments at June 30, 2019 and December 31, 2018 (in thousands):
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Fair Value Measurement Using Significant Other Observable Inputs (Level 2) |
||||
|
|
June 30, |
|
December 31, |
||
Description |
|
2019 |
|
2018 |
||
Warrants |
|
$ |
468 |
|
$ |
524 |
Total |
|
$ |
468 |
|
$ |
524 |
The table below represents a roll -forward of Level 2 financial instruments from January 1, 2018 to June 30, 2019 (in thousands):
The Level 2 inputs used to value the Company’s financial instruments were determined using prices that can be directly observed or corroborated in active markets. Although the fair value of this obligation is calculated using the observable market price of the Company’s common stock, an active market for this financial instrument does not exist and therefore the Company has classified the fair value of this liability as a Level 2 liability in the table above.
Warrants Outstanding
The following table summarizes information about warrants outstanding at June 30, 2019 and December 31, 2018:
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Warrants |
|
Weighted Average
|
|
Balance, December 31, 2018 |
|
11,999,852 |
|
$ |
5.97 |
Granted |
|
— |
|
|
— |
Exercised |
|
— |
|
|
— |
Forfeited |
|
— |
|
|
— |
Balance, June 30, 2019 |
|
11,999,852 |
|
$ |
5.97 |
17
7 . Inventories
Inventories are stated at the lower of cost or n et realizable value (on a first-in, first- out basis) using standard costs. Standard costs include an allocation of overhead rates, which include those costs attributable to managing the supply chain and are evaluated regularly. Variances are expensed as incurred.
The Company regularly reviews the expiration dates of its inventories and maintains a reserve for inventories that are probable to expire before shipment. Inventories recorded on the Company’s consolidated balance sheets are net of a reserve for expirable inventory of $3.0 million and $2.2 million at June 30, 2019 and December 31, 2018 , respectively. The Company expensed inventory that it believes will not be sold prior to reaching its expiration date totaling $0.9 million during each of the three and six months ended June 30, 2019, and $0.1 million and $0.2 million during the three and six months ended June 30, 2018 , respectively . If the amount and timing of future sales differ from management’s assumptions, adjustments to the estimated inventory reserves may be required.
Inventories Produced in Preparation for Product Launches
The Company capitalizes inventories produced in preparation for product launches sufficient to support estimated initial market demand. Typically, capitalization of such inventory begins when positive results have been obtained for the clinical trials that the Company believes are necessary to support regulatory approval, uncertainties regarding ultimate regulatory approval have been significantly reduced and the Company has determined it is probable that these capitalized costs will provide some future economic benefit in excess of capitalized costs. The material factors considered by the Company in evaluating these uncertainties include the receipt and analysis of positive clinical trial results for the underlying product candidate, results from meetings with the relevant regulatory authorities prior to the filing of regulatory applications and the compilation of the regulatory application. The Company closely monitors the status of each product within the regulatory approval process, including all relevant communication with regulatory authorities. If the Company is aware of any specific material risks or contingencies other than the normal regulatory review and approval process or if there are any specific issues identified relating to safety, efficacy, manufacturing, marketing or labeling, the related inventory would generally not be capitalized.
For inventories that are capitalized in preparation of product launch, anticipated future sales, expected approval date and shelf lives are evaluated in assessing realizability. The shelf life of a product is determined as part of the regulatory approval process; however , in evaluating whether to capitalize pre-launch inventory production costs, the Company considers the product stability data of all of the pre-approval production to date to determine whether there is adequate expected shelf life for the capitalized pre-launch production costs.
The Company has concluded that KD034, its generic version of trientine hydrochloride, is commercially viable since it is the chemical equivalent of the original drug approved by the U.S. Food and Drug Administration (“FDA”). T he Company has submitted two Abbreviated New Drug Applications with the FDA, and determined that receiving economic benefits of the pre-launch inventory re c orded at June 30, 2019 is probable. Accordingly, the pre-launch costs are realizable as the Company expects the inventory will be sold or used prior to expiration. An assessment of likelihood that regulatory approval will not be obtained will be made at each reporting period. If at any time regulatory approval is deemed to not be probable, the inventory will be written down to its net realizable value, which is presumably zero, as the product would have no alternative future use. During the three and six months ended June 30, 2019, the Company expensed inventory that it believes will not be sold prior to reaching its expiration date totaling $0.9 million. The Company maintained $0.2 million and $0.9 million of work-in-process inventory related to KD034 at June 30, 2019 and December 31, 2018 , respectively.
Inventories are comprised of the following (in thousands):
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
June 30, |
|
December 31, |
||
|
|
2019 |
|
2018 |
||
Raw materials |
|
$ |
— |
|
$ |
— |
Work-in-process |
|
|
183 |
|
|
886 |
Finished goods, net |
|
|
45 |
|
|
39 |
Total inventories |
|
$ |
228 |
|
$ |
925 |
18
8. Leases
On January 1, 2019, the Company adopted ASC 842 using the modified retrospective transition app roach allowed under ASU 2018-11, “Leases (Topic 842: Targeted Improvements”), which releases companies from presenting comparative periods and related disclosures under ASC 842 and requires a cumulative-effect adjustment to the opening balance of retained earnings in the period of adoption (Note 2) . The Company is party to six operating leases for of fice or laboratory space and three finance leases for office IT equipment . The Company’s finance leases are immaterial both individually and in the aggregate. The Company has elected to apply the short-term lease exception to all leases of one year or less. As of June 30, 2019 , this exception applied to two operating leases for office space, which are each for a term of one year. Further, the Company has applie d the guidance in ASC 842 to its corporate offic e and laboratory leases and has determined that these should be classified as operating leases. Consequently, as a result of the adoption of ASC 842, the Company recognized a ROU lease asset of approximately $22.7 million with a corresponding lease liability of approximately $27.0 million based on the present value of the minimum rental payments of such leases. In accordance with ASC 842, the beginning balance of the ROU lease asset was reduced by the existing deferred rent liability at inception of approximately $4.3 million. In the consolidated balance sheets at June 30, 2019, the Company has a ROU asset balance of $21.2 million and a current and non-current lease liability of $3.8 million and $21.7 million, respectively, relating to the ROU lease asset. The balance of both the ROU lease asset and the lease liabilities primarily consists of future payments under the Company’s office lease in New York, New York.
The Company is party to an operating lease in New York, New York for office and laboratory space for its headquarters. The lease commenced in October 2010 , its initial term is set to expire in February 2021 , and the Company opened a secured letter of credit with a third party financial institution in lieu of providing a security deposit of $2.0 million , which letter of credit is included in restricted cash at June 30, 2019. As of June 30, 2019, there were six amendments to this lease agreement, which altered office and laboratory capacity and extended the lease term through October 2025, with total lease cost of $1.1 million and $2.3 million for the three and six months ended June 30, 2019, respectively. This office lease contains the ability to extend portions of the lease at fair market value but does not have any renewal options.
The Company is party to an operating lease in Warrendale, Pennsylvania for the Company’s special ty-focused commercial operation . In March 2019, the Company entered into an amendment to this lease , which extended the lease term to September 30, 2022, with two five -year renewal options , which would extend the term to September 30, 2032, if exercised. Rental payments under the renewal period would be at market rates determined from the average rentals of similar tenants in the same industrial park. The option to renew this office lease was not considered when assessing the value of the ROU asset because the Company was not reasonably certain that it would assert its option to renew the lease. Total lease cost for this lease was $0.1 million and $0.3 million for the three and six months ended June 30, 2019, respectively.
In August 2015, the Company entered into an operating office lease agreeme nt in Cambridge, Massachusetts for the Company’s clinical office effective January 2016 and expiring in April 2023. The Company opened a secured letter of credit with a third party financial institution in lieu of providing a security deposit of $0.1 million, which letter of credit is included in restricted cash at June 30, 2019. The Company is also party to an operating lease for laboratory space in Princeton, N ew Jersey , which expires in February 2021. Neither of these office leases contain any renewal options. Total lease cost for these leases was $0.1 million and $0.2 million for the three and six months ended June 30, 2019, respectively.
19
Quantitative information regarding the Company’s leases for the three and six months ended June 30, 2019 is as follows (in thousands) :
|
(a) |
|
Includes short-term lease costs and finance lease costs, which are immaterial. |
|
(b) |
|
Includes sublease income related to MeiraGTx (Note 11) . |
Future lease payments under noncancellable leases are as follows (in thousands) at June 30, 2019:
Note: As most of the Company’s leases do not provide an implicit rate, the Company use s its incremental borrowing rate based on the information available at commencement date in determining the present value of lease payments. The Company uses the incremental borrowing rate on January 1, 2019 for operating leases that commenced prior to that date .
