异动解读｜Celcuity Inc夜盘下跌5.45%，FDA批准核心药物后市场兑现获利

行情直击07-15

7月15日，Celcuity Inc夜盘下跌5.45%，报105.0美元/股，成交额4229.8美元。

消息面上，FDA正式批准公司核心药物REVTORPYK（gedatolisib）用于HR+/HER2-、PIK3CA野生型局部晚期或转移性乳腺癌，批准基于III期VIKTORIA-1试验数据（中位无进展生存期9.3个月 vs 对照组2.0个月）。然而该股此前已因FDA审评日临近大幅上涨，盘中一度涨超5%，正式获批后资金呈典型"利好兑现"式抛售。此外，当前获批适应症仅限PIK3CA野生型患者，针对PIK3CA突变患者的补充申请尚需于第三季度提交，市场对适应症范围或存在预期差。公司预计将于第三季度末启动商业化。

（以上内容均基于市场公开消息，由程序或算法智能生成，仅作为股价异动提醒，不作为投资建议或交易依据。）

免责声明：本文观点仅代表作者个人观点，不构成本平台的投资建议，本平台不对文章信息准确性、完整性和及时性做出任何保证，亦不对因使用或信赖文章信息引发的任何损失承担责任。

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