Outlook Therapeutics 宣布 Lytenava™ 获 FDA 批准:成为首个且唯一用于治疗湿性 AMD 的眼用贝伐珠单抗

美股速递
Jul 25

Outlook Therapeutics 正式宣布,其药物 Lytenava™ 已获得美国食品药品监督管理局(FDA)批准。这是首款、也是唯一一款获 FDA 许可、专用于治疗湿性年龄相关性黄斑变性(湿性 AMD)的眼用贝伐珠单抗。

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