Fosun Pharma (02196.HK): Controlled Subsidiary’s HLX3902 Injection Obtains Clinical Trial Approval

NewTimeSpace News: Fosun Pharma announced on June 17 that its controlled subsidiary Henlius has received approval from the National Medical Products Administration (NMPA) to conduct Phase I clinical trials for its self-developed HLX3902 Injection (STEAP1×CD3×CD28 trispecific antibody) in the treatment of metastatic castration-resistant prostate cancer and other advanced solid tumors.

NewTimeSpace News: On June 17, 2026, Fosun Pharma (02196.HK) issued an announcement stating that its controlled subsidiary Shanghai Henlius Biotech, Inc. has secured approval from the National Medical Products Administration to launch a Phase I clinical trial of HLX3902 Injection for the treatment of metastatic castration-resistant prostate cancer (mCRPC) and other advanced solid tumors.

The candidate drug has previously obtained clinical trial notification clearance from the Therapeutic Goods Administration (TGA) of Australia, and its Phase I clinical trial protocol has been approved by the relevant ethics committee.

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