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Bioxcel Therapeutics Inc.

0.7606

-0.0432-5.37%

盘后：0.77930.0187+2.46%19:57 EDT

成交量：112.31万

成交额：88.06万

市值：2,381.10万

市盈率：-0.24

高：0.8330

开：0.8000

低：0.7510

收：0.8038

52周最高：5.25

52周最低：0.7365

股本：3,130.55万

流通股本：2,688.93万

量比：0.80

换手率：4.18%

股息：- -

股息率：- -

每股收益(TTM):-3.1505

每股收益(LYR):-5.7255

净资产收益率：-1766.94%

总资产收益率：-102.43%

市净率：-0.21

市盈率(LYR):-0.13

数据加载中...

总览公司新闻资讯公告

BioXcel Therapeutics于2026年8月21日签署信贷协议第十三次修订案——SEC文件披露

BioXcel Therapeutics 必须在2026年8月21日前达成协议以偿还债务或寻求替代资本方案——SEC文件揭示

BioXcel Therapeutics 贷款方放宽最低流动性限制：从625万美元降至300万美元——SEC文件显示

Bioxcel Therapeutics：贷款方同意将本金还款推迟至2026年8月31日；根据SEC文件，到期应付本息合计902万美元外加应计利息

BioXcel Therapeutics需在2026年8月10日前达成最终协议——SEC文件披露

BioXcel Therapeutics在2026年ASCP年会上公布SERENITY At-Home 3期试验新数据，针对双相情感障碍或精神分裂症相关激越

BUZZ--美国股票走势-达美、GATX、Humana

BUZZ-创伤受害者应激障碍药物试验启动，BioXcel 股价上涨

BioXcel Therapeutics宣布首批患者入组美国国防部资助的Bxcl501（舌下右美托咪定）治疗急性应激反应研究

BioXcel Therapeutics Inc：FDA为Igalmi新药申请设定PDUFA目标审评日期为2026年11月14日——SEC文件披露

BioXcel Therapeutics宣布FDA受理Igalmi®居家使用补充新药申请

BUZZ-BioXcel股价跳涨，中期试验显示药物可缓解阿片类药物戒断症状

BioXcel Therapeutics股价盘前飙升21.1%，实验性阿片类药物戒断疗法中期试验显效

BioXcel Therapeutics Inc.：Bxcl501在治疗阿片类药物戒断症状中展现出临床获益与良好耐受性

BioXcel Therapeutics公布哥伦比亚大学主导的Bxcl501治疗阿片戒断二期研究积极顶线结果

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Therapeutics在短期内面临的资金链压力有所缓解。它可能在当前阶段获得更多战略调整空间，以应对研发支出或市场波动。\n监管文件明确披露了这一变动。对于密切关注该公司股票表现及未来发展路径的投资者而言，这无疑是一个重要的信号。","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":"","news_rank":0,"length":0,"strategy_id":0,"source":null,"symbols":["BK4139","BTAI"],"isVideo":false,"video":null,"gpt_icon":0},{"id":"1117292485","title":"Bioxcel Therapeutics：贷款方同意将本金还款推迟至2026年8月31日；根据SEC文件，到期应付本息合计902万美元外加应计利息","url":"https://stock-news.laohu8.com/highlight/detail?id=1117292485","media":"美股速递","labels":[],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/1117292485?lang=zh_cn&edition=fundamental","pubTime":"2026-08-03 19:07","pubTimestamp":1785755227,"startTime":"0","endTime":"0","summary":"Bioxcel Therapeutics Inc.迎来关键财务进展。根据最新提交的SEC文件披露，该公司已与贷款方达成协议，将原定到期的本金还款义务推迟至2026年8月31日。这一调整意味着，届时公司需一次性支付约902万美元的本金，同时还需结清这笔债务在此期间产生的全部应计利息。此次延期协议的签署，为Bioxcel Therapeutics提供了宝贵的现金流缓冲空间。","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":["BTAI","BK4139"],"isVideo":false,"video":null,"gpt_icon":0},{"id":"1154078824","title":"BioXcel Therapeutics需在2026年8月10日前达成最终协议——SEC文件披露","url":"https://stock-news.laohu8.com/highlight/detail?id=1154078824","media":"美股速递","labels":[],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/1154078824?lang=zh_cn&edition=fundamental","pubTime":"2026-08-03 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Therapeutics的核心产品线提供了重要支持，特别是在满足精神健康领域对有效且便捷的急性干预措施的迫切需求方面。