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Celcuity Inc

83.45

-2.0400-2.39%

盤後：85.001.55+1.86%19:46 EDT

成交量：86.34萬

成交額：7,255.65萬

市值：40.70億

市盈率：-19.31

高：87.01

開：86.38

低：83.24

收：85.49

52周最高：151.02

52周最低：44.42

股本：4,876.63萬

流通股本：2,971.92萬

量比：1.08

換手率：2.91%

股息：- -

股息率：- -

每股收益(TTM):-4.3223

每股收益(LYR):-3.7900

淨資產收益率：-1433.70%

總資產收益率：-25.78%

市淨率：-318.41

市盈率(LYR):-22.02

資料載入中...

總覽公司新聞公告

王長俊現場推進重點項目建設

Celcuity向FDA提交Revtorpyk™（Gedatolisib）補充新藥申請，用於HR+/HER2-、PIK3CA突變局部晚期或轉移性乳腺癌治療

美國研究綜述-思科、福克斯公司、塔吉特

美國研究綜述-思科、福克斯公司、塔吉特

獲FDA新批准的Revtorpyk™（Gedatolisib）被納入NCCN® HR+/HER2-局部晚期或轉移性乳腺癌臨床實踐指南

FDA批准Celcuity旗下Revtorpyk用於治療無PIK3CA突變的HR+/HER2-晚期乳腺癌

美國研究綜述-黑石集團、哈特福德保險公司、澤夫拉治療公司

異動解讀｜Celcuity Inc盤中下跌22.15%，FDA批准核心藥物後利好兑現引發深度拋售

異動解讀｜Celcuity Inc盤前下跌5.59%，FDA批准核心藥物後市場兑現獲利

美國研究綜述-Equinix、高盛、摩根大通

異動解讀｜Celcuity Inc夜盤下跌5.45%，FDA批准核心藥物後市場兑現獲利

Celcuity公司宣佈FDA批准Revtorpyk™ (gedatolisib) 用於治療HR+/HER2-、PIK3CA野生型局部晚期或轉移性乳腺癌

異動解讀｜Celcuity Inc盤後下跌6.75%，報106.79美元

美國食品藥品監督管理局批准Celcuity公司的乳腺癌藥物

FDA批准Gedatolisib聯合氟維司群，聯用或不聯用哌柏西利，用於HR陽性、HER2陰性局部晚期或轉移性乳腺癌

異動解讀｜Celcuity盤中上漲5.22%，FDA關鍵審評日臨近催化市場預期

異動解讀｜Celcuity盤中下跌5.37%，FDA審評目標日期臨近多空博弈加劇

異動解讀｜Celcuity盤中上漲5.02%，核心藥物FDA審評目標日期臨近

市場快訊——美股行情動態-聯合健康集團、Pinterest、Celcuity

Celcuity Inc. 定價增發5億美元、2032年到期的0.25%可轉換優先票據

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塔吉特公司TGT.N：杰富瑞将目标价从161美元上调至177美元以下是路透周五报导的针对美国公司的研究行动摘要。","market":"hk","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://api.refinitiv.com/data/news/v1/stories/urn:newsml:reuters.com:20260814:nL4T44B0HP:1","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":["EPAI","HAUS","HTFL","RDVI","OPTZ","TPR","IPAR","LUMA","BURL","SPRX","CSCS","CHEF","FOXA","COHX","MSGE","AEHR","NERV","QQQG","MSGS","BJ","CSCO","TGT","DE","LGN","EGGY","FTAG","AIQ","RSPR","AMAT","CTRE","SJM","XYZG","ESS","FOTO","IYF","WSM","KTB","XYZ","HEI","WDAY","KBWB","ROKT","SNDK","CELC","TDV","SPHR","LTC","COHR","ENVX","CIBR"],"isVideo":false,"video":null,"gpt_icon":0},{"id":"2659111341","title":"美國研究綜述-思科、福克斯公司、塔吉特","url":"https://stock-news.laohu8.com/highlight/detail?id=2659111341","media":"路透中文","labels":[],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2659111341?lang=zh_tw&edition=fundamental","pubTime":"2026-08-14 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塔吉特公司TGT.N：杰富瑞将目标价从161美元上调至177美元以下是路透周五报道的针对美国公司的研究行动摘要。","market":"us","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://api.refinitiv.com/data/news/v1/stories/urn:newsml:reuters.com:20260814:nL4S44B0HP:1","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":["WUGI","KROP","DE","CELC","SOXQ","XYZ","CSCO","AMAT","FTXO","TMSL","VEGI","NERV","EGGY","SNDG","IPAR","TDV","CHEF","MSGS","SCHM","COHR","XYZY","ESS","BURL","SPRX","TPR","AEHR","MSGE","BJ","COHC","HEI","CTRE","PTF","HTFL","SCHA","SJM","LUMA","SHOC","FOXA","SPHR","LTC","RDVY","TGT","SNDK","WDAY","WSM","CSCS","XYZG","LGN","KTB","ENVX"],"isVideo":false,"video":null,"gpt_icon":0},{"id":"1162791330","title":"獲FDA新批准的Revtorpyk™（Gedatolisib）被納入NCCN® HR+/HER2-局部晚期或轉移性乳腺癌臨床實踐指南","url":"https://stock-news.laohu8.com/highlight/detail?id=1162791330","media":"美股速递","labels":["policyRegulatory"],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/1162791330?lang=zh_tw&edition=fundamental","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":["BK4139","CELC"],"isVideo":false,"video":null,"gpt_icon":0},{"id":"1184889176","title":"FDA批准Celcuity旗下Revtorpyk用於治療無PIK3CA突變的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://ttm.financial/m/news/1184889176?lang=zh_tw&edition=fundamental","pubTime":"2026-07-30 