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VistaGen Therapeutics, Inc.

0.2264

+0.00040.18%

盤後：0.23060.0042+1.86%19:14 EDT

成交量：115.07萬

成交額：25.83萬

市值：928.97萬

市盈率：-0.12

高：0.2345

開：0.2230

低：0.2191

收：0.2260

52周最高：5.14

52周最低：0.1980

股本：4,103.25萬

流通股本：3,504.05萬

量比：1.73

換手率：3.28%

股息：- -

股息率：- -

每股收益(TTM):-1.8303

每股收益(LYR):-1.8303

淨資產收益率：-131.59%

總資產收益率：-67.84%

市淨率：0.26

市盈率(LYR):-0.12

資料載入中...

總覽公司新聞公告

VistaGen公佈Fasedienol治療社交焦慮症的Palisade-4三期公眾演講挑戰試驗頂線及事後分析數據

Vistagen股價暴跌，因治療社交焦慮症的藥物在後期臨牀試驗中未達到主要目標

VistaGen公司事後分析顯示，Fasedienol在極重度社恐亞組中達到名義統計顯著性

VistaGen公佈Fasedienol治療社交焦慮障礙急性期Palisade-4三期公開演講挑戰試驗的頂線及事後分析數據

VistaGen Therapeutics公司：Fasedienol在主要及次要終點上未實現統計學顯著改善

VistaGen計劃與FDA會晤，探討Fasedienol的註冊路徑及未來三期試驗

VistaGen Therapeutics公佈積極安全性及耐受性數據與既往臨牀試驗結果一致

VistaGen Therapeutics, Inc.旗下Fasedienol用於社交焦慮障礙急性治療的臨牀項目達到ICH最低安全暴露推薦標準

VistaGen Therapeutics, Inc. 旗下Fasedienol鼻噴霧劑耐受性良好，12個月後無新增安全性發現

Vistagen披露Palisade-3三期研究開放標籤擴展部分初步積極數據，Fasedienol用於社交焦慮障礙急性治療

VistaGen獲FDA批准開展Refisolone新藥臨牀研究，推進更年期血管舒縮症狀（潮熱）二期臨牀試驗

BUZZ-Vistagen 裁員 20% 以延長現金跑道，股價下跌

VistaGen Therapeutics披露：被裁員工或獲現金遣散費及臨時醫保

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公布的一项事后分析结果显示，其候选药物 Fasedienol 在针对极重度社交焦虑障碍亚组患者的研究中，达到了名义上的统计学显著性。该分析聚焦于病情程度最为严重的患者群体，数据显示，与安慰剂相比，Fasedienol 在这一特定亚组中展现出具有前景的疗效信号。名义统计显著性意味着，在未对多重检验进行调整的情况下，结果达到了预设的统计阈值。这一发现为 Fasedienol 的后续临床开发路径提供了新的见解。","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":["VTGN","BK4139"],"isVideo":false,"video":null,"gpt_icon":0},{"id":"1128069424","title":"VistaGen公佈Fasedienol治療社交焦慮障礙急性期Palisade-4三期公開演講挑戰試驗的頂線及事後分析數據","url":"https://stock-news.laohu8.com/highlight/detail?id=1128069424","media":"美股速递","labels":["dataReport"],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/1128069424?lang=zh_tw&edition=fundamental","pubTime":"2026-06-30 20:01","pubTimestamp":1782820910,"startTime":"0","endTime":"0","summary":"VistaGen Therapeutics, Inc. (VTGN) 公布了其候选药物Fasedienol用于社交焦虑障碍急性期治疗的三期临床试验Palisade-4的顶线数据及事后分析结果。该试验采用公开演讲挑战模型进行评估。\n数据显示，在主要终点和关键次要终点上，Fasedienol治疗组与安慰剂组相比，未达到统计学显著性差异。然而，公司进行的探索性事后分析指出，在预先设定的亚组人群中观察到了具有临床意义的改善信号。\n此次公布的数据为后续临床开发策略提供了重要参考。公司表示将继续深入分析完整数据集，以进一步明确Fasedienol的潜在治疗价值。","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":["VTGN","BK4139"],"isVideo":false,"video":null,"gpt_icon":0},{"id":"1150037136","title":"VistaGen Therapeutics公司：Fasedienol在主要及次要終點上未實現統計學顯著改善","url":"https://stock-news.laohu8.com/highlight/detail?id=1150037136","media":"美股速递","labels":["dataReport"],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/1150037136?lang=zh_tw&edition=fundamental","pubTime":"2026-06-30 20:01","pubTimestamp":1782820902,"startTime":"0","endTime":"0","summary":"VistaGen Therapeutics, Inc. (VTGN) 近日公布，其候选药物Fasedienol在关键临床试验中，未能于主要及次要疗效终点上展现出统计学意义上的显著改善。