Israel
|
2834
|
81-3676773
|
(State or other jurisdiction of
incorporation or organization)
|
(Primary Standard Industrial
Classification Code Number)
|
(I.R.S. Employer
Identification No.)
|
|
|
|
Brent D. Fassett
Jesse F. Schumaker
Wilson Sonsini Goodrich & Rosati, P.C.
1881 9th Street, Suite 110
Boulder, CO 80023
(303) 256-5900
|
David S. Glatt
Ronen Bezalel
Jonathan M. Nathan Matthew Rudolph
Meitar | Law Offices 16 Abba Hillel Rd. Ramat Gan 5250608, Israel +972 (3) 610-3100 |
Anthony W. Basch
J. Britton Williston
Kaufman & Canoles, P.C.
Two James Center, 14th Floor 1021 E. Cary St.
Richmond, VA 23219
+1.804.771.5700
|
Large accelerated filer
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☐
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Accelerated filer
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☐
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Non-accelerated filer
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☒
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Smaller reporting company
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☒
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Emerging growth company
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☒
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Per Unit
|
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Per Pre-Funded Unit
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Total
|
|
Public offering price
|
$
|
|
$
|
$
|
|
Underwriting discounts (1)
|
$
|
|
$
|
$
|
|
Proceeds, before expenses, to us(2)
|
$
|
|
$
|
$
|
(1)
|
See “Underwriting” beginning on page 50 of this prospectus for a description of the compensation payable to the underwriter.
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(2)
|
The amount of proceeds, before expenses, to us does not give effect to the exercise of the Warrants.
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Aegis Capital Corp.
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Page
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1
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7 | |
8
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12
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13 |
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14
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15
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16
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17
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18
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24
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31
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33
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38
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46
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53 | |
57
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57 | |
58
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59
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59 |
• |
We have incurred significant losses since inception and anticipate that we will continue to incur increasing levels of operating losses over the next several years and for the foreseeable future. We are unable to predict the
extent of any future losses or when we will become profitable, if at all. Even if we become profitable, we may not be able to sustain or increase our profitability on a quarterly or annual basis.
|
• |
We have a limited operating history and funding, which may make it difficult to evaluate our prospects and likelihood of success.
|
• |
Our business is highly dependent on the success of our lead product candidate, CM-101, and any other product candidates that we advance into clinical studies. All of our programs will require significant additional clinical
development.
|
• |
Our central objective is to design and develop targeted treatments for inflammation and fibrosis with an initial focus on the antagonism of CCL24 signaling, which is known to regulate fibrotic and inflammatory processes. While
several studies are currently underway, our approach in the area of fibrotic diseases is novel and unproven and may not result in marketable products.
|
• |
The successful completion of clinical studies is a prerequisite to submitting a marketing application to the FDA and similar marketing applications to comparable foreign regulatory authorities, for each product candidate and,
consequently, the ultimate approval and commercial marketing of any product candidates. We may experience negative or inconclusive results, which may result in us deciding, or regulators requiring us, to conduct additional
clinical studies or trials or abandon some or all of its product development programs, which could have a material adverse effect on our business.
|
• |
We may encounter difficulties enrolling patients in our clinical studies, including due to the continuing effects of the COVID-19 pandemic, or other public health emergencies and related clinical development activities could be
delayed or otherwise adversely affected.
|
• |
Our ongoing and future clinical studies may reveal significant adverse events or immunogenicity-related responses and may result in a safety profile that could delay or prevent regulatory approval or market acceptance of our
product candidate.
|
• |
The regulatory approval processes of the FDA and comparable foreign authorities are lengthy, time consuming and inherently unpredictable, and if we are ultimately unable to obtain regulatory approval for CM-101 or any other
product candidates, our business will be substantially harmed.
|
• |
If we do not achieve our projected development and commercialization goals in the timeframes we announce and expect, the commercialization of our product candidates may be delayed and our business will be harmed.
|
• |
We face substantial competition, which may result in others discovering, developing or commercializing products before or more successfully than us.
|
• |
We have been granted Orphan Drug Designation for CM-101 in connection with three indications and may seek Orphan Drug Designation for other indications or product candidates, and we may be unable to maintain the benefits
associated with Orphan Drug Designation, including the potential for market exclusivity, and may not receive Orphan Drug Designation for other indications or for its other product candidates.
|
• |
We expect to experience significant growth in the number of our employees over time and the scope of our operations, particularly in the areas of product candidate development, regulatory affairs and sales and marketing. We
will therefore need to expand our organization, and we may experience difficulties in managing this growth, which could disrupt our operations.
|
• |
If we are unable to protect our patents or other proprietary rights, or if we infringe the patents or other proprietary rights of others, our competitiveness and business prospects may be materially damaged. In addition,
changes in patent laws or patent jurisprudence could diminish the value of patents in general, thereby impairing our ability to protect our product candidates.
|
• |
Risks related to our operations in Israel could materially adversely impact our business, financial condition and results of operations.
|
• |
Our principal executive offices are located in Israel and certain of our product candidates may be manufactured at third-party facilities located in Europe. In addition, our business strategy includes potentially expanding
internationally if any of its product candidates receives regulatory approval. A variety of risks associated with operating internationally could materially adversely affect our business.
|
• |
Holders of ADSs are not treated as holders of our ordinary shares.
|
• |
Holders of ADSs may not have the same voting rights as the holders of our ordinary shares and may not receive voting materials in time to be able to exercise their right to vote.
|
• |
Holders of ADSs may be subject to limitations on the transfer of their ADSs and the withdrawal of the underlying ordinary shares.
|
• |
We are entitled to amend the deposit agreement and to change the rights of ADS holders under the terms of such agreement, or to terminate the deposit agreement, without the prior consent of the ADS holders.
|
• |
ADSs holders may not be entitled to a jury trial with respect to claims arising under the deposit agreement, which could result in less favorable outcomes to the plaintiff(s) in any such action.
|
• |
We presently anticipate that we will be classified as a passive foreign investment company, which could result in adverse U.S. federal income tax consequences to U.S. Holders of our ordinary shares.
|
• |
The Warrants are speculative in nature.
|
• |
There is no established market for the Warrants being offered in this offering.
|
• |
Holders of the Warrants will have no rights as a shareholder until they acquire our ordinary shares.
|
• |
The Warrants offered by this prospectus may not have any value.
|
• |
As our Warrant holders exercise their Warrants into Warrant ADSs and underlying ordinary shares, our shareholders’ ownership will be diluted.
|
• |
CM-101 appeared to be safe and well tolerated when administered subcutaneously. Most reported adverse events observed were mild, with one unrelated serious adverse event reported. No significant injection site reactions were
reported and no anti-drug antibodies were detected.
|
• |
CM-101 administered subcutaneously demonstrated favorable pharmacokinetics and target engagement profiles as expected, and were similar to what the company has previously reported.
|
• |
CM-101-treated patients showed greater improvements than the placebo group in a number of liver fibrosis-related biomarkers, including ProC-3, ProC-4, ProC-18, TIMP-1 and ELF.
|
• |
A majority of CM-101-treated patients showed improvements in multiple liver fibrosis-related biomarkers—almost 60% of CM-101 patients were “multiple responders”, responding in at least three biomarkers at week 20, compared to
no patients in the placebo group.
