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VNDA 万达生物制药
休市中 04-10 16:00:00 EDT
7.22
-0.11
-1.50%
盘后
7.18
-0.04
-0.55%
19:03 EDT
最高
7.35
最低
7.06
成交量
85.45万
今开
7.35
昨收
7.33
日振幅
3.96%
总市值
4.27亿
流通市值
3.57亿
总股本
5,910万
成交额
612.05万
换手率
1.73%
流通股本
4,948万
市净率
--
ROE
--
每股收益
0.00
52周最高
--
52周最低
--
市盈率
--
股息
--
股息收益率
--
ROA
--
分时
五日
日K
周K
月K
数据加载中...
北京优虎网络科技有限公司
资讯
新帖
简况
万达生物制药敦促FDA撤回2027财年立法议程中延长药物审评时限的提案
美股速递 · 04-09
万达生物制药敦促FDA撤回2027财年立法议程中延长药物审评时限的提案
万达生物制药启动Thetis研究:评估Nereus™预防GLP-1受体激动剂所致呕吐的临床试验
美股速递 · 04-09
万达生物制药启动Thetis研究:评估Nereus™预防GLP-1受体激动剂所致呕吐的临床试验
欧洲药品管理局人用药品委员会:确认拒绝Hetlioz(塔西美尔通)营销授权变更的建议
美股速递 · 03-27
欧洲药品管理局人用药品委员会:确认拒绝Hetlioz(塔西美尔通)营销授权变更的建议
万达生物制药呼吁FDA加速推动动物试验向人体相关方法转型
美股速递 · 03-20
万达生物制药呼吁FDA加速推动动物试验向人体相关方法转型
欧洲药管局拒绝Hetlioz新增史密斯-马吉利斯综合征成人夜间睡眠障碍适应症的申请
美股速递 · 03-18
欧洲药管局拒绝Hetlioz新增史密斯-马吉利斯综合征成人夜间睡眠障碍适应症的申请
Vanda Pharmaceuticals Inc.盘中异动 大幅上涨5.07%报8.29美元
市场透视 · 03-09
Vanda Pharmaceuticals Inc.盘中异动 大幅上涨5.07%报8.29美元
万达生物制药宣布美国FDA为Hetlioz®时差障碍适应症召开里程碑式听证会,系40余年来首次新药审批听证
美股速递 · 03-03
万达生物制药宣布美国FDA为Hetlioz®时差障碍适应症召开里程碑式听证会,系40余年来首次新药审批听证
EMA人用医药产品委员会:万达生物制药的伊洛哌酮获负面意见 用于精神分裂症治疗
美股速递 · 02-27
EMA人用医药产品委员会:万达生物制药的伊洛哌酮获负面意见 用于精神分裂症治疗
万达生物制药盘前股价上涨2.3%,FDA受理其罕见皮肤病药物审查申请
美股速递 · 02-25
万达生物制药盘前股价上涨2.3%,FDA受理其罕见皮肤病药物审查申请
万达生物制药宣布美国FDA受理imsidolimab治疗泛发性脓疱型银屑病的生物制品许可申请
投资观察 · 02-25
万达生物制药宣布美国FDA受理imsidolimab治疗泛发性脓疱型银屑病的生物制品许可申请
万达生物制药宣布美国FDA受理Imsidolimab治疗泛发性脓疱型银屑病的生物制品许可申请
美股速递 · 02-25
万达生物制药宣布美国FDA受理Imsidolimab治疗泛发性脓疱型银屑病的生物制品许可申请
万达生物制药更新Bysanti安全警告:老年痴呆相关精神病患者死亡率上升
美股速递 · 02-21
万达生物制药更新Bysanti安全警告:老年痴呆相关精神病患者死亡率上升
万达生物制药宣布Bysanti™(米沙哌隆)获FDA批准用于治疗双相I型障碍和精神分裂症——新化学实体开启精神科创新新纪元
美股速递 · 02-21
万达生物制药宣布Bysanti™(米沙哌隆)获FDA批准用于治疗双相I型障碍和精神分裂症——新化学实体开启精神科创新新纪元
万达生物制药公布年度营收指引:现有商业化产品收入预计达2.3亿至2.6亿美元
美股速递 · 02-12
万达生物制药公布年度营收指引:现有商业化产品收入预计达2.3亿至2.6亿美元
美国FDA拒绝时差症药物申请,万达生物制药盘前股价重挫近12%
美股速递 · 01-08
美国FDA拒绝时差症药物申请,万达生物制药盘前股价重挫近12%
万达生物制药宣布收到美国食品药品监督管理局关于Hetlioz®时差障碍补充新药申请的决定函
美股速递 · 01-08
万达生物制药宣布收到美国食品药品监督管理局关于Hetlioz®时差障碍补充新药申请的决定函
美股异动 | 止吐新药Nereus获FDA批准 万达生物制药(VNDA.US)涨超32%
智通财经 · 2025-12-31
美股异动 | 止吐新药Nereus获FDA批准 万达生物制药(VNDA.US)涨超32%
万达生物制药:预防运动诱发性呕吐的药物已获FDA批准
老虎资讯综合 · 2025-12-31
万达生物制药:预防运动诱发性呕吐的药物已获FDA批准
盘前|VNDA暴涨20%,特斯拉快速拉升,英伟达、台积电曝重磅消息
老虎资讯综合 · 2025-12-31
盘前|VNDA暴涨20%,特斯拉快速拉升,英伟达、台积电曝重磅消息
盘前异动|万达生物制药暴涨22%,贵金属概念普跌,小鹏汽车跌超4%
老虎资讯综合 · 2025-12-31
盘前异动|万达生物制药暴涨22%,贵金属概念普跌,小鹏汽车跌超4%
公司概况
公司名称:
万达生物制药
所属市场:
NASDAQ
上市日期:
--
主营业务:
Vanda Pharmaceuticals Inc.于2002年在特拉华州注册成立。该公司是一家全球领先的生物制药公司,专注于创新疗法的开发和商业化,以解决高度未满足的医疗需求并改善患者的生活。该公司努力推进新的方法,通过负责任的创新将重要的新药推向市场。该公司致力于在药物发现、临床试验和产品的商业定位中使用支持健全科学的技术,包括遗传学和基因组学。
发行价格:
--