Future minimum rental payments under noncancellable leases are as follows (in thousands) at December 31, 2018:
|
|
|
|
|
|
|
|
Year ending December 31, |
|
Amount |
|
2019 |
|
$ |
4,672 |
2020 |
|
|
4,204 |
2021 |
|
|
4,177 |
2022 |
|
|
4,286 |
2023 |
|
|
4,153 |
Thereafter |
|
|
7,731 |
Total |
|
$ |
29,223 |
20
9. Fixed Assets
Fixed assets consisted of the following (in thousands):
Depreciation and amortization of fixed assets totaled $0.9 million and $0.7 million for the six months ended June 30, 2019 and 2018 , respectively , and $0.4 million for each of the three months ended June 30, 2019 and 2018. Unamortized computer software costs were $0.5 million and $0.7 million at June 30, 2019 and December 31, 2018 , respectively . The amortization of computer software costs amounted to $0.2 million and $0.1 million for the six months ended June 30, 2019 and 2018 , respectively, and $0.1 million for each of the three months ended June 30, 2019 and 2018.
10. Goodwill
The Company’s goodwill relates to the 2010 acquisition of Kadmon Pharmaceuticals , LLC , a Pennsylvania limited liability company that was formed in April 2000. There were no changes in the carrying amount of goodwill for the six months ended June 30, 2019 or the year ended December 31, 2018 .
11. Investment in MeiraGTx
On June 12, 2018, MeiraGTx completed its initial public offering (the “MeiraGTx IPO”) whereby it sold 5,000,000 shares of common stock at an initial public offering price of $15.00 per share. MeiraGTx, a limited company under the laws of the Cayman Islands, is a clinical-stage biotech nology company developing novel gene therapy treatments for a wide range of inherited and acquired disorders for which there are no effective treatments available. The shares began trading on the Nasdaq Global Select Market on June 7, 2018 under the symbol “MGTX.”
Prior to the MeiraGTx IPO, for the period beginning January 1, 2018 through June 12, 2018, the Company recorded its share of MeiraGTx’s net loss under the equity method of accounting of $1.2 million. T he Company had no remaining basis in any of the investments held in MeiraGTx prior to the MeiraGTx IPO . Upon completion of the MeiraGTx IPO, the Company’s investment was diluted to a 13.0% ownership in MeiraGTx common stock and the Company no longer had the ability to exert significant influence over MeiraGTx. The Company discontinued the equ ity method of accounting for its investment in MeiraGTx on June 12, 2018 and determined that the remaining investment was an equity security accounted for in accordance with ASC 321 , Investments – Equity Securities, at the date th e investment no longer qualified for the equity method of accounting. ASC 321 requires the investment to be recorded at cost, less any impairment, plus or minus changes resulting from observable price changes in orderly transactions for the identical or similar investment of the same issuer. As the Company’s investm ent in MeiraGTx common stock had a readily determinable market value, the Company recorded an unrealized gain of $40.5 million for the three and six months ended June 30, 2018 related to the fair value of its ownership of common stock of MeiraGTx. As of June 30, 2019 and December 31, 2018, the Company maintained a 10.6% and 12.9% ownership , respectively, in the common stock of MeiraGTx with a fair value of $95.0 million and $34.1 million , respectively, recorded as a noncurrent in vestment in equity securities since depending on certain circumstances, the Company may, at times, be deemed to be an affiliate of MeiraGTx. The Company has recorded an unrealized gain on the MeiraGTx common stock investment of $34.1 million and $60.9 million for the three and six months ended June 30, 2019 , respectively. The investment in MeiraGTx is valued using Level 1 inputs , which includes quoted price s in active markets for identic al assets in accordance with the fair value hierarchy (Note 6). The Company has not realized any gains related to the investment in common stock of MeiraGTx.
21
The Company was party to a TSA with MeiraGTx , which expired in April 2018. Upon expiration of the TSA, the Company continued to provide office space to MeiraGTx. On October 1, 2018, the Company and MeiraGTx entered into a sublease agreement , which is effective from October 1, 2018 for a period of two months and is automatically renewed on a monthly basis unless MeiraGTx provides 30 days ’ prior written notice. The Company’s accounting for this sublease as a lessor was not impacted by the adoption of the new leasing standard ASC 842 (Note 2). As part of the TSA and sublease agreement with MeiraGTx, the Company recognized $0.2 million and $0.3 million to other revenue during each of the three and six months ended June 30, 2019 and 2018 . The Company received cash payments of $0.3 million and $1. 1 million, respectively, from MeiraGTx for the six months ended June 30, 2019 and 2018 . The Company ha d no amounts receivable from MeiraGTx at June 30, 2019 or December 31, 2018.
1 2 . License Agreements
The Company has entered into several license agreements for products currently under devel opment. The Company’s license agreements are disclosed in the audited financial statements included in Item 8 of its Annual Report on Form 10-K for the year ended December 31, 2018 . Since the date of such financial statements, there have been no significant changes to the Company’s license agreements.
Contingent License Agreement Milestones
The Company may be obligated in future periods to make additional payments, which would become due and payable only upon the achievement of certain research and development, regulatory and approval milestones. The specific timing of such milestones cannot be predicted and depends upon future discretionary clinical developments as well as regulatory agency actions which cannot be predicted with certainty (including action which may never occur). These additional contingent milestone payments aggregate to $215.9 million at June 30, 2019 . Any payments made prior to FDA approval will be expensed as research and development. Payments made after FDA approval will be capitalized.
Further, under the terms of certain licensing agreements, the Company may be obligated to pay commercial milestones contingent upon the realization of sales revenues and subli cense revenues. Due to the long- range nature of such commercial milestones, they are neither probable at this time nor predictable, and consequently are not included in the additional contingent milestone payment amount.
13. Share-based Compensation
2016 Equity Incentive Plan
A total of 11,668,905 shares of the Company’s common stock were authorized and reserved for issuance under the Company’s 2016 Equity Incentive Plan, as amended (the “2016 Equity Plan”) at December 31, 2018. This reserve automatically increased to 16,194,138 on January 1, 2019 and will automatically increase each subsequent anniversary through January 1, 2025, by an amount equal to the smaller of (a) 4% of the number of shares of common stock issued and outstanding on the immediately preceding December 31, or (b) an amount determined by the Company’s board of directors. At June 30, 2019, there were options to purchase an aggregate of 10,578,920 shares of common stock outstanding at a weighted average price of $5.80 per share under the 2016 Equity Plan.
Total unrecognized compensation expense related to unvested options granted under the Company’s share-based compensation plan was $5.7 million and $6.8 million at June 30, 2019 and December 31, 2018, respectively. That expense is expected to be recognized over a weighted average period of 1.3 years and 1.5 years as of June 30, 2019 and December 31, 2018, respectively. The Company recorded share-based compensation expense under the 2016 Equity Plan of $ 4.1 million and $5.6 million for the six months ended June 30, 2019 and 2018, respectively, and $1.9 million and $3.0 million for the three months ended June 30, 2019 and 2018, respectively.
22
The following table summarizes information about stock options outstanding, not including performance stock options, at June 30, 2019 and December 31, 2018:
The aggregate intrinsic value in the table above represents the total pre-tax intrinsic value calculated as the difference between the fair value of the Company’s common stock at June 30, 2019 ( $2.06 per share) and the exercise price, multiplied by the related in-the-money options that would have been received by the option holders had they exercised their options at the end of the period. This amount changes based on the fair value of the Company’s common stock. There were no options exercised during the six months ended June 30, 2019 and 2018.
There were 1,293,973 stock options granted during the six months ended June 30, 2019 with a weighted-average exercise price of $2.25 . During the six months ended June 30, 2018, 80,924 stock options were granted with a weighted ‑average exercise price of $7.75 . The fair value of each stock option award, not including performance stock options, was estimated at the date of grant using the Black-Scholes option-pricing model and the assumptions noted in the following table:
Performance Awards
On April 3, 2018 , the Company granted 1,597,500 nonqualified performance-based stock options ( the “Performance Options”) to certain executive officers (each, a “Grantee”) under the 20 16 Equity Plan, which represent the maximum number of Performance Options that may be earned if all three performance milestones (each, a “Performance Goal”) are achieved during the three -year period following the g rant d ate (the “Performance Period”). The Performance Options may be earned based on the achievement of three separate Performance Goals related to the Company’s operating and research and development activities during the Performance Period, subject to the Grantee’s employment through the achievement date. If no Performance Goals are achieved during the Performance Period, the Performance Options will be forfeited. Each Performance Option was granted with an exercise price of $4.06 per share and does not contain any voting rights. No other Performance Options have been granted under the 2016 Equity Plan.
The weighted-average fair value of the Performance Options granted was $2.71 and was estimated at the date of grant using the Black-Scholes option-pricing model with the following assumptions: risk-free interest rate of 2.67% , expected term of 6.0 years, expected volatility of 74.50% and a dividend rate of 0% .
Compensation expense for the Performance Options is recognized on a straight-line basis over the awards’ requisite service period. The Performance Options vest upon the satisfaction of both a service condition and the satisfaction of one or more performance conditions, therefore the Company initially determined which outcomes are probable of achievement. The Company believes that the three-year service condition (explicit service period) and all three performance conditions (implicit service periods) will be satisfied. The requisite service period would be three years as that is the longest period of both the explicit service period and the implicit service periods. The first two performance conditions were satisfied during 2018 and the third performance condition is expected to be satisfied in the third quarter of 2019.
