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Valion Bio Inc

1.65

-0.4929-23.03%

成交量：18.13万

成交额：33.26万

市值：320.82万

市盈率：-0.01

高：2.14

开：2.13

低：1.62

收：2.14

52周最高：76.50

52周最低：1.62

股本：194.78万

流通股本：194.49万

量比：1.37

换手率：9.32%

股息：- -

股息率：- -

每股收益(TTM):-210.1984

每股收益(LYR):-192.0762

净资产收益率：-459.52%

总资产收益率：-57.13%

市净率：0.76

市盈率(LYR):-0.01

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新闻资讯

Valion Bio Inc宣布高层任命：Lisa Wolf出任总裁兼首席运营官，并继续兼任首席财务官

Valion Bio突发人事变动：CEO Michael K. Handley被解职，8月16日正式生效

乌克兰卫生部依据监管等效路径正式受理Entolimod档案进行审评

Afrri/Niaid 设计专有PBI-BM2.5方案，评估Valion Bio（纳斯达克：VBIO）的Entolimod作为首个且唯一GI-ARS疗法

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Handley已被终止职务，该决定将于今年8月16日正式生效。作为一家生物科技企业，Valion Bio在业内一直备受关注，而此番高层变动无疑为公司的未来走向增添了新的不确定性。不过，截至目前，公司方面尚未就此次人事变动的具体原因作出进一步说明。Valion Bio接下来如何平稳过渡、谁将接任这一关键职位，都将成为市场关注的焦点。","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":"executive","news_rank":0,"length":0,"strategy_id":0,"source":null,"symbols":["VBIO","BK4082","BK4139"],"isVideo":false,"video":null,"gpt_icon":0},{"id":"1108799602","title":"乌克兰卫生部依据监管等效路径正式受理Entolimod档案进行审评","url":"https://stock-news.laohu8.com/highlight/detail?id=1108799602","media":"美股速递","labels":[],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/1108799602?lang=zh_cn&edition=fundamental","pubTime":"2026-07-22 19:46","pubTimestamp":1784720777,"startTime":"0","endTime":"0","summary":"乌克兰卫生部已正式接受Entolimod（一种用于治疗急性辐射综合征的候选药物）的注册档案，并依据其监管等效性路径启动正式审评程序。此举标志着该药物在乌克兰的监管审批进程迈出了关键一步。\nEntolimod由Valion Bio Inc开发，此次档案受理意味着该药物在乌克兰的上市申请已进入实质性审查阶段。监管等效性路径允许乌克兰主管部门参考其他严格监管机构（如美国FDA或欧洲EMA）的审评数据与决策，以加速本国审批流程。\n这一进展为Entolimod未来在乌克兰市场的潜在获批奠定了基础，也为Valion Bio Inc拓展其全球布局提供了新的监管机遇。","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":["BK4082","BK4139","VBIO"],"isVideo":false,"video":null,"gpt_icon":0},{"id":"1161118562","title":"Afrri/Niaid 设计专有PBI-BM2.5方案，评估Valion Bio（纳斯达克：VBIO）的Entolimod作为首个且唯一GI-ARS疗法","url":"https://stock-news.laohu8.com/highlight/detail?id=1161118562","media":"美股速递","labels":[],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/1161118562?lang=zh_cn&edition=fundamental","pubTime":"2026-06-25 19:46","pubTimestamp":1782387982,"startTime":"0","endTime":"0","summary":"美国陆军放射生物学研究所与国立过敏和传染病研究所联合设计了一项专有的PBI-BM2.5研究方案，旨在评估Valion Bio Inc（纳斯达克股票代码：VBIO）旗下药物Entolimod，将其作为首个也是目前唯一用于治疗胃肠道急性辐射综合征的候选疗法。这项专门设计的方案旨在验证该药物的有效性与安全性，标志着针对这一严重辐射损伤的治疗开发迈出了关键一步。若最终评估结果积极，Entolimod有望填补该治疗领域长期存在的空白，为受辐射影响的胃肠道系统提供首个靶向治疗方案。","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":["VBIO","BK4139","BK4082"],"isVideo":false,"video":null,"gpt_icon":0}],"pageSize":4,"totalPage":2,"pageCount":1,"totalSize":5,"code":"91000000","status":"200"}],"@#url:\"https://hq.skytigris.cn/market/plate/belongs/VBIO\",params:#limit:6,delay:false,,,undefined,":[]}}