1月2日,中国国家药监局(NMPA)官网最新公示,吉利德科学公司申报的来那帕韦片和来那帕韦注射液上市申请已获得批准。来那帕韦将为HIV感染者提供一种每年仅需给药两次的全新治疗方案。 该药此前已在欧盟、美国等地获批上市。在长效治疗HIV感染的适应症获批后,来那帕韦在预防HIV感染方面的临床研究也在今年有了重要进展。2024年7月,来那帕韦一项名为PURPOSE1的三期临床试验中期结果在《新英格兰...
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