Press Release

INVESTOR ALERT: Law Offices of Howard G. Smith Announces the Filing of a Securities Class Action on Behalf of Checkpoint Therapeutics, Inc. (CKPT) Investors

BENSALEM, Pa.–(BUSINESS WIRE)–Law Offices of Howard G. Smith announces that a class action lawsuit has been filed on behalf of investors who purchased Checkpoint Therapeutics, Inc. (โ€œCheckpointโ€ or the โ€œCompanyโ€) (NASDAQ: CKPT) securities between March 10, 2021 and December 15, 2023, inclusive (the โ€œClass Periodโ€). Checkpoint investors have until June 4, 2024 to file a lead plaintiff motion.

Investors suffering losses on their Checkpoint investments are encouraged to contact the Law Offices of Howard G. Smith to discuss their legal rights in this class action at 888-638-4847 or by email to [email protected].

On December 18, 2023, Checkpoint disclosed that the U.S. Food and Drug Administration (โ€œFDAโ€) had not approved the Biologics License Application (โ€œBLAโ€) that the Company had submitted for its metastatic cutaneous squamous cell carcinoma (โ€œcSCCโ€) treatment, cosibelimab. Specifically, the Company stated that the FDA had issued a complete response letter which โ€œcites findings that arose during a multi-sponsor inspection of Checkpointโ€™s third-party [CMO] as approvability issues to address in a resubmission.โ€

On this news, Checkpointโ€™s stock price fell $1.49, or 44.9%, to close at $1.83 per share on December 18, 2023, thereby injuring investors.

The complaint filed in this class action alleges that throughout the Class Period, Defendants made materially false and/or misleading statements, as well as failed to disclose material adverse facts about the Companyโ€™s business, operations, and prospects. Specifically, Defendants failed to disclose to investors that: (1) Checkpoint had overstated its oversight of, and/or its establishment of adequate manufacturing standards and controls over, its third-party contract manufacturers; (2) accordingly, there were one or more issues with the Companyโ€™s third-party contract manufacturing organization (โ€œCMOโ€) for cosibelimab; (3) all the foregoing reduced the likelihood that the FDA would approve the cosibelimab BLA in its present form; (4) as a result, the manufacturing, regulatory, and commercial prospects of cosibelimab were overstated; and (5) as a result, Defendantsโ€™ positive statements about the Companyโ€™s business, operations, and prospects were materially misleading and/or lacked a reasonable basis at all relevant times.

If you purchased Checkpoint securities, have information or would like to learn more about these claims, or have any questions concerning this announcement or your rights or interests with respect to these matters, please contact Howard G. Smith, Esquire, of Law Offices of Howard G. Smith, 3070 Bristol Pike, Suite 112, Bensalem, Pennsylvania 19020, by telephone at (215) 638-4847 or by email to [email protected], or visit our website at www.howardsmithlaw.com.

This press release may be considered Attorney Advertising in some jurisdictions under the applicable law and ethical rules.

Contacts

Law Offices of Howard G. Smith

Howard G. Smith, Esquire

215-638-4847

[email protected]
www.howardsmithlaw.com

Author

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