绿叶制药:新药LY03020在美国获准开展临床试验

E公司
14 Jan

e公司讯,绿叶制药在港交所公告,该集团自主开发的新一代抗精神病药物LY03020已获得美国食品药品监督管理局(“FDA”)许可开展临床试验,拟用于治疗精神分裂症。LY03020基于该集团新分子实体/新治疗实体技术平台开发,是全球首个痕量胺相关受体1和5-羟色胺2C受体双靶点激动剂。LY03020亦在中国进入临床阶段。

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