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 06-11 13:37:32 EDT

90.35

+2.11

+2.39%

最高91.49	最低85.54	成交量51.90万
今开89.46	昨收88.24	日振幅6.74%
总市值44.06亿	流通市值26.78亿	总股本4,877万
成交额4,590万	换手率1.75%	流通股本2,965万
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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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":"","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":"","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":"","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 - SEC文件披露","url":"https://stock-news.laohu8.com/highlight/detail?id=1169917585","media":"投资观察","labels":["dataReport"],"top":-1,"itemType":null,"share":"https://www.laohu8.com/m/news/1169917585?lang=zh_cn&edition=full","pubTime":"2026-06-02 20:34","pubTimestamp":1780403640,"startTime":"0","endTime":"0","summary":"Celcuity公司近期通过提交给美国证券交易委员会的文件，公布了其关键III期VIKTORIA-1临床试验中针对PIK3CA突变患者队列的详细数据。安全性方面，gedatolisib相关治疗方案普遍耐受性良好，报告的大多数不良事件为低级别。美国食品药品监督管理局已授予Celcuity公司gedatolisib的新药申请优先审评资格，并设定了处方药用户付费法案目标日期为2026年7月17日。公司表示，若获得FDA批准，正按计划推进gedatolisib在2026年第三季度的商业化上市准备工作。","market":"us","thumbnail":"","type":0,"news_type":0,"thumbnails":[],"rights":null,"property":[],"language":"zh","translate_title":"","themeId":"","theme_name":"","theme_type":"","isJumpTheme":false,"source_url":"","is_publish_highlight":false,"source_rank":0,"column":"","sentiment":"0","news_top_title":null,"news_tag":"dataReport","news_rank":0,"length":0,"strategy_id":0,"source":null,"symbols":["BK4139","CELC"],"isVideo":false,"video":null,"gpt_icon":0},{"id":"1107864078","title":"FDA授予Celcuity公司Gedatolisib新药申请优先审评资格；PDUFA目标日期定于2026年7月17日","url":"https://stock-news.laohu8.com/highlight/detail?id=1107864078","media":"美股速递","labels":["productRelease"],"top":-1,"itemType":null,"share":"https://www.laohu8.com/m/news/1107864078?lang=zh_cn&edition=full","pubTime":"2026-06-02 20:16","pubTimestamp":1780402573,"startTime":"0","endTime":"0","summary":"美国食品药品监督管理局（FDA）已授予Celcuity公司旗下药物Gedatolisib的新药申请（NDA）优先审评资格。根据提交至美国证券交易委员会（SEC）的文件，该申请的处方药使用者付费法案（PDUFA）目标日期设定为2026年7月17日。此举标志着该药物在监管审批流程中迈出了关键一步，有望加速其上市进程。","market":"us","thumbnail":"","type":0,"news_type":0,"thumbnails":[],"rights":null,"property":[],"language":"zh","translate_title":"","themeId":"","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":["CELC","BK4139"],"isVideo":false,"video":null,"gpt_icon":0},{"id":"1134324033","title":"Celcuity：Gedatolisib三联疗法对比Alpelisib联合Fulvestrant，中位无进展生存期达11.1个月 vs 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.laohu8.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":"","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.laohu8.com/m/news/1179894923?lang=zh_cn&edition=full","pubTime":"2026-06-02 20:15","pubTimestamp":1780402516,"startTime":"0","endTime":"0","summary":"根据一份提交给美国证券交易委员会（SEC）的文件，Celcuity Inc 在其临床研究中评估的Gedatolisib治疗方案展现出积极的耐受性特征。数据显示，该治疗方案总体上被患者良好耐受，所报告的大多数不良事件严重程度较低，属于低级别范畴。这一发现为后续的临床开发提供了支持性数据。","market":"us","thumbnail":"","type":0,"news_type":0,"thumbnails":[],"rights":null,"property":[],"language":"zh","translate_title":"","themeId":"","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":["BK4139","CELC"],"isVideo":false,"video":null,"gpt_icon":0},{"id":"1113606237","title":"Celcuity公司将于2026年6月2日召开电话会议，讨论Gedatolisib方案针对HR+/HER-晚期乳腺癌的3期Viktoria-1临床试验中PIK3CA突变队列的结果","url":"https://stock-news.laohu8.com/highlight/detail?id=1113606237","media":"美股速递","labels":["conferences"],"top":-1,"itemType":null,"share":"https://www.laohu8.com/m/news/1113606237?lang=zh_cn&edition=full","pubTime":"2026-06-01 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Inc：预计现金、现金等价物、投资及信贷额度提款将支撑运营至2027年","url":"https://stock-news.laohu8.com/highlight/detail?id=1122239009","media":"美股速递","labels":[],"top":-1,"itemType":null,"share":"https://www.laohu8.com/m/news/1122239009?lang=zh_cn&edition=full","pubTime":"2026-05-15 04:04","pubTimestamp":1778789052,"startTime":"0","endTime":"0","summary":"Celcuity Inc 