|
• |
CM-101-treated patients with higher CCL24 levels at baseline showed greater reductions in fibrosis-related biomarkers than patients with lower levels of CCL24 at baseline. More CM-101-treated patients with higher CCL24 levels
also were “multiple responders”, responding in three or more of the fibrosis-related biomarkers, compared to patients with lower CCL24 levels at baseline. These findings further add to the growing body of evidence validating the
role of CCL24 in the pathophysiology of fibrotic liver disease.
|
• |
A higher proportion of patients in the CM-101-treated group showed improvement in a physiologic measure of liver stiffness as compared to placebo (reduction of at least one grade of fibrosis score as assessed by the
non-invasive elastography method known as FibroScan®).
|
• |
After completion of the study, the unblinded data showed that patients in the CM-101-treated group had higher baseline levels of fibrosis compared to placebo patients. The impact of this difference on the results, if any, is
unknown.
|
Over-allotment Option
|
We have granted the underwriter an option to purchase from us, at the public offering price, less the underwriting discounts, up to
986,842 additional ADSs and/or Pre-Funded Warrants, and/or up to 986,842 over-allotment Warrants, within 30 days after the closing of this offering to cover over-allotments, if any. The underwriter may exercise the
over-allotment option with respect to ADSs only, Pre-Funded Warrants only, Warrants only, or any combination thereof.
|
ADSs outstanding prior to this offering
|
11,049,812 ADSs.
|
ADSs outstanding after this offering
|
17,628,759 ADSs (assuming full exercise of the Pre-Funded Warrants).
|
Use of proceeds
|
We estimate the net proceeds from this offering will be approximately $8.8 million, after deducting estimated underwriting discounts and commissions and estimated offering expenses
payable by us. We intend to use the net proceeds from this offering for continued clinical development of our product candidates, research activities, and for other general corporate purposes. See “Use of Proceeds” on page 12 of
this prospectus.
|
Risk factors
|
See “Risk Factors” beginning on page 8 for a discussion of factors you should carefully consider before deciding to invest in our securities.
|
ADS depositary
|
The Bank of New York Mellon.
|
Nasdaq Capital Market symbol
|
The ADSs are listed on Nasdaq under the symbol “CMMB.” We do not intend to list the Warrants on any securities exchange or nationally recognized trading system.
|
|
●
|
1,747,077 ADSs issuable upon the exercise of outstanding options to purchase ADSs, at a weighted average exercise price of $6.60 per ADS;
|
|
|
|
|
●
|
an aggregate of 655,869 ADSs reserved for future issuance under the Chemomab Ltd. 2015 Share Incentive Plan (the “2015 Plan”), which was assumed by the Company upon effectiveness of the
Merger, and the 2017 Equity-Based Incentive Plan (the “2017 Plan” and together with the 2015 Plan, the “Share Incentive Plans”), as of December 31, 2022, as well as any automatic increases in the number of ADSs reserved
for future issuance under the 2017 Plan;
|
|
|
|
|
●
|
261,929 ADSs issuable upon the exercise of outstanding warrants to purchase ADSs at a weighted average exercise price of $17.35088 per ADS, which warrants are expected to remain
outstanding at the consummation of this offering; and
|
|
●
|
6,578,947 ADSs issuable upon exercise of the Warrants issued in this offering.
|
1. |
Ablin, J. N., M. Entin-Meer, V. Aloush, S. Oren, O. Elkayam, J. George, and I. Barshack. 2010. 'Protective effect of eotaxin-2 inhibition in adjuvant-induced arthritis', Clin Exp Immunol, 161: 276-83.
|
2. |
Bhattacharyya, S., J. Wei, and J. Varga. 2011. 'Understanding fibrosis in systemic sclerosis: shifting paradigms, emerging opportunities', Nat Rev Rheumatol, 8: 42-54.
|
3. |
Bocchino, V., G. Bertorelli, C. P. Bertrand, P. D. Ponath, W. Newman, C. Franco, A. Marruchella, S. Merlini, M. Del Donno, X. Zhuo, and D. Olivieri. 2002. 'Eotaxin and CCR3 are up-regulated in exacerbations of chronic bronchitis',
Allergy, 57: 17-22.
|
4. |
Henderson, N. C., F. Rieder, and T. A. Wynn. 2020. 'Fibrosis: from mechanisms to medicines', Nature, 587: 555-66.
|
5. |
Jimenez, S. A., E. Hitraya, and J. Varga. 1996. 'Pathogenesis of scleroderma. Collagen', Rheum Dis Clin North Am, 22: 647-74.
|
6. |
Jose, P. J., D. A. Griffiths-Johnson, P. D. Collins, D. T. Walsh, R. Moqbel, N. F. Totty, O. Truong, J. J. Hsuan, and T. J. Williams. 1994. 'Eotaxin: a potent eosinophil chemoattractant cytokine detected in a guinea pig model of
allergic airways inflammation', J Exp Med, 179: 881-7.
|
7. |
Karlsen, T. H., T. Folseraas, D. Thorburn, and M. Vesterhus. 2017. 'Primary sclerosing cholangitis - a comprehensive review', J Hepatol, 67: 1298-323.
|
8. |
Kitaura, M., T. Nakajima, T. Imai, S. Harada, C. Combadiere, H. L. Tiffany, P. M. Murphy, and O. Yoshie. 1996. 'Molecular cloning of human eotaxin, an eosinophil-selective CC chemokine, and identification of a specific eosinophil
eotaxin receptor, CC chemokine receptor 3', J Biol Chem, 271: 7725-30.
|
9. |
Kohan, M., I. Puxeddu, R. Reich, F. Levi-Schaffer, and N. Berkman. 2010. 'Eotaxin-2/CCL24 and eotaxin-3/CCL26 exert differential profibrogenic effects on human lung fibroblasts', Ann Allergy Asthma Immunol, 104: 66-72.
|
10. |
Mor, A. , Afek, A. , Entin-Meer, M. , Keren, G. and George, J. 2013. 'Anti eotaxin-2 antibodies attenuate the initiation and progression of experimental atherosclerosis.', World Journal of Cardiovascular Diseases, 3: 339-46.
|
11. |
Mor, A., M. Segal Salto, A. Katav, N. Barashi, V. Edelshtein, M. Manetti, Y. Levi, J. George, and M. Matucci-Cerinic. 2019. 'Blockade of CCL24 with a monoclonal antibody ameliorates experimental dermal and pulmonary fibrosis', Ann
Rheum Dis, 78: 1260-68.
|
12. |
Ponath, P. D., S. Qin, D. J. Ringler, I. Clark-Lewis, J. Wang, N. Kassam, H. Smith, X. Shi, J. A. Gonzalo, W. Newman, J. C. Gutierrez-Ramos, and C. R. Mackay. 1996. 'Cloning of the human eosinophil chemoattractant, eotaxin.
