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万达生物制药

5.73

-0.1500-2.55%

盘后：5.70-0.0300-0.52%19:09 EDT

成交量：94.46万

成交额：540.70万

市值：3.45亿

市盈率：-1.41

高：5.93

开：5.88

低：5.61

收：5.88

52周最高：9.94

52周最低：4.14

股本：6,013.51万

流通股本：5,419.93万

量比：0.92

换手率：1.74%

股息：- -

股息率：- -

每股收益(TTM):-4.0548

每股收益(LYR):-3.7413

净资产收益率：-60.48%

总资产收益率：-18.81%

市净率：1.23

市盈率(LYR):-1.53

数据加载中...

总览公司新闻公告

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万达生物制药宣布Nereus™（Tradipitant）在美国上市，系40余年来首款晕动症新药

万达生物制药：持有效处方患者可获Nereus药物现金支付价为每剂85美元

万达生物制药宣布Nereus™（Tradipitant）在美国上市，系四十余年来首款晕动症新药

BUZZ-旺达敦促美国食品药品管理局放弃延长药品审查时限的建议；股价下跌

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

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

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

BUZZ-美国食品及药物管理局罕见地就时差药竞标举行听证会后，万达股价上涨

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

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

BUZZ-FDA接受罕见皮肤病药物审查申请，万达股价上涨

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

BUZZ--美国股票走势-礼来、达美乐、诺和诺德

BUZZ-美国 FDA 批准新型抗精神病药，万达医药一跃而起

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公司称美国食品药品管理局将举行罕见的公开听证会，审查其扩大睡眠药物Hetlioz治疗时差紊乱的申请** 当长途旅行扰乱了人体的内部时钟，导致疲劳和睡眠不佳时，就会出现时差现象。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":"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:20260303:nL4T3ZR19F:1","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":["VNDA","BK4139"],"isVideo":false,"video":null,"gpt_icon":0},{"id":"1146152400","title":"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","url":"https://stock-news.laohu8.com/highlight/detail?id=1146152400","media":"美股速递","labels":["productRelease"],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/1146152400?lang=zh_cn&edition=fundamental","pubTime":"2026-03-03 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制药商称美国FDA接受了其对imsidolimab的审查申请，该药用于治疗泛发性脓疱型银屑病，一种会导致皮肤出现疼痛脓疱、发烧和疲劳的罕见疾病。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":"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:20260225:nL4T3ZL16T: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":["VNDA","BK4139"],"isVideo":false,"video":null,"gpt_icon":0},{"id":"1130498462","title":"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","url":"https://stock-news.laohu8.com/highlight/detail?id=1130498462","media":"投资观察","labels":[],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/1130498462?lang=zh_cn&edition=fundamental","pubTime":"2026-02-25 20:41","pubTimestamp":1772023308,"startTime":"0","endTime":"0","summary":"万达生物制药公司宣布，美国食品药品监督管理局已正式受理其候选药物imsidolimab用于治疗泛发性脓疱型银屑病的生物制品许可申请。\nFDA已为该申请设定了目标审评日期为2026年12月12日。","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":["VNDA","BK4139"],"isVideo":false,"video":null,"gpt_icon":0},{"id":"1177212007","title":"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","url":"https://stock-news.laohu8.com/highlight/detail?id=1177212007","media":"美股速递","labels":["policyRegulatory"],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/1177212007?lang=zh_cn&edition=fundamental","pubTime":"2026-02-25 20:30","pubTimestamp":1772022603,"startTime":"0","endTime":"0","summary":"万达生物制药近日宣布，其针对泛发性脓疱型银屑病治疗的生物制剂Imsidolimab的生物制品许可申请，已获得美国食品药品监督管理局的正式受理。这一进展标志着该药物向获批上市迈出了关键一步。","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":"2613782199","title":"BUZZ--美国股票走势-礼来、达美乐、诺和诺德","url":"https://stock-news.laohu8.com/highlight/detail?id=2613782199","media":"路透中文","labels":["event"],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2613782199?lang=zh_cn&edition=fundamental","pubTime":"2026-02-23 21:22","pubTimestamp":1771852942,"startTime":"0","endTime":"0","summary":".N** 礼来公司LLLY.N：BUZZ - 诺和诺德肥胖症药物在哥本哈根试验中表现不佳，导致该公司股价上涨。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:20260223:nL4T3ZJ0WD:1","is_publish_highlight":false,"source_rank":0,"column":"","sentiment":"0","news_top_title":null,"news_tag":"event","news_rank":0,"length":0,"strategy_id":0,"source":null,"symbols":["LU1629891620.HKD","COIW","ELIS","COIG","RTYY","IMRA","ACLX","CONY","VNDA","BK4534","WDAY","LU1551013425.SGD","CONI","DE","VFC","DOCU","MARO","DPZ","COII","LDOS","MLTX","MRAL","LU0345781412.USD","COIA","COIO","LLYZ","RIOX","MRK","SGXZ81514606.USD","FIAT","LU0210536198.USD","LLII","LU2361044949.HKD","IE00BBT3K403.USD","ELIL","ICOI","MNDY","MAAY","LLYX","COYY","RIOT","CDE","FBIN","HL","LLY","FRSH","CONX"],"isVideo":false,"video":null,"gpt_icon":1},{"id":"2613789898","title":"BUZZ-美国 FDA 批准新型抗精神病药，万达医药一跃而起","url":"https://stock-news.laohu8.com/highlight/detail?id=2613789898","media":"路透中文","labels":["productRelease"],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2613789898?lang=zh_cn&edition=fundamental","pubTime":"2026-02-23 19:32","pubTimestamp":1771846325,"startTime":"0","endTime":"0","summary":"2月23日 - ** Vanda Pharmaceuticals VNDA.O股价盘前上涨37%至7.91美元** 周五晚些时候，美国 FDA 批准了  VNDA 用于治疗两种严重精神疾病的药物** 该药名为 Bysanti，是一种抗精神病药，主要用于治疗精神分裂症和急性双相情感障碍。** H.C. Wainwright 分析师表示：\"Bysanti 的市场独占期预计将延长至 2044 年，这为长期创新和患者获益奠定了坚实的基础。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":"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:20260223:nL4T3ZJ0NQ:1","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}],"pageSize":20,"totalPage":3,"pageCount":1,"totalSize":44,"code":"91000000","status":"200"}]}}