恒瑞医药公告,近日公司及子公司成都盛迪医药有限公司收到国家药品监督管理局核准签发关于HRS-5041片的《药物临床试验批准通知书》,将于近期开展临床试验。HRS-5041是公司开发的新型、高效、选择性的AR-PROTAC(雄激素受体-蛋白降解靶向嵌合体)小分子,拟用于治疗前列腺癌。截至目前,HRS-5041片相关项目累计研发投入约6919万元。
恒瑞医药公告,近日公司及子公司成都盛迪医药有限公司收到国家药品监督管理局核准签发关于HRS-5041片的《药物临床试验批准通知书》,将于近期开展临床试验。HRS-5041是公司开发的新型、高效、选择性的AR-PROTAC(雄激素受体-蛋白降解靶向嵌合体)小分子,拟用于治疗前列腺癌。截至目前,HRS-5041片相关项目累计研发投入约6919万元。
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