Lindsay A. Md Rosenwald - May 28, 2025 Form 4 Insider Report for Checkpoint Therapeutics, Inc. (CKPT)

Role
Director
Signature
/s/ James F. Oliviero, Attorney-in-Fact
Stock symbol
CKPT
Transactions as of
May 28, 2025
Transactions value $
$64,500
Form type
4
Date filed
5/30/2025, 11:19 AM
Previous filing
Jan 3, 2025
Next filing
Jul 7, 2025

Reporting Owners (1)

Name Relationship Address Signature Signature date CIK
ROSENWALD LINDSAY A MD Director 95 SAWYER ROAD, SUITE 110, WALTHAM /s/ James F. Oliviero, Attorney-in-Fact 2025-05-30 0000941841

Transactions Table

Type Sym Class Transaction Value $ Shares Change % * Price $ Shares After Date Ownership Footnotes
transaction CKPT COMMON STOCK Award $0 +12.2K +8.42% $0.00 157K May 28, 2025 Direct F1
transaction CKPT COMMON STOCK Award $64.5K +50K +31.85% $1.29 207K May 29, 2025 Direct
transaction CKPT COMMON STOCK Disposition pursuant to a tender of shares in a change of control transaction -207K -100% 0 May 30, 2025 Direct F2
* An asterisk sign (*) next to the price indicates that the price is likely invalid.

Lindsay A. Md Rosenwald is no longer subject to Section 16 filing requirements. Form 4 or Form 5 obligations may continue.

Explanation of Responses:

Id Content
F1 Includes restricted shares of Common Stock which vest over various time periods, subject to Mr. Rosenwald's continued service on the board.
F2 Disposed of in connection with an offer made pursuant to the Agreement and Plan of Merger, dated as of March 9, 2025 and as amended on April 14, 2025 (the "Merger Agreement"), in exchange for $4.10 per share, net to the holder in cash, plus one contractual contingent value right ("CVR") per share. Each CVR represents the right to receive a payment ranging from $0.20 to $0.70 pursuant to certain milestone payments as defined in the Merger Agreement relating to the regulatory approval for cosibelimab in the European Union. The CVR milestone must be achieved within thirty-six (36) months after the date on which a marketing authorization application or equivalent application for cosibelimab receives a positive validation outcome by the European Medicines Agency.