Expression, receptor binding, and functional properties suggest a mechanism for the selective recruitment of eosinophils', J Clin Invest, 97: 604-12.
|
13. |
Segal-Salto, M., N. Barashi, A. Katav, V. Edelshtein, A. Aharon, S. Hashmueli, J. George, Y. Maor, M. Pinzani, D. Haberman, A. Hall, S. Friedman, and A. Mor. 2020. 'A blocking monoclonal antibody to CCL24 alleviates liver fibrosis
and inflammation in experimental models of liver damage', JHEP Rep, 2: 100064.
|
14. |
Wynn, T. A. 2008. 'Cellular and molecular mechanisms of fibrosis', J Pathol, 214: 199-210.
|
|
•
|
|
on an actual basis; and
|
|
•
|
|
on an as adjusted basis to give effect to the sale of 6,578,947 ADSs in this offering, at an assumed public offering price of $1.52 per ADS and accompanying Warrant, and after deducting
the estimated underwriting discounts and commissions and estimated offering expenses payable by us.
|
|
As of December 31 , 2022
|
|||||||
|
(in thousands)(unaudited)
|
|||||||
|
Actual
|
As Adjusted
|
||||||
|
||||||||
Cash and cash equivalents and short-term bank deposits
|
$
|
39,970
|
48,743
|
|||||
Shareholders’ equity
|
||||||||
Ordinary Shares, no par value - Authorized: 650,000,000 ordinary shares as of December 31, 2022
|
—
|
|||||||
Issued and outstanding: 232,636,700 ordinary shares issued and outstanding actual; 373,280,480 ordinary shares issued and outstanding as adjusted
|
||||||||
Additional paid-in capital
|
101,260
|
110,033
|
||||||
Treasury stock at cost
|
(1,218
|
)
|
(1,218
|
)
|
||||
Accumulated deficit
|
(63,819
|
)
|
(63,819
|
)
|
||||
Total shareholders’ equity
|
$
|
36,223
|
$
|
44,996
|
||||
Total liabilities and shareholders’ equity
|
$
|
43,063
|
$
|
51,836
|
|
●
|
1,747,077 ADSs issuable upon the exercise of outstanding options to purchase ADSs, at a weighted average exercise price of $6.60 per ADS;
|
|
|
|
|
●
|
an aggregate of 655,869 ADSs reserved for future issuance under our Share Incentive Plans, as of December 31,2022, as well as any automatic increases in the number of ADSs reserved for future issuance
under the 2017 Plan;
|
|
|
|
|
●
|
261,929 ADSs issuable upon the exercise of outstanding warrants to purchase ADSs at a weighted average exercise price of $17.35088 per ADS, which warrants are expected to remain
outstanding at the consummation of this offering; and
|
|
|
|
|
●
|
6,578,947 ADSs issuable upon exercise of the Warrants issued in this offering.
|
Assumed offering price per ADS and accompanying Warrant
|
|
|
|
|
$
|
1.52
|
|
|
Net tangible book value per ADS as of December 31, 2022
|
|
$
|
3.28
|
|
|
|
|
|
Net dilution in net tangible book value per ADS attributable to existing shareholders
|
|
$
|
(0.73
|
)
|
|
$
|
|
|
As adjusted net tangible book value per ADS after this offering
|
|
|
|
|
|
$
|
2.55
|
|
Net increase in net tangible book value per ADS to new investors in this offering
|
|
|
|
|
|
$
|
1.03
|
|
|
●
|
1,747,077 ADSs issuable upon the exercise of outstanding options to purchase ADSs, at a weighted average exercise price of $6.60 per ADS;
|
|
|
|
|
●
|
an aggregate of 655,869 ADSs reserved for future issuance under our Share Incentive Plans, as of December 31,2022, as well as any automatic increases in the number of ADSs reserved for future issuance
under the 2017 Plan;
|
|
|
|
|
●
|
261,929 ADSs issuable upon the exercise of outstanding warrants to purchase ADSs at a weighted average exercise price of $17.35088 per ADS, which warrants are expected to remain
outstanding at the consummation of this offering; and
|
|
|
|
|
●
|
6,578,947 ADSs issuable upon exercise of the Warrants issued in this offering.
|
• |
expenses incurred under agreements with clinical research organizations and contract manufacturing organizations, as well as investigative sites and consultants that conduct our clinical trials, preclinical studies and other
scientific development services;
|
• |
manufacturing scale-up expenses and the cost of acquiring and manufacturing preclinical and clinical trial materials;
|
• |
employee-related expenses, including salaries, related benefits, travel and share-based compensation expenses for employees engaged in research and development functions, as well as external costs, such as fees paid to outside
consultants engaged in such activities;
|
• |
license maintenance fees and milestone fees incurred in connection with various license agreements;
|
• |
costs related to compliance with regulatory requirements; and
|
• |
depreciation and other expenses.
|
Year ended December 31,
|
||||||||
2022
|
2021
|
|||||||
Operating Expenses:
|
(in thousands)
|
|||||||
Research and development
|
$
|
16,977
|
$
|
6,334
|
||||
General and administrative
|
11,556
|
6,033
|
||||||
Total operating expenses
|
28,533
|
12,367
|
||||||
Financing (income) expense, net
|
(353
|
)
|
111
|
|||||
Loss before taxes
|
28,180
|
12,478
|
||||||
Taxes on income (benefit)
|
(534
|
)
|
-
|
|||||
Net loss
|
$
|
27,646
|
$
|
12,478
|
Year ended
December 31, |
Increase/(decrease)
|
|||||||||||||||
2022
|
2021
|
$ |
%
|
|||||||||||||
(in thousands)
|
||||||||||||||||
Net cash used in operating activities
|
$
|
(20,370
|
)
|
$
|
(12,374
|
)
|
$
|
(7,996
|
)
|
65
|
%
|
|||||
Net cash provided by (used in) investing activities
|
19,533
|
(45,186
|
)
|
64,719
|
(143
|
)%
|
||||||||||
Net cash provided by (used in) financing activities
|
(808
|
)
|
61,074
|
(61,882
|
)
|
(101
|
)%
|
|||||||||
Net increase (decrease) in cash, cash equivalents and restricted cash
|
$
|
(1,645
|
)
|
$
|
3,514
|
$
|
(5,159
|
)
|
(147
|
)%
|
• |
the progress and costs of our preclinical and clinical trials and other research and development activities;
|
• |
the scope, prioritization and number of our preclinical and clinical trials and other research and development programs;
|
• |
the amount of revenues and contributions we receive under future licensing, collaboration, development and commercialization arrangements with respect to our product candidates;
|
• |
the costs of development and expansion of our operational infrastructure;
|
• |
the costs and timing of obtaining regulatory approval for one or more of our product candidates
|
• |
our ability, or that of our collaborators, to achieve development milestones, marketing approval and other events or developments under potential future licensing agreements;
|
• |
the costs of filing, prosecuting, enforcing and defending patent claims and other intellectual property rights;
|
• |
the costs and timing of securing manufacturing arrangements for clinical or commercial production;
|
• |
the costs of contracting with third parties to provide sales and marketing capabilities for us or establishing such capabilities ourselves;
|
• |
the costs of acquiring or undertaking development and commercialization efforts for any future products, product candidates or technology;
|
• |
the magnitude of our general and administrative expenses; and
|
• |
any additional costs that we may incur under future in- and out-licensing arrangements relating to one or more of our product candidates.
