7月17日，据CDE官网消息，上海复旦张江生物医药股份有限公司联合申请药品“注射用FDA018抗体偶联剂”，获得临床试验默示许可，受理号CXSB2400041。
公示信息显示，药品“注射用FDA018抗体偶联剂”适应症：晚期实体瘤。
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上海复旦张江生物医药股份有限公司药品申请临床试验默示许可获受理
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The above content is for informational or educational purposes only and does not constitute any investment advice related to Futu. Although we strive to ensure the truthfulness, accuracy, and originality of all such content, we cannot guarantee it.
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Risk Disclaimer
The above content is for informational or educational purposes only and does not constitute any investment advice related to Futu. Although we strive to ensure the truthfulness, accuracy, and originality of all such content, we cannot guarantee it.
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