23
During the year ended December 31, 2018, 307,500 Performance Options were forfeited. A total of 1,290,000 Performance Options are outstanding at both June 30, 2019 and December 31, 2018 with an exercise price of $4.06 per share and no intrinsic value. The weighted average remaining contractual life of outstanding Performance Options at June 30, 2019 was 8.8 years. At June 30, 2019, there was $0.9 million of total unrecognized compensation expense related to unvested Performance Options, which is expected to be recognized over a weighted-average period of 1.5 years. As of June 30, 2019, 430,002 Performance Options had vested and became exercisable during the second quarter of 2019 in accordance with the terms of the awards.
S tock Appreciation Rights
A total of 835,000 stock appreciation rights (“SARs”) were outstanding at both June 30, 2019 and December 31, 2018, with an exercise price of $3.64 per share and no intrinsic value. The weighted average remaining contractual life of outstanding SARs at June 30, 2019 was 8.5 years. Compensation expense for SARs is recognized on a straight-line basis over the awards’ requisite service period. At June 30, 2019, there was $1.0 million of total unrecognized compensation cost related to unvested SARs which is expected to be recognized over a weighted-average period of 1.4 years. At both June 30, 2019 and December 31, 2018, 278,335 SARs had vested and no SARs ha d been exercised.
2 014 Long-term Incentive Plan ( the “LTIP”)
A total of 9,750 units have been granted under the LTIP as of both June 30, 2019 and December 31, 2018. The LTIP is payable upon the fair market value of the Company’s common stock exceeding 333% of the $6.00 grant price ( $20.00 ) per share prior to December 7, 2024. The holders of the LTIP awards have no right to demand a particular form of payment, and the Company reserves the right to make payment in the form of cash or common stock. No LTIP awards were exercisable or ha d been exercised at June 30, 2019.
2016 Employee Stock Purchase Plan
A total of 2,551,180 shares of the Company’s common stock were reserved for issuance under the 2016 Employee Stock Purchase Plan, as amended (the “2016 ESPP”) at December 31, 2018. The Board elected not to increase the shares reserved for issuance under the 2016 ESPP on January 1, 2019. The Company issued 32,273 and 22,958 shares under the 2016 ESPP during the six months ended June 30, 2019 and 2018, respectively. No meaningful compensation expense was recognized for the ESPP during the six months ended June 30, 2019 and 2018.
14 . Accrued Expenses
Short- term accrued expenses at June 30, 2019 and December 31, 2018 include the following (in thousands):
Commission p ayable
The Company recorded $2.4 million in accrued liabilities at both June 30, 2019 and December 31, 2018 relating to commissions to third parties for Class E redeemable convertible unit raises during 2014 and 2015.
24
Compensation, benefits and severance
Compensation, benefits and severance represent earned and unpaid employee wages and bonus es , as well as contractual s everance to be paid to former employees . At June 30, 2019 and December 31, 2018 , these accrued expenses totaled $2.5 million and $3.8 million, respectively . A separation agreement with Dr. Samuel D. Waksal , which expired on February 8, 2019, contained severance payments and certain supplement conditional payments . The Company paid $0.1 million o f severance payments during the six months ended June 30, 2019 related to amounts accrued at December 31, 2018 and has not recorded any expense related to these conditional payments as of June 30, 2019 , as none of the conditional payments were met as of the expiration of the agreement on February 8, 2019.
Research and development
The Company has contracts with third part ies for the development of the C ompany’s product candidates. The timing of the expenses varies depending upon the timing of initiation of clinical trials and enrollment of patients in clinical trials. At June 30, 2019 and December 31, 2018 , accrued research and development expenses for which the Company has not yet been invoiced totaled $6.2 million and $4.8 million, respectively .
15 . Commitments
The Company’s commitments are disclosed in the audited financial statements included in Item 8 of the Annual Report on Form 10-K for the year ended December 31, 2018 . Since the date of such financial statements, there have been no material changes to the Company’s commitments . Further, the Company’s commitments related to lease agreements are disclosed in Note 8 .
16 . Contingencies
The Company has been subject to various legal proceedings that arise from time to time in the ordinary course of its business. Although the Company believes that the various proceedings brought against it have been without merit, and that it has adequate product liability and other insurance to cover any claims, litigation is subject to many factors which are difficult to predict and there can be no assurance that the Company will not incur material costs in the resolution of legal matters. Should the Company determine that any future obligations will exist, the Company will record expense equal to the amount which is deemed probable and estimable . The Company has no significant contingencies related to leg al proceedings at June 30, 2019 .
17 . Related Party Transactions
The Company’s related party transactions are disclosed in the audited financial statements included in Item 8 of the Annual Report on Form 10-K for the year ended December 31, 201 8 . Since the date of such financial statements, there have been no changes to the Company’s related party transactions other than those related to MeiraGTx (Note 11) .
18 . Income Taxes
The Company files a consolidated tax return for Kadmon Holdings, Inc. and its domestic subsidiaries and the required information returns for its international subsidiaries, all of which are wholly owned. Where permitted, the Company files combined state returns, but in some instances separate company returns for certain subsidiaries on a stand- alone basis are required.
Deferred income taxes reflect the net effects of temporary differences between the carrying amounts of assets and liabilities for financial reporting purposes and the amounts used for income tax purposes. The Company’s deferred tax assets relate primarily to its net operating loss (“NOL”) carryforwards and other balance sheet basis differences. In accordance with ASC 740, “Income Taxes,” the Company recorded a valuation allowance to fully offset the gross deferred tax asset, because it is more likely than not that the Company will not realize future benefits associated with these deferred tax assets at June 30, 2019 and December 31, 2018.
The Tax Cuts and Jobs Act (the “ Tax Act”) was enacted in December 2017. The Tax Act reduces the U.S. federal corporate tax rate from 35 percent to 21 percent, requires companies to pay a one-time transition tax on earnings of certain foreign subsidiaries that were previously tax deferred, creates new taxes on certain foreign earnings and reduces the orphan drug tax credit. In accordance with the Tax Act, the Company determined it necessary to reduce the recorded deferred tax liability by $0.6 million during the six months ended June 30, 2018 to allow naked credit deferred tax liabilities to be used as a source of taxable income in the future. This change in deferred tax liability was recognized as income tax benefit in the consolidated financial statements of operations for the three and six months ended June 30, 2018. T here was no change in
25
deferred tax liability f or the three and six months ended June 30, 2019 and no income tax expense was recorded for the three and six months ended June 30, 2019 .
At December 31, 2018, the Company ha d unused federal and state NOL carry forwards of $460.3 million and $404.3 million, respectively, that may be applied against future taxable income. The Company has fully reserved the deferred tax asset related to these NOL carry forwards as reflected in its consolidated financial statements. These carry forwards expire at various dates through December 31, 2037, with the exception of approximately $44.0 million of federal NOL carry forwards that will not expire. The 20- year limitation was eliminated for losses generated after January 1, 2018, giving the taxpayer the ability to carry forward losses i ndefinitely. However, NOL carry forward s arising after January 1, 2018, will now be limited to 80 percent of taxable income.
Th e use of the Company’s NOL carry forwards may, however, be subject to limitations as a result of an ownership change. A corporation undergoes an “ownership change,” in general, if a greater than 50% change (by value) in its equi t y ownership by one or more five- percent stockh olders (or certain groups of non-five- pe rcent stockholders) over a three - year period occurs. After such an ownership change, t he corporation’s use of its pre-change NOL carry forwards and other pre- change t a x attributes to offset its post- change income is subject to an annual limitation determined by the equity value of the corporation on the date the ownership change occurs multiplied by a rate determined monthly by the Internal Revenue Service. This rate for April 2019 equals 2. 20 percent. The Company experienced ownership changes under Section 382 of the Internal Revenue Code of 1986, as amended, in 2010, 2011 and 2016, but the Company did not reduce the gross deferred tax assets related to the NOL carry forwards because the limitations do not hinder the Company’s ability to potential ly utilize all of the NOL carry forwards.
The Company is likely to experience another ownership change in the future, possibly in 2019, as a result of shifts in stock ownership due to any future equity offerings. A renewed ownership change will likely materially and substantially reduce the Company’s ability to fully utilize the NOL carry forwards and, consequently, will likely reduce the gross deferred tax assets related to the NOL carry forwards. If an ownership change occurred and if the Comp any earned net taxable income, its ability to use the pre- change NOLs to offset U.S. federal taxable income would be subject to these limitations, which could potentially result in increased future tax liability compared to the tax liability the Company would incur if the use of NOL carr y forwards were not so limited.
26
I tem 2. Management’s Discussion and Analysis of Financial Condition and Results of Operations.
You should read the following discussion and analysis of our financial condition and results of operations together with our financial statements and related notes appearing in this Quarterly Report on Form 10-Q and t hose in included in Item 8 of our Annual Report on Form 10-K for the year ended December 31, 2018. Some of the information contained in this discussion and analysis or set forth elsewhere in this Quarterly Report, including information with respect to our plans and strategy for our business and related financing, includes forward-looking statements that involve risks and uncertainties. As a result of many factors, including those factors set forth in t his report and our most recent Annual Report on Form 10-K , our actual results could differ materially from the results described in, or implied by, the forward-looking statements contained in the following discussion and analysis.
