复星医药(600196.SH)子公司HLX3902注射液获准于澳大利亚开展临床试验

智通财经05-21

智通财经APP讯，复星医药(600196.SH)发布公告，近日，公司控股子公司上海复宏汉霖生物技术股份有限公司及其控股子公司(合称“复宏汉霖”)自主研发的HLX3902注射液(即STEAP1xCD3xCD28三特异性抗体)用于转移性去势抵抗性前列腺癌及其他晚期实体瘤治疗的Ⅰ期临床试验方案获得相关人类研究伦理委员会的批准、并通过澳大利亚药品管理局(Therapeutic Goods Administration)备案，系该药品于全球范围内取得的首个临床试验许可。复宏汉霖拟于条件具备后于澳大利亚开展该药品的相关临床研究。

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