Shandong Boan Biotechnology Co. Ltd. Receives FDA Approval to Initiate Clinical Trials for BA1302 in the U.S

Reuters
2025/06/17
Shandong Boan Biotechnology Co. Ltd. Receives FDA Approval to Initiate Clinical Trials for BA1302 in the U.S

Shandong Boan Biotechnology Co. Ltd. has announced that it has received approval from the U.S. Food and Drug Administration (FDA) to initiate clinical trials for its novel antibody-drug conjugate $(ADC)$, BA1302, targeting CD228 for the treatment of various solid tumors. BA1302 has previously been granted Orphan Drug Designations by the FDA for squamous non-small cell lung cancer and pancreatic cancer. Currently, a Phase 1 clinical trial is ongoing in China, with development progress leading similar projects globally. The company is committed to accelerating the clinical development of BA1302 worldwide, aiming to explore its potential as a monotherapy and in combination with other treatments, thereby offering new hope for targeted cancer treatment. This announcement marks a significant step forward in Shandong Boan Biotechnology's efforts to provide innovative cancer therapies.

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. Shandong Boan Biotechnology Co. Ltd. published the original content used to generate this news brief on June 17, 2025, and is solely responsible for the information contained therein.

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