公司表示，这些数据将有助于推进该疗法的后续监管沟通与开发计划。","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":["BK4139","BTAI"],"isVideo":false,"video":null,"gpt_icon":0},{"id":"2625945239","title":"BUZZ--美国股票走势-达美、GATX、Humana","url":"https://stock-news.laohu8.com/highlight/detail?id=2625945239","media":"路透中文","labels":[],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2625945239?lang=zh_cn&edition=fundamental","pubTime":"2026-04-08 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该公司称已开始招募患者参加BXCL501治疗急性应激反应的试验，急性应激反应是一种短期心理健康问题，包括创伤事件后的焦虑、睡眠障碍和疼痛。","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:20260408:nL4T40R0YY:1","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","BTAI"],"isVideo":false,"video":null,"gpt_icon":0},{"id":"1192848839","title":"BioXcel Therapeutics宣布首批患者入组美国国防部资助的Bxcl501（舌下右美托咪定）治疗急性应激反应研究","url":"https://stock-news.laohu8.com/highlight/detail?id=1192848839","media":"美股速递","labels":[],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/1192848839?lang=zh_cn&edition=fundamental","pubTime":"2026-04-08 19:01","pubTimestamp":1775646113,"startTime":"0","endTime":"0","summary":"BioXcel Therapeutics公司宣布，首批患者已正式入组一项由美国国防部资助的临床研究。该研究旨在评估其核心候选药物Bxcl501（舌下右美托咪定）用于治疗急性应激反应的有效性与安全性。这一进展标志着该创新疗法在应对创伤后应激障碍等急性应激相关病症的探索中迈出了关键一步。","market":"us","thumbnail":"","type":0,"news_type":0,"thumbnails":[],"rights":null,"property":[],"language":"zh","translate_title":"","themeId":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":["BK4139","BTAI"],"isVideo":false,"video":null,"gpt_icon":0},{"id":"1161815906","title":"BioXcel Therapeutics Inc：FDA为Igalmi新药申请设定PDUFA目标审评日期为2026年11月14日——SEC文件披露","url":"https://stock-news.laohu8.com/highlight/detail?id=1161815906","media":"美股速递","labels":["productRelease"],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/1161815906?lang=zh_cn&edition=fundamental","pubTime":"2026-04-01 19:00","pubTimestamp":1775041218,"startTime":"0","endTime":"0","summary":"根据一份提交给美国证券交易委员会（SEC）的文件披露，BioXcel Therapeutics Inc. 已获得美国食品药品监督管理局（FDA）就其Igalmi新药申请设定的处方药使用者付费法案（PDUFA）目标审评日期。该关键日期定于2026年11月14日，标志着监管机构完成审评的最后期限。\n这一进展为该公司针对Igalmi的审批路径提供了明确的时间表，是药物研发过程中的一个重要监管里程碑。","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","BTAI"],"isVideo":false,"video":null,"gpt_icon":0},{"id":"1176205883","title":"BioXcel Therapeutics宣布FDA受理Igalmi®居家使用补充新药申请","url":"https://stock-news.laohu8.com/highlight/detail?id=1176205883","media":"美股速递","labels":["productRelease"],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/1176205883?lang=zh_cn&edition=fundamental","pubTime":"2026-04-01 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(BTAI) 近日宣布，美国食品药品监督管理局（FDA）已正式受理其旗下药物Igalmi®用于居家环境的补充新药申请（sNDA）。