预计，其现有的现金及现金等价物、投资组合，以及通过信贷额度进行的潜在提款，将共同为公司运营提供资金支持，直至2027年。","market":"us","thumbnail":"","type":0,"news_type":0,"thumbnails":[],"rights":null,"property":[],"language":"zh","translate_title":"","themeId":"","theme_name":"","theme_type":"","isJumpTheme":false,"source_url":"","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":null,"symbols":["CELC","BK4139"],"isVideo":false,"video":null,"gpt_icon":0},{"id":"1147706263","title":"异动解读 | 新药获FDA优先审评且临床试验扩大，Celcuity盘中大涨6.23%","url":"https://stock-news.laohu8.com/highlight/detail?id=1147706263","media":"异动解读","labels":["movement"],"top":-1,"itemType":null,"share":"https://www.laohu8.com/m/news/1147706263?lang=zh_cn&edition=full","pubTime":"2026-05-14 22:13","pubTimestamp":1778768010,"startTime":"0","endTime":"0","summary":"Celcuity Inc今日盘中股价大涨6.23%，引起了市场的广泛关注。首先，Celcuity 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":"sg","thumbnail":"","type":0,"news_type":0,"thumbnails":[],"rights":null,"property":[],"language":"zh","translate_title":"","themeId":"","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 19:31","pubTimestamp":1778758282,"startTime":"0","endTime":"0","summary":"Celcuity Inc 宣布，其针对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。该申请的处方药用户付费法案目标审评日期定为2026年7月17日。此项决定标志着该药物在监管审批流程中迈出了关键一步。","market":"us","thumbnail":"","type":0,"news_type":0,"thumbnails":[],"rights":null,"property":[],"language":"zh","translate_title":"","themeId":"","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":"1155265476","title":"Celcuity公司Gedatolisib一线治疗HR+/HER2-晚期乳腺癌的III期Viktoria-2试验将扩大至纳入内分泌敏感患者","url":"https://stock-news.laohu8.com/highlight/detail?id=1155265476","media":"美股速递","labels":["dataReport"],"top":-1,"itemType":null,"share":"https://www.laohu8.com/m/news/1155265476?lang=zh_cn&edition=full","pubTime":"2026-05-14 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20:31","pubTimestamp":1768912276,"startTime":"0","endTime":"0","summary":"Celcuity Inc 宣布，其候选药物Gedatolisib针对HR阳性、HER2阴性且PIK3CA基因为野生型的晚期乳腺癌患者所提交的新药申请，已获得美国食品药品监督管理局的正式受理。此次受理标志着该药物在审批流程中迈出了关键一步。","market":"us","thumbnail":"","type":0,"news_type":0,"thumbnails":[],"rights":null,"property":[],"language":"zh","translate_title":"","themeId":"","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":"1151282268","title":"Celcuity在2025年圣安东尼奥乳腺癌研讨会上展示Pik3CA野生型队列的Viktoria-1三期试验更新结果","url":"https://stock-news.laohu8.com/highlight/detail?id=1151282268","media":"美股速递","labels":["dataReport"],"top":-1,"itemType":null,"share":"https://www.laohu8.com/m/news/1151282268?lang=zh_cn&edition=full","pubTime":"2025-12-12 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Inc C/Wts 13/02/2029 、Geovax Labs Inc C/Wts 29/09/2025涨幅较大，Cyclerion Therapeutics, Inc.、Nls Pharmaceutics Ltd.、Silexion Therapeutics Corp较为活跃，换手率分别为2126.43%、1938.99%、182.85%，振幅较大的相关个股有Nls Pharmaceutics Ltd C/Wts 02/02/2026、Cyclerion Therapeutics, Inc.、Psyence Biomedical Ltd C/Wts 25/01/2029，振幅分别为80.00%、56.30%、52.24%。Celcuity Inc.公司简介：Celcuity Inc 是一家致力于开发肿瘤学方向的临床阶段生物技术公司。","market":"us","thumbnail":null,"type":0,"news_type":0,"thumbnails":[],"rights":{"source":"tencent","url":"http://gu.qq.com/resources/shy/news/detail-v2/index.html#/?id=nesSN20250201005026a2355b48&s=b","rn_cache_url":null,"customStyle":"body{padding-top:10px;}#news_title{font-weight:bold;#titleStyle#;}#news_description span{font-size:12px;#descriptionStyle#;}.footer-note{#statement#}","selectors":".mod-LoadTzbdNews, body","filters":".relate-stock, .hot-list, .recom-box, 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Bio Co.涨幅较大，Windtree Therapeutics, Inc.、Phio Pharmaceuticals Corp.、Oncolytics Biotech Inc.较为活跃，换手率分别为184.95%、52.43%、35.39%，振幅较大的相关个股有Klotho Neurosciences, Inc.、Vincerx Pharma, Inc.、Viracta Therapeutics, Inc.，振幅分别为12.00%、10.72%、9.48%。Celcuity Inc.公司简介：Celcuity Inc 是一家致力于开发肿瘤学方向的临床阶段生物技术公司。","market":"us","thumbnail":null,"type":0,"news_type":0,"thumbnails":[],"rights":{"source":"tencent","url":"http://gu.qq.com/resources/shy/news/detail-v2/index.html#/?id=nesSN20250115223209a222fe03&s=b","rn_cache_url":null,"customStyle":"body{padding-top:10px;}#news_title{font-weight:bold;#titleStyle#;}#news_description span{font-size:12px;#descriptionStyle#;}.footer-note{#statement#}","selectors":".mod-LoadTzbdNews, body","filters":".relate-stock, .hot-list, .recom-box, 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