
Apr 02,2026
Kexing Biopharm’s Innovative Drug GB19 Received Approval From FDA To Conduct Clinical Trials
Recently, GB19 Injection, independently developed by Shenzhen Kexing Pharmaceutical Co., Ltd., a wholly-owned subsidiary of Kexing Biopharm, has officially received an Investigational New Drug (IND) approval notice from the U.S. Food and Drug Administration (FDA), allowing clinical trials to be conducted in the United States. The indication is for the treatment of cutaneous lupus erythematosus (CLE) and systemic lupus erythematosus (SLE).
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