As filed with the Securities and Exchange Commission
on August 19, 2024.
Registration No. 333-
UNITED STATES
SECURITIES AND EXCHANGE COMMISSION
Washington, D.C. 20549
FORM S-3
REGISTRATION STATEMENT
UNDER
THE SECURITIES ACT OF 1933
CHECKPOINT THERAPEUTICS, INC.
(Exact Name of Registrant as Specified in Its
Charter)
Delaware
(State or Other Jurisdiction of
Incorporation or Organization) |
47-2568632
(I.R.S. Employer
Identification Number) |
95 Sawyer Road, Suite 110
Waltham, Massachusetts 02453
(781) 652-4500
(Address, Including Zip Code, and Telephone
Number, Including Area Code, of Registrant’s Principal Executive Offices)
James F. Oliviero III
President & Chief Executive Officer
95 Sawyer Road, Suite 110
Waltham, Massachusetts 02453
(781) 652-4500
(Name, Address, Including Zip Code, and
Telephone Number, Including Area Code, of Agent For Service)
Copies to:
Matthew W. Mamak, Esq.
Alston & Bird LLP
90 Park Avenue
New York, NY 10016
(212) 210-9400
Approximate
date of commencement of proposed sale to the public: As soon as practicable after the effective date of this Registration
Statement.
If
the only securities being registered on this Form are being offered pursuant to dividend or interest reinvestment plans, please
check the following box: ¨
If
any of the securities being registered on this form are to be offered on a delayed or continuous basis pursuant to Rule 415 under
the Securities Act of 1933, other than securities offered only in connection with dividend or interest reinvestment plans, check the
following box. x
If
this form is filed to register additional securities for an offering pursuant to Rule 462(b) under the Securities Act, check
the following box and list the Securities Act registration statement number of the earlier effective registration statement for the same
offering. ¨
If
this form is a post-effective amendment filed pursuant to Rule 462(c) under the Securities Act, check the following box and
list the Securities Act registration statement number of the earlier effective registration statement for the same offering. ¨
If
this Form is a registration statement pursuant to General Instruction I.D. or a post-effective amendment thereto that shall become
effective upon filing with the Commission pursuant to Rule 462(e) under the Securities Act, check the following box. ¨
If
this Form is a post-effective amendment to a registration statement filed pursuant to General Instruction I.D. filed to register
additional securities or additional classes of securities pursuant to Rule 413(b) under the Securities Act, check the following
box. ¨
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 definition of “large accelerated filer,” “accelerated filer,” “smaller reporting company”
and “emerging growth company” in Rule 12b-2 of the Exchange Act.
Large accelerated filer ¨ |
Accelerated filer ¨ |
Non-accelerated filer x |
Smaller reporting company x |
|
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. ¨
The Registrant hereby
amends this registration statement on such date or dates as may be necessary to delay its effective date until the Registrant shall file
a further amendment which specifically states that this registration statement shall thereafter become effective in accordance with Section 8(a) of
the Securities Act of 1933 or until the registration statement shall become effective on such date as the Securities and Exchange Commission,
acting pursuant to said Section 8(a), may determine.
The information in this prospectus is not complete and
may be changed. We may not sell these securities until the registration statement filed with the Securities and Exchange Commission is
effective. This prospectus is not an offer to sell these securities and we are not soliciting offers to buy these securities in any jurisdiction
where the offer or sale is not permitted.
Subject To Completion, Dated August 19,
2024
PROSPECTUS
6,204,879 Shares of Common Stock underlying
certain Common Warrants and Placement Agent Warrants
This prospectus relates to
the resale from time to time by certain selling stockholders identified herein of up to 5,853,659 shares of common stock, $0.0001 par
value (“Common Stock”), underlying those certain Common Stock warrants (the “Common Warrants”) and 351,220 shares
of Common Stock, $0.0001 par value, underlying those certain Placement Agent Warrants (the “Placement Agent Warrants,” and
together with the Common Warrants, the “Warrants”). We refer to the 6,204,879 shares of Common Stock underlying the Warrants
being registered herein as the “Registered Securities.”
The offering price per share
of Common Stock and accompanying warrant was $2.05. The Common Warrants will be exercisable beginning on the effective date of stockholder
approval of the issuance of the shares upon exercise of the Common Warrants, will expire five (5) years following the issuance date
and have an exercise price of $2.05 per share. The Placement Agent Warrants were exercisable immediately upon issuance and will expire
five (5) years following the issuance date and have an exercise price of $2.5625 per share.
The selling stockholders
may offer, sell or distribute all or a portion of the Registered Securities publicly or through private transactions at prevailing market
prices or at negotiated prices. The selling stockholders may retain underwriters, dealers or agents from time to time. See “Plan
of Distribution” for more information about how the selling stockholders may sell the Registered Securities.
We will not receive any proceeds
from the sale of the Registered Securities, but we agreed to bear the expenses relating to the registration of the Registered Securities.
Our Common Stock is listed for trading on the Nasdaq Capital Market
under the symbol “CKPT.” On August 16, 2024, the last reported sale price of our Common Stock on the Nasdaq Capital Market
was $2.21 per share.
Investing in our securities
involves a high degree of risk. See the information contained under “Risk Factors” on page 6 of this prospectus and
in the documents incorporated herein by reference. You should read this entire prospectus carefully before you make your investment decision.
Neither the Securities
and Exchange Commission nor any state securities commission has approved or disapproved of these securities or passed upon the accuracy
or adequacy of this prospectus. Any representation to the contrary is a criminal offense.
The date of this prospectus is , 2024.
TABLE OF CONTENTS
Page
IMPORTANT INFORMATION ABOUT THIS PROSPECTUS
This prospectus is part of
a registration statement that we have filed with the SEC pursuant to which the selling stockholders named herein may, from time to time,
offer and sell or otherwise dispose of the shares of our Common Stock, $0.0001 par value covered by this prospectus. You should not assume
that the information contained in this prospectus is accurate on any date subsequent to the date set forth on the front cover of this
prospectus or that any information we have incorporated by reference is correct on any date subsequent to the date of the document incorporated
by reference, even though this prospectus is delivered or shares of Common Stock are sold or otherwise disposed of on a later date. It
is important for you to read and consider all information contained in this prospectus, including the documents incorporated by reference
therein, in making your investment decision. You should also read and consider the information in the documents to which we have referred
you under “Where You Can Find More Information” and “Incorporation of Certain Documents by Reference” in this
prospectus.
We have not authorized anyone
to give any information or to make any representation to you other than those contained or incorporated by reference in this prospectus.
You must not rely upon any information or representation not contained or incorporated by reference in this prospectus. This prospectus
does not constitute an offer to sell or the solicitation of an offer to buy any of our shares of Common Stock other than the shares of
our Common Stock covered hereby, nor does this prospectus constitute an offer to sell or the solicitation of an offer to buy any securities
in any jurisdiction to any person to whom it is unlawful to make such offer or solicitation in such jurisdiction. Persons who come into
possession of this prospectus in jurisdictions outside the United States are required to inform themselves about, and to observe, any
restrictions as to the offering and the distribution of this prospectus applicable to those jurisdictions.
Unless we have indicated
otherwise, or the context otherwise requires, references in this prospectus to “Checkpoint,” the “Company,” “we,”
“us” and “our” refer to Checkpoint Therapeutics, Inc.
|
SUMMARY |
|
Our
Business |
|
We are a clinical-stage immunotherapy and targeted oncology company focused on the acquisition, development and commercialization of
novel treatments for patients with solid tumor cancers. We are evaluating our lead antibody product candidate, cosibelimab, an anti-programmed
death-ligand 1 antibody licensed from the Dana-Farber Cancer Institute, in an ongoing global, open-label, multicohort Phase 1 clinical
trial in checkpoint therapy-naïve patients with selected recurrent or metastatic cancers, including ongoing cohorts in locally advanced
and metastatic cutaneous squamous cell carcinoma (“CSCC”) intended to support one or more applications for marketing approval.