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Pharmaceuticals)近日呼吁美国食品药品监督管理局(FDA)从其2027财年立法议程中撤销一项旨在延长药物审评时间表的提案。该公司认为,此举可能对药物研发进程产生不利影响。","market":"us","thumbnail":"","type":0,"news_type":0,"thumbnails":[],"rights":null,"property":[],"language":"zh","translate_title":"","themeId":"","theme_name":"","theme_type":"","isJumpTheme":false,"source_url":"","is_publish_highlight":false,"source_rank":0,"column":"","sentiment":"2","news_top_title":null,"news_tag":"policyRegulatory","news_rank":0,"length":0,"strategy_id":0,"source":null,"symbols":["VNDA","BK4139"],"isVideo":false,"video":null,"gpt_icon":0},{"id":"1118743082","title":"万达生物制药启动Thetis研究:评估Nereus™预防GLP-1受体激动剂所致呕吐的临床试验","url":"https://stock-news.laohu8.com/highlight/detail?id=1118743082","media":"美股速递","labels":[],"top":-1,"itemType":null,"share":"https://www.laohu8.com/m/news/1118743082?lang=zh_cn&edition=full","pubTime":"2026-04-09 04:46","pubTimestamp":1775681177,"startTime":"0","endTime":"0","summary":"万达生物制药宣布正式启动名为\"Thetis研究\"的临床试验,该试验旨在评估其创新药物Nereus对GLP-1受体激动剂引发的呕吐症状的预防效果。这项研究将针对使用GLP-1受体激动剂治疗时出现胃肠道不良反应的患者群体,探索Nereus在控制药物相关性呕吐方面的潜在疗效。若试验结果积极,Nereus有望成为首款专门针对GLP-1类药物相关呕吐症状的预防性疗法,为全球数百万相关患者提供新的解决方案。","market":"us","thumbnail":"","type":0,"news_type":0,"thumbnails":[],"rights":null,"property":[],"language":"zh","translate_title":"","themeId":"","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","VNDA"],"isVideo":false,"video":null,"gpt_icon":0},{"id":"1146656831","title":"欧洲药品管理局人用药品委员会:确认拒绝Hetlioz(塔西美尔通)营销授权变更的建议","url":"https://stock-news.laohu8.com/highlight/detail?id=1146656831","media":"美股速递","labels":[],"top":-1,"itemType":null,"share":"https://www.laohu8.com/m/news/1146656831?lang=zh_cn&edition=full","pubTime":"2026-03-27 19:45","pubTimestamp":1774611912,"startTime":"0","endTime":"0","summary":"欧洲药品管理局人用药品委员会(CHMP)已确认其建议,拒绝批准对Hetlioz(塔西美尔通)营销授权的变更申请。该决定维持了委员会早前的立场,意味着相关制药公司——万达生物制药(Vanda Pharmaceuticals)——此次申请未获通过。","market":"us","thumbnail":"","type":0,"news_type":0,"thumbnails":[],"rights":null,"property":[],"language":"zh","translate_title":"","themeId":"","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","VNDA"],"isVideo":false,"video":null,"gpt_icon":0},{"id":"1106740354","title":"万达生物制药呼吁FDA加速推动动物试验向人体相关方法转型","url":"https://stock-news.laohu8.com/highlight/detail?id=1106740354","media":"美股速递","labels":[],"top":-1,"itemType":null,"share":"https://www.laohu8.com/m/news/1106740354?lang=zh_cn&edition=full","pubTime":"2026-03-20 04:37","pubTimestamp":1773952632,"startTime":"0","endTime":"0","summary":"万达生物制药近日公开敦促美国食品药品监督管理局采取实质性行动,加快医药研发领域从传统动物试验向更具人体相关性的替代方法转变。