海创药业一款在研新药在美国获快速通道认定，用于AR三阴乳腺癌

新京报07-01

新京报讯(记者张兆慧)6月30日，海创药业宣布，其在研1类新药蛋白降解靶向嵌合体HP518片获得美国食品药品监督管理局(FDA)授予“快速通道认定”，用于治疗雄激素受体(AR)阳性三阴乳腺癌。目前国内外均无同类靶点产品获批上市。三阴乳腺癌约占所有乳腺癌的10%-15%，具有侵袭性强、复发率高和预后较差的特点。AR阳性三阴乳腺癌患者约占三阴乳腺癌患者的15%-50%。AR通过非配体依赖的全新机理调节...

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