海创药业申请HP568片临床试验获FDA批准

财中社2024-12-30

财中社12月30日电海创药业（688302）发布自愿披露公告，宣布其自主研发的口服PROTAC药物HP568片已获得美国FDA批准，用于治疗ER+/HER2-晚期乳腺癌的临床试验。此前，该药物的临床试验申请于2024年10月获得中国国家药品监督管理局批准。截至公告披露日，国内外无同类PROTAC产品获批上市。HP568是针对雌激素受体α的靶向药物，具有良好的抗增殖活性和安全性。全球2022年乳腺癌...

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