Shanghai Henlius Biotech Inc. announced that the National Medical Products Administration (NMPA) has approved the investigational new drug $(IND)$ application for HLX15-SC, a recombinant anti-CD38 fully human monoclonal antibody injection intended for subcutaneous administration, for the treatment of multiple myeloma. The IND approval allows the company to proceed with a phase 1 clinical trial of HLX15-SC, which has been independently developed by Shanghai Henlius Biotech Inc.
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