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Inc盤中下跌22.15%，FDA批准核心藥物後利好兑現引發深度拋售","url":"https://stock-news.laohu8.com/highlight/detail?id=1123499084","media":"行情直击","labels":["productRelease"],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/1123499084?lang=zh_tw&edition=fundamental","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":"異動解讀｜Celcuity Inc盤前下跌5.59%，FDA批准核心藥物後市場兑現獲利","url":"https://stock-news.laohu8.com/highlight/detail?id=1179546739","media":"行情直击","labels":[],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/1179546739?lang=zh_tw&edition=fundamental","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":"2651043069","title":"美國研究綜述-Equinix、高盛、摩根大通","url":"https://stock-news.laohu8.com/highlight/detail?id=2651043069","media":"路透中文","labels":[],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2651043069?lang=zh_tw&edition=fundamental","pubTime":"2026-07-15 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Inc夜盤下跌5.45%，FDA批准核心藥物後市場兑現獲利","url":"https://stock-news.laohu8.com/highlight/detail?id=1103001250","media":"行情直击","labels":[],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/1103001250?lang=zh_tw&edition=fundamental","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公司宣佈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":"異動解讀｜Celcuity Inc盤後下跌6.75%，報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://ttm.financial/m/news/1124500511?lang=zh_tw&edition=fundamental","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":"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":"2651486846","title":"美國食品藥品監督管理局批准Celcuity公司的乳腺癌藥物","url":"https://stock-news.laohu8.com/highlight/detail?id=2651486846","media":"路透中文","labels":["productRelease"],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2651486846?lang=zh_tw&edition=fundamental","pubTime":"2026-07-15 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03:21","pubTimestamp":1784056876,"startTime":"0","endTime":"0","summary":"美国食品药品监督管理局（FDA）已批准Gedatolisib与氟维司群联合治疗方案，可选择性地加用哌柏西利，用于治疗激素受体（HR）阳性、人表皮生长因子受体2（HER2）阴性的局部晚期或转移性乳腺癌患者。这一批准为这类特定亚型的乳腺癌患者提供了新的治疗选择。","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":"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":"1123253973","title":"異動解讀｜Celcuity盤中上漲5.22%，FDA關鍵審評日臨近催化市場預期","url":"https://stock-news.laohu8.com/highlight/detail?id=1123253973","media":"行情直击","labels":[],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/1123253973?lang=zh_tw&edition=fundamental","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":"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":"1160136010","title":"異動解讀｜Celcuity盤中下跌5.37%，FDA審評目標日期臨近多空博弈加劇","url":"https://stock-news.laohu8.com/highlight/detail?id=1160136010","media":"行情直击","labels":[],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/1160136010?lang=zh_tw&edition=fundamental","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":"異動解讀｜Celcuity盤中上漲5.02%，核心藥物FDA審評目標日期臨近","url":"https://stock-news.laohu8.com/highlight/detail?id=1197009110","media":"行情直击","labels":[],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/1197009110?lang=zh_tw&edition=fundamental","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":"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":"2640166952","title":"市場快訊——美股行情動態-聯合健康集團、Pinterest、Celcuity","url":"https://stock-news.laohu8.com/highlight/detail?id=2640166952","media":"路透中文","labels":["event"],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2640166952?lang=zh_tw&edition=fundamental","pubTime":"2026-06-04 23:47","pubTimestamp":1780588076,"startTime":"0","endTime":"0","summary":"美国东部时间11:30，道琼斯工业平均指数 .DJI 上涨1.75%，报51,575.56点。标普500指数 .SPX 上涨0.27%，报7,573.97点；纳斯达克综合指数 .IXIC 下跌0.19%，报26,801.49点。","market":"hk","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://api.refinitiv.com/data/news/v1/stories/urn:newsml:reuters.com:20260604:nL4S42C1FS:1","is_publish_highlight":false,"source_rank":0,"column":"","sentiment":"0","news_top_title":null,"news_tag":"event","news_rank":0,"length":0,"strategy_id":0,"source":null,"symbols":["LU1674673428.USD","LU2362540622.SGD","LU0011850046.USD","LU0820561909.HKD","LU0348723411.USD","LU1674673691.USD","LU2279689827.SGD","LU0187121727.USD","LU2347655156.SGD","LU2491049909.HKD","SG9999013999.USD","LU0683600562.USD","BK4533","LU1267930490.SGD","LU0345770308.USD","LU0354030511.USD","LU1153585028.USD","UNH","IE0002270589.USD","LU0342679015.USD","IE00BKPKM429.USD","IE0005OL40V9.USD","SG9999018857.SGD","IE00BFSS7M15.SGD","IE00BZ1G4Q59.USD","LU0234572021.USD","LU2324357040.USD","IE00B19Z3581.USD","BK4548","LU2089284900.SGD","LU0053666078.USD","LU2089283258.USD","LU0353189763.USD","LU0553294199.USD","BK4588","LU0417517546.SGD","LU0949170772.SGD","IE00B19Z8X17.USD","IE00B894F039.SGD","LU0079474960.USD","IE00B4JS1V06.HKD","SG9999002224.SGD","SGXZ51526630.SGD","IE00BKVL7J92.USD","LU0708994859.HKD","LU0861579265.USD","LU1037948541.HKD","LU0689472784.USD","LU1720051017.SGD","LU1814569148.SGD","LU0029864427.USD","IE00B19Z3B42.SGD","IE00B7KXQ091.USD","SGXZ31699556.SGD","LU1732800096.USD","IE000M9KFDE8.USD","LU0128525929.USD","LU1074936037.SGD","LU1778281490.HKD","SG9999002232.USD","LU0820562030.AUD","IE00B19Z9P08.USD","LU1854103824.USD","BK4154","BK4534","IE00BJT1NW94.SGD","LU2357305700.SGD","LU0345770993.USD","LU0496365809.HKD","LU0238689110.USD","IE00BFXG1179.USD","LU1791710582.SGD","LU1267930227.SGD","LU1267930573.SGD","LU0354030438.USD","SGXZ99366536.SGD","LU1057294990.SGD","LU1989771016.USD","LU0149725797.USD","LU2089984988.USD","BK4581","LU0432979614.USD","SG9999014880.SGD","LU0251132253.USD","LU1084165304.USD","BK4139","IE00BJJMRZ35.SGD","LU1934455863.HKD","UNHG","LU1548497426.USD","LU1323610961.USD","LU0316494557.USD","LU1066051811.HKD","PINS","LU2111349929.HKD","LU0943347566.SGD","LU2244417387.USD","LU0738911758.USD","LU2362541513.USD","IE00BFSS8