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Betta Pharmaceuticals: National Medical Products Administration approves the launch of Patuzumab Injection
Betta Pharmaceuticals announces that the company has received the “Drug Registration Certificate” issued by the National Medical Products Administration (Approval Number: GuoYaoZhunZi S20260009), approving the launch of Patuzumab Injection (brand name: Bezetin) developed in cooperation with Hangzhou Bozhi Rui Biopharmaceutical Co., Ltd. Bezetin is indicated for early-stage and metastatic breast cancer patients. The drug is a biosimilar of Patuzumab independently developed by Borui Bio, used to treat early-stage and metastatic breast cancer. After obtaining the registration certificate, the company can proceed with the commercialization of Bezetin.