Based on top-line and interim results in metastatic and locally advanced CSCC, respectively, Checkpoint submitted a Biologics License
Application (“BLA”) to the U.S. Food and Drug Administration (“FDA”) for these indications in January 2023.
On December 15, 2023, the FDA issued a complete response letter (“CRL”) for the
treatment of patients with metastatic or locally advanced CSCC who are not candidates or curative surgery or radiation. The CRL only
cites findings that arose during a multi-sponsor inspection of our third-party contract manufacturing organization as approvability issues
to address in a resubmission. In July 2024, we announced that we had completed a resubmission of the BLA to the FDA for cosibelimab
to potentially address the issues cited in the CRL. The resubmission was accepted by the FDA as a complete response and the FDA has set
a Prescription Drug User Fee Act goal date of December 28, 2024. |
|
In
addition, we are evaluating our lead small-molecule, targeted anti-cancer agent, olafertinib (formerly CK-101), a third-generation
epidermal growth factor receptor (“EGFR”) inhibitor, as a potential new treatment for patients with EGFR mutation-positive
non-small cell lung cancer. |
|
In
January 2022, we announced top-line results from a registration-enabling cohort of our multi-regional, Phase 1 clinical trial
of cosibelimab in patients with metastatic CSCC. The cohort met its primary endpoint, with cosibelimab demonstrating a confirmed
objective response rate (“ORR”) of 47.4% (95% CI: 36.0, 59.1) based on independent central review of 78 patients enrolled
in the metastatic CSCC cohort using Response Evaluation Criteria in Solid Tumors version 1.1 (“RECIST 1.1”). |
|
In
June 2022, we announced interim results from a registration-enabling cohort of our multi-regional, Phase 1 clinical trial of
cosibelimab in patients with locally advanced CSCC that are not candidates for curative surgery or radiation. Cosibelimab demonstrated
a confirmed ORR of 54.8% (95% CI: 36.0, 72.7) based on independent central review of 31 patients enrolled in the cohort. |
|
In
July 2023, we announced longer-term results for cosibelimab from its pivotal studies in locally advanced and metastatic CSCC.
These results demonstrated a deepening of response over time, resulting in complete response rates of 26% and 13% in locally advanced
and metastatic CSCC, respectively. Additionally, the confirmed ORR in metastatic CSCC increased to 50.0% based on independent central
review using RECIST 1.1. Furthermore, responses continue to remain durable over time with the median duration of response not yet
reached in either group. Updated safety data across 247 patients enrolled and treated with cosibelimab in all cohorts of the ongoing
study remain consistent with those previously reported. |
|
To
date, we have not received approval for the sale of any product candidate in any market and, therefore, have not generated any product
sales from any product candidates. In addition, we have incurred substantial operating losses since our inception, and expect to
continue to incur significant operating losses for the foreseeable future and may never become profitable. As of June 30, 2024,
we have an accumulated deficit of $331.9 million. |
|
We
are a majority-controlled subsidiary of Fortress Biotech, Inc (“Fortress”). |
|
|
About
this Offering |
|
On
July 2, 2024, we entered into a securities purchase agreement (the “Purchase Agreement”) with a single
healthcare-dedicated institutional investor. The Purchase Agreement provided for the sale and issuance by us of an aggregate
of: (i) 1,230,000 shares (the “Shares”) of our Common Stock, (ii) Pre-Funded Warrants to purchase up to 4,623,659
Shares of our Common Stock, (iii) Common Warrants to purchase up to 5,853,659 shares of our Common Stock, and (iv) Placement
Agent Warrants to purchase up to 351,220 shares of our Common Stock. The offering price per share of Common Stock and accompanying
warrant was $2.05. The Pre-Funded Warrants were exercisable immediately upon issuance and will expire when exercised in full and
have an exercise price of $2.0499 per share. The Common Warrants will be exercisable beginning on the effective date of stockholder
approval of the issuance of the shares upon exercise of the Common Warrants, will expire five (5) years following the issuance
date and have an exercise price of $2.05 per share. The Placement Agent Warrants were exercisable immediately upon issuance and will
expire five (5) years following the issuance date and have an exercise price of $2.5625 per share. |
|
The
Shares and Pre-Funded Warrants described above were offered pursuant to an effective shelf registration statement on Form S-3
(Registration No. 333-270843) and a related prospectus supplement filed with the Securities and Exchange Commission (the “Registered
Direct Offering”). The Common Warrants and Placement Agent Warrants described above were issued in a concurrent private placement
(the “Private Placement” and together with the Registered Direct Offering, the “Offerings”). The Offerings
closed on July 3, 2024. |
|
We
agreed to register the Registered Securities. |
|
Company
Information |
|
Checkpoint
Therapeutics, Inc. was incorporated in Delaware on November 10, 2014, and commenced principal operations in March 2015.
Our principal executive offices are located at 95 Sawyer Road, Suite 110, Waltham, MA 02453, and our telephone number is (781)
652-4500. We maintain a website on the Internet at www.checkpointtx.com and our e-mail address is ir@checkpointtx.com. Our internet
website, and the information contained on it, are not to be considered part of this prospectus. For further information regarding
us and our financial information, you should refer to our recent filings with the SEC. See “Where You Can Find More Information”
and “Incorporation of Certain Documents by Reference.” |
|
A
certificate of amendment of Checkpoint’s certificate of incorporation for a 1-for-10 reverse split of Checkpoint’s issued
and outstanding Common Stock was effective as of December 6, 2022. Unless otherwise indicated, all share numbers herein, including
Common Stock and all securities convertible into Common Stock, give effect to the Reverse Stock Split. |
|
Our
Common Stock is listed on the Nasdaq Capital Market under the symbol “CKPT”. |
|
SPECIAL NOTE REGARDING FORWARD-LOOKING STATEMENTS
Certain matters discussed
in this prospectus may constitute forward-looking statements for purposes of the Securities Act of 1933, as amended, or the Securities
Act, and the Securities Exchange Act of 1934, as amended, or the Exchange Act, and involve known and unknown risks, uncertainties and
other factors that may cause our actual results, performance or achievements to be materially different from the future results, performance
or achievements expressed or implied by such forward-looking statements. The words “anticipate,” “believe,” “estimate,”
“may,” “expect,” “will,” “could,” “project,” “intend” and similar
expressions are generally intended to identify forward-looking statements. Our actual results may differ materially from the results
anticipated in these forward-looking statements due to a variety of factors, including, without limitation, those discussed under the
caption “Risk Factors” contained in this prospectus, any prospectus supplement, any applicable free writing prospectus, or
under similar heading in the other documents that are incorporated by reference into this prospectus. All written or oral forward-looking
statements attributable to us are expressly qualified in their entirety by these cautionary statements. Such forward-looking statements
include, but are not limited to, statements about our:
· |
expectations for increases
or decreases in expenses; |
· |
expectations for the clinical
and pre-clinical development, manufacturing, regulatory approval, and commercialization of our pharmaceutical product candidates
or any other products we may acquire or in-license; |
· |
use of clinical research
centers and other contractors; |
· |
expectations as to the
timing of commencing or completing pre-clinical and clinical trials and the expected outcomes of those trials; |
· |
intention to use data from
our ongoing Phase 1 clinical trial of cosibelimab to support the submissions of one or more U.S. Biologics License Applications (“BLAs”)
and relatedly, our assumption that exclusively foreign clinical data may be acceptable to support marketing approval under U.S. Food
and Drug Administration (“FDA”) regulations; |
|
|
· |
expectations that
the FDA will agree that our BLA resubmission addresses the approvability issues identified in the complete response letter (“CRL”)
received from the FDA on December 15, 2023; |
|
|
· |
expectations regarding
the potential differentiation of cosibelimab, including a potentially favorable study profile as compared to the currently available
anti-PD-1 therapies, the two-fold mechanism of action of cosibelimab translating into potential enhanced efficacy, and the projections
of publication and regulatory submission timelines; |
|
|
· |
expectations for incurring
capital expenditures to expand our research and development and manufacturing capabilities; |
· |
expectations for generating
revenue or becoming profitable on a sustained basis; |
· |
expectations or ability
to enter into marketing and other partnership agreements; |
· |
expectations or ability
to enter into product acquisition and in-licensing transactions; |
· |
expectations or ability
to build our own commercial infrastructure to manufacture, market and sell our product candidates; |
· |
expectations for the acceptance
of our products by doctors, patients or payors; |
· |
ability to compete against
other companies and research institutions; |
· |
ability to secure adequate
protection for our intellectual property; |
· |
ability to attract and
retain key personnel; |
· |
ability to obtain reimbursement
for our products; |
· |
estimates of the sufficiency
of our existing cash and cash equivalents and investments to finance our operating requirements, including expectations regarding
the value and liquidity of our investments; |
· |
stock price and the volatility
of the equity markets; |
· |
expected losses; and |
|
|
· |
expectations for future
capital requirements. |
The forward-looking statements
contained in this prospectus reflect our views and assumptions only as of the date of this prospectus. Except as required by law, we
assume no responsibility for updating any forward-looking statements. We qualify all of our forward-looking statements by these cautionary
statements. New risks and uncertainties arise from time to time, and it is impossible for us to predict these events or how they may
affect us. In addition, with respect to all of our forward-looking statements, we claim the protection of the safe harbor for forward-looking
statements contained in the Private Securities Litigation Reform Act of 1995.