Q28.SGD","BK4508","LU1261432733.SGD","IE00BJJMRX11.SGD","LU0048584097.USD","LU1291159041.SGD","LU2023251221.USD","LU2133065610.SGD","LU1064131342.USD","LU0107464264.USD","LU0882574055.USD","IE00B1XK9C88.USD","LU0256863811.USD","IE00B7SZLL34.SGD","LU1119994496.HKD","LU0965509101.SGD","LU2271345857.HKD","SGXZ57979304.SGD","SG9999018865.SGD","LU1914381329.SGD","LU0211328371.USD","UNHW","LU2242649171.HKD","LU1037948897.HKD","LU0820561818.USD","LU0094547139.USD","LU2362541273.HKD","IE00BJJMRY28.SGD","LU1003077747.HKD","LU0289739699.SGD","LU2361044949.HKD","IE00B1BXHZ80.USD","LU0052756011.USD","LU0787776722.HKD","LU1035773651.USD","BK4532","LU2236285917.USD","LU0077335932.USD","LU0708995401.HKD","LU2264538146.SGD","SG9999001176.USD","LU0672654240.SGD","LU2360032135.SGD","LU0198837287.USD","IE0004445015.USD","LU0965509010.AUD","LU1496350502.SGD","GB00BDT5M118.USD","LU1934455194.USD","LU0965508806.USD","LU1718418525.SGD","LU2491050071.SGD","LU2125154778.USD","LU1551013425.SGD","IE00B3T34201.USD","SGXZ81514606.USD","LU2552382058.USD","IE0004445239.USD","BK4551","LU0211326839.USD","BK4077","LU0545039389.USD","LU2361045086.USD","IE00B4R5TH58.HKD","LU0109391861.USD","LU0310799852.SGD","SG9999014898.SGD","SG9999014906.USD","LU0557290698.USD","LU0912757837.SGD","SG9999001176.SGD","LU2087625088.SGD","LU0320765059.SGD","LU1551013342.USD","LU0097036916.USD","LU0661504455.SGD","LU0456855351.SGD","LU0965509283.SGD","LU1988902786.USD","IE00BFTCPJ56.SGD","LU2468319806.SGD","LU2552382132.HKD","LU0795875086.SGD","LU1506573853.SGD","SG9999014914.USD","LU0823416689.USD","LU0122379950.USD","LU0795875169.SGD","LU0353189680.USD","LU0310800379.SGD","LU1061106388.HKD","LU0203347892.USD","LU0058720904.USD","LU0211326755.USD","LU1791710400.SGD","IE00B19Z8W00.USD","LU1066053197.SGD","LU0128525689.USD","LU2317271919.USD","IE0009355771.USD","LU0158827781.USD","IE00B775H168.HKD","IE00BSNM7G36.USD","IE00BWXC8680.SGD","LU0266013472.USD","LU0976567544.SGD","LU1670627923.USD","IE0002141913.USD","IE00B19Z9505.USD","LU1732799900.SGD","LU1854104046.USD","LU2125154935.USD","IE00B2B36J28.USD","LU2552382215.SGD","LU2491050154.USD","BK4566","IE00B19Z9Z06.USD","LU0211327993.USD","LU0203345920.USD","LU1066051225.USD","LU1983299246.USD","LU2361044865.SGD","SG9999017495.SGD","LU1023059063.AUD","LU2028103732.USD","LU1066051498.USD","LU1934455277.USD","LU2461242641.AUD","CELC","BK4585","LU1670628061.USD","LU1720051108.HKD","LU0114720955.EUR","LU1069347547.HKD","LU2112291526.USD","LU1267930730.SGD","LU0158827948.USD","LU2211815571.USD","LU0310800965.SGD","IE00BN29S564.USD","IE00BZ9MQY76.HKD","LU0528227936.USD"],"isVideo":false,"video":null,"gpt_icon":0},{"id":"1187497120","title":"Celcuity Inc. 定價增發5億美元、2032年到期的0.25%可轉換優先票據","url":"https://stock-news.laohu8.com/highlight/detail?id=1187497120","media":"投资观察","labels":["shareholding"],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/1187497120?lang=zh_tw&edition=fundamental","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":["BK4139","CELC"],"isVideo":false,"video":null,"gpt_icon":0}],"pageSize":20,"totalPage":2,"pageCount":1,"totalSize":35,"code":"91000000","status":"200"}]}}