这一进展标志着该药物在拓展临床应用场景方面迈出重要一步。","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","BTAI"],"isVideo":false,"video":null,"gpt_icon":0},{"id":"2617542668","title":"BUZZ-BioXcel股价跳涨，中期试验显示药物可缓解阿片类药物戒断症状","url":"https://stock-news.laohu8.com/highlight/detail?id=2617542668","media":"路透中文","labels":["dataReport"],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2617542668?lang=zh_cn&edition=fundamental","pubTime":"2026-03-05 20:40","pubTimestamp":1772714401,"startTime":"0","endTime":"0","summary":"由于自动化翻译可能有误，或未能包含所需语境，路透不保证自动化翻译文本的准确性，仅是为了便利读者而提供自动化翻译。对于因为使用自动化翻译功能而造成的任何损害或损失，路透不承担任何责任。","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:20260305:nL4T3ZT16T:1","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","BTAI"],"isVideo":false,"video":null,"gpt_icon":0},{"id":"1186310919","title":"BioXcel Therapeutics股价盘前飙升21.1%，实验性阿片类药物戒断疗法中期试验显效","url":"https://stock-news.laohu8.com/highlight/detail?id=1186310919","media":"美股速递","labels":["dataReport"],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/1186310919?lang=zh_cn&edition=fundamental","pubTime":"2026-03-05 20:35","pubTimestamp":1772714114,"startTime":"0","endTime":"0","summary":"BioXcel Therapeutics Inc. (BTAI) 股价在盘前交易中大幅上涨21.1%，此前该公司宣布其用于治疗阿片类药物戒断的实验性药物在一项中期临床试验中显示出积极疗效。这一积极数据显著提振了投资者信心，推动该公司股价强势上扬。","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":"dataReport","news_rank":0,"length":0,"strategy_id":0,"source":null,"symbols":["BK4139","BTAI"],"isVideo":false,"video":null,"gpt_icon":0},{"id":"1115086186","title":"BioXcel Therapeutics Inc.：Bxcl501在治疗阿片类药物戒断症状中展现出临床获益与良好耐受性","url":"https://stock-news.laohu8.com/highlight/detail?id=1115086186","media":"美股速递","labels":[],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/1115086186?lang=zh_cn&edition=fundamental","pubTime":"2026-03-05 20:10","pubTimestamp":1772712603,"startTime":"0","endTime":"0","summary":"BioXcel Therapeutics Inc.公布的最新临床数据显示，其研究性药物Bxcl501在治疗阿片类药物戒断症状方面表现出显著的临床益处和良好的耐受性特征。该结果突显了该疗法在应对这一严峻公共卫生挑战方面的潜力。","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":["BTAI","BK4139"],"isVideo":false,"video":null,"gpt_icon":0},{"id":"1145611771","title":"BioXcel Therapeutics公布哥伦比亚大学主导的Bxcl501治疗阿片戒断二期研究积极顶线结果","url":"https://stock-news.laohu8.com/highlight/detail?id=1145611771","media":"美股速递","labels":["dataReport"],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/1145611771?lang=zh_cn&edition=fundamental","pubTime":"2026-03-05 20:04","pubTimestamp":1772712277,"startTime":"0","endTime":"0","summary":"BioXcel Therapeutics宣布，由哥伦比亚大学主导的Bxcl501用于治疗阿片戒断的二期临床研究取得积极顶线结果。该研究达到了主要终点，显示Bxcl501能显著缓解戒断症状。公司计划基于这些数据与监管机构讨论后续开发路径。","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":"dataReport","news_rank":0,"length":0,"strategy_id":0,"source":null,"symbols":["BTAI","BK4139"],"isVideo":false,"video":null,"gpt_icon":0}],"pageSize":20,"totalPage":1,"pageCount":1,"totalSize":15,"code":"91000000","status":"200"}]}}