RISK FACTORS
Investment
in our securities involves risks. Before deciding whether to invest in our securities, you should consider carefully the risk factors
discussed below and those contained in the section entitled “Risk Factors” contained in our Annual Report on Form 10-K for the year ended December 31, 2023, as filed with the SEC on March 22, 2024, which is incorporated herein
by reference in its entirety, as well as any amendment or update to our risk factors reflected in subsequent filings with the SEC. If
any of the risks or uncertainties described in our SEC filings actually occurs, our business, financial condition, results of operations
or cash flow could be materially and adversely affected. This could cause the trading price of our Common Stock to decline, resulting
in a loss of all or part of your investment. The risks and uncertainties we have described are not the only ones facing our company.
Additional risks and uncertainties not presently known to us or that we currently deem immaterial may also affect our business operations.
Risks Related to Our Common Stock and This
Offering
The
resale of our Common Stock by the selling stockholders could adversely affect the prevailing market price of our Common Stock and may
cause substantial dilution to our existing stockholders.
We are registering for resale
by the selling stockholders 5,853,659 shares of Common Stock, $0.0001 par value, underlying those certain Common Warrants and 351,220
shares of Common Stock, $0.0001 par value, underlying those certain Placement Agent Warrants. We refer to the 6,204,879 shares of Common
Stock underlying the Warrants being registered herein as the “Registered Securities.”
The number of shares of Common
Stock ultimately offered for sale by the selling stockholders under this prospectus is dependent upon the number of shares of Common
Stock the selling stockholders elects to sell from time to time. Depending upon market liquidity at the time, sales of shares of our
Common Stock upon the exercise of the Warrants, may cause the trading price of our Common Stock to decline.
The selling stockholders
may sell all, some or none of the shares that they hold or come to hold upon the exercise of the Warrants. Sales by the selling stockholders
of the shares acquired upon such exercise and sold under the registration statement of which this prospectus is a part, may result in
dilution to the interests of other holders of our Common Stock. The sale of a substantial number of shares of our Common Stock by the
selling stockholders in this offering, or anticipation of such sales, could make it more difficult for us to sell equity or equity-related
securities in the future at a time and at a price that we might otherwise wish to effect sales.
Holders
of Warrants will have no rights as a common stockholder until they acquire our Common Stock.
The Warrants do not confer
any rights of Common Stock ownership on their holders but rather merely represent the right to acquire shares of our Common Stock at
a fixed price for a limited period of time. Only upon exercise of the Warrants will a holder be entitled to exercise the rights of a
holder of our Common Stock.
The trading price of our Common Stock could be highly volatile,
which could result in substantial losses for holders of our Common Stock.
Our stock price is volatile.
The stock market in general and the market for pharmaceutical and biotechnology companies in particular have experienced extreme volatility
that has often been unrelated to the operating performance of particular companies. As a result of this volatility, you may lose some
or all of your investment. The market price for our Common Stock may be influenced by many factors, including:
· |
announcements relating
to the clinical development of our product candidates; |
· |
announcements concerning
the progress of our efforts to obtain regulatory approval for and commercialize our product candidates or any future product candidate,
including any requests we receive from the FDA, or comparable regulatory authorities outside the United States, for additional studies
or data that result in delays or additional costs in obtaining regulatory approval or launching these product candidates, if approved; |
· |
the depth and liquidity
of the market for our Common Stock; |
· |
investor perceptions about
us and our business; |
· |
market conditions
in the pharmaceutical and biotechnology sectors or the economy as a whole, which may be impacted by economic or other crises or external
factors; |
· |
price
and volume fluctuations in the overall stock market; |
· |
the
failure of one or more of our product candidates or any future product candidate, if approved, to achieve commercial success; |
· |
announcements
of the introduction of new products by us or our competitors; |
· |
developments
concerning product development results or intellectual property rights of others; |
· |
litigation
or public concern about the safety of our potential products; |
· |
actual
fluctuations in our quarterly operating results, and concerns by investors that such fluctuations may occur in the future; |
· |
deviations
in our operating results from the estimates of securities analysts or other analyst comments; |
· |
additions
or departures of key personnel; |
· |
health
care reform legislation, including measures directed at controlling the pricing of pharmaceutical products, and third-party coverage
and reimbursement policies; |
· |
developments
concerning current or future strategic collaborations; and |
· |
discussion
of us or our stock price by the financial and scientific press and in online investor communities. |
In the past, securities class
action litigation has often been brought against a company following a decline in the market price of its securities. This risk is especially
relevant for pharmaceutical and biotechnology companies, which have experienced significant stock price volatility in recent years.
You may experience future dilution as a result of future equity
offerings.
In order to raise additional
capital, we may in the future offer additional shares of our Common Stock or other securities convertible into or exchangeable for our
Common Stock at prices different from the price you paid. We may sell shares or other securities in any other offering at a price per
share that is less than the price per share paid by investors in this offering, and investors purchasing shares or other securities in
the future could have rights superior to existing stockholders. If we sell Common Stock, convertible securities, or other equity securities,
investors may be materially diluted by subsequent sales.
We cannot guarantee that the resubmission
of the BLA for cosibelimab will address all issues identified in the CRL to support approval.
On July 2, 2024, we announced that we had completed the resubmission
of the cosibelimab BLA potentially addressing the approvability issues cited in the CRL. The resubmission was accepted by the FDA as a
complete response and the FDA has set a Prescription Drug User Fee Act goal date of December 28, 2024. While we believe the BLA resubmission
addresses all the issues identified in the CRL, there is no guarantee that the FDA will ultimately agree that such issues have been successfully
addressed and resolved or that new approvability issues will not be raised during the BLA resubmission review. Any inability to successfully
work with the FDA to find a satisfactory solution to address any issues or concerns in a timely manner or at all during the review process
for the BLA, including any inability to provide the FDA with data, analysis or other information sufficient to support an approval of
the BLA, may adversely impact the prospects for FDA approval. In addition, an FDA inspection or re-inspection of any facility, including
those of our third party contract manufacturing organization (“CMO”) or otherwise, may further delay, or adversely impact,
potential approval. We cannot guarantee that any of our facilities, including our third-party CMO’s facility, will pass any such
inspection or reinspection. If we and our CMO are unable to adequately respond to and address any approvability issues or observations
raised by FDA during the resubmission review, the approval of cosibelimab could be delayed or a second CRL could be issued. Therefore,
it remains unclear when the FDA will approve our BLA, if at all. The previously received CRL, any additional CRLs, and any subsequent
resulting delay in the development and approval of cosibelimab may prevent, decrease and/or delay expected revenue. Any of these risks
could have a material impact on our business, operating results, and financial condition.