|
Name and Principal Position
|
Year
|
Salary (1) ($)
|
Bonus (2) ($)
|
Option
Awards (3) ($) |
All Other
Compensation (4) ($)
|
Total ($)
|
||||||||||||||||
Dale Pfost
|
2021
|
182,557
|
-
|
300,000
|
22,868
|
505,425
|
||||||||||||||||
Chief Executive Officer and Chairman (5)
|
2022
|
600,000
|
300,000
|
1,500,000
|
75,160
|
2,475,160
|
||||||||||||||||
|
|
|||||||||||||||||||||
Adi Mor
|
2021
|
248,547
|
167,000
|
8,000
|
64,453
|
488,000
|
||||||||||||||||
Chief Scientific Officer, Director and Previous Chief Executive Officer (6)
|
2022
|
298,470
|
120,000
|
-
|
16,926
|
435,396
|
||||||||||||||||
|
|
|||||||||||||||||||||
Donald Marvin
|
2021
|
88,276
|
-
|
102,390
|
11,590
|
202,256
|
||||||||||||||||
Chief Financial Officer, Executive Vice President and Chief Operating Officer (7)
|
2022
|
460,000
|
207,000
|
660,252
|
60,397
|
1,387,649
|
||||||||||||||||
|
|
|||||||||||||||||||||
Sigal Fattal
|
2021
|
127,050
|
122,000
|
616,000
|
8,952
|
874,002
|
||||||||||||||||
Previous Interim Chief Financial Officer (8)
|
|
|
Option awards
|
||||||||||||
Name
|
Number of securities
underlying unexercised options (#) exercisable |
Number of
securities underlying unexercised options (#) unexercsiable |
Option
exercise price ($) |
Option expiration
date |
|||||||||
Dale Pfost, Chief Executive Officer and Chairman of the Board
|
133,977
|
325,376
|
(1)
|
10.05
|
October 25, 2031
|
||||||||
|
|
||||||||||||
Adi Mor, Chief Scientific Officer, Director and Previous Chief Executive Officer
|
131,698
|
-
|
1.49
|
March 15, 2028
|
|||||||||
|
|
||||||||||||
Donald Marvin, Chief Financial Officer, Executive Vice President and Chief Operating Officer
|
53,320
|
143,555
|
(2)
|
9.77
|
November 8, 2031
|
Name
|
Fees earned or paid
in cash ($) |
Option
awards ($) |
Total ($)
|
|||||||||
Nissim Darvish
|
47,000
|
76,000
|
(1)
|
123,000
|
||||||||
Jill Quigley
|
23,000
|
15,000
|
(2)
|
38,000
|
||||||||
Alan Moses
|
43,000
|
76,000
|
(3)
|
119,000
|
||||||||
Claude Nicaise
|
47,000
|
76,000
|
(4)
|
123,000
|
||||||||
Neil Cohen
|
47,000
|
76,000
|
(5)
|
123,000
|
|
Option awards
|
||||||||||||
Name
|
Number of ADSs
underlying unexercised options (#) exercisable |
Number of
ADSs underlying unexercised options (#) unexercsiable |
Option
exercise price ($) |
Option expiration
date |
|||||||||
Nissim Darvish
|
10,123
|
-
|
0.80
|
October 27, 2026
|
|||||||||
Nissim Darvish
|
6,932
|
4,952
|
27.26
|
April 19, 2031
|
|||||||||
Nissim Darvish
|
-
|
6,820
|
3.53
|
March 7, 2032
|
|||||||||
|
|
||||||||||||
Alan Moses
|
6,932
|
4,952
|
27.26
|
April 19, 2031
|
|||||||||
Alan Moses
|
-
|
6,820
|
3.53
|
March 7, 2032
|
|||||||||
|
|
||||||||||||
Claude Nicaise
|
6,932
|
4,952
|
27.26
|
April 19, 2031
|
|||||||||
Claude Nicaise
|
-
|
6,820
|
3.53
|
March 7, 2032
|
|||||||||
|
|
||||||||||||
Neil Cohen
|
515
|
173
|
13.20
|
July 16, 2030
|
|||||||||
Neil Cohen
|
6,932
|
4,952
|
27.26
|
April 19, 2031
|
|||||||||
Neil Cohen
|
-
|
6,820
|
3.53
|
March 7, 2032
|
|||||||||
|
|
||||||||||||
Jill Quigley
|
2,273
|
11,367
|
3.25
|
June 16, 2032
|
|
•
|
each person who is known by us to own beneficially more than 5% of our ordinary shares;
|
|
•
|
each director;
|
|
•
|
each executive officer; and
|
|
•
|
all of our directors and executive officers collectively.
|
NAME OF BENEFICIAL OWNER
|
Total
Beneficial
Ownership (ADSs)
|
Percentage of
ADSs Beneficially
Owned†
|
||||||
5% and Greater Shareholders
|
||||||||
OrbiMed Israel (1)
|
2,270,091
|
20.5
|
%
|
|||||
The Centillion Fund(2)
|
661,370
|
6.0
|
%
|
|||||
Rivendell Investments 2017-9(3)
|
1,131,563
|
10.2
|
%
|
|||||
Kobi George(4)
|
747,445
|
6.7
|
%
|
|||||
Apeiron Group(5)
|
770,388
|
6.9
|
%
|
|||||
Directors and Executive Officers
|
||||||||
Dale Pfost (6)
|
174,757
|
1.6
|
%
|
|||||
Donald Marvin (7)
|
75,828
|
*
|
%
|
|||||
Adi Mor (8)
|
747,445
|
6.7
|
%
|
|||||
Neil Cohen (9)
|
25,702
|
*
|
||||||
Nissim Darvish (10)
|
26,395
|
*
|
||||||
Alan Moses (11)
|
15,072
|
*
|
||||||
Claude Nicaise (12)
|
15,072
|
*
|
||||||
Jill Quigley (13)
|
3,788
|
*
|
||||||
Matthew Frankel
|
-
|
-
|
||||||
All current executive officers and directors as a group (9 persons)
|
1,084,059
|
9.40
|
%
|
(1) |
Pursuant to a Schedule 13D/A filed with the SEC by OrbiMed Israel BioFund GP Limited Partnership (“OrbiMed BioFund”) and OrbiMed Israel GP Ltd. (“OrbiMed GP”, and together with OrbiMed BioFund, “OrbiMed Israel”) on January 5, 2023,
such amount consists of (i) 2,241,274 ADSs and (ii) 28,817 ADSs issuable upon the exercise of warrants to purchase ADSs. OrbiMed GP, a company that acts as general partner of certain limited partnerships, is the general partner of
OrbiMed BioFund, which is the general partner of OrbiMed Israel Partners Limited Partnership, which is the entity that holds the foregoing securities. The address of OrbiMed Israel is 89 Medinat HaYehudim St., Build E, 11th Floor,
Herzliya 46766 Israel.
|
(2) |
The address of Centillion Fund, Inc. is 10 Manoel Street, Castries, Saint Lucia.
|
(3) |
Represents 1,108,509 ADSs, representing 22,170,180 ordinary shares, held by Rivendell Investments 2017-9 LLC, or Rivendell, as reported by Rivendell on Schedule 13G filed with the SEC on March 26, 2021, and 23,054 ADSs,
representing 461,080 Ordinary Shares, issuable upon the exercise of warrants. Rivendell is the shareholder of record. Peter Thiel is the beneficial owner of Rivendell and has sole voting and investment power over the securities held
by Rivendell. The address of Rivendell is 1209 Orange Street, Wilmington, Delaware 19801.
