Celcuity Inc(CELC)_个股概要_股票价格_最新资讯_行情走势_历史数据 - 老虎社区

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CELC Celcuity Inc

交易中 09-29 15:41:02 EDT

77.79

-1.85

-2.32%

最高80.52	最低77.26	成交量51.50万
今开79.64	昨收79.64	日振幅4.10%
总市值37.94亿	流通市值23.12亿	总股本4,877万
成交额4,025万	换手率1.73%	流通股本2,972万
市净率--	ROE--	每股收益0.00
52周最高--	52周最低--	市盈率--
股息--	股息收益率--	ROA--

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北京优虎网络科技有限公司

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23:01","pubTimestamp":1789052460,"startTime":"0","endTime":"0","summary":"9月10日，县委书记王长俊现场推进重点项目建设。王长俊与企业负责人深入交流，详细了解项目规划、要素保障、施工筹备等推进情况，要求相关部门主动靠前服务、全程跟踪跟进，扎实做好审批办理、要素配套各项保障工作，对置换项目加快原地块建筑拆除、场地清理等工作，尽快实现净地交付，确保新项目10月份能够开工建设。","market":"other","thumbnail":null,"type":0,"news_type":0,"thumbnails":[],"rights":null,"property":[],"language":"zh","translate_title":"","themeId":null,"theme_name":"","theme_type":"","isJumpTheme":false,"source_url":"https://finance.sina.com.cn/wm/2026-09-10/doc-inirkiyn2622862.shtml","is_publish_highlight":false,"source_rank":0,"column":"","sentiment":"0","news_top_title":null,"news_tag":"","news_rank":0,"length":0,"strategy_id":0,"source":"sina","symbols":["CELC","BK4139"],"isVideo":false,"video":null,"gpt_icon":0},{"id":"1188384409","title":"Celcuity向FDA提交Revtorpyk™（Gedatolisib）补充新药申请，用于HR+/HER2-、PIK3CA突变局部晚期或转移性乳腺癌治疗","url":"https://stock-news.laohu8.com/highlight/detail?id=1188384409","media":"美股速递","labels":["productRelease"],"top":-1,"itemType":null,"share":"https://www.laohunote.com/m/news/1188384409?lang=zh_cn&edition=full","pubTime":"2026-08-26 20:31","pubTimestamp":1787747481,"startTime":"0","endTime":"0","summary":"Celcuity公司近日宣布，已正式向美国食品药品监督管理局提交了Revtorpyk的补充新药申请。此番申请针对的适应症为HR阳性、HER2阴性且携带PIK3CA突变的局部晚期或转移性乳腺癌患者群体。Revtorpyk作为一种潜在的治疗方案，其开发聚焦于特定的生物标志物定义人群——即在HR+/HER2-乳腺癌中检测到PIK3CA基因突变的患者。Celcuity此次提交的sNDA，若获FDA批准，将为这一特定患者亚群提供新的治疗选项。目前，FDA将对该补充新药申请进行审评，审评周期及最终决定时间尚待公布。","market":"us","thumbnail":"","type":0,"news_type":0,"thumbnails":[],"rights":null,"property":[],"language":"zh","translate_title":"","themeId":null,"theme_name":"","theme_type":"","isJumpTheme":false,"source_url":"","is_publish_highlight":false,"source_rank":0,"column":"","sentiment":"1","news_top_title":null,"news_tag":"productRelease","news_rank":0,"length":0,"strategy_id":0,"source":null,"symbols":["BK4139","CELC"],"isVideo":false,"video":null,"gpt_icon":0},{"id":"1162791330","title":"获FDA新批准的Revtorpyk™（Gedatolisib）被纳入NCCN® HR+/HER2-局部晚期或转移性乳腺癌临床实践指南","url":"https://stock-news.laohu8.com/highlight/detail?id=1162791330","media":"美股速递","labels":["policyRegulatory"],"top":-1,"itemType":null,"share":"https://www.laohunote.com/m/news/1162791330?lang=zh_cn&edition=full","pubTime":"2026-07-30 20:31","pubTimestamp":1785414676,"startTime":"0","endTime":"0","summary":"近日，一款新获美国食品药品监督管理局（FDA）批准的药物——Revtorpyk™（通用名：Gedatolisib），已被正式纳入美国国家综合癌症网络®（NCCN®）的临床实践指南。