USE OF PROCEEDS
We will not receive any proceeds
from the sale of the Registered Securities by the selling stockholders. We will bear all other costs, fees and expenses incurred by us,
or by the selling stockholders, in effecting the registration of the Registered Securities. The selling stockholders, however, will pay
any other expenses incurred in selling their Registered Securities, including any brokerage commissions or costs of sale.
SELLING STOCKHOLDERS
The Common Stock being offered
by the selling stockholders are those previously issued to the selling stockholders in the Offerings, and those issuable to the selling
stockholders upon exercise of the Warrants. For additional information regarding the Offerings, see “Summary - About this Offering.”
We are registering the Registered Securities in order to permit the selling stockholders to offer such securities for sale from time
to time. Except for the ownership of the Registered Securities issued in the Offerings, the selling stockholders have not had any material
relationship with us within the past three years.
The table below lists the
selling stockholders and other information regarding the beneficial ownership of our Common Stock of each of the selling stockholders.
The second column lists the number of shares of Common Stock beneficially owned by each selling stockholder, based on its ownership of
the Warrants and our Common Stock, as of August 1, 2024, assuming exercise of all Warrants held by such selling stockholder on that
date, without regard to any limitations on exercise.
This prospectus generally
covers the resale of the maximum number of shares of Common Stock issuable upon exercise of the Warrants, determined as if the outstanding
Warrants were exercised in full as of the trading day immediately preceding the date the registration statement of which this prospectus
forms a part was initially filed with the SEC, each as of the trading day immediately preceding the applicable date of determination
and all subject to adjustment as provided in the registration right agreement, without regard to any limitations on the exercise of the
Warrants. The third column assumes the sale of all of the shares of Common Stock offered by the selling securityholders pursuant to this
prospectus.
Under the terms of the Warrants,
a selling securityholder may not exercise the Warrants to the extent such exercise would cause such selling securityholder, together
with its affiliates and attribution parties, to beneficially own a number of shares of Common Stock which would exceed 4.99% (or, at
the direction of the selling securityholder, 9.99%), of our then outstanding shares of Common Stock following such exercise, excluding
for purposes of such determination of the shares of Common Stock issuable upon exercise of such Warrants which have not been exercised.
The number of shares of Common Stock in the columns below do not reflect this limitation. The selling securityholders may sell all, some
or none of their shares of Common Stock in this offering. See “Plan of Distribution.”
Name of Selling
Shareholder |
|
Number
of
shares of
Common Stock
Owned
Prior to
Offering (1) |
|
|
Maximum
Number of
shares of
Common Stock
to be Sold
Pursuant to this
Prospectus (2) |
|
|
Number
of
shares of
Common Stock
Owned
After
Offering (3) |
|
|
Percentage
of
Beneficial
Ownership
After
Offering (3) |
|
Armistice Capital, LLC
(4) |
|
|
3,208,000 |
|
|
|
5,853,659 |
|
|
|
3,862,341 |
(5) |
|
|
9.30 |
% |
Michael Vasinkevich (6)(7)(8) |
|
|
675,265 |
|
|
|
225,220 |
|
|
|
900,485 |
|
|
|
2.17 |
% |
Noam Rubinstein (6)(7)(8) |
|
|
370,092 |
|
|
|
110,634 |
|
|
|
480,726 |
|
|
|
1.16 |
% |
Craig Schwabe (6)(7)(8) |
|
|
51,509 |
|
|
|
11,854 |
|
|
|
63,363 |
|
|
|
0.15 |
% |
Charles Worthman (6)(7)(8) |
|
|
15,262 |
|
|
|
3,512 |
|
|
|
18,774 |
|
|
|
0.05 |
% |
(1) |
All of the shares of Common
Stock that are exercisable for the shares underlying the Warrants offered hereby contain certain beneficial ownership limitations,
which provide that a holder of the securities will not have the right to exercise any portion of its Warrants if such holder, together
with its affiliates and attribution parties, would beneficially own in excess of 4.99% or 9.99%, as applicable, of the number of
shares of Common Stock outstanding immediately after giving effect to such exercise, provided that upon at least 61 days’ prior
notice to us, a holder may increase or decrease such limitation up to a maximum of 9.99% of the number of shares of Common Stock
outstanding. Additionally, stockholders may have acquired shares on the open market without the Company’s knowledge that may
not be reflected. |
(2) |
Represents shares of Common
Stock underlying the Warrants issued to the selling stockholders in the private placement and offered hereby. |
(3) |
We do not know when or
in what amounts a selling stockholder may offer shares for sale. The selling stockholders might not sell any or might sell all of
the shares offered by this prospectus. Because the selling stockholders may offer all or some of the shares pursuant to this offering,
and because there are currently no agreements, arrangements or understandings with respect to the sale of any of the shares, we cannot
estimate the number of the shares that will be held by the selling stockholders after completion of the offering. However, for purposes
of this table, we have assumed that, after completion of the offering, none of the shares covered by this prospectus will be held
by the selling stockholders, including Common Stock issuable upon exercise of the Warrants issued in the Offering. |
(4) |
These securities are directly
held by Armistice Capital Master Fund, Ltd. (the “Master Fund”), a Cayman Islands exempted company, and may be deemed
to be indirectly beneficially owned by Armistice Capital, LLC (“Armistice”), as the investment manager of the Master
Fund; and Steven Boyd, as the Managing Member of Armistice. Armistice and Steven Boyd disclaim beneficial ownership of the reported
securities except to the extent of their respective pecuniary interest therein. The Warrants are subject to a 4.99% beneficial ownership
limitation that precludes the Master Fund from exercising any portion of the Warrants to the extent that, following such exercise,
the Master Fund’s beneficial ownership of our then outstanding Common Stock would exceed 4.99%. The number of shares set forth
in the above table do not reflect the application of this limitation, but the percentages in the table do give effect to such beneficial
ownership limitation. The address of the Master Fund is c/o Armistice Capital, LLC, 510 Madison Avenue, 7th
Floor, New York, NY 10022. |
(5) |
The beneficial ownership
excludes an aggregate of 29,487,603 shares of Common Stock issuable upon the exercise of certain warrants currently held in abeyance
due to a 4.99% beneficial ownership blocker, 5,853,659 shares of Common Stock issuable upon the exercise of certain warrants shares
currently held in abeyance due to a 9.99% beneficial ownership blocker, and 4,623,659 shares of Common Stock issuable upon the exercise
of certain pre-funded warrants currently held in abeyance due to a 9.99% ownership blocker. |
(6) |
The selling stockholder
purchased or received the Warrants in the ordinary course of business and, at the time of purchase of the securities that are registered
for resale, the selling stockholders had no agreements or understanding, directly or indirectly with any person to distribute securities. |
(7) |
Each of the selling stockholders
is affiliated with H.C. Wainwright & Co., LLC, a registered broker dealer having a registered address of 430 Park Avenue,
3rd Floor, New York, NY 10022, and has the sole voting and dispositive power
over the securities held. H.C. Wainwright & Co., LLC acted as our exclusive placement agent in connection with our financings
consummated in December 2022, February 2023, April 2023, May 2023, July 2023, October 2023, January 2024,
and July 2024. |
(8) |
Consists of warrants to
purchase shares of our Common Stock. |
PLAN OF DISTRIBUTION
We are registering the Registered
Securities on behalf of the selling stockholders. The selling stockholders and any of their pledgees, assignees, distributees, and successors-in-interest
in the Registered Securities received after the date of this prospectus from the selling stockholders as a partnership distribution,
gift, pledge, or other transfer, may, from time to time, sell, transfer, or otherwise dispose of any or all of the shares of our Common
Stock covered hereby on the Nasdaq Capital Market or any other stock exchange, market or trading facility on which the Common Stock is
traded or in private transactions. These dispositions may be at fixed prices, at prevailing market prices at the time of the sale, at
varying prices determined at the time of sale, or at negotiated prices. The selling stockholders may use any one or more of the following
methods when selling Common Stock:
· |
ordinary brokerage transactions
and transactions in which the broker-dealer solicits purchasers; |
· |
block trades in which the
broker-dealer will attempt to sell the Common Stock as agent but may position and resell a portion of the block as principal to facilitate
the transaction; |
· |
purchases by a broker-dealer
as principal and resale by the broker-dealer for its account; |
· |
exchange distributions
in accordance with the rules of the applicable exchange; |
· |
privately negotiated transactions; |
· |
settlement of short sales; |
· |
transactions through broker-dealers
that agree with the selling stockholders to sell a specified number of such Common Stock at a stipulated price per security; |
· |
through the writing or
settlement of options or other hedging transactions, whether through an options exchange or otherwise; |
· |
a combination of any such
methods of sale; or |
· |
any other method permitted
pursuant to applicable law. |
The selling stockholders
may, from time to time, pledge or grant a security interest in some or all of the Registered Securities owned by them and, if they default
in the performance of their secured obligations, the pledgees or secured parties may offer and sell the Registered Securities, from time
to time, under this prospectus, or under an amendment to this prospectus under Rule 424(b)(3) or other applicable provision
of the Securities Act amending the list of selling stockholders to include the pledgee, transferee or other successors in interest as
selling stockholders under this prospectus. The selling stockholders also may transfer the Registered Securities in other circumstances,
in which case the transferees, pledgees or other successors in interest will be the selling beneficial owners for purposes of this prospectus.