|
(4) |
Consists of (i) 257,247 ADSs owned directly by Dr. George, (ii) 324,775 ADSs owned by Dr. Adi Mor (Dr. George’s spouse), (iii) 33,725 options to purchase 33,725 ADSs issued directly to Dr. George, issuable upon the exercise of
options, and (iv) 131,698 options to purchase 131,698 ADSs, issued to Dr. Mor, (Dr. George’s spouse), as reported by Dr. Adi Mor on Schedule 13D/A filed with the SEC on November 17, 2022.
|
(5) |
The Apeiron Group consists of (i) Apeiron SICAV Ltd. - Presight Capital Fund One, of which owns 438,993 ADSs, (ii) Apeiron Presight Capital Fund II, LP, of which owns 288,170 ADSs and 28,817 ADSs issuable upon the exercise of
warrants and (iii) Apeiron Investment Group Ltd., of which owns 14,408 ADSs issuable upon the exercise of warrants. Each of Fabian Hansen and Christian Angermayer may be deemed to share voting and investment power with respect to the
ADSs held by the Apeiron Group.
|
(6) |
Includes 2,500 ADSs and 172,257 ADSs issuable upon the exercise of options within 60 days of the date hereof as reported by Dr. Dale Pfost on Form 4 filed with the SEC on March 15, 2022.
|
(7) |
Includes 2,000 ADSs and 73,828 ADSs issuable upon the exercise of options within 60 days of the date hereof as reported by Mr. Donald Marvin on Form 4 filed with the SEC on June 21, 2022.
|
(8) |
Consists of (i) 324,775 ADSs owned directly by Dr. Mor, (ii) 257,247 ADSs owned by Dr. George, (Dr. Mor’s spouse), (iii) 131,698 ADSs issued to Dr. Mor, issuable upon the exercise of options within 60 days of the date hereof, and
(iv) 33,725 options to purchase 33,725 ADSs issued to Dr. George, (Dr. Mor’s spouse) issuable upon the exercise of options within 60 days of the date hereof, as reported by Dr. Adi Mor on Schedule 13D/A filed with the SEC on November
17, 2022.
|
(9) |
Includes 10,000 ADSs, and 15,702 ADSs issuable upon the exercise of options within 60 days of the date hereof, as reported by Mr. Neil Cohen on Form 4 filed with the SEC on November 11, 2022.
|
(10) |
Includes 1,200 ADSs, and 25,195 ADSs issuable upon the exercise of options within 60 days of the date hereof, as reported by Dr. Nissim Darvish on Form 4 filed with the SEC on March 14, 2022.
|
(11) |
Represents 15,072 ADSs issuable upon the exercise of options within 60 days of the date hereof, as reported by Dr. Alan Moses on Form 4 filed with the SEC on March 9, 2022.
|
(12) |
Represents 15,072 ADSs issuable upon the exercise of options within 60 days of the date hereof, as reported by Dr. Claude Nicaise on Form 4 filed with the SEC on March 9, 2022.
|
(13) |
Represents 3,788 ADSs issuable upon the exercise of options within 60 days of the date hereof, as reported by Ms. Jill Quigley on Form 4 filed with the SEC on June 16, 2022.
|
|
•
|
amendments to our amended and restated articles of association;
|
|
•
|
appointment, terms of service or and termination of service of our auditors;
|
|
•
|
appointment of directors, including external directors (if applicable);
|
|
•
|
approval of certain related party transactions;
|
|
•
|
increases or reductions of our authorized share capital;
|
|
•
|
a merger; and
|
|
•
|
the exercise of our board of directors’ powers by a general meeting, if our board of directors is unable to exercise its powers and the exercise of any of its powers is required for our
proper management.
|
Persons depositing or withdrawing ordinary shares or ADS holders must pay
|
|
For
|
|
$5.00 (or less) per 100 ADSs (or portion of 100 ADSs)
|
|
Issuance of ADSs, including issuances resulting from a distribution of ordinary shares or rights or other property
Cancellation of ADSs for the purpose of withdrawal, including if the deposit agreement terminates
|
|
|
|
|
|
$.05 (or less) per ADS
|
|
Any cash distribution to ADS holders
|
|
|
|
|
|
A fee equivalent to the fee that would be payable if securities distributed to you had been ordinary shares and the ordinary shares had been deposited for issuance of ADSs
|
|
Distribution of securities distributed to holders of deposited securities (including rights) that are distributed by the depositary to ADS holders
|
|
|
|
|
|
$.05 (or less) per ADS per calendar year
|
|
Depositary services
|
|
Persons depositing or withdrawing ordinary shares or ADS holders must pay
|
|
For
|
|
Registration or transfer fees
|
|
Transfer and registration of ordinary shares on our share register to or from the name of the depositary or its agent when you deposit or withdraw ordinary shares
|
|
|
|
|
|
Expenses of the depositary
|
|
Cable, telex and facsimile transmissions (when expressly provided in the deposit agreement)
Converting foreign currency to U.S. dollars
|
|
|
|
|
|
Taxes and other governmental charges the depositary or the custodian has to pay on any ADSs or ordinary shares underlying ADSs, such as stock transfer taxes, stamp duty or withholding
taxes
|
|
As necessary
|
|
|
|
|
|
Any charges incurred by the depositary or its agents for servicing the deposited securities
|
|
As necessary
|
|
• |
90 days have passed since the depositary told us it wants to resign but a successor depositary has not been appointed and accepted its appointment;
|
• |
we delist the ADSs from an exchange on which they were listed and do not list the ADSs on another exchange within a reasonable time;
|
• |
the depositary has reason to believe that the ADSs have become, or will become, ineligible for registration on Form F-6 under the Securities Act.
|
• |
we appear to be insolvent or enter insolvency proceedings;
|
• |
all or substantially all the value of the deposited securities has been distributed either in cash or in the form of securities;
|
• |
there are no deposited securities underlying the ADSs or the underlying deposited securities have become apparently worthless; or
|
• |
there has been a replacement of deposited securities.
|
• |
are only obligated to take the actions specifically set forth in the deposit agreement without negligence or bad faith and the depositary will not be a fiduciary or have any fiduciary duty to holders of ADSs;
|
• |
are not liable if we are or it is prevented or delayed by law or circumstances beyond our or its control from performing our or its obligations under the deposit agreement;
|
• |
are not liable if we exercise or it exercises discretion permitted under the deposit agreement;
|
• |
are not liable for the inability of any holder of ADSs to benefit from any distribution on deposited securities that is not made available to holders of ADSs under the terms of the deposit agreement, or for any special, consequential
or punitive damages for any breach of the terms of the deposit agreement;
|
• |
have no obligation to become involved in a lawsuit or other proceeding related to the ADSs or the deposit agreement on your behalf or on behalf of any other person;
|
• |
are not liable for the acts or omissions of any securities depository, clearing agency or settlement system;
|
• |
may rely upon any documents we believe or it believes in good faith to be genuine and to have been signed or presented by the proper person; and
|
• |
the depositary has no duty to make any determinations or provide any information as to our status, or any liability for any tax consequences that may be incurred by ADS holders as a result of owning or holding ADSs or liable for the
inability or failure of an ADS holder to obtain the benefit of a foreign tax credit reduced rate of withholdings or refund of amounts withheld in respect of tax or any other tax benefit.