该指南针对的是HR+/HER2-局部晚期或转移性乳腺癌患者。这一纳入标志着这款药物在肿瘤治疗领域的权威性认可迈出了关键一步。该消息由Celcuity Inc（CELC）公司对外披露。Revtorpyk™的加入，为特定类型的乳腺癌患者提供了全新的治疗选择与希望。指南的更新，将有助于临床医生在制定个体化治疗方案时，有更多循证依据可供参考。","market":"us","thumbnail":"","type":0,"news_type":0,"thumbnails":[],"rights":null,"property":[],"language":"zh","translate_title":"","themeId":null,"theme_name":"","theme_type":"","isJumpTheme":false,"source_url":"","is_publish_highlight":false,"source_rank":0,"column":"","sentiment":"1","news_top_title":null,"news_tag":"policyRegulatory","news_rank":0,"length":0,"strategy_id":0,"source":null,"symbols":["CELC","BK4139"],"isVideo":false,"video":null,"gpt_icon":0},{"id":"1184889176","title":"FDA批准Celcuity旗下Revtorpyk用于治疗无PIK3CA突变的HR+/HER2-晚期乳腺癌","url":"https://stock-news.laohu8.com/highlight/detail?id=1184889176","media":"美股速递","labels":["productRelease"],"top":-1,"itemType":null,"share":"https://www.laohunote.com/m/news/1184889176?lang=zh_cn&edition=full","pubTime":"2026-07-30 20:31","pubTimestamp":1785414675,"startTime":"0","endTime":"0","summary":"2026年7月14日，美国食品药品监督管理局（FDA）正式批准了Celcuity公司开发的药物Revtorpyk。该药物针对的是一种特定类型的晚期乳腺癌——激素受体阳性（HR+）、人表皮生长因子受体2阴性（HER2-），且不携带PIK3CA基因突变。这一里程碑式的决定，为原本治疗选择有限的这部分患者群体，开辟了全新的治疗路径。","market":"us","thumbnail":"","type":0,"news_type":0,"thumbnails":[],"rights":null,"property":[],"language":"zh","translate_title":"","themeId":null,"theme_name":"","theme_type":"","isJumpTheme":false,"source_url":"","is_publish_highlight":false,"source_rank":0,"column":"","sentiment":"1","news_top_title":null,"news_tag":"productRelease","news_rank":0,"length":0,"strategy_id":0,"source":null,"symbols":["BK4139","CELC"],"isVideo":false,"video":null,"gpt_icon":0},{"id":"1123499084","title":"异动解读｜Celcuity Inc盘中下跌22.15%，FDA批准核心药物后利好兑现引发深度抛售","url":"https://stock-news.laohu8.com/highlight/detail?id=1123499084","media":"行情直击","labels":["productRelease"],"top":-1,"itemType":null,"share":"https://www.laohunote.com/m/news/1123499084?lang=zh_cn&edition=full","pubTime":"2026-07-15 21:33","pubTimestamp":1784122391,"startTime":"0","endTime":"0","summary":"7月15日，Celcuity Inc盘中下跌22.15%，报91.795美元/股，成交额4476.92万美元。消息面上，FDA正式批准公司核心药物REVTORPYK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。然而该股此前已因PDUFA审评日临近大幅走高，盘中一度涨超5%至109.21美元，正式获批后资金呈典型\"利好兑现\"式抛售并持续加深。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，适应症范围窄于部分市场预期，加剧了卖压。","market":"hk","thumbnail":"","type":0,"news_type":0,"thumbnails":[],"rights":null,"property":[],"language":"zh","translate_title":"","themeId":null,"theme_name":"","theme_type":"","isJumpTheme":false,"source_url":"","is_publish_highlight":false,"source_rank":0,"column":"","sentiment":"-2","news_top_title":null,"news_tag":"productRelease","news_rank":0,"length":0,"strategy_id":0,"source":null,"symbols":["CELC"],"isVideo":false,"video":null,"gpt_icon":0},{"id":"1179546739","title":"异动解读｜Celcuity Inc盘前下跌5.59%，FDA批准核心药物后市场兑现获利","url":"https://stock-news.laohu8.com/highlight/detail?id=1179546739","media":"行情直击","labels":[],"top":-1,"itemType":null,"share":"https://www.laohunote.com/m/news/1179546739?lang=zh_cn&edition=full","pubTime":"2026-07-15 18:59","pubTimestamp":1784113147,"startTime":"0","endTime":"0","summary":"7月15日，Celcuity Inc盘前下跌5.59%，报104.84美元/股，成交额9.01万美元。然而该股此前已因FDA审评日临近而大幅走高，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。","market":"us","thumbnail":"","type":0,"news_type":0,"thumbnails":[],"rights":null,"property":[],"language":"zh","translate_title":"","themeId":null,"theme_name":"","theme_type":"","isJumpTheme":false,"source_url":"","is_publish_highlight":false,"source_rank":0,"column":"","sentiment":"-1","news_top_title":null,"news_tag":"","news_rank":0,"length":0,"strategy_id":0,"source":null,"symbols":["CELC"],"isVideo":false,"video":null,"gpt_icon":0},{"id":"1103001250","title":"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","url":"https://stock-news.laohu8.com/highlight/detail?id=1103001250","media":"行情直击","labels":[],"top":-1,"itemType":null,"share":"https://www.laohunote.com/m/news/1103001250?lang=zh_cn&edition=full","pubTime":"2026-07-15 08:32","pubTimestamp":1784075567,"startTime":"0","endTime":"0","summary":"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。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。","market":"us","thumbnail":"","type":0,"news_type":0,"thumbnails":[],"rights":null,"property":[],"language":"zh","translate_title":"","themeId":null,"theme_name":"","theme_type":"","isJumpTheme":false,"source_url":"","is_publish_highlight":false,"source_rank":0,"column":"","sentiment":"-1","news_top_title":null,"news_tag":"","news_rank":0,"length":0,"strategy_id":0,"source":null,"symbols":["CELC"],"isVideo":false,"video":null,"gpt_icon":0},{"id":"1124036184","title":"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","url":"https://stock-news.laohu8.com/highlight/detail?id=1124036184","media":"美股速递","labels":["productRelease"],"top":-1,"itemType":null,"share":"https://www.laohunote.com/m/news/1124036184?lang=zh_cn&edition=full","pubTime":"2026-07-15 04:54","pubTimestamp":1784062483,"startTime":"0","endTime":"0","summary":"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。","market":"us","thumbnail":"","type":0,"news_type":0,"thumbnails":[],"rights":null,"property":[],"language":"zh","translate_title":"","themeId":null,"theme_name":"","theme_type":"","isJumpTheme":false,"source_url":"","is_publish_highlight":false,"source_rank":0,"column":"","sentiment":"2","news_top_title":null,"news_tag":"productRelease","news_rank":0,"length":0,"strategy_id":0,"source":null,"symbols":["CELC","BK4139"],"isVideo":false,"video":null,"gpt_icon":0},{"id":"1124500511","title":"异动解读｜Celcuity Inc盘后下跌6.75%，报106.79美元","url":"https://stock-news.laohu8.com/highlight/detail?id=1124500511","media":"行情直击","labels":[],"top":-1,"itemType":null,"share":"https://www.laohunote.com/m/news/1124500511?lang=zh_cn&edition=full","pubTime":"2026-07-15 04:43","pubTimestamp":1784061822,"startTime":"0","endTime":"0","summary":"7月15日，Celcuity Inc盘后下跌6.75%，报106.79美元/股，成交额332.07万美元。