In connection with the sale
of the Registered Securities, the selling stockholders may enter into hedging transactions with broker-dealers or other financial institutions,
which may in turn engage in short sales of the Registered Securities in the course of hedging the positions they assume. To the extent
permitted by applicable securities laws, the selling stockholders may also sell the Registered Securities short and deliver these securities
to close out their short positions, or loan or pledge the Registered Securities to broker-dealers that in turn may sell these securities.
The selling stockholders may also enter into option or other transactions with broker-dealers or other financial institutions or the
creation of one or more derivative securities which require the delivery to such broker-dealer or other financial institution of the
Registered Securities offered by this prospectus, which Registered Securities such broker-dealer or other financial institution may resell
pursuant to this prospectus (as supplemented or amended to reflect such transaction).
The aggregate proceeds to
the selling stockholders from the sale of the Registered Securities offered by them will be the purchase price of the Registered Securities
less discounts or commissions, if any. Each of the selling stockholders reserves the right to accept and, together with their agents
from time to time, to reject, in whole or in part, any proposed purchase of the Registered Securities to be made directly or through
agents. We will not receive any of the proceeds from this offering.
The selling stockholders
also may resell all or a portion of the Registered Securities in open market transactions in reliance upon Rule 144 under the Securities
Act, provided that they meet the criteria and conform to the requirements of that rule.
The selling stockholders
and any underwriters, broker-dealers or agents that participate in the sale of the Registered Securities or interests therein may be
“underwriters” within the meaning of Section 2(11) of the Securities Act. Any discounts, commissions, concessions or
profit they earn on any resale of the Registered Securities covered by this prospectus may be underwriting discounts and commissions
under the Securities Act. Selling stockholders who are “underwriters” within the meaning of Section 2(11) of the Securities
Act will be subject to the prospectus delivery requirements of the Securities Act.
To the extent required, the
Registered Securities to be sold, the names of the selling stockholders, the respective purchase prices and public offering prices, the
names of any agents, dealer or underwriter, any applicable commissions or discounts with respect to a particular offer will be set forth
in an accompanying prospectus supplement or, if appropriate, a post-effective amendment to the registration statement that includes this
prospectus.
In order to comply with the
securities laws of some states, if applicable, the Registered Securities may be sold in these jurisdictions only through registered or
licensed brokers or dealers. In addition, in some states the Registered Securities may not be sold unless it has been registered or qualified
for sale or an exemption from registration or qualification requirements is available and is complied with.
Description
of Securities
Description of Capital Stock
The following description
summarizes the material terms of Checkpoint capital stock. Because it is only a summary, it does not contain all the information that
may be important to you. For a complete description of our capital stock, you should refer to our certificate of incorporation, our bylaws
and to the provisions of applicable Delaware law.
Common Stock
Our Common Stock is traded
on The Nasdaq Capital Market, or the Exchange, under the symbol “CKPT”.
The authorized capital stock
of Checkpoint consists of 175,000,000 shares of Common Stock, of which 700,000 shares have been designated as Class A Common Stock.
The description of our Class A Common Stock in this item is for information purposes only. All of the Class A Common Stock
has been issued to Fortress. Class A Common Stock is identical to common stock other than as to voting rights, the election of directors
for a definite period, and conversion rights. On any matter presented to our stockholders for their action or consideration at any meeting
of our stockholders (or by written consent of stockholders in lieu of meeting), each holder of outstanding shares of Class A Common
Stock will be entitled to cast for each share of Class A Common Stock held by such holder as of the record date for determining
stockholders entitled to vote on such matter, the number of votes that is equal to one and one-tenth (1.1) times a fraction, the numerator
of which is the sum of the shares of outstanding Common Stock and the denominator of which is the number of shares of outstanding Class A
Common Stock. Thus, the Class A Common Stock will at all times constitute a voting majority. For a period of ten (10) years
from the date of the first issuance of shares of Class A Common Stock expiring in 2025 (the “Class A Director Period”),
the holders of record of the shares of Class A Common Stock (or other capital stock or securities issued upon conversion of or in
exchange for the Class A Common Stock), exclusively and as a separate class, will be entitled to appoint or elect the majority of
the directors of Checkpoint (the “Class A Directors”). Finally, each share of Class A Common Stock is convertible,
at the option of the holder, into one fully paid and nonassessable share of Common Stock (the “Conversion Ratio”), subject
to certain adjustments.
If Checkpoint at any time
effects a subdivision of the outstanding Common Stock (or other capital stock or securities at the time issuable upon conversion of the
Class A Common Stock) by any stock split, stock dividend, recapitalization or otherwise, the applicable Conversion Ratio in effect
immediately before that subdivision will be proportionately decreased so that the number of shares of Common Stock (or other capital
stock or securities at the time issuable upon conversion of the Class A Common Stock) issuable on conversion of each share of Class A
Common Stock will be increased in proportion to such increase in the aggregate number of shares of common stock (or other capital stock
or securities at the time issuable upon conversion of the Class A Common Stock) outstanding. If Checkpoint at any time combines
the outstanding shares of common stock, the applicable Conversion Ratio in effect immediately before the combination will be proportionately
increased so that the number of shares of Common Stock (or other capital stock or securities at the time issuable upon conversion of
the Class A Common Stock) issuable on conversion of each share of Class A Common Stock will be decreased in proportion to such
decrease in the aggregate number of shares of Common Stock (or other capital stock or securities at the time issuable upon conversion
of the Class A Common Stock) outstanding. Additionally, if any reorganization, recapitalization, reclassification, consolidation
or merger involving Checkpoint occurs in which the Common Stock (but not the Class A Common Stock) is converted into or exchanged
for securities, cash or other property (other than a transaction involving the subdivision or combination of the Common Stock), then,
following any such reorganization, recapitalization, reclassification, consolidation or merger, each share of Class A Common Stock
becomes convertible into the kind and amount of securities, cash or other property which such Class A Stockholder would have been
entitled to receive had he or she converted the Class A Shares immediately before said transaction. In such case, appropriate adjustment
(as determined in good faith by the Board of Directors of Checkpoint) will be made in the application of the provisions of Checkpoint’s
Amended and Restated Certificate of Incorporation relating the subdivision or combination of the Common Stock with respect to the rights
and interests thereafter of the holders of the Class A Common Stock, such that the provisions set forth in of Checkpoint’s
Amended and Restated Certificate of Incorporation relating to the subdivision or combination of the Common Stock (including the provisions
with respect to changes in and other adjustments of the applicable Conversion Ratio) will thereafter be applicable, as nearly as reasonably
may be, in relation to any securities or other property thereafter deliverable upon the conversion of the Class A Common Stock.
