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VistaGen Therapeutics, Inc.

0.2432

+0.00622.62%

盤後：0.24320.00000.00%16:15 EDT

成交量：23.70萬

成交額：5.84萬

市值：1,079.25萬

市盈率：-0.15

高：0.2497

開：0.2490

低：0.2418

收：0.2370

52周最高：5.14

52周最低：0.1980

股本：4,437.69萬

流通股本：4,142.29萬

量比：0.56

換手率：0.57%

股息：- -

股息率：- -

每股收益(TTM):-1.6559

每股收益(LYR):-1.8303

淨資產收益率：-166.46%

總資產收益率：-83.21%

市淨率：0.44

市盈率(LYR):-0.13

資料載入中...

總覽公司新聞資訊公告

VistaGen第一財季每股虧損0.30美元

Vistagen公布Fasedienol重複劑量研究用於社交焦慮症急性治療的頂線結果

Vistagen Therapeutics 旗下Fasedienol在主要與次要終點均展現療效信號

Vistagen Therapeutics：法西地諾重複給藥展現與單次給藥相當的安全性及耐受性

Vistagen Therapeutics 在重度社交焦慮症患者中顯示出名義上的統計顯著改善

VistaGen公布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床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公布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公布積極安全性及耐受性數據與既往臨床試驗結果一致

VistaGen Therapeutics, Inc.旗下Fasedienol用於社交焦慮障礙急性治療的臨床項目達到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新藥臨床研究，推進更年期血管舒縮症狀（潮熱）二期臨床試驗

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Therapeutics：法西地諾重複給藥展現與單次給藥相當的安全性及耐受性","url":"https://stock-news.laohu8.com/highlight/detail?id=1189830212","media":"美股速递","labels":[],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/1189830212?lang=zh_tw&edition=fundamental","pubTime":"2026-08-06 20:31","pubTimestamp":1786019481,"startTime":"0","endTime":"0","summary":"Vistagen Therapeutics 公司宣布，其核心药物法西地诺（Fasedienol）在重复给药试验中，表现出与单次给药同样良好的安全性与耐受性。这一发现，为这款候选药物的后续开发提供了关键性支持。无论是单次应用还是多次给药，法西地诺均未引发显著差异的不良反应，其耐受性特征保持高度一致。这意味着，在反复用药的场景下，该药物的安全性轮廓并未出现意料之外的恶化。对于Vistagen Therapeutics而言，这无疑是一个积极信号。它进一步巩固了法西地诺作为一种潜在治疗选择的地位，特别是在那些需要长期或周期性用药的适应症领域。目前，公司正基于这些数据，积极推进后续的临床研究计划。","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":"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},{"id":"1122815029","title":"Vistagen Therapeutics 在重度社交焦慮症患者中顯示出名義上的統計顯著改善","url":"https://stock-news.laohu8.com/highlight/detail?id=1122815029","media":"美股速递","labels":[],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/1122815029?lang=zh_tw&edition=fundamental","pubTime":"2026-08-06 20:31","pubTimestamp":1786019480,"startTime":"0","endTime":"0","summary":"Vistagen Therapeutics 公布了一项临床研究结果，针对重度社交焦虑症患者，该公司疗法展现出名义上的统计显著改善。这一数据为治疗这类严重心理障碍领域带来了新的希望。尽管改善幅度被标记为“名义上”显著，但依然凸显了潜在的治疗价值。患者群体处于病情严重状态，任何积极信号都值得关注。VistaGen Therapeutics 正致力于推进其核心管线，探索更有效的干预方案。此次发现无疑增强了市场对其研发方向的预期。然而，后续还需更大规模验证，以确认疗效的稳定性与临床意义。整体来看，这一进展传递出积极信号，但距离实际应用仍有关键节点待突破。","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":"1106146048","title":"VistaGen公布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","url":"https://stock-news.laohu8.com/highlight/detail?id=1106146048","media":"投资观察","labels":[],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/1106146048?lang=zh_tw&edition=fundamental","pubTime":"2026-07-06 15:26","pubTimestamp":1783322808,"startTime":"0","endTime":"0","summary":"VistaGen Therapeutics Inc.宣布了其候选药物Fasedienol用于社交焦虑症急性治疗的Palisade-4三期公众演讲挑战试验的顶线结果及事后分析数据。试验数据显示，Fasedienol在主要和次要终点上均未达到统计学意义上的显著改善。\n然而，该药物的安全性和耐受性数据良好，与先前的临床试验结果保持一致。\n公司计划与美国食品药品监督管理局（FDA）会面，就Fasedienol的未来三期试验及注册路径进行讨论。\n值得注意的是，一项事后分析表明，在非常严重的社交焦虑症患者亚组中，Fasedienol显示出名义上的统计学显著性。","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":"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":"2647055698","title":"Vistagen股價暴跌，因治療社交焦慮症的藥物在後期臨床試驗中未達到主要目標","url":"https://stock-news.laohu8.com/highlight/detail?id=2647055698","media":"路透中文","labels":["dataReport"],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2647055698?lang=zh_tw&edition=fundamental","pubTime":"2026-06-30 20:43","pubTimestamp":1782823400,"startTime":"0","endTime":"0","summary":"BUZZ-Vistagen股价暴跌，因治疗社交焦虑症的药物在后期临床试验中未达到主要目标6月30日-** Vistagen（VTGN.O）股价在盘前交易中暴跌67%，至0.25美元** 这家生物技术公司表示，其用于治疗社交焦虑障碍（一种以对社交场合产生强烈恐惧为特征的疾病）的实验性鼻喷雾剂，在后期临床试验中未能优于安慰剂** 该公司称，在模拟公开演讲测试中，接受法塞迪诺尔治疗的患者其焦虑程度降低幅","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:20260630:nL4S432100:1","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","VTGN"],"isVideo":false,"video":null,"gpt_icon":0},{"id":"1142107877","title":"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","url":"https://stock-news.laohu8.com/highlight/detail?id=1142107877","media":"美股速递","labels":[],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/1142107877?lang=zh_tw&edition=fundamental","pubTime":"2026-06-30 20:03","pubTimestamp":1782821010,"startTime":"0","endTime":"0","summary":"VistaGen Therapeutics 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":["BK4139","VTGN"],"isVideo":false,"video":null,"gpt_icon":0},{"id":"1128069424","title":"VistaGen公布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":["VTGN","BK4139"],"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":["BK4139","VTGN"],"isVideo":false,"video":null,"gpt_icon":0},{"id":"1109937075","title":"VistaGen Therapeutics公布積極安全性及耐受性數據 與既往臨床試驗結果一致","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床項目達到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 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