这一结果标志着该药物在特定治疗路径上遭遇了重大挫折，引发了市场对公司研发管线进展的重新评估。","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","VTGN"],"isVideo":false,"video":null,"gpt_icon":0},{"id":"1168620088","title":"VistaGen計劃與FDA會晤，探討Fasedienol的註冊路徑及未來三期試驗","url":"https://stock-news.laohu8.com/highlight/detail?id=1168620088","media":"美股速递","labels":["conferences"],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/1168620088?lang=zh_tw&edition=fundamental","pubTime":"2026-06-30 20:01","pubTimestamp":1782820900,"startTime":"0","endTime":"0","summary":"VistaGen Therapeutics公司宣布，计划与美国食品药品监督管理局（FDA）会面，商讨其候选药物Fasedienol的注册申报路径以及未来的三期临床试验规划。此次会议旨在为后续的临床开发与监管提交确定清晰的路线图。","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":"conferences","news_rank":0,"length":0,"strategy_id":0,"source":null,"symbols":["VTGN","BK4139"],"isVideo":false,"video":null,"gpt_icon":0},{"id":"1109937075","title":"VistaGen Therapeutics公佈積極安全性及耐受性數據 與既往臨牀試驗結果一致","url":"https://stock-news.laohu8.com/highlight/detail?id=1109937075","media":"美股速递","labels":["dataReport"],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/1109937075?lang=zh_tw&edition=fundamental","pubTime":"2026-06-30 20:01","pubTimestamp":1782820894,"startTime":"0","endTime":"0","summary":"VistaGen Therapeutics披露的最新数据显示，其药物在安全性及耐受性方面的表现令人鼓舞，这一结果与先前开展的临床试验所得结论高度吻合。该积极数据进一步巩固了公司研发管线的可靠性，为后续的临床开发路径提供了有力支持。","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","VTGN"],"isVideo":false,"video":null,"gpt_icon":0},{"id":"1198088723","title":"VistaGen Therapeutics, Inc.旗下Fasedienol用於社交焦慮障礙急性治療的臨牀項目達到ICH最低安全暴露推薦標準","url":"https://stock-news.laohu8.com/highlight/detail?id=1198088723","media":"美股速递","labels":[],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/1198088723?lang=zh_tw&edition=fundamental","pubTime":"2026-06-09 20:32","pubTimestamp":1781008339,"startTime":"0","endTime":"0","summary":"VistaGen Therapeutics, Inc.宣布，其用于治疗社交焦虑障碍急性发作的候选药物Fasedienol，在整个临床开发项目中已达到国际人用药品注册技术协调会（ICH）关于最低安全暴露的推荐标准。这一进展标志着该药物在安全性数据积累方面取得了重要里程碑，为其后续的临床推进和监管沟通奠定了关键基础。","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":["VTGN","BK4139"],"isVideo":false,"video":null,"gpt_icon":0},{"id":"1114884667","title":"VistaGen Therapeutics, Inc. 旗下Fasedienol鼻噴霧劑耐受性良好，12個月後無新增安全性發現","url":"https://stock-news.laohu8.com/highlight/detail?id=1114884667","media":"美股速递","labels":[],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/1114884667?lang=zh_tw&edition=fundamental","pubTime":"2026-05-12 19:31","pubTimestamp":1778585476,"startTime":"0","endTime":"0","summary":"VistaGen Therapeutics, Inc. 宣布，其Fasedienol鼻喷雾剂在为期12个月的观察期内展现出良好的耐受性，未发现新的安全性问题。","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","VTGN"],"isVideo":false,"video":null,"gpt_icon":0},{"id":"1172520288","title":"Vistagen披露Palisade-3三期研究開放標籤擴展部分初步積極數據，Fasedienol用於社交焦慮障礙急性治療","url":"https://stock-news.laohu8.com/highlight/detail?id=1172520288","media":"美股速递","labels":["dataReport"],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/1172520288?lang=zh_tw&edition=fundamental","pubTime":"2026-05-12 19:31","pubTimestamp":1778585475,"startTime":"0","endTime":"0","summary":"Vistagen公司宣布，在其Palisade-3三期研究中，关于Fasedienol用于社交焦虑障碍急性治疗的开放标签扩展部分，获得了初步的积极数据。