格隆汇7月9日|近日,复宏汉霖(2696.HK)创新型程序性死亡-配体1(PD-L1)抗体偶联药物(ADC)注射用HLX43全球开发再度取得重要进展,该产品已获得中国国家药品监督管理局(NMPA)、美国食品药品监督管理局(FDA)、澳大利亚药品管理局(TGA)及日本药品医疗器械综合机构(PMDA)许可,开展针对晚期非小细胞肺癌(NSCLC)的国际多中心II期临床研究,并于此前在中国境内完成首例...
Source Link格隆汇7月9日|近日,复宏汉霖(2696.HK)创新型程序性死亡-配体1(PD-L1)抗体偶联药物(ADC)注射用HLX43全球开发再度取得重要进展,该产品已获得中国国家药品监督管理局(NMPA)、美国食品药品监督管理局(FDA)、澳大利亚药品管理局(TGA)及日本药品医疗器械综合机构(PMDA)许可,开展针对晚期非小细胞肺癌(NSCLC)的国际多中心II期临床研究,并于此前在中国境内完成首例...
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