UNITED STATES
SECURITIES AND EXCHANGE COMMISSION
Washington, D.C. 20549
FORM
CURRENT REPORT
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Item 1.01 Entry into a Material Definitive Agreement.
On March 12, 2024, IDEAYA Biosciences, Inc. (the “Company”) announced that it had entered into a Clinical Trial Collaboration and Supply Agreement (the “Agreement”), dated March 8, 2024, with MSD International Business GmbH (“MSD”), to evaluate the Company’s investigational IDE161 compound in combination with KEYTRUDA® (pembrolizumab) Merck’s anti-PD-1 therapy (the “Study”). Pursuant to the Agreement, the Company is the sponsor of the Study and the Company will provide the Company’s IDE161 compound and will pay for the costs of the Study. Merck will provide KEYTRUDA for the Study at no cost to the Company. The Company and MSD will jointly own clinical data from the Study and all inventions relating to the combined use of IDE161 and pembrolizumab. Each party retains commercial rights to its respective compounds, including with respect to use as a monotherapy or combination agent.
The foregoing is only a summary description of the terms of the Agreement, does not purpose to be complete and is qualified in its entirety by reference to the Agreement, which will be filed as an exhibit to the Company’s Quarterly Report on Form 10-Q for the fiscal quarter ending March 31, 2024.
(d) Exhibits.
Exhibit No.
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Description
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99.1 |
SIGNATURES
Pursuant to the requirements of the Securities Exchange Act of 1934, as amended, the registrant has duly caused this report to be signed on its behalf by the undersigned hereunto duly authorized.
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IDEAYA BIOSCIENCES, INC. |
Date: March 12, 2024 |
By: /s/ Yujiro Hata Yujiro Hata President and Chief Executive Officer |