|
• |
payment of stock transfer or other taxes or other governmental charges and transfer or registration fees charged by third parties for the transfer of any ordinary shares or other deposited securities;
|
• |
satisfactory proof of the identity and genuineness of any signature or other information it deems necessary; and
|
• |
compliance with regulations it may establish, from time to time, consistent with the deposit agreement, including presentation of transfer documents.
|
• |
when temporary delays arise because: (i) the depositary has closed its transfer books or we have closed our transfer books; (ii) the transfer of ordinary shares is blocked to permit voting at a shareholders’ meeting; or (iii) we are
paying a dividend on our shares;
|
• |
when you owe money to pay fees, taxes and similar charges; or
|
• |
when it is necessary to prohibit withdrawals in order to comply with any laws or governmental regulations that apply to ADSs or to the withdrawal of ordinary shares or other deposited securities.
|
Underwriter
|
|
Number of
Units |
|
Number of Pre-Funded Units
|
|
Aegis Capital Corporation
|
|
|
|
|
|
Total
|
|
|
|
|
|
|
|
Per Unit
|
Per Pre-Funded Unit
|
|
Total No Exercise
|
Total Full Exercise
|
|||
Public offering price
|
|
$
|
$
|
$
|
$
|
||||
Underwriting discounts (1)
|
|
$
|
$
|
$
|
$
|
||||
Proceeds, before expenses, to us
|
|
$
|
$
|
$
|
$
|
•
|
Stabilizing transactions — The underwriter may make bids or purchases for the purpose of pegging, fixing or maintaining the price of the ADSs, so long as stabilizing bids do not
exceed a specified maximum.
|
•
|
Syndicate covering transactions — The underwriter may sell more ADSs in connection with this offering than the number of ADSs that it has committed to purchase. This over-allotment
creates a short position for the underwriter. This short sales position may involve either “covered” short sales or “naked” short sales. Covered short sales are short sales made in an amount not greater than the underwriter’s
over-allotment option to purchase additional ADSs, if applicable. The underwriter may close out any covered short position either by exercising its over-allotment option, if applicable, or by purchasing ADSs in the open market. To
determine how they will close the covered short position, the underwriter will consider, among other things, the price of ADSs available for purchase in the open market, as compared to the price at which it may purchase ADSs through
the over-allotment option, if applicable. Naked short sales are short sales in excess of the over-allotment option, if applicable. The underwriter must close out any naked short position by purchasing ADSs in the open market. A naked
short position is more likely to be created if the underwriter is concerned that, in the open market after pricing, there may be downward pressure on the price of the ADSs that could adversely affect investors who purchase ADSs in
this offering.
|
•
|
Penalty bids — If the underwriter purchases ADSs in the open market in a stabilizing transaction or syndicate covering transaction, it may reclaim a selling concession from the
underwriter and selling group members who sold those ADSs as part of this offering.
|
•
|
Passive market making — Market makers in the ADSs who is the underwriter or prospective underwriters may make bids for or purchases of ADSs, subject to limitations, until the time, if
ever, at which a stabilizing bid is made.
|
(a) |
by an investment firm, bank or intermediary permitted to conduct such activities in Italy in accordance with Legislative Decree No. 58 of 24 February 1998 and Legislative Decree No. 385 of 1 September 1993 (the “Banking Act”);
|
(b) |
in compliance with Article 129 of the Banking Act and the implementing guidelines of the Bank of Italy; and
|
(c) |
in compliance with any other applicable laws and regulations and other possible requirements or limitations which may be imposed by Italian authorities.
|
(a) |
to legal entities which are authorized or regulated to operate in the financial markets or, if not so authorized or regulated, whose corporate purpose is solely to invest in securities;
|
(b) |
to any legal entity which has two or more of (1) an average of at least 250 employees during the last financial year; (2) a total balance sheet of more than €43,000,000 and (3) an annual net turnover of more than €50,000,000, as
shown in its last annual or consolidated accounts;
|
(c) |
by the representative to fewer than 100 natural or legal persons (other than qualified investors as defined in the Prospectus Directive); or
|
(d) |
in any other circumstances falling within Article 3(2) of the Prospectus Directive, provided that no such offer of ADSs shall result in a requirement for the publication by the company or any underwriter of a prospectus pursuant to
Article 3 of the Prospectus Directive.
|
(a) |
it has only communicated or caused to be communicated and will only communicate or cause to be communicated any invitation or inducement to engage in investment activity (within the meaning of section 21 of the Financial Services and
Markets Act 2000 (the FSMA)) received by it in connection with the issue or sale of any ADSs in circumstances in which section 21(1) of the FSMA does not apply to the company; and
|
(b) |
it has complied with and will comply with all applicable provisions of the FSMA with respect to anything done by it in relation to the ADSs in, from or otherwise involving the United Kingdom.
|
|
•
|
the judgment was rendered by a court which was, according to the laws of the state of the court, competent to render the judgment;
|
|
|
|
|
•
|
the obligation imposed by the judgment is enforceable according to the rules relating to the enforceability of judgments in Israel and the substance of the judgment is not contrary to
public policy; and
|
|
|
|
|
•
|
the judgment is executory in the state in which it was given.
|
|
•
|
the judgment was given in a state whose laws do not provide for the enforcement of judgments of Israeli courts (subject to exceptional cases);
|
|
|
|
|
•
|
the enforcement of the judgment is likely to prejudice the sovereignty or security of the State of Israel;
|
|
|
|
|
•
|
the judgment was obtained by fraud;
|
|
|
|
|
•
|
the opportunity given to the defendant to bring its arguments and evidence before the court was not reasonable in the opinion of the Israeli court;
|
|
|
|
|
•
|
the judgment was rendered by a court not competent to render it according to the laws of private international law as they apply in Israel;
|
|
|
|
|
•
|
the judgment is contradictory to another judgment that was given in the same matter between the same parties and that is still valid; or
|
|
|
|
|
•
|
at the time the action was brought in the foreign court, a lawsuit in the same matter and between the same parties was pending before a court or tribunal in Israel.
|
|
•
|
The Registrant’s Annual Report on Form 10-K for the fiscal year ended
December 31, 2022, filed with the SEC on March 20, 2023 (the “Annual Report”);
|
|
•
|
The Company’s Current Reports on Form 8-K, as filed with the SEC on January
3, 2023, January 11, 2023, February 21, 2023 and February 21, 2023;
|
|
•
|
The description of our share capital, which is set forth in exhibit 4.1 of our Annual Report, and as may be further updated or amended in any amendment or report filed for such purpose;
and
|
|
|
|
|
•
|
All other reports filed pursuant to Section 13(a) or 15(d) of the Securities Exchange Act of 1934, as amended (the “Exchange Act”), since the end of the fiscal year covered by the
Annual Report.
|
Aegis Capital Corp.
