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 07-27 11:03:11 EDT

83.07

+0.45

+0.54%

最高85.05	最低81.01	成交量49.91万
今开84.11	昨收82.62	日振幅4.89%
总市值40.51亿	流通市值24.85亿	总股本4,877万
成交额4,174万	换手率1.67%	流通股本2,991万
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--

数据加载中...

北京优虎网络科技有限公司

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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":"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"],"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.laohu8.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":"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":"-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 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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":"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":"-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) 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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.laohu8.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.laohu8.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.laohu8.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.laohu8.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. 定价增发5亿美元、2032年到期的0.25%可转换优先票据","url":"https://stock-news.laohu8.com/highlight/detail?id=1187497120","media":"投资观察","labels":["shareholding"],"top":-1,"itemType":null,"share":"https://www.laohu8.com/m/news/1187497120?lang=zh_cn&edition=full","pubTime":"2026-06-04 10:23","pubTimestamp":1780539808,"startTime":"0","endTime":"0","summary":"6月3日 - 生物技术公司 Celcuity Inc. 宣布，已为其增发的2032年到期、利率为0.250%的可转换优先票据完成定价。此次发行规模最终确定为5亿美元。\n该笔票据的发行规模较原计划有所扩大，凸显了市场对其融资条款的认可。可转换票据为投资者提供了未来将债务转换为公司股权的选择权，是成长型公司常见的融资工具之一。","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":"shareholding","news_rank":0,"length":0,"strategy_id":0,"source":null,"symbols":["CELC","BK4139"],"isVideo":false,"video":null,"gpt_icon":0},{"id":"1187515046","title":"Celcuity Inc宣布公开发行2032年到期的可转换优先票据","url":"https://stock-news.laohu8.com/highlight/detail?id=1187515046","media":"投资观察","labels":["shareholding"],"top":-1,"itemType":null,"share":"https://www.laohu8.com/m/news/1187515046?lang=zh_cn&edition=full","pubTime":"2026-06-03 19:39","pubTimestamp":1780486794,"startTime":"0","endTime":"0","summary":"Celcuity Inc于6月3日宣布，将公开发行一批于2032年到期的可转换优先票据。此举旨在为公司运营及战略发展募集资金。","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":"0","news_top_title":null,"news_tag":"shareholding","news_rank":0,"length":0,"strategy_id":0,"source":null,"symbols":["BK4139","CELC"],"isVideo":false,"video":null,"gpt_icon":0},{"id":"1199488490","title":"异动解读｜Celcuity盘中下跌23.24%，III期VIKTORIA-1临床数据公布后股价承压","url":"https://stock-news.laohu8.com/highlight/detail?id=1199488490","media":"行情直击","labels":["dataReport"],"top":-1,"itemType":null,"share":"https://www.laohu8.com/m/news/1199488490?lang=zh_cn&edition=full","pubTime":"2026-06-03 00:20","pubTimestamp":1780417249,"startTime":"0","endTime":"0","summary":"6月2日，Celcuity盘中下跌23.24%，报93.69美元/股，成交额3.2亿美元。消息面上，公司通过SEC文件公布了III期VIKTORIA-1试验PIK3CA突变队列结果：Gedatolisib三联疗法中位无进展生存期为11.1个月，对照组Alpelisib联合Fulvestrant为5.6个月；安全性方面不良事件多为低级别。FDA已授予其新药申请优先审评资格，PDUFA目标日期定为7月17日。尽管临床数据及监管进展积极，股价仍大幅回落，提示市场此前或已充分定价甚至对数据抱有更高预期。","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":"dataReport","news_rank":0,"length":0,"strategy_id":0,"source":null,"symbols":["CELC"],"isVideo":false,"video":null,"gpt_icon":0},{"id":"1169917585","title":"Celcuity公布III期VIKTORIA-1试验PIK3CA突变队列结果 - 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Inc宣布，其针对核心药物Gedatolisib的新药申请已获得美国食品药品监督管理局的优先审评资格，关键审评日期定于2026年7月17日，这标志着该药物在监管审批流程中迈出了关键一步，有望加速上市进程。与此同时，公司另一则公告显示，其针对Gedatolisib作为HR+/HER2-晚期乳腺癌一线疗法的III期Viktoria-2临床试验，将扩大招募范围，将内分泌敏感患者群体也纳入其中。","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":"movement","news_rank":0,"length":0,"strategy_id":0,"source":"ai_movement_cn","symbols":["CELC"],"isVideo":false,"video":null,"gpt_icon":0},{"id":"1142039438","title":"Celcuity Inc 新药申请获FDA优先审评资格，关键审评日期定于2026年7月17日","url":"https://stock-news.laohu8.com/highlight/detail?id=1142039438","media":"美股速递","labels":["productRelease"],"top":-1,"itemType":null,"share":"https://www.laohu8.com/m/news/1142039438?lang=zh_cn&edition=full","pubTime":"2026-05-14 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