这项研究目前仍在进行中。","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":["VTGN","BK4139"],"isVideo":false,"video":null,"gpt_icon":0},{"id":"1100851891","title":"VistaGen獲FDA批准開展Refisolone新藥臨牀研究，推進更年期血管舒縮症狀（潮熱）二期臨牀試驗","url":"https://stock-news.laohu8.com/highlight/detail?id=1100851891","media":"美股速递","labels":["productRelease"],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/1100851891?lang=zh_tw&edition=fundamental","pubTime":"2026-04-22 20:35","pubTimestamp":1776861341,"startTime":"0","endTime":"0","summary":"VistaGen Therapeutics宣布，美国食品药品监督管理局（FDA）已就其Refisolone新药临床申请发出“研究可继续进行”许可函，这意味着公司可进一步开展针对更年期引发的血管舒缩症状（即潮热）的二期临床开发计划。\n此次监管绿灯为Refisolone的临床推进扫清了关键障碍，标志着该创新疗法在解决更年期女性潮热问题方面迈出实质性一步。公司计划基于这一许可加速推进二期临床试验，探索Refisolone在缓解更年期相关症状方面的潜力与安全性。","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":["VTGN","BK4139"],"isVideo":false,"video":null,"gpt_icon":0},{"id":"2618694094","title":"BUZZ-Vistagen 裁員 20% 以延長現金跑道，股價下跌","url":"https://stock-news.laohu8.com/highlight/detail?id=2618694094","media":"路透中文","labels":["executive","shareholding"],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2618694094?lang=zh_tw&edition=fundamental","pubTime":"2026-03-11 21:10","pubTimestamp":1773234648,"startTime":"0","endTime":"0","summary":"BUZZ-Vistagen 裁员 20% 以延长现金跑道，股价下跌3月11日 - ** 药物开发商Vistagen Therapeutics VTGN.O股价盘前下跌3%至0.60美元** 该公司称已于3月5日裁员20%，以管理现金并支持Palisade项目的临床研究** 预计现金跑道将持续到 2027 年** Palisade 计划包括针对精神疾病的实验性鼻腔喷雾研究，旨在提供起效更快的治疗方案 - VTGN** 该公司表示，裁员的成本不大，受影响的员工可能会获得现金遣散费和临时医疗保险** 2025 年，VTGN 下跌了约 66%(为便利非英文母语者，路透将其报导自动化翻译为数种其他语言。","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:20260311:nL4T3ZZ1AG:1","is_publish_highlight":false,"source_rank":0,"column":"","sentiment":"-1","news_top_title":null,"news_tag":"executive,shareholding","news_rank":0,"length":0,"strategy_id":0,"source":null,"symbols":["VTGN","BK4139"],"isVideo":false,"video":null,"gpt_icon":0},{"id":"1187789740","title":"VistaGen Therapeutics披露：被裁員工或獲現金遣散費及臨時醫保","url":"https://stock-news.laohu8.com/highlight/detail?id=1187789740","media":"美股速递","labels":[],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/1187789740?lang=zh_tw&edition=fundamental","pubTime":"2026-03-11 19:07","pubTimestamp":1773227259,"startTime":"0","endTime":"0","summary":"根据最新提交至美国证券交易委员会（SEC）的文件显示，生物制药公司VistaGen Therapeutics, Inc. 正为其裁员计划中的受影响员工提供补偿方案。该方案可能包括一次性现金遣散费以及过渡期的医疗保险覆盖。\n这一举措反映了公司在业务调整过程中对员工权益的保障。通过提供经济补偿和延续医疗保障，VistaGen旨在减轻岗位变动对员工生活的短期冲击。SEC文件披露的细节表明，公司已就裁员补偿制定了具体实施框架。\n（注：根据公开信息，VistaGen Therapeutics为临床阶段生物制药企业，专注于开发新型神经科学疗法。此次人员调整或与公司战略重心优化相关。）","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","VTGN"],"isVideo":false,"video":null,"gpt_icon":0}],"pageSize":20,"totalPage":1,"pageCount":1,"totalSize":13,"code":"91000000","status":"200"}]}}