Overview
We are a fully integrated biopharmaceutical company engaged in the discovery, development and commercialization of small molecules and biologics to address significant u nmet medical needs, with a near- term clinical focus on autoimmune, inflammatory and fibrotic diseases. Our team, which has a proven track record of successful drug development and commercialization, identifies and develops novel candidates from our small molecule and biologics platf orms as well as develops our in- licensed product candidates. By retaining global commercial rights to our lead product candidates, we believe that we have the ability to progress these candidates ourselves while maintaining flexibility for commercial and licensing arrangements . We expect to continue to progress our clinical candidates and have further clinical trial data to report in the second half of 2019 and in 2020 .
Our operations to date have been focused on developing first-in-class innovative therapies for indications with significant unmet medical needs while leveraging our commercial infrastructure. We have never been profitable and had an accumulated deficit of $257.9 million at June 30, 2019. Our net income was $9.2 million and $12.8 million for the three and six months ended June 30, 2019, respectively, and $21.5 million and $1.1 million for the three and six months ended June 30, 2018, respectively. Our net inc ome for each of these periods was primarily driven by non-cash unrealized gains related to our investment in MeiraGTx common stock.
Although our commercial business generates revenue, the revenues generated for the three and six months ended June 30, 2019 and 2018 were not significant, and we expect to incur significant losses for the foreseeable future and expect these losses to increase as we continue our development of, and seek regulatory approvals for, our additional product candidates, hire additional personnel and initiate commercialization of any products that receive regulatory approval. We anticipate that our expenses will increase substantially if, or as, we:
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invest significantly to further develop our most advanced product candidates; |
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initiate clinical trials and preclinical studies for our other product candidates; |
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seek regulatory approval for any of our product candidates that successfully complete clinical trials; |
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continue to invest in our research discovery platforms; |
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seek to identify and develop additional product candidates; |
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scale up our sales, marketing and distribution infrastructure and product sourcing capabilities; |
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acquire or in-license other product candidates and technologies; |
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scale up our operational, financial and management information systems and personnel, including personnel to support our product development; |
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make milestone or other payments under any in-license agreements; or |
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maintain , expand and protect our intellectual property portfolio. |
27
Components of Statement of Operations
Revenue
Our revenue is substantially derived from sales of our portfolio of products, including ribavirin and tetrabenazine. We also recognize service revenue from our TSA and sublease agreement with MeiraGTx.
Cost of Sales
Cost of sales consists of product costs, including ingredient costs and costs of contract manufacturers for production, and shipping and handling of the products. Also included are costs related to quality release testing and stability testing of the products. Other costs included in cost of sales are packaging costs, warehousing costs and certain allocated costs re lated to management, facilities and other expenses associated with supply chain logistics.
Research and Development Expenses
Research and development expenses consist primarily of costs incurred for the development of our product candidates, which include:
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license fees related to the license and collaboration agreements; |
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research and development-based employee- related expenses, including salaries, benefits, travel and other compensation expenses; |
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expenses incurred under our agreements with contract rese arch organizations that conduct nonclinical and preclinical studies, and clinical sites and consultants that conduct our clinical trials; |
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costs associated with regulatory filings; |
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costs of laboratory supplies and the acquisition, development and manufacture of preclinical and clinical study m aterials and study drugs; and |
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allocated facility-related expenses. |
Our research and development expenses may vary substantially from period to period based on the timing of our research and development activities, including due to timing of initiation of clinical trials and enrollment of patients in clinical trial s. We do not allocate personnel- related costs, including share - based compensation, costs associated with broad technology platform improvements and other indirect costs to specific product candidates. We do not allocate these costs to specific product candidates because they are deployed across multiple overlapping projects under development, making it difficult to specifically and accurately allocate such costs to a particular product candidate.
The successful development of our product candidates is highly uncertain and subject to numerous risks , including, but not limited to:
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the scope, rate of progress and expense of our research and development activities; |
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clinical trial results; |
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the scope, terms and timing of regulatory approvals; |
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the expense of filing, prosecuting, defending and enforcing patent claims and other intellectual property rights; |
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the cost, timing and our ability to acquire sufficient clinical and commercial supplies for any product candidates and prod ucts that we may develop; and |
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the risks disclosed in this report and our most recent Annual Report on Form 10-K . |
A change in the outcome of any of these variables could mean a significant change in the expenses and timing associated with the development of any product candidate.
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Selling, G eneral and Administrative E xpenses
Selling, general and administrative expenses consist primarily of sa laries and related costs for non- res earch personnel, including stock- based compensation and travel expenses for our employees in executive, operational, finance, legal, commercial, regulatory, pharmacovigilance and human resource functions. Other selling, general and administ rative expenses include facility- related costs, business insurance, director compensation, accounting and legal services, consulting costs and programs and marketing costs to s upport the commercial business.
O ther Income (E xpense)
Other income (expense) comprises interest income earned on cash and cash equivalents and restricted cash and interest expense on our outstan ding indebtedness, including non- cash interest related to the amortization of debt discount, debt premium and deferred financing costs associated with our indebtedness. Our loss on equity method investment in MeiraGTx, as well as gains and losses arising from changes in fair value of our common stock ownership in MeiraGTx are recognized in other income (expense) in the consolidated statements of operations. Changes in the fair value of financial instruments , based upon the fair value of the underlying security at t he end of each reporting period as calculated using th e Black- Scholes option pricing model, are also recognized in other income (expense). Such financial instruments include warrant liabilities for which cash settlement features exist.
In addition, we operate in currencies other than the U.S. dollar to fund certain research and development and commercial activ ities performed by various third- party vendors. The translation of these currencies into U.S. dollars results in foreign currency gains or losses, depending on the change in value of these currencies against the U.S. dollar. These gains and losses are included in other income (expense).
I ncome T axes
We file a consolidated tax return for Kadmon Holdings, Inc. and its domestic subsidiaries and the required information returns for its international subsidiaries, all of which are wholly owned. Where permitted, we file combined state returns, but in some instances separate company returns for certain subsidiaries on a stand alone basis are required. At both June 30, 2019 and December 31, 2018 , we had a deferred tax liability of $ 0.4 million and a full valuation allowance for our deferred tax assets.
Critical Accounting Policies and Significant Judgments and Estimates
Management’s discussion and analysis of our financial condition and results of operations is based on our financial statements, which have been prepared in accordance with accounting principles generally accepted in the United States of America (“GAAP”). The preparation of these consolidated financial statements requires us to make estimates and judgments that affect the reporting amounts of assets, liabilities and expenses and the disclosure of contingent assets and liabilities in our financial statements. On an ongoing basis, we evaluate our estimates and judgments, including those related to investments, goodwill, fair value of financial instruments, share- based compensation and accrued expenses. We base our estimates on historical experience, known trends and events and various other factors that we believe to be reasonable under the circumstances, the results of which form the basis for making judgments about the carrying value of assets and liabilities that are not readily apparent from other sources. Actual results may differ from these estimates under different assumptions or conditions.
Critical A ccounting P olicies
The Company’s significant accounting policies are disclosed in the audited financial statements for the year ended December 31, 2018 included in the Company’s Annual Report on Form 10-K filed on March 7 , 201 9 with the Securities Exchange Commission (“SEC”). Since the date of such financial statements, there have been no changes to the Company’s significant accounting policies except for the change in lease accounting upon adoption of ASC 842 (See Note 2 and Note 8 to our unaudited consolidated financial statements included elsewhere in this Quarterly Report on Form 10-Q ).
Recent Accounting Pronouncements
See Note 2 of the notes to our unaudited consolidated financial statements included elsewhere in this Quarterly Report on Form 10-Q for a summary of recently issued and adopted accounting pronouncements.
29
Results of Operations
Three and Six Months Ended June 30, 2019 and 2018
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Three Months Ended |
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Six Months Ended |
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June 30, |
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June 30, |
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2019 |
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2018 |
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2019 |
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2018 |
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(unaudited) |
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(unaudited) |
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(in thousands) |
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(in thousands) |
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Revenues |
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Net sales |
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$ |
47 |
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$ |
161 |
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$ |
114 |
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$ |
435 |
Other revenue |
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|
179 |
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|
198 |
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|
353 |
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|
357 |
Total revenue |
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226 |
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|
359 |
|
|
467 |
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|
792 |
Cost of sales |
|
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45 |
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103 |
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|
76 |
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302 |
Write ‑ down of inventory |
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|
932 |
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98 |
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|
932 |
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245 |
Gross profit |
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(751) |
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158 |
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(541) |
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245 |
Operating expenses: |
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Research and development |
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15,108 |
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10,178 |
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30,099 |
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19,958 |
Selling, general and administrative |
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8,981 |
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8,812 |
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16,927 |
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17,062 |
Total operating expenses |
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24,089 |
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18,990 |
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47,026 |
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37,020 |
Loss from operations |
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(24,840) |
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(18,832) |
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(47,567) |
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(36,775) |
Total other income |
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34,000 |
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39,775 |
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60,319 |
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37,277 |
Income tax benefit |
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— |
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|
562 |
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— |
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|
562 |
Net income |
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$ |
9,160 |
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$ |
21,505 |
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$ |
12,752 |
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$ |
1,064 |
Deemed dividend on convertible preferred stock |
|
|
508 |
|
|
491 |
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|
1,023 |
|
|
981 |
Net income attributable to common stockholders |
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$ |
8,652 |
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$ |
21,014 |
|
$ |
11,729 |
|
$ |
83 |
Revenues
Total revenue decreased by 37.0% , or approximately $0.2 million, from $0.4 million for the three months ended June 30, 2018 to $0.2 million for the three months ended June 30, 2019 . The decrease in total revenue was primarily attributable to a decline in sales of tetrabenazine of $0.1 million for the three months ended June 30, 2018 as compared to the three months ended June 30, 2019 . Total revenue also included service and sublease revenue from MeiraGTx of $0.2 million for each of the three months ended June 30, 2019 and 2018 .