Checkpoint is not authorized to issue preferred stock.
Dividends
The holders of outstanding
shares of our Common Stock, including Class A Common Stock, are entitled to receive dividends out of funds legally available at
the times and in the amounts that our board of directors may determine. All dividends are non-cumulative.
Voting Rights
The holders of our Common
Stock are entitled to one vote for each share of Common Stock held on all matters submitted to a vote of the stockholders, including
the election of directors, except as to the Class A Directors during the Class A Director Period. Our certificate of incorporation
and bylaws do not provide for cumulative voting rights.
Liquidation and Dissolution
Upon our liquidation, dissolution,
or winding-up, the assets legally available for distribution to our stockholders would be distributable ratably among the holders of
our Common Stock, including Class A Common Stock, outstanding at that time after payment of other claims of creditors, if any.
Other
The holders of our Common
Stock have no preemptive, conversion, or subscription rights, and there are no redemption or sinking fund provisions applicable to our
Common Stock.
All of the outstanding shares
of our common stock, including Class A Common Stock, are duly issued, fully paid and non-assessable.
DIVIDEND POLICY
We have never declared or
paid any dividends. We currently intend to retain earnings, if any, for use in our business. We do not anticipate paying dividends in
the foreseeable future. Any future determination to declare dividends will be made at the discretion of our board of directors and will
depend on our financial condition, operating results, capital requirements, general business conditions, and other factors that our board
of directors may deem relevant.
LEGAL MATTERS
The validity of the securities
offered hereby will be passed upon for us by Alston & Bird LLP, New York, New York. Additional legal matters may be passed upon
for us or any underwriters, dealers or agents, by counsel that we will name in any applicable prospectus supplement.
EXPERTS
The financial statements
of Checkpoint Therapeutics, Inc. as of December 31, 2023 and 2022 and for each of the years in the two-year period ended December 31
2023, have been incorporated by reference herein in reliance upon the report of KPMG LLP, independent registered public accounting firm,
incorporated by reference herein, and upon the authority of said firm as experts in accounting and auditing.
The audit report covering
the December 31, 2023 financial statements contains an explanatory paragraph that states that the Company’s recurring losses
from operations and net capital deficiency raise substantial doubt about the entity’s ability to continue as a going concern. The
financial statements do not include any adjustments that might result from the outcome of that uncertainty.
WHERE YOU CAN FIND MORE INFORMATION
We file reports with the
SEC on an annual basis using Form 10-K, quarterly reports on Form 10-Q and current reports on Form 8-K. The SEC maintains
a website that contains annual, quarterly, and current reports, proxy statements, and other information that issuers (including us) file
electronically with the SEC. The SEC’s website address is www.sec.gov. You can also obtain copies of materials we file with the
SEC from our internet website found at www.checkpointtx.com. Our stock is quoted on the Nasdaq Capital Market under the symbol “CKPT”.
This prospectus is only part
of a registration statement on Form S-3 that we have filed with the SEC under the Securities Act and therefore omits certain information
contained in the registration statement. We have also filed exhibits and schedules with the registration statement that are excluded
from this prospectus, and you should refer to the applicable exhibit or schedule for a complete description of any statement referring
to any contract or other document. You may inspect a copy of the registration statement, including the exhibits and schedules, without
charge, at the SEC’s website.
INCORPORATION OF CERTAIN DOCUMENTS BY REFERENCE
The SEC allows us to “incorporate
by reference” the information we file with them, which means that we can disclose important information to you by referring you
to those documents instead of having to repeat the information in this prospectus and any prospectus supplement. The information incorporated
by reference is considered to be part of this prospectus, and later information that we file with the SEC will automatically update and
supersede this information. This prospectus incorporates by reference the documents listed below (other than, unless otherwise specifically
indicated, current reports furnished under Item 2.02 or Item 7.01 of Form 8-K and exhibits filed on such form that are related to
such items):
a) |
Our Annual Report on Form 10-K
for the year ended December 31, 2023, filed with the SEC on March 22, 2024; |
|
|
b) |
Our Quarterly Reports on
Form 10-Q for the quarters ended March 31, 2024 and June 30, 2024, filed with the SEC on May 10, 2024 and August 12, 2024, respectively; |
|
|
c) |
Our Current reports on
Form 8-K filed with the SEC on January 5, 2024, January 30, 2024, February 2, 2024, March 18, 2024,
May 14, 2024, June 24, 2024, July 3, 2024, and July 25, 2024; and |
|
|
d) |
Description of our common
stock, which is contained in the Registration Statement on Form 10-12G/A, as filed with the SEC on August 19, 2016,
as supplemented by the description of common stock found on page 13 of this prospectus. |
All reports and other documents
we subsequently file pursuant to Section 13(a), 13(c), 14 or 15(d) of the Exchange Act prior to the termination of this offering,
including all such documents we may file with the SEC after the date of the initial registration statement and prior to the effectiveness
of the registration statement, but excluding any information furnished to, rather than filed with, the SEC, will also be incorporated
by reference into this prospectus and deemed to be part of this prospectus from the date of the filing of such reports and documents.
We will provide to each person,
including any beneficial owner, to whom a copy of this prospectus is delivered, a copy of any or all of the information that we have
incorporated by reference into this prospectus and any related prospectus, but not delivered with this prospectus and any related prospectus.
We will provide this information upon written or oral request at no cost to the requester. You may request this information by contacting
our corporate headquarters at the following address: 95 Sawyer Road, Suite 110, Waltham, Massachusetts 02453, Attn: Chief Financial
Officer, or by calling (781) 652-4500.
![](https://www.sec.gov/Archives/edgar/data/1651407/000110465924090904/tm2421765d1_s3sp1img001.jpg)
Checkpoint Therapeutics, Inc.
6,204,879 Shares of Common Stock underlying
certain Common Warrants and Placement Agent Warrants
PROSPECTUS
, 2024
PART II
INFORMATION NOT REQUIRED IN PROSPECTUS
Item 14. Other Expenses of Issuance and Distribution
|
|
Amount
to
Be Paid |
|
U.S. Securities and Exchange
Commission registration fee |
|
$ |
2,097.28 |
|
Legal fees and expenses |
|
|
25,000.00 |
* |
Accounting fees and expenses |
|
|
25,000.00 |
* |
Miscellaneous |
|
|
1,000.00 |
* |
Total |
|
|
53,097.28 |
* |
* These fee and expense amounts are estimated.
Item 15. Indemnification of Directors and Officers
Under the General Corporation
Law of the State of Delaware (“DGCL”), a corporation may include provisions in its certificate of incorporation that will
relieve its directors of monetary liability for breaches of their fiduciary duty to the corporation, except under certain circumstances,
including a breach of the director’s duty of loyalty, acts or omissions of the director not in good faith or which involve intentional
misconduct or a knowing violation of law, the approval of an improper payment of a dividend or an improper purchase by the corporation
of stock or any transaction from which the director derived an improper personal benefit. The Company’s Amended and Restated Certificate
of Incorporation eliminates the personal liability of directors to the Company or its stockholders for monetary damages for breach of
fiduciary duty as a director with certain limited exceptions set forth in the DGCL.