Celcuity Inc所在的生物科技行业中，个股中，艾伯维公司跌0.03%，Nextcure Inc.跌12.61%，渤健公司涨0.45%，吉利德科学涨0.17%，Revolution Medicines, Inc.跌0.52%。Celcuity Inc.是一家临床阶段的生物技术公司，专注于开发针对实体瘤的靶向疗法。其主要候选药物gedatolisib是一种PI3K/AKT/mTOR通路激酶抑制剂，目前正在进行针对HR+/HER2-晚期乳腺癌及其他适应症的3期临床试验。","market":"us","thumbnail":"","type":0,"news_type":0,"thumbnails":[],"rights":null,"property":[],"language":"zh","translate_title":"","themeId":null,"theme_name":"","theme_type":"","isJumpTheme":false,"source_url":"","is_publish_highlight":false,"source_rank":0,"column":"","sentiment":"-1","news_top_title":null,"news_tag":"","news_rank":0,"length":0,"strategy_id":0,"source":null,"symbols":["CELC"],"isVideo":false,"video":null,"gpt_icon":0},{"id":"1123253973","title":"异动解读｜Celcuity盘中上涨5.22%，FDA关键审评日临近催化市场预期","url":"https://stock-news.laohu8.com/highlight/detail?id=1123253973","media":"行情直击","labels":[],"top":-1,"itemType":null,"share":"https://www.laohunote.com/m/news/1123253973?lang=zh_cn&edition=full","pubTime":"2026-07-15 03:15","pubTimestamp":1784056548,"startTime":"0","endTime":"0","summary":"7月15日，Celcuity盘中上涨5.22%，报109.21美元/股，成交额1.0亿美元。消息面上，FDA此前已受理Celcuity核心候选药物gedatolisib的新药申请并授予优先审评资格，PDUFA目标审评日期定于7月17日，距当前仅两日。市场对该药获批前景的乐观预期推动股价走强。此前公布的III期Viktoria-1试验数据显示，gedatolisib三联疗法将疾病进展或死亡风险降低50%，中位无进展生存期达11.1个月，远超对照组的5.6个月，客观缓解率分别为48.9%和35.7%，安全性整体良好。","market":"us","thumbnail":"","type":0,"news_type":0,"thumbnails":[],"rights":null,"property":[],"language":"zh","translate_title":"","themeId":null,"theme_name":"","theme_type":"","isJumpTheme":false,"source_url":"","is_publish_highlight":false,"source_rank":0,"column":"","sentiment":"1","news_top_title":null,"news_tag":"","news_rank":0,"length":0,"strategy_id":0,"source":null,"symbols":["CELC"],"isVideo":false,"video":null,"gpt_icon":0},{"id":"1160136010","title":"异动解读｜Celcuity盘中下跌5.37%，FDA审评目标日期临近多空博弈加剧","url":"https://stock-news.laohu8.com/highlight/detail?id=1160136010","media":"行情直击","labels":[],"top":-1,"itemType":null,"share":"https://www.laohunote.com/m/news/1160136010?lang=zh_cn&edition=full","pubTime":"2026-07-09 00:21","pubTimestamp":1783527689,"startTime":"0","endTime":"0","summary":"7月9日，Celcuity盘中下跌5.37%，报110.27美元/股，成交额5625.14万美元。该股前一交易日曾上涨5.02%。消息面上，公司核心候选药物gedatolisib的FDA处方药用户付费法案目标审评日期定于7月17日，距今不足10天。该药物已获FDA新药申请优先审评资格，用于HR+/HER2-/PIK3CA突变晚期乳腺癌治疗，III期Viktoria-1试验数据显示三联疗法将疾病进展或死亡风险降低50%，中位无进展生存期达11.1个月。