Total revenue decreased by 41.0% , or approximately $0.3 million, from $0.8 million for the six months ended June 30, 2018 to $0.5 million for the six months ended June 30, 2019 . The decrease in total revenue was primarily attributable to the decline in sales of tetrabenazine from $0.3 million for the six months ended June 30, 2018 to $0.1 million for the six months ended June 30, 2019 . Total revenue also included service and sublease revenue from MeiraGTx of $0.3 million for each of the six months ended June 30, 2019 and 2018 .
Cost of sales and write-down of inventory
Cost of sales was less than $0.1 million for each of the three months ended June 30, 2019 and 2018 , and $0.1 million and $0.3 million for the six months ended June 30, 2019 and 2018 , respectively. We recognized $0.9 million of inventory write-downs during each of the three and six months ended June 30, 2019 of our pre-launch KD034 inventory based on our expectation that such inventory will not be sold prior to reaching its product expiration date. We recognized $0.1 million and $0.2 million of inventory write-downs during the three and six months ended June 30, 2018 , respectively, of our Ribasphere inventory based on our expectation that such inventory will not be sold prior to reaching its product expiration date.
Research and development expenses
Research and development expenses increased by 48.4% , or approximately $4.9 million, to $15.1 million for the three months ended June 30, 2019 from $10.2 million for the three months ended June 30, 2018 . The increase in research and development expense for the three months ended June 30, 2019 as compared to the three months ended June 30, 2018 was primarily related to development of the Company’s most advanced product candidate KD025, as well as the development of KD033 and KD045.
30
Research and development expenses increased by 50.8% , or approximately $10.1 million, to $30.1 million for the six months ended June 30, 2019 from $20.0 million for the six months ended June 30, 2018 . The increase in research and development expense for the six months ended June 30, 2019 as compared to the six months ended June 30, 2018 was primarily related to development of the Company’s most advanced product candidate , KD025 , as well as the development of KD033 and KD045.
Selling, general and administrative expenses
Selling , general and administrative expenses remained generally consistent for the three and six months ended June 30, 2019 as compared to the three and six months ended June 30, 2018. Selling, general and administrative expenses increased by 1.9% , or approximately $0.2 million, to $9.0 million for the three months ended June 30, 2019 from $8.8 million for the three months ended June 30, 2018 , while s elling, general and administrative expenses decreased by 0.8% , or approximately $0.1 million, to $16.9 million for the six months ended June 30, 2019 from $17.1 million for the six months ended June 30, 2018 .
Total o ther income
The following table provides components of other income:
For the three and six months ended June 30, 2019 , other income consisted primarily of unrealized gains related to our investment in MeiraGTx common stock of $34.1 million and $60.9 million, respectively, and interest income of $0.5 million and $1.2 million, respectively, partially offset by a change in the fair value of financial instruments of $0.3 million and $0.1 million, respectively , and interest expense and other costs related to our debt of $0.9 million and $1.9 million, respectively.
For the three and six months ended June 30, 2018, other income consisted primarily of a change in the fair value of financial instruments of $0.5 million and $0.6 million, respectively, and unrealized gains related to our investment in MeiraGTx common stock of $40.5 million for each of the three and six months ended June 30, 2018, partially offset by interest expense and other costs related to our debt of $1.3 million and $2.8 million for the three and six months ended June 30, 2018, respectively.
Income tax benefit
No income tax expense was recorded for the three and six months ended June 30, 2019 . The Tax Cuts and Jobs Act (the “ Tax Act”) was enacted in December 2017. In accordance with the Tax Act, the Company determined it necessary to reduce the recorded deferred tax liability by $0.6 million during the second quarter of 2018 to allow naked credit deferred tax liabilities to be used as a source of taxable income in the future. The change in deferred tax liability has been recognized as income tax benefit in the consolidated financial statements of operations for the three and six months ended June 30, 2018.
31
Deemed dividend
We have 28,708 shares of 5% convertible preferred stock outstanding , which accrue divide nds at a rate of 5% and convert into shares of our common stock at a 20% discount to the initial public offering price per share of common stock in the Company’s IPO of $12.00 per share . In May 2019, the holders of 1,292 shares of 5% convertible preferred stock exercised their right to convert the ir convertible preferred shares into 154,645 shares of the Company’s common stock . T he Company accrued dividends on the 5% convertible preferred stock of $0.4 million and $0.8 million during the three and six months ended June 30, 2019 and 2018 , respectively. T he Company calculated a deemed dividend of $0.1 million on the $0.4 million of accrued dividends during each of the three months ended June 30, 2019 and 2018 , and $0.2 million on the $0.8 million of accrued dividends during each of the six months ended June 30, 2019 and 2018 , which is a beneficial conversion feature. The stated liquidation preference amount on the 5% convertible preferred stock totaled $33.1 million at June 30, 2019 .
Liquidity and Capital Resources
Overview
We maintained cash and cash equivalents of $86.2 million at June 30, 2019 . We had an accumulated deficit of $257.9 million and working capital of $58.9 million at June 30, 2019 . We entered into a Sales Agreement with Cantor Fitzgerald & Co. in August 2017 under which we may sell up to $40.0 million in shares of our common stock in one or more placements at prevailing market prices for our common stock (the “ATM Offering”). Any such sales would be effected pursuant to our registration statement on Form S-3 (File No. 333-222364), declared effective by the SEC on January 10, 2018. In January 2019, we sold 13,778,705 shares of common stock at a weighted average price of $2.17 per share through the ATM Offering and received total gross proceeds of $ 29.9 million ($29.0 million net of $0.9 million of commissions). In April , 2019, we sold 2, 5 38 , 1 00 shares of common stock at a price of $2. 7 0 per share through the ATM Offering and received total gross proceeds of $6. 9 million ($6. 7 million net of $0.2 million of commissions payable by us ). Our existing cash and cash equiv alents are expected to enable us to advance our Phase 2 clinical studies of KD025 and advance certain of our other pipeline product candidates and provide for other working capital purposes.
Our plans include continuing to finance operations through the issuance of additional equity securities , monetization of assets and increasing our commercial portfo lio through the development of our current pipeline or through strategic collaborations. Any transactions which occur may contain covenants that restrict the ability of our management to operate the business or may have rights, preferences or privileges senior to the our common stock and may dilute our current stockholders.
Going Concern
The accompanying financial statements have been prepared in conformity with accounting principles generally accepted in the United States of America, which contemplate our continuation as a going concern. We have not established a source of revenues sufficient to cover our operating costs, and as such, have been dependent on funding operations through the issuance of debt and sale of equity securities. Since inception, we have experienced significant loses and incurred negative cash flows from operations. We expect to incur further losses over the next several years as we develop our business. We have spent, and expect to continue to spend, a substantial amount of funds in connection with implementing our business strategy, including our planned product development efforts, preparation for our planned clinical trials, performance of clinical trials and our research and discovery efforts.
Our cash and cash equivalents are not expected to be sufficient to enable us to meet our long-term expected plans, including commercialization of clinical pipeline products, if approved, or initiation or completion of future registrational studies. We have no commitments for any additional financing and may not be successful in our efforts to raise additional funds or achieve profitable operations , and there can be no assurance that additional financing will be available to us on commercially acceptable terms or at all . Any amounts raised will be used for further development of our product candidates, for marketing and promotion, to secure ad ditional property and equipment and for other working capital purposes.
If we are unable to obtain additional capital, our long-term business plan may not be accomplished and we may be forced to curtail or cease operations. The 2015 Credit Agreement contains certain developmental milestones, as well as a minimum liquidity covenant. The Company’s failure to achieve these milestones [as anticipated] by December 31, 2019 or its violation of its minimum liquidity covenant would constitute an event of default under the 2015 Credit Agreement. Upon an event of default, the Lender may terminate the commitments under the 2015 Credit Agreement and declare the loans then outstanding under the 2015 Credit Agreement to be due and payable in whole or in part, together with any applicable fees and accrued interest thereon. The Company considers some of these developmental milestones to be outside of its control. As a
32
result, if an event of default arises under the Credit Agreement, the Company may need to use cash and cash equivalents on hand to fund certain repayment commitments under the 2015 Credit Agreement .
These factors individually and collectively continue to raise substantial doubt about our ability to continue as a going concern. The accompanying financial statements do not include any adjustments or classifications that may result from the possible inability of us to continue as a going concern .