Section 145 of the DGCL
grants to corporations the power to indemnify each officer and director against liabilities and expenses incurred by reason of the fact
that he or she is or was an officer or director of the corporation if he or she acted in good faith and in a manner he or she reasonably
believed to be in or not opposed to the best interests of the corporation and, with respect to any criminal action or proceeding, had
no reasonable cause to believe his or her conduct was unlawful. The Company’s Amended and Restated Certificate of Incorporation
and Bylaws provide for indemnification of each officer and director of the Company to the fullest extent permitted by the DGCL. Section 145
of the DGCL also empowers corporations to purchase and maintain insurance on behalf of any person who is or was an officer or director
of the corporation against liability asserted against or incurred by him in any such capacity, whether or not the corporation would have
the power to indemnify such officer or director against such liability under the provisions of Section 145 of the DGCL.
Item 16. Exhibits and Financial Statement Schedules
The exhibits to the Registration
Statement are listed in the Exhibit Index attached hereto and incorporated by reference herein.
Item 17. Undertakings
(a) |
The undersigned registrant
hereby undertakes: |
1. |
To file, during any period
in which offers or sales are being made, a post-effective amendment to this registration statement: |
(i) To
include any prospectus required by Section 10(a)(3) of the Securities Act of 1933;
(ii)
To reflect in the prospectus any facts or events arising after the effective date of 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 Commission pursuant to Rule 424(b) if, in the aggregate, the changes
in volume and price represent no more than 20% change in the maximum aggregate offering price set forth in the “Calculation of
Registration Fee” table in the effective registration statement;
(iii) 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;
provided,
however, that paragraphs (1)(i), (1)(ii) and (1)(iii) of this section do not apply if the information required to
be included in a post-effective amendment by those paragraphs is contained in reports filed with or furnished to the SEC by the registrant
pursuant to Section 13 or Section 15(d) of the Securities Exchange Act of 1934 that are incorporated by reference in the
registration statement, or is contained in a form of prospectus filed pursuant to Rule 424(b) that is part of the registration
statement.
2. |
That, for the purpose of
determining any liability under the Securities Act of 1933, each such post-effective amendment shall be deemed to be a new registration
statement relating to the securities offered therein, and the offering of such securities at that time shall be deemed to be the
initial bona fide offering thereof. |
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 of 1933 to any purchaser: |
(i) Each
prospectus filed by the registrant pursuant to Rule 424(b)(3) shall be deemed to be part of the registration statement as of
the date the filed prospectus was deemed part of and included in the registration statement; and
(ii)
Each prospectus required to be filed pursuant to Rule 424(b)(2), (b)(5), or (b)(7) as part of a registration statement in reliance
on Rule 430B relating to an offering made pursuant to Rule 415(a)(1)(i), (vii), or (x) for the purpose of providing the
information required by Section 10(a) of the Securities Act of 1933 shall be deemed to be part of and included in the registration
statement as of the earlier of the date such form of prospectus is first used after effectiveness or the date of the first contract of
sale of securities in the offering described in the prospectus. As provided in Rule 430B, for liability purposes of the issuer and
any person that is at that date an underwriter, such date shall be deemed to be a new effective date of the registration statement relating
to the securities in the registration statement to which that prospectus relates, and the offering of such securities at that time shall
be deemed to be the initial bona fide offering thereof. 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
effective date, 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 effective date.
5. |
That, for the purpose of
determining liability of the registrant under the Securities Act of 1933 to any purchaser in the initial distribution of the securities,
the undersigned registrant undertakes that in a primary offering of securities of the undersigned registrant pursuant to this registration
statement, regardless of the underwriting method used to sell the securities to the purchaser, if the securities are offered or sold
to such purchaser by means of any of the following communications, the undersigned registrant will be a seller to the purchaser and
will be considered to offer or sell such securities to such purchaser: |
(i) Any
preliminary prospectus or prospectus of the undersigned registrant relating to the offering required to be filed pursuant to Rule 424;
(ii)
Any free writing prospectus relating to the offering prepared by or on behalf of the undersigned registrant or used or referred to by
the undersigned registrant;
(iii) The
portion of any other free writing prospectus relating to the offering containing material information about the undersigned registrant
or its securities provided by or on behalf of the undersigned registrant; and
(iv) Any
other communication that is an offer in the offering made by the undersigned registrant to the purchaser.
(b) |
The undersigned registrant
hereby undertakes that, for purposes of determining any liability under the Securities Act of 1933, each filing of the registrant’s
annual report pursuant to Section 13(a) or 15(d) of the Securities Exchange Act of 1934 (and, where applicable, each
filing of an employee benefits plan’s annual report pursuant to Section 15(d) of the Securities Exchange Act of 1934)
that is incorporated by reference in the registration statement shall be deemed to be a new registration statement relating to the
securities offered therein, and the offering of such securities at that time shall be deemed to be the initial bona fide offering
thereof. |
(c) |
The undersigned registrant
hereby undertakes to supplement the prospectus, after the expiration of the subscription period, to set forth the results of the
subscription offer, the transactions by the underwriters during the subscription period, the amount of unsubscribed securities to
be purchased by the underwriters, and the terms of any subsequent reoffering thereof. If any public offering by the underwriters
is to be made on terms differing from those set forth on the cover page of the prospectus, a post-effective amendment will be
filed to set forth the terms of such offering. |
(d) |
Insofar as indemnification
for liabilities arising under the Securities Act of 1933 may be permitted to directors, officers and controlling persons of the registrant
pursuant to the foregoing provisions, or otherwise, the registrant has been advised that in the opinion of the Securities and Exchange
Commission such indemnification is against public policy as expressed in the Securities Act of 1933, as amended, and is, therefore,
unenforceable. In the event that a claim for indemnification against such liabilities (other than the payment by the registrant of
expenses incurred or paid by a director, officer or controlling person of the registrant in the successful defense of any action,
suit or proceeding) is asserted by such director, officer or controlling person in connection with the securities being registered,
the registrant will, unless in the opinion of its counsel the matter has been settled by controlling precedent, submit to a court
of appropriate jurisdiction the question of whether such indemnification by it is against public policy as expressed in the Securities
Act of 1933, as amended, and will be governed by the final adjudication of such issue. |
SIGNATURES
Pursuant to the requirements
of the Securities Act of 1933, the registrant has duly caused this registration statement to be signed on its behalf by the undersigned,
thereunto duly authorized.
|
CHECKPOINT THERAPEUTICS, INC. |
|
|
Date: August 19,
2024 |
By: |
/s/
James. F. Oliviero |
|
Name: |
James F. Oliviero |
|
Title: |
President and Chief Executive
Officer |
POWER OF ATTORNEY
We, the undersigned directors
and/or executive officers of Checkpoint Therapeutics, Inc., hereby severally constitute and appoint James F. Oliviero, acting singly,
his or her true and lawful attorney-in-fact and agent, with full power of substitution and resubstitution, for him or her in any and
all capacities, to sign this registration statement and to file the same, with all exhibits thereto and other documents in connection
therewith, with the Securities and Exchange Commission, granting unto said attorney-in-fact and agent full power and authority to do
and perform each and every act and thing necessary or appropriate to be done in connection therewith, as fully for all intents and purposes
as he or she might or could do in person, hereby approving, ratifying and confirming all that said attorney-in-fact and agent, or his
substitute, may lawfully do or cause to be done by virtue hereof.
Pursuant to the requirements
of the Securities Act of 1933, this registration statement has been signed below by the following persons on behalf of the registrant
and in the capacities and on the dates indicated.
