IDEAYA Biosciences Inc. has received clearance from the U.S. Food and Drug Administration (FDA) for its investigational new drug $(IND)$ application to initiate a Phase 1 clinical trial of IDE034, a potential first-in-class bispecific B7H3/PTK7 TOP1 antibody-drug conjugate $(ADC)$. The trial is expected to begin enrolling patients with solid tumors that express B7H3 and PTK7, including lung, colorectal, head and neck, and ovarian/gynecological cancers, in the first quarter of 2026.
Disclaimer: This news brief was created by Public Technologies (PUBT) using generative artificial intelligence. While PUBT strives to provide accurate and timely information, this AI-generated content is for informational purposes only and should not be interpreted as financial, investment, or legal advice. IDEAYA Biosciences Inc. published the original content used to generate this news brief via PR Newswire (Ref. ID: SF35497) on December 01, 2025, and is solely responsible for the information contained therein.
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