|
|
Amount Paid
or to be Paid |
|||
SEC registration fee
|
$
|
3,306
|
||
FINRA filing fee
|
$
|
1,050
|
||
Legal fees and expenses (including underwriters' legal fees)
|
$
|
300,000
|
||
Accounting fees and expenses
|
$
|
65,710
|
||
Printing expenses
|
$
|
15,000
|
||
Depositary and transfer agent fees and expenses
|
$
|
151,312
|
||
Miscellaneous
|
$
|
10,000
|
||
Total
|
$
|
546,378
|
• |
reasonable litigation expenses, including attorneys’ fees, incurred by the office holder as a result of an investigation or proceeding instituted against him or her by an authority authorized to conduct such investigation or
proceeding, provided that (i) no indictment was filed against such office holder as a result of such investigation or proceeding; and (ii) no financial liability, such as a criminal penalty (as defined in the Companies Law), was imposed
upon him or her as a substitute for the criminal proceeding as a result of such investigation or proceeding or, if such financial liability was imposed, it was imposed with respect to an offense that does not require proof of criminal
intent or in connection with a monetary sanction;
|
• |
reasonable litigation expenses, including attorneys’ fees, incurred by the office holder or imposed by a court (i) in proceedings instituted against him or her by the company, on its behalf or by a third party, or (ii) in connection
with criminal proceedings in which the office holder was acquitted, or (iii) as a result of a conviction for a crime that does not require proof of criminal intent;
|
• |
a financial liability imposed on him or her in favor of another person pursuant to a judgment, including a settlement or arbitrator’s award approved by a court. However, if an undertaking to indemnify an office holder with respect to
such liability is provided in advance, then such an undertaking must be limited to events which, in the opinion of the board of directors, can be foreseen based on the company’s activities when the undertaking to indemnify is given, and
to an amount or according to criteria determined by the board of directors as reasonable under the circumstances, and such undertaking shall detail the abovementioned events and amount or criteria; and
|
• |
expenses, including reasonable litigation expenses and legal fees, incurred by an office holder in relation to an administrative proceeding instituted against such office holder, or certain compensation payments made to an injured
party imposed on an office holder by an administrative proceeding, pursuant to certain provisions of the Israeli Securities Law.
|
• |
a breach of duty of care to the company or to a third party, including a breach arising out of the negligent conduct of an office holder;
|
• |
a breach of duty of loyalty to the company, provided the director or officer acted in good faith and had a reasonable basis to believe that the act would not prejudice the interests of the company;
|
• |
financial liabilities imposed on the office holder for the benefit of a third party;
|
• |
financial liabilities imposed in an administrative proceeding on the office holder in favor of a third party harmed by a breach, pursuant to certain provisions of the Israeli Securities Law; and
|
• |
expenses, including reasonable litigation expenses and legal fees, incurred by the office holder as a result of an administrative proceeding instituted against him or her, pursuant to certain provisions of the Israeli Securities Law.
|
• |
a breach of duty of loyalty, except to the extent that the office holder acted in good faith and had a reasonable basis to believe that the act would not prejudice the company;
|
• |
a breach of duty of care committed intentionally or recklessly, excluding a breach arising out of the negligent conduct of the office holder;
|
• |
an act or omission committed with intent to derive unlawful personal benefit; or
|
• |
a fine, monetary sanction, penalty or forfeit levied against the office holder.
|
1. |
To file, during any period in which offers or sales are being made, a post-effective amendment to this registration statement:
|
a. |
To include any prospectus required by Section 10(a)(3) of the Securities Act;
|
b. |
To reflect in the prospectus any facts or events arising after the effective date of the registration statement (or the most recent post-effective amendment thereof) which, individually or in the aggregate, represent a fundamental
change in the information set forth in the registration statement. Notwithstanding the foregoing, any increase or decrease in volume of securities offered (if the total dollar value of securities offered would not exceed that which was
registered) and any deviation from the low or high end of the estimated maximum offering range may be reflected in the form of prospectus filed with the SEC pursuant to Rule 424(b) if, in the aggregate, the changes in volume and price
represent no more than a 20% change in the maximum aggregate offering price set forth in the “Calculation of Registration Fee” table in the effective registration statement; and
|
c. |
To include any material information with respect to the plan of distribution not previously disclosed in the registration statement or any material change to such information in the registration statement.
|
2. |
That, for the purpose of determining any liability under the Securities Act, each such post-effective amendment shall be deemed to be a new registration statement relating to the securities offered therein, and the offering of such
securities at that time shall be deemed to be the initial bona fide offering thereof.
|
3. |
To remove from registration by means of a post-effective amendment any of the securities being registered which remain unsold at the termination of the offering.
|
4. |
That, for the purpose of determining liability under the Securities Act to any purchaser, each prospectus filed pursuant to Rule 424(b) as part of a registration statement relating to an offering, other than registration statements
relying on Rule 430B or other than prospectuses filed in reliance on Rule 430A, shall be deemed to be part of and included in the registration statement as of the date it is first used after effectiveness. Provided, however, that no
statement made in a registration statement or prospectus that is part of the registration statement or made in a document incorporated or deemed incorporated by reference into the registration statement or prospectus that is part of the
registration statement will, as to a purchaser with a time of contract of sale prior to such first use, supersede or modify any statement that was made in the registration statement or prospectus that was part of the registration
statement or made in any such document immediately prior to such date of first use.
|
5. |
That, for the purpose of determining liability of the registrant under the Securities Act to any purchaser in the initial distribution of the securities, the undersigned registrant undertakes that in a primary offering of securities
of the undersigned registrant pursuant to this registration statement, regardless of the underwriting method used to sell the securities to the purchaser, if the securities are offered or sold to such purchaser by means of any of the
following communications, the undersigned registrant will be a seller to the purchaser and will be considered to offer or sell such securities to such purchaser.
|
a. |
Any free writing prospectus relating to the offering prepared by or on behalf of the undersigned registrant or used or referred to by the undersigned registrant;
|
b. |
The portion of any other free writing prospectus relating to the offering containing material information about the undersigned registrant or its securities provided by or on behalf of the undersigned registrant; and
|
c. |
Any other communication that is an offer in the offering made by the undersigned registrant to the purchaser.
|
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CHEMOMAB THERAPEUTICS LTD.
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By:
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/s/ Dale Pfost
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Dale Pfost
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Chairman of the Board,
Chief Executive Officer
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Signature
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Title
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Date
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/s/ Dale Pfost
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Chairman of the Board and
Chief Executive Officer
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March 21, 2023
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Dale Pfost
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(Principal Executive Officer)
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/s/ Donald Marvin
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Chief Financial Officer, Executive Vice President and Chief Operating Officer
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March 21, 2023
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Donald Marvin
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(Principal Financial and Accounting Officer)
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*
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Director
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March 21, 2023
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Adi Mor
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*
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Director
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March 21, 2023
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Nissim Darvish
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*
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Director
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March 21, 2023
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Alan Moses
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*
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Director
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March 21, 2023
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Claude Nicaise
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*
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Director
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March 21, 2023
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Neil Cohen
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*
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Director
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March 21, 2023
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Jill M. Quigley
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/s/ Dale Pfost
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Dale Pfost
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Attorney in Fact
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CHEMOMAB THERAPEUTICS, INC.
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By:
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/s/ Dale Pfost
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Dale Pfost
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Chairman of the Board,
Chief Executive Officer
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Very truly yours,
CHEMOMAB THERAPEUTICS LTD.