Sources of Liquidity
Since our inception through June 30, 2019 , we have raised net proceeds from the issuance of equity and debt. At June 30, 2019 , we had $28.0 million of outstanding loans under the 2015 Credit Agreement , which matures in July 2020 . As of the date hereof, we are not in default under the terms of the 2015 Credit Agreement. We maintained cash and cash equivalents of $86.2 million at June 30, 2019 .
The following table sets forth the primary sources and uses of cash and cash equivalents for each period set forth below:
Operating Activities
The net cash used in operating activities was $43.9 million for the six months ended June 30, 2019 , and consisted primarily of a net income of $12.8 million adjusted for $53.2 million in net non- cash items, including unrealized gain on equity securities of $60.9 million, offset by the depreciation and amortization of fixed assets and right-of- use lease assets of $ 2.6 million, amortizat ion of deferred financing costs and debt discount of $0.2 million, write-down of inventory of $0.9 million, change in fair va lue of financial instruments of $(0.1) million and share- based compensation expense of $4.1 million, as well as a net decrease in operating assets and liabilities of $3.5 million . Once adjusted for the non- cash items above, the cash used in operating activities for the six months ended June 30, 2019 was primarily driven by selling, general and administrative expenses of $11.4 million , research and development expense related to the advancement of our clinical product candidates of $28.0 million and interest paid on our debt of $1.7 million .
The net cash used in operating activities was $35.3 million for the six months ended June 30, 2018, and consisted primarily of a net income of $1.1 million adjusted for $33.1 million in net non ‑cash items, including the depreciation and amortization of fixed assets of $0.7 million, amortization of deferred financing costs, debt discount and debt premium of $0.9 million, loss on equity me thod investment of $1.2 million and share ‑based compensation expense of $5.6 million , offset by an unrealized gain on equity securities of $40.5 million, change in deferred tax liability of $0.6 million, as well as a net decrease in operating assets and liabilities of $3.4 million. The significant items in the change in operating assets and liabilities include a decrease of $2.9 million in accounts payable, accrued expenses and other liabilities, an increase in prepaid and other assets of $0.5 million due to timing of payments for certain services, and a decrease in inventories of $0.7 million, partially offset by a decrease in accounts receivable of $0.6 million due to timing of collections from our customers. The net income was primarily driven by an unrealized gain on equity securities related to our investment in MeiraGTx of $40.5 million, offset by selling, general and administrative expenses of $17.1 million, research and development expense related to the advancement of our clinical product candidates of $20.0 million and interest paid on our debt of $1.9 million.
Investing Activities
Net cash used in investing activities was $0.4 million for the six months ended June 30, 2019 consisting of costs related to leasehold improvements at our clinical office in Cambridge, Massachusetts and the purchase of laboratory equipment. Net cash used in investing activities was $0.5 million for the six months ended June 30, 2018 , consisting of costs related to the purchase of property and equipment, primarily related to in ‑house software and laboratory equipment.
33
Financing Activities
Net cash provided by financing activities for the six months ended June 30, 2019 was $35.8 million, c onsisting primarily of net proceeds from the issuance of common stock through the ATM Offering of $ 35.7 million. Net cash provided by financing activities for the six months ended June 30, 2018 was $99.8 million, consisting primarily of proceeds from the issuance of common stock in our June 2018 public o ffering of shares of our common stock .
Future Funding Requirements
We expect our expenses to increase compared to prior periods in connection with our ongoing activities, particularly as we continue research and development, continue and initiate clinical trials and seek regulatory approvals for our product candidates. In anticipation of regulatory approval for any of our product candidates , we expect to incur significant pre- commercialization expenses related to product sales, marketing, distribution and manufacturing.
The expected use of our cash and cash equivalents at June 30, 2019 represents our intentions based upon our current plans and business conditions, which could change in the future as our plans and busines s conditions evolve. The amount and timing of our actual expenditures may vary significantly depending on numerous factors , including the progress of our development, the status of, and results from, clinical trials, the potential need to conduct additional clinical trials to obtain approval of our product candidates for all intended indications, as well as any additional collaborations that we may enter into with third parties for our product candidates and any unforeseen cash needs. As a result, our management will retain broad discretion over the allocation of our existing cash and cash equivalents. In addition, we anticipate the need to raise additional funds from the issuance of additional equity securities and monetization of assets , and our management will retain broad discretion over the allocation of those funds as well .
Contractual Obligations and Commitments
There have been no material changes in our contractual obligations and commitments during the six months ended June 30, 2019 from those set forth in our Annual Report on Form 10-K for the year ended December 31, 2018 .
Off- balance Sheet Arrangements
During the periods presented we did not have, and we do not currently have, any off- balance sheet ar rangements, as defined under SEC rules.
Ite m 3. Quantitative and Qualitative Disclosures about Market Risk
Our market risks as of June 30, 2019 have not changed materially from those discussed in Item 7A of our Annual Report on Form 10-K for the year ended Decemb er 31, 201 8 .
Ite m 4. Controls and Procedures
Management’s Evaluation of our Disclosure Controls and Procedures
We maintain disclosure controls and procedures that are designed to ensure that information required to be disclosed in the reports that we file or submit under the Securities and Exchange Act of 1934, as amended, is (1) recorded, processed, summarized, and reported within the time periods specified in the SEC’s rules and forms and (2) accumulated and communicated to our management, including our principal executive officer and principal financial officer, to allow timely decisions regarding required disclosure.
As of June 30, 2019 , our management, with the participation of our principal executive officer and principal financial officer, evaluated the effectiveness of our disclosure controls and procedures (as defined in Rules 13a-15(e) and 15d-15(e) under the Securities and Exchange Act of 1934, as amended). Our management recognizes that any controls and procedures, no matter how well designed and operated, can provide only reasonable assurance of achieving their objectives, and management necessarily applies its judgment in evaluating the cost-benefit relationship of possible controls and procedures. Our principal executive officer and principal financial officer have concluded based upon the evaluation described above that, as of June 30, 2019 , our disclosure controls and procedures were effective at the reasonable assurance level.
34
Changes in Internal Control over Financial Reporting
No change in our internal control over financial reporting (as defined in Rules 13a-15(f) and 15d-15(f) under the Securities and Exchange Act of 1934, as amended ) occurred during the fiscal quarter ended June 30, 2019 that has materially affected, or is reasonably likely to materially affect, our internal control over financial reporting.
Please refer to Note 1 6 of the notes to our unaudited consolidated financial state ments included elsewhere in this Quarterly Report on Form 10-Q for a discussion related to our legal proceedings.
Investing in our securities involves a high degree of risk. In addition to the other information contained elsewhere in this Quarterly Report on Form 10-Q , you should carefully consider the factors discussed in “Part I, Item 1A. Risk Factors” in our Annual Report on Form 10-K for the year ended D ecember 31, 2018, which could materially and adversely affect our business, financial condition or future results. These risks and uncertainties are not the only ones we face. You should recognize that other significant risks and uncertainties may arise in the future, which we cannot foresee at this time. Also, t he risks that we currently foresee might affect us to a greater or different degree than expected. Certain risks and uncertainties, including ones that we currently deem immaterial or that are similar to those faced by other companies in our industry or business in general, may also affect our business. If any of the risks actually occur, our business, financial condition or results of operations could be materially and adversely affected. As of June 30, 2019, there we re no material changes to the risk factors described in our Annual Report on Form 10-K for the year ended December 31, 2018.
Item 2. Unre gistered Sales of Equity Securities and Use of Proceeds
Recent Sales of Unregistered Equity Securities
None .
I tem 3. Defaults Upon Senior Securities
None.
Ite m 4. Mine Safety Disclosures
Not applicable.
None.
The exhibits filed as part of this Quarterly Report on Form 10-Q are set forth on the Exhibit Index, which is incorporated herein by reference.
35
EXHIBIT INDEX
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Exhibit
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Description of Exhibit |
3.1* |
Restated Certificate of Incorporation of Kadmon Holdings, Inc. |
3.2 | |
3.3 | |
31.1* |
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31.2* |
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32.1** |
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32.2** |
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101* |
The following materials from the Kadmon Holdings, Inc. Form 10-Q for the quarter ended June 30, 2019, formatted in Extensible Business Reporting Language (XBRL): (i) Consolidated Balance Sheets as of June 30, 2019 and December 31, 2018, (ii) Consolidated Statements of Operations for the three and six months ended June 30, 2019 and 2018, (iii) Consolidated Statements of Cash Flows for the six months ended June 30, 2019 and 2018, and (iv) Notes to the Financial Statements. |
* |
Filed herewith. |
** |
Furnished herewith. |
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36
Pursuant to the requirements of Section 13 or 15(d) of the Securities Exchange Act of 1934, the registrant has duly caused this report to be signed on its behalf by the undersigned, thereunto duly authorized.
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Date: August 5 , 2019 |
By: |
/s/ Harlan W. Waksal
Harlan W. Waksal
(Principal Executive Officer) |
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Date: August 5 , 2019 |
By: |
/s/ Steven Meehan
Steven Meehan
(Principal Financial Officer)
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Date: August 5 , 2019 |
By: |
/s/ Kyle Carver |
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Kyle Carver
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(Principal Accounting Officer) |
37
RESTATED CERTIFICATE OF INCORPORATION
OF
KADMON HOLDINGS, INC.
