Celcuity公司宣布FDA批准Revtorpyk™ (gedatolisib) 用于治疗HR+/HER2-、PIK3CA野生型局部晚期或转移性乳腺癌

美股速递07-15

Celcuity公司今日宣布，其新药Revtorpyk™ (gedatolisib) 已获得美国食品药品监督管理局（FDA）的批准。该药物获准用于治疗激素受体阳性、HER2阴性，且PIK3CA基因呈野生型的局部晚期或转移性乳腺癌患者。此项批准标志着针对这一特定乳腺癌亚型患者群体的一项重要治疗新选择。

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