临近重大二元催化事件，市场多空博弈加剧，股价出现回调。","market":"us","thumbnail":"","type":0,"news_type":0,"thumbnails":[],"rights":null,"property":[],"language":"zh","translate_title":"","themeId":null,"theme_name":"","theme_type":"","isJumpTheme":false,"source_url":"","is_publish_highlight":false,"source_rank":0,"column":"","sentiment":"-1","news_top_title":null,"news_tag":"","news_rank":0,"length":0,"strategy_id":0,"source":null,"symbols":["CELC"],"isVideo":false,"video":null,"gpt_icon":0},{"id":"1197009110","title":"异动解读｜Celcuity盘中上涨5.02%，核心药物FDA审评目标日期临近","url":"https://stock-news.laohu8.com/highlight/detail?id=1197009110","media":"行情直击","labels":[],"top":-1,"itemType":null,"share":"https://www.laohunote.com/m/news/1197009110?lang=zh_cn&edition=full","pubTime":"2026-07-08 00:07","pubTimestamp":1783440465,"startTime":"0","endTime":"0","summary":"7月8日，Celcuity盘中上涨5.02%，报114.03美元/股，成交额5562.87万美元。消息面上，公司核心候选药物gedatolisib的FDA处方药用户付费法案目标审评日期定于7月17日，距今仅约一周。该药物此前已获FDA新药申请优先审评资格，用于HR+/HER2-/PIK3CA突变晚期乳腺癌治疗。III期Viktoria-1试验数据显示，gedatolisib三联疗法将疾病进展或死亡风险降低50%，中位无进展生存期达11.1个月，较对照组5.6个月近乎翻倍。市场对即将到来的FDA审批决定持乐观预期，推动股价走强。","market":"us","thumbnail":"","type":0,"news_type":0,"thumbnails":[],"rights":null,"property":[],"language":"zh","translate_title":"","themeId":null,"theme_name":"","theme_type":"","isJumpTheme":false,"source_url":"","is_publish_highlight":false,"source_rank":0,"column":"","sentiment":"1","news_top_title":null,"news_tag":"","news_rank":0,"length":0,"strategy_id":0,"source":null,"symbols":["CELC"],"isVideo":false,"video":null,"gpt_icon":0},{"id":"1187497120","title":"Celcuity Inc. 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5.6个月","url":"https://stock-news.laohu8.com/highlight/detail?id=1134324033","media":"美股速递","labels":["dataReport"],"top":-1,"itemType":null,"share":"https://www.laohunote.com/m/news/1134324033?lang=zh_cn&edition=full","pubTime":"2026-06-02 20:15","pubTimestamp":1780402521,"startTime":"0","endTime":"0","summary":"根据一份提交给美国证券交易委员会的文件，Celcuity Inc 公布的数据显示，其Gedatolisib三联疗法在关键试验中取得了显著成果。\n该疗法展现出的中位无进展生存期达到11.1个月，而对照组使用Alpelisib联合Fulvestrant方案的中位无进展生存期仅为5.6个月。这一对比数据突显了Gedatolisib三联疗法的潜在优势。","market":"us","thumbnail":"","type":0,"news_type":0,"thumbnails":[],"rights":null,"property":[],"language":"zh","translate_title":"","themeId":null,"theme_name":"","theme_type":"","isJumpTheme":false,"source_url":"","is_publish_highlight":false,"source_rank":0,"column":"","sentiment":"1","news_top_title":null,"news_tag":"dataReport","news_rank":0,"length":0,"strategy_id":0,"source":null,"symbols":["CELC","BK4139"],"isVideo":false,"video":null,"gpt_icon":0},{"id":"1179894923","title":"Celcuity公司：Gedatolisib治疗方案总体耐受性良好，不良事件多为低级别","url":"https://stock-news.laohu8.com/highlight/detail?id=1179894923","media":"美股速递","labels":["dataReport"],"top":-1,"itemType":null,"share":"https://www.laohunote.com/m/news/1179894923?lang=zh_cn&edition=full","pubTime":"2026-06-02 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