By: ________________________________
Name:
Title:
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Underwriter
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Number of Firm Units to Be
Purchased |
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Number of Option Securities
to Be Purchased if the Maximum Over-Allotment Option Is Exercised |
Aegis Capital Corp.
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Common Units: [NUMBER]
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[NUMBER]
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Pre-funded Units: [NUMBER]
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Total:
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[NUMBER]
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[NUMBER]
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Warrant ADSs: [●]
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Initial Exercise Date: [●], 2023
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Issue Date: [●], 2023
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(A) = |
as applicable: (i) the VWAP on the Trading Day immediately preceding the date of the applicable Notice of Exercise if such Notice of Exercise is (1) both executed and
delivered pursuant to Section 2(a) hereof on a day that is not a Trading Day or (2) both executed and delivered pursuant to Section 2(a) hereof on a Trading Day prior to the opening of “regular trading hours” (as defined in Rule 600(b) of
Regulation NMS promulgated under the federal securities laws) on such Trading Day, (ii) at the option of the Holder, either (y) the VWAP on the Trading Day immediately preceding the date of the applicable Notice of Exercise or (z) the Bid
Price of the ADSs on the principal Trading Market as reported by Bloomberg L.P. as of the time of the Holder’s execution of the applicable Notice of Exercise if such Notice of Exercise is executed during “regular trading hours” on a Trading
Day and is delivered within two (2) hours thereafter (including until two (2) hours after the close of “regular trading hours” on a Trading Day) pursuant to Section 2(a) hereof or (iii) the VWAP on the date of the applicable Notice of
Exercise if the date of such Notice of Exercise is a Trading Day and such Notice of Exercise is both executed and delivered pursuant to Section 2(a) hereof after the close of “regular trading hours” on such Trading Day;
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(B) = |
the Exercise Price of this Warrant, as adjusted hereunder; and
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(X) = |
the number of Warrant ADSs that would be issuable upon exercise of this Warrant in accordance with the terms of this Warrant if such exercise were by means of a cash
exercise rather than a cashless exercise.
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CHEMOMAB THERAPEUTICS LTD.
By: ______________________________
Name: Dale
Pfost
Its: Chief
Executive Officer
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Name of Investing Entity:
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Signature of Authorized
Signatory of Investing Entity:
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Name of Authorized Signatory:
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Title of Authorized Signatory:
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Date:
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Name:
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(Please Print)
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Address:
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Phone Number:
Email Address:
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(Please Print)
______________________________________
______________________________________
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Dated: _______________ __, ______
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Holder’s Signature:
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Holder’s Address:
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Warrant ADSs: [●]
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Initial Exercise Date: [●], 2023
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Issue Date: [●], 2023
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(A) = |
as applicable: (i) the VWAP on the Trading Day immediately preceding the date of the applicable Notice of Exercise if such Notice of Exercise is (1) both executed and delivered pursuant to Section 2(a) hereof on a day that is not a Trading
Day or (2) both executed and delivered pursuant to Section 2(a) hereof on a Trading Day prior to the opening of “regular trading hours” (as defined in Rule 600(b) of Regulation NMS promulgated under the federal securities laws) on such
Trading Day, (ii) at the option of the Holder, either (y) the VWAP on the Trading Day immediately preceding the date of the applicable Notice of Exercise or (z) the Bid Price of the ADSs on the principal Trading Market as reported by
Bloomberg L.P. as of the time of the Holder’s execution of the applicable Notice of Exercise if such Notice of Exercise is executed during “regular trading hours” on a Trading Day and is delivered within two (2) hours thereafter (including
until two (2) hours after the close of “regular trading hours” on a Trading Day) pursuant to Section 2(a) hereof or (iii) the VWAP on the date of the applicable Notice of Exercise if the date of such Notice of Exercise is a Trading Day and
such Notice of Exercise is both executed and delivered pursuant to Section 2(a) hereof after the close of “regular trading hours” on such Trading Day;
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(B) = |
the Exercise Price of this Warrant, as adjusted hereunder; and
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(X) = |
the number of Warrant ADSs that would be issuable upon exercise of this Warrant in accordance with the terms of this Warrant if such exercise were by means of a cash exercise rather than a cashless exercise.
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CHEMOMAB THERAPEUTICS LTD.
By: ______________________________
Name: Dale Pfost
Its: Chief Executive Officer
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Name of Investing Entity:
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Signature of Authorized Signatory of Investing Entity:
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Name of Authorized Signatory:
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Title of Authorized Signatory:
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Date:
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Name:
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(Please Print)
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Address:
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Phone Number:
Email Address:
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(Please Print)
______________________________________
______________________________________
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Dated: _______________ __, ______
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Holder’s Signature:
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Holder’s Address:
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Very truly yours,
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/s/ Meitar Law Offices
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Meitar Law Offices
|
![]() |
Wilson
Sonsini Goodrich & Rosati
Professional Corporation 1881
9th Street, Suite 110
Boulder,
CO 80302
O: 303-256-5900
F: 866.974.7329 |
Very truly yours,
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/s/ Wilson Sonsini Goodrich & Rosati
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WILSON SONSINI GOODRICH & ROSATI
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Professional Corporation
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/s/ Somekh Chaikin
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Member Firm of KPMG International
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Form S-1
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(Form Type)
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CHEMOMAB THERAPEUTICS LTD.
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|
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(Exact Name of Registrant as Specified in its Charter)
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|
Security
Type |
Security
Class Title |
Fee
Calculation or Carry Forward Rule |
Maximum
Aggregate Offering Price(1)(2) |
Fee
Rate |
Amount of
Registration Fee |
|||||||||||||
Newly Registered Securities
|
||||||||||||||||||
Fees to be Paid
|
Equity
|
Units consisting of (i) either one American Depositary Share or one Pre-Funded Warrant to purchase one American Depositary Share
and (ii) one Warrant to Purchase one American Depositary Share (2)(3)
|
(1
|
)
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$
|
11,500,000.00
|
$
|
.0001102
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$
|
1,267.30
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||||||||
Fees to be Paid
|
Equity
|
American Depositary Shares issuable upon exercise of Pre-Funded Warrants and Warrants (2)
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(1
|
)
|
$
|
11,500,000.00
|
$
|
.0001102
|
$
|
1,267.30
|
||||||||
Total Offering Amounts
|
$
|
23,000,000.00
|
$
|
2,534.60
|
||||||||||||||
Total Fees Previously Paid
|
$
|
3,306.00
|
||||||||||||||||
Total Fee Offsets
|
-
|
|||||||||||||||||
Net Fee Due
|
$
|
0.00
|
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(1)
|
Estimated solely for the purpose of computing the amount of the registration fee pursuant to Rule 457(o) under the Securities
Act of 1933, as amended.
|
|
|
|
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(2)
|
Each ADS represents twenty (20) ordinary shares of the registrant. ADSs issuable upon deposit of the ordinary shares registered
hereby have been registered pursuant to a separate registration statement on Form F-6 (File No. 333-229522).
|
|
|
|
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(3)
|
Calculated in accordance with Rule 457(g) under the Securities Act, because the ADSs of the registrant underlying the warrants are
registered hereby.
|