(Pursuant to Sections 242 and 245 of the
General Corporation Law of the State of Delaware)
Kadmon Holdings, Inc., a corporation organized and existing under the Delaware General Corporation Law (the “ Delaware General Corporation Law ”),
DOES HEREBY CERTIFY:
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ARTICLE I |
The name of the corporation is Kadmon Holdings, Inc. (hereinafter referred to as the “ Corporation ”).
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ARTICLE II |
The address of the registered office of the Corporation in the State of Delaware is 2711 Centerville Road, Suite 400, in the City of Wilmington, County of New Castle, 19808. The name of the registered agent at such address is Corporation Service Company.
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ARTICLE III |
The purpose of the Corporation is to engage in any lawful act or activity for which a corporation may be organized under the Delaware General Corporation Law.
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ARTICLE IV |
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A. The total number of shares of capital stock of all classes which the Corporation shall have authority to issue is 410,000,000 shares, consisting of: 400,000,000 shares of common stock, $0.001 par value per share (the “ Common Stock ”) and 10,000,000 shares of preferred stock, par value $0.001 per share (“ Preferred Stock ”). |
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B. Except as otherwise restricted by this Certificate of Incorporation (this “ Certificate ”), the Corporation is authorized to issue, from time to time, all or any portion of the capital stock of the Corporation which may have been authorized but not issued, to such person or persons and for such lawful consideration as it may deem appropriate, and generally in its absolute discretion to determine the terms and manner of any disposition of such authorized but unissued capital stock. |
Any and all such shares issued for which the full consideration has been paid or delivered shall be deemed fully paid shares of capital stock, and the holder of such shares shall not be liable for any further call or assessment or any other payment thereon.
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C. The designations and the powers, preferences and rights and qualifications, limitations or restrictions of the shares of each class of stock are as follows: |
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1. Common Stock |
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(a) General . The voting, dividend and liquidation rights of the holders of the Common Stock are subject to the rights of the holders of any series of Preferred Stock then outstanding. |
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2. Preferred Stock . The shares of Preferred Stock shall initially be undesignated and may be issued from time to time in one or more additional series by the Board of Directors of the Corporation (the “ Board of Directors ”). The Board of Directors is hereby authorized, subject to any limitations prescribed by law, to determine or alter the rights, preferences, privileges and restrictions granted to or imposed upon a wholly-unissued series of Preferred Stock, and the number of shares constituting any such series and the designation thereof, or any of them; and to increase or decrease the number of shares constituting any such series and the designation thereof, or any of them; and to increase or decrease the number of shares of any series subsequent to the issue of shares of that series, but, in respect of decreases, not below the number of shares of such series then outstanding. In case the number of shares of any series should be so decreased, the shares constituting such decrease shall resume the status which they had prior to the adoption of the resolutions originally fixing the number of shares of such series. The number of authorized shares of Preferred Stock may be increased or decreased (but not below the number of shares thereof then outstanding) by the affirmative vote of the holders of a majority of the outstanding shares of Common Stock without a vote of the holders of the Preferred Stock, or of any series thereof, unless a vote of any such holders is required pursuant to the certificate or certificates establishing any series of Preferred Stock. |
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ARTICLE V |
The name and mailing address of the sole incorporator are as follows:
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NAME |
MAILING ADDRESS |
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Steven N. Gordon, Esq. |
Kadmon Holdings, Inc. |
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450 East 29th Street |
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New York, NY 10016 |
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Attention: Steven N. Gordon, Esq. |
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ARTICLE VI |
The Corporation is to have a perpetual existence.
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ARTICLE VII |
The following provisions are inserted for the management of the business and the conduct of the affairs of the Corporation, and for further definition, limitation and regulation of the powers of the Corporation and of its directors and stockholders:
A. The business and affairs of the Corporation shall be managed by or under the direction of the Board of Directors. In addition to the powers and authority expressly conferred upon them by law or by this Certificate or the bylaws of the Corporation, as the same may be amended from time to time (the “ Bylaws ”), the directors are hereby empowered to exercise all such powers and do all such acts and things as may be exercised or done by the Corporation.
B. The directors of the Corporation need not be elected by written ballot unless the Bylaws so provide.
C. Subject to the rights of the holders of any series of Preferred Stock, any action required or permitted to be taken by the stockholders of the Corporation must be effected at a duly called annual or special meeting of stockholders of the Corporation and may not be effected by any consent in writing by such stockholders.
D. Subject to the rights of the holders of any series of Preferred Stock then outstanding, special meetings of stockholders of the Corporation may be called only by the Board of Directors pursuant to a resolution adopted by a majority of the total number of authorized directors (whether or not there exist any vacancies in previously authorized directorships at the time any such resolution is presented to the Board for adoption).
E. The number of directors shall be set at nine (9) and, thereafter, shall be fixed from time to time exclusively by the Board of Directors pursuant to a resolution adopted by a majority of the total number of authorized directors (whether or not there exist any vacancies in previously authorized directorships at the time any such resolution is presented to the Board of Directors for adoption). All directors shall hold office until the expiration of the term for which elected, and until their respective successors are elected, except in the case of the death, resignation, or removal of any director.
F. Subject to the rights of the holders of any series of Preferred Stock then outstanding, newly created directorships resulting from any increase in the authorized number of directors or any vacancies in the Board of Directors resulting from death, resignation or other cause (including removal from office by a vote of the stockholders described in Article VI I (G) below) may, except as otherwise required by law, be filled only by a majority vote of the directors then in office, though less than a quorum, or by the sole remaining director, and directors so chosen shall hold office for a term expiring at the next annual meeting of stockholders at which the term of office of the class to which they have been elected expires, and until their respective successors are elected, except in the case of the death, resignation, or removal of any director. No decrease in the number of directors constituting the Board of Directors shall shorten the term of any incumbent director.
G. Subject to the rights of the holders of any series of Preferred Stock then outstanding, any directors, or the entire Board of Directors, may be removed from office at any time, but only by the affirmative vote of the holders of at least a majority of the voting power of all of the then outstanding shares of capital stock entitled to vote generally in the election of directors, voting together as a single class. Vacancies in the Board of Directors resulting from such removal may, except as otherwise required by law, be filled by a majority of the directors then in office, though less than a quorum, or by the sole remaining director. Directors so chosen shall hold office for a term expiring at the next annual meeting of stockholders at which the term of office of the class to which they have been elected expires, and until their respective successors are elected, except in the case of the death, resignation, or removal of any director.
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ARTICLE VIII |
No person shall be personally liable to the Corporation or its stockholders for monetary damages for breach of his or her fiduciary duty as a director of the Corporation, except for liability (i) for any breach of the director’s duty of loyalty to the Corporation or its stockholders, (ii) for any acts or omissions not in good faith or which involve intentional misconduct or a knowing violation of law, (iii) under Section 174 of the Delaware General Corporation Law or (iv) for any transaction from which the director derived an improper personal benefit. If the Delaware General Corporation Law hereafter is amended to authorize further elimination or limitation of the liability of directors, then the liability of a director of the Corporation, in addition to the limitation on personal liability provided herein, shall be limited to the fullest extent permitted by the amended Delaware General Corporation Law. Any repeal or modification of this paragraph by the stockholders of the Corporation shall be prospective only, and shall not adversely affect any limitation on the personal liability of a director of the Corporation existing at the time of such repeal or modification.
The Corporation shall indemnify any director or officer to the fullest extent permitted by Delaware law.
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ARTICLE IX |
All of the powers of the Corporation, insofar as the same may be lawfully vested by this Certificate in the Board of Directors, are hereby conferred upon the Board of Directors.
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ARTICLE X |
The Board of Directors is expressly empowered to adopt, amend or repeal the Bylaws. Any adoption, amendment or repeal of the Bylaws by the Board of Directors shall require the approval of a majority of the total number of authorized directors (whether or not there exist any vacancies in previously authorized directorships at the time any resolution providing for adoption, amendment or repeal is presented to the Board of Directors). The stockholders shall also have power to adopt, amend or repeal the Bylaws. Subject to the rights of the holders of any series of Preferred Stock then outstanding, any adoption, amendment or repeal of Bylaws by the stockholders shall require, in addition to any vote of the holders of any class or series of stock of the Corporation required by law or by this Certificate, the affirmative vote of the holders of at least a majority of the voting power of all of the then outstanding shares of the capital stock of the Corporation entitled to vote generally in any election of directors, voting together as a single class.
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ARTICLE XI |
The Corporation reserves the right to amend or repeal any provision contained in this Certificate in the manner prescribed by the laws of the State of Delaware and all rights conferred upon stockholders are granted subject to this reservation; provided , that , notwithstanding any other provision of this Certificate or any provision of law which might otherwise permit a lesser vote or no vote, but subject to the rights of the holders of any series of Preferred Stock then outstanding and in addition to any vote of the holders of any class or series of the stock of this Corporation required by law or by this Certificate, the affirmative vote of the holders of at least a majority of the voting power of all of the then outstanding shares of the capital stock of the Corporation entitled to vote generally in any election of directors, voting together as a single class, shall be required to amend or repeal any of the Articles in this Certificate.