该公司指出,当前基于人类生物学的新型检测技术已展现出更精准预测药物反应的潜力,此举将有望重构药物安全评估体系,提升临床转化效率。","market":"us","thumbnail":"","type":0,"news_type":0,"thumbnails":[],"rights":null,"property":[],"language":"zh","translate_title":"","themeId":"","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":["VNDA","BK4139"],"isVideo":false,"video":null,"gpt_icon":0},{"id":"1152286791","title":"欧洲药管局拒绝Hetlioz新增史密斯-马吉利斯综合征成人夜间睡眠障碍适应症的申请","url":"https://stock-news.laohu8.com/highlight/detail?id=1152286791","media":"美股速递","labels":["policyRegulatory"],"top":-1,"itemType":null,"share":"https://www.laohu8.com/m/news/1152286791?lang=zh_cn&edition=full","pubTime":"2026-03-18 00:17","pubTimestamp":1773764233,"startTime":"0","endTime":"0","summary":"欧洲药品管理局近日正式否决了关于拓展Hetlioz(塔司普雷酮)营销授权的申请,该申请旨在将史密斯-马吉利斯综合征成人患者的夜间睡眠障碍纳入治疗范围。此次决定意味着由万达生物制药开发的这款褪黑素受体激动剂暂无法在欧洲市场扩大其临床适用范围。","market":"us","thumbnail":"","type":0,"news_type":0,"thumbnails":[],"rights":null,"property":[],"language":"zh","translate_title":"","themeId":"","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","VNDA"],"isVideo":false,"video":null,"gpt_icon":0},{"id":"2618675841","title":"Vanda Pharmaceuticals Inc.盘中异动 大幅上涨5.07%报8.29美元","url":"https://stock-news.laohu8.com/highlight/detail?id=2618675841","media":"市场透视","labels":[],"top":-1,"itemType":null,"share":"https://www.laohu8.com/m/news/2618675841?lang=zh_cn&edition=full","pubTime":"2026-03-09 23:33","pubTimestamp":1773070438,"startTime":"0","endTime":"0","summary":"北京时间2026年03月09日23时33分,Vanda Pharmaceuticals Inc.股票出现波动,股价急速拉升5.07%。Vanda Pharmaceuticals Inc.股票所在的生物技术行业中,整体涨幅为0.50%。Vanda Pharmaceuticals Inc.公司简介:万达生物制药有限公司是一家生物制药公司,该公司致力于开发和商业化疗法,以满足大量未满足的医疗需求,并改善患者的生活。大部分收入来自 Fanapt 产品销售。","market":"us","thumbnail":null,"type":0,"news_type":0,"thumbnails":[],"rights":{"source":"tencent","url":"http://gu.qq.com/resources/shy/news/detail-v2/index.html#/?id=nesSN2026030923335897ab39f2&s=b","rn_cache_url":null,"customStyle":"body{padding-top:10px;}#news_title{font-weight:bold;#titleStyle#;}#news_description span{font-size:12px;#descriptionStyle#;}.footer-note{#statement#}","selectors":".mod-LoadTzbdNews, body","filters":".relate-stock, .hot-list, .recom-box, 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21:04","pubTimestamp":1772543085,"startTime":"0","endTime":"0","summary":"万达生物制药宣布,美国食品药品监督管理局已为其药物Hetlioz®用于治疗时差障碍的申请召开了一次具有里程碑意义的听证会。此次听证会是FDA超过40年来首次针对新药审批举行的听证会,标志着监管程序的一个重要突破。","market":"us","thumbnail":"","type":0,"news_type":0,"thumbnails":[],"rights":null,"property":[],"language":"zh","translate_title":"","themeId":"","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":["BK4139","VNDA"],"isVideo":false,"video":null,"gpt_icon":0},{"id":"1119330741","title":"EMA人用医药产品委员会:万达生物制药的伊洛哌酮获负面意见 用于精神分裂症治疗","url":"https://stock-news.laohu8.com/highlight/detail?id=1119330741","media":"美股速递","labels":["policyRegulatory"],"top":-1,"itemType":null,"share":"https://www.laohu8.com/m/news/1119330741?lang=zh_cn&edition=full","pubTime":"2026-02-27 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