ImmuneOnco Biopharmaceuticals Announces FDA Clearance to Initiate Phase I Clinical Trial for IMM2510/AXN-2510 in the U.S

Reuters
07-30
ImmuneOnco Biopharmaceuticals Announces FDA Clearance to Initiate Phase I Clinical Trial for IMM2510/AXN-2510 in the U.S

ImmuneOnco Biopharmaceuticals (Shanghai) Inc. has announced the initiation of a Phase I clinical trial for IMM2510/AXN-2510 in the United States, following clearance from the U.S. Food and Drug Administration (FDA). IMM2510/AXN-2510 is a PD-L1 and VEGF bispecific antibody currently under development. The trial's commencement marks a significant milestone in the company's collaboration with Axion Bio, a wholly-owned subsidiary of Instil Bio, Inc. As part of this development, ImmuneOnco has received a milestone payment of US$10 million from Instil Bio. To date, total payments under their License and Collaboration Agreement have reached US$30 million. Results from this trial are expected to be presented in the future.

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. Immuneonco Biopharmaceuticals (Shanghai) Co. Ltd. published the original content used to generate this news brief on July 30, 2025, and is solely responsible for the information contained therein.

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