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ARTICLE XII |
To the fullest extent permitted by law, the Court of Chancery of the State of Delaware shall be the sole and exclusive forum for (i) any derivative action or proceeding brought on behalf of the Corporation, (ii) any action asserting a claim of breach of a fiduciary duty owed by any director or officer of the Corporation to the Corporation or the Corporation’s stockholders, (iii) any action asserting a claim against the Corporation arising pursuant to any provision of the Delaware General Corporation Law, this Certificate or the Bylaws, or (iv) any action asserting a claim against the Corporation governed by the internal affairs doctrine.
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ARTICLE XIII |
The Corporation elects to be governed by Section 203 of the DGCL (or any successor provision thereto).
IN WITNESS WHEREOF, the Corporation has caused this Restated Certificate of Incorporation to be signed by the undersigned officer, thereun to duly authorized, on this 5th day of August , 2019.
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KADMON HOLDINGS, INC. |
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By: |
/s/ Harlan W. Waksal |
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Name: |
Harlan W. Waksal |
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Title: |
President and Chief Executive Officer |
CERTIFICATION OF CHIEF EXECUTIVE OFFICER PURSUANT TO EXCHANGE ACT RULES 13a-14 AND 15d-14, AS ADOPTED PURSUANT TO SECTION 302 OF SARBANES-OXLEY ACT OF 2002
I, Harlan W. Waksal , certify that:
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1. |
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I have reviewed this Quarterly Report on Form 10-Q of Kadmon Holdings , Inc.; |
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2. |
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Based on my knowledge, this report does not contain any untrue statement of a material fact or omit to state a material fact necessary to make the statements made, in light of the circumstances under which such statements were made, not misleading with respect to the period covered by this report; |
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3. |
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Based on my knowledge, the financial statements, and other financial information included in this report, fairly present in all material respects the financial condition, results of operations and cash flows of the registrant as of, and for, the periods presented in this report; |
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4. |
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The registrant’s other certifying officer and I are responsible for establishing and maintaining disclosure controls and procedures (as defined in the Securities Exchange Act of 1934, as amended, Rules 13a-15(e) and 15d-15(e)) and internal control over financial reporting (as defined in Exchange Act Rules 13a-15(f) and 15d-15(f)) for the registrant and have: |
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a) |
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Designed such disclosure controls and procedures, or caused such disclosure controls and procedures to be designed under our supervision, to ensure that material information relating to the registrant, including its consolidated subsidiaries, is made known to us by others within those entities, particularly during the period in which this report is being prepared; |
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b) |
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Designed such internal control over financial reporting, or caused such internal control over financial reporting to be designed under our supervision, to provide reasonable assurance regarding the reliability of financial reporting and the preparation of financial statements for external purposes in accordance with generally accepted accounting principles; |
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c) |
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Evaluated the effectiveness of the registrant’s disclosure controls and procedures and presented in this report our conclusions about the effectiveness of the disclosure controls and procedures, as of the end of the period covered by this report based on such evaluation; and |
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d) |
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Disclosed in this report any change in the registrant’s internal control over financial reporting that occurred during the registrant’s most recent fiscal quarter (the registrant’s fourth fiscal quarter in the case of an annual report) that has materially affected, or is reasonably likely to materially affect, the registrant’s internal control over financial reporting; and |
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5. |
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The registrant’s other certifying officer and I have disclosed, based on our most recent evaluation of internal control over financial reporting, to the registrant’s auditors and the audit committee of the registrant’s board of directors (or persons performing the equivalent functions): |
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a) |
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All significant deficiencies and material weaknesses in the design or operation of internal control over financial reporting which are reasonably likely to adversely affect the registrant’s ability to record, process, summarize and report financial information; and |
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b) |
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Any fraud, whether or not material, that involves management or other employees who have a significant role in the registrant’s internal control over financial reporting. |
x |
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Dated: August 5 , 201 9 |
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/s/ Harlan W. Waksal |
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Harlan W. Waksal |
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President and Chief Executive Officer |
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CERTIFICATION OF CHIEF FINANCIAL OFFICER PURSUANT TO EXCHANGE ACT RULES 13a-14 AND 15d-14, AS ADOPTED PURSUANT TO SECTION 302 OF SARBANES-OXLEY ACT OF 2002
I, Steven Meehan , certify that:
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1. |
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I have reviewed this Quarterly Report on Form 10-Q of Kadmon Holdings , Inc.; |
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2. |
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Based on my knowledge, this report does not contain any untrue statement of a material fact or omit to state a material fact necessary to make the statements made, in light of the circumstances under which such statements were made, not misleading with respect to the period covered by this report; |
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3. |
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Based on my knowledge, the financial statements, and other financial information included in this report, fairly present in all material respects the financial condition, results of operations and cash flows of the registrant as of, and for, the periods presented in this report; |
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4. |
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The registrant’s other certifying officer and I are responsible for establishing and maintaining disclosure controls and procedures ( as defined in the Securities Exchange Act of 1934, as amended, Rules 13a-15(e) and 15d-15(e)) and internal control over financial reporting (as defined in Exchange Act Rules 13a-15(f) and 15d-15(f)) for the registrant and have: |
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a) |
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Designed such disclosure controls and procedures, or caused such disclosure controls and procedures to be designed under our supervision, to ensure that material information relating to the registrant, including its consolidated subsidiaries, is made known to us by others within those entities, particularly during the period in which this report is being prepared; |
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b) |
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Designed such internal control over financial reporting, or caused such internal control over financial reporting to be designed under our supervision, to provide reasonable assurance regarding the reliability of financial reporting and the preparation of financial statements for external purposes in accordance with generally accepted accounting principles; |
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c) |
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Evaluated the effectiveness of the registrant’s disclosure controls and procedures and presented in this report our conclusions about the effectiveness of the disclosure controls and procedures, as of the end of the period covered by this report based on such evaluation; and |
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d) |
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Disclosed in this report any change in the registrant’s internal control over financial reporting that occurred during the registrant’s most recent fiscal quarter (the registrant’s fourth fiscal quarter in the case of an annual report) that has materially affected, or is reasonably likely to materially affect, the registrant’s internal control over financial reporting; and |
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5. |
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The registrant’s other certifying officer and I have disclosed, based on our most recent evaluation of internal control over financial reporting, to the registrant’s auditors and the audit committee of the registrant’s board of directors (or persons performing the equivalent functions): |
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a) |
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All significant deficiencies and material weaknesses in the design or operation of internal control over financial reporting which are reasonably likely to adversely affect the registrant’s ability to record, process, summarize and report financial information; and |
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b) |
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Any fraud, whether or not material, that involves management or other employees who have a significant role in the registrant’s internal control over financial reporting. |
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Dated: August 5 , 201 9 |
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/s/ Steven Meehan |
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Steven Meehan |
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Executive Vice President, Chief Financial Officer |
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CERTIFICATION OF CHIEF EXECUTIVE OFFICER PURSUANT TO 18 U.S.C. SECTION 1350, AS ADOPTED PURSUANT TO SECTION 906 OF THE SARBANES-OXLEY ACT OF 2002
In connection with the Quarterly Report on Form 10-Q of Kadmon Holdings , Inc. (the “Company”) for the period ended June 30 , 201 9 as filed with the Securities and Exchange Commission on the date hereof (the “Report”), the undersigned, Harlan W. Waksal , President and Chief Executive Officer of the Company, hereby certifies, pursuant to 18 U.S.C. Section 1350, that to his knowledge:
(1) the Report fully complies with the requirements of Section 13(a) or 15(d) of the Securities Exchange Act of 1934; and
(2) the information contained in the Report fairly presents, in all material respects, the financial condition and results of operations of the Company.
A signed original of this written statement has been provided to Kadmon Holdings , Inc. and will be retained by Kadmon Holdings , Inc. and furnished to the Securities and Exchange Commission or its staff upon request.
x |
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Dated: August 5 , 201 9 |
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/s/ Harlan W. Waksal |
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Harlan W. Waksal |
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President and Chief Executive Officer |
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CERTIFICATION OF CHIEF FINANCIAL OFFICER PURSUANT TO 18 U.S.C. SECTION 1350, AS ADOPTED PURSUANT TO SECTION 906 OF THE SARBANES-OXLEY ACT OF 2002
In connection with the Quarterly Report on Form 10-Q of Kadmon Holdings, Inc. (the “Company”) for the period ended June 30 , 201 9 as filed with the Securities and Exchange Commission on the date hereof (the “Report”), the undersigned, Steven Meehan , Executive Vice President, Chief Financial Officer o f the Company, hereby certifies, pursuant to 18 U.S.C. Section 1350, that to his knowledge:
(1) the Report fully complies with the requirements of Section 13(a) or 15(d) of the Securities Exchange Act of 1934; and
(2) the information contained in the Report fairly presents, in all material respects, the financial condition and results of operations of the Company.
A signed original of this written statement has been provided to Kadmon Holdings, Inc. and will be retained by Kadmon Holdings, Inc. and furnished to the Securities and Exchange Commission or its staff upon request.
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Dated: August 5 , 201 9 |
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/s/ Steven Meehan |
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Steven Meehan |
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Executive Vice President, Chief Financial Officer |
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