Abpro Holdings Inc. announced that its lead multispecific antibody oncology program, ABP-102 / CT-P72, recently received Investigational New Drug $(IND)$ clearance from the U.S. Food and Drug Administration (FDA). This regulatory approval enables the initiation of a global Phase 1 clinical trial to evaluate ABP-102 / CT-P72 in patients with HER2-positive solid tumors. The study is expected to commence in the first half of 2026 through Abpro's strategic collaboration with Celltrion.
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. Abpro Holdings Inc. published the original content used to generate this news brief via GlobeNewswire (Ref. ID: GNW9626264-en) on January 15, 2026, and is solely responsible for the information contained therein.