Fosun Pharma: Henlius HLX17 receives U.S. FDA approval for clinical trials

Henlius HLX17 receives U.S. FDA approval for clinical trials

September 9, 2025 Source: drugdu 93

Fosun Pharma announced on the evening of September 8th that its controlling subsidiary, Shanghai Henlius Biotech Co., Ltd., and its subsidiaries (collectively, " Henlius "), have recently received approval from the U.S. Food and Drug Administration (FDA) to conduct a Phase I clinical trial of HLX17 (a recombinant anti-PD-1 humanized monoclonal antibody injection) for the treatment of patients with various resected solid tumors. Henlius intends to conduct this international, multicenter clinical study in the United States once conditions permit.
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