Signature |
|
Title |
|
Date |
|
|
|
|
|
/s/
James. F. Oliviero |
|
Chief
Executive Officer and President |
|
August 19,
2024 |
James F. Oliviero |
|
(Principal Executive Officer) |
|
|
|
|
|
|
|
/s/ Garrett
Gray |
|
Chief Financial Officer |
|
August 19, 2024 |
Garrett Gray |
|
(Principal Financial Officer) |
|
|
|
|
|
|
|
/s/ Michael
S. Weiss |
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Chairman of the Board |
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August 19, 2024 |
Michael S. Weiss |
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/s/ Lindsay
A. Rosenwald, M.D. |
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Director |
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August 19, 2024 |
Lindsay A. Rosenwald, M.D. |
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/s/ Neil
Herskowitz |
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Director |
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August 19, 2024 |
Neil Herskowitz |
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/s/ Barry
Salzman |
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Director |
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August 19, 2024 |
Barry Salzman |
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/s/ Christian
Béchon |
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Director |
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August 19, 2024 |
Christian Béchon |
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/s/ Amit
Sharma, M.D. |
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Director |
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August 19, 2024 |
Amit Sharma, M.D. |
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EXHIBIT INDEX
Exhibit 5.1
90 Park Avenue
New York, NY 10016
212-210-9400 | Fax: 212-210-9444
Matthew W. Mamak |
Direct Dial: 212-210-1256 |
Email: matthew.mamak@alston.com |
August 19, 2024
Checkpoint Therapeutics, Inc.
95 Sawyer Road, Suite 110,
Waltham, MA 02453
|
Re: |
Registration Statement on Form S-3 |
Ladies and Gentlemen:
We are acting as counsel to
Checkpoint Therapeutics, Inc., a Delaware corporation (the “Company”) in connection with the registration statement
(the “Registration Statement”) on Form S-3 filed today by the Company with the Securities and Exchange Commission (the
“Commission”) to register under the Securities Act of 1933, as amended (the “Securities Act”), 6,204,879
shares of the Company’s common stock, $0.0001 par value per share (the “Shares”). The Shares being registered
are shares of the Company’s common stock underlying certain warrants as follows: 5,853,659 Shares underlying certain Common Warrants
and 351,220 Shares underlying certain Placement Agent Warrants (the "Warrants," and the agreements under which they are
governed, the “Warrant Agreements”). This opinion is furnished to you
at your request in accordance with the requirements of Item 601(b)(5) of Regulation S-K promulgated under the Securities Act.
We have examined the Warrant
Agreements, the Amended and Restated Certificate of Incorporation of the Company, as amended, the Bylaws of the Company, records of proceedings
of the Board of Directors of the Company, or committees thereof, and records of proceedings of the stockholders, deemed by us to be relevant
to this opinion letter and the Registration Statement. We also have made such further legal and factual examinations and investigations
as we deemed necessary for purposes of expressing the opinion set forth herein. In our examination, we have assumed the genuineness of
all signatures, the legal capacity of all natural persons, the authenticity of all documents submitted to us as original documents and
the conformity to original documents of all documents submitted to us as certified, conformed, facsimile, electronic or photostatic copies.
As to certain factual matters
relevant to this opinion letter, we have relied conclusively upon originals or copies, certified or otherwise identified to our satisfaction,
of such records, agreements, documents and instruments, including certificates or comparable documents of officers of the Company and
of public officials, as we have deemed appropriate as a basis for the opinion hereinafter set forth. Except to the extent expressly set
forth herein, we have made no independent investigations with regard to matters of fact, and, accordingly, we do not express any opinion
as to matters that might have been disclosed by independent verification.
Our opinion set forth below
is limited to the General Corporation Law of the State of Delaware, applicable provisions of the Constitution of the State of Delaware
and reported judicial decisions interpreting such General Corporation Law and Constitution that, in our professional judgment, are normally
applicable to transactions of the type contemplated by the Plan, the laws of the State of New York, and the federal law of the United
States, and we do not express any opinion herein concerning any other laws.
Alston & Bird LLP | www.alston.com |
Atlanta | Beijing | Brussels | Charlotte | Dallas | Fort Worth | London | Los Angeles | New York
| Raleigh | San Francisco | Silicon Valley | Washington, D.C.
This opinion letter is
provided for use in connection with the transactions contemplated by the Registration Statement and may not be used, circulated,
quoted or otherwise relied upon for any other purpose without our express written consent. The only opinion rendered by us consists
of those matters set forth in the sixth paragraph hereof, and no opinion may be implied or inferred beyond the opinion expressly
stated. This opinion letter is rendered as of the date hereof and we make no undertaking and expressly disclaim any duty to
supplement or update the opinions rendered herein, if, after the date hereof, facts or circumstances come to our attention or
changes in the law occur which could affect such opinions.
Based on the foregoing, it
is our opinion that, when issued following the proper exercise and payment for the Warrants pursuant to the Warrant Agreements, the Shares
to be issued pursuant to such Warrant Agreements will be duly authorized, validly issued, fully paid and non-assessable.
We consent to the filing of
this opinion letter as an exhibit to the Registration Statement. In giving such consent, we do not thereby admit that we are within the
category of persons whose consent is required under Section 7 of the Securities Act or the rules and regulations of the Commission thereunder.
|
ALSTON & BIRD LLP |
|
|
|
By: |
/s/ Matthew W. Mamak |
|
|
Matthew W. Mamak |
|
|
Partner |
Exhibit 23.1
Consent of Independent Registered Public Accounting
Firm
We
consent to the use of our report dated March 22, 2024, with respect to the financial statements of Checkpoint Therapeutics, Inc., incorporated
herein by reference, and to the reference to our firm under the heading “Experts” in the prospectus.
Boston, Massachusetts
August 19, 2024
Exhibit 107
Calculation of Filing Fee Table
Form S-3
(Form Type)
Checkpoint Therapeutics, Inc.
(Exact Name of Registrant as Specified in its Charter)
Table 1: Newly Registered Securities
|
|
Security
Type |
|
Security
Class
Title |
|
Fee
Calculation
Rule |
|
|
Amount
Registered |
|
|
Proposed
Maximum
Offering
Price Per
Unit |
|
|
Proposed Maximum
Aggregate
Offering Price |
|
Fee Rate |
|
Amount of
Registration
Fee |
|
Fees to be paid |
|
Equity |
|
Common Stock, par value $0.0001 per share |
|
|
457(c) |
|
|
6,204,879 |
(1) |
|
$ |
2.29 |
(2) |
|
$ |
14,209,172.9 |
|
$ |
0.00014760 |
|
$ |
2,097.28 |
|
|
|
|
|
Total Offering Amounts |
|
|
|
|
|
|
|
|
|
$ |
14,209,172.9 |
|
|
|
|
$ |
2,097.28 |
|
|
|
|
|
Total Fee Offsets |
|
|
|
|
|
|
|
|
|
|
-- |
|
|
|
|
|
-- |
|
|
|
|
|
Net Fee Due |
|
|
|
|
|
|
|
|
|
$ |
14,209,172.9 |
|
|
|
|
$ |
2,097.28 |
|
(1) |
Consists of an aggregate of 6,204,879 shares of Common Stock registered for sale by certain of the selling stockholders named in this registration statement consisting of: 5,853,659 shares of Common Stock, $0.0001 par value, underlying those certain Common Warrants and 351,220 shares of Common Stock, $0.0001 par value, underlying those certain Placement Agent Warrants. |
|
|
(2) |
Determined pursuant to Rule 457(c) and 457(h) under the Securities Act of 1933, as amended, solely for the purpose of calculating the registration fee, based on the average of the high and low prices of the Company’s Common Stock on the Nasdaq Capital Market on August 13, 2024. |
Table 2: Fee Offset Claims and Sources
N/A
Table 3: Combined Prospectuses
N/A
Checkpoint Therapeutics (NASDAQ:CKPT)
Gráfica de Acción Histórica
De Jul 2024 a Ago 2024
Checkpoint Therapeutics (NASDAQ:CKPT)
Gráfica de Acción Histórica
De Ago 2023 a Ago 2024