美股詳情

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Savara Inc

5.30

-0.0200-0.38%

盤後：5.300.00000.00%19:30 EDT

成交量：106.37萬

成交額：565.49萬

市值：10.85億

市盈率：-9.17

高：5.40

開：5.38

低：5.27

收：5.32

52周最高：7.01

52周最低：3.34

股本：2.05億

流通股本：1.98億

量比：0.87

換手率：0.54%

股息：- -

股息率：- -

每股收益(TTM):-0.5782

每股收益(LYR):-0.5344

淨資產收益率：-105.48%

總資產收益率：-50.15%

市淨率：7.55

市盈率(LYR):-9.92

資料載入中...

總覽公司新聞公告

Savara將在2026年歐洲呼吸學會大會上再度呈現Molgramostim吸入溶液治療自身免疫性肺泡蛋白沉積症（aPAP）的III期臨床試驗結果

Savara旗下Molbreevi MAAS同步接受EMA與英國MHRA審查，預計分別於2027年Q1與2026年Q4揭曉結果

Savara宣佈歐洲和澳大利亞專利局授予Molbreevi*液體制劑專利，保護期至2041年3月

Savara公司首席財務及行政官Dave Lowrance將於2026年7月15日卸任

Savara在美國胸科學會2026年國際會議上公布其Molgramostim吸入溶液用於自身免疫性肺泡蛋白沉積症的Impala-2三期臨床試驗新生物標誌物數據

Savara公布IMPALA-2三期臨床試驗中莫格司亭吸入溶液治療自身免疫性肺泡蛋白沉積症的新運動能力數據

Savara Inc：處方藥使用者付費法案目標審評日期延長三個月至2026年11月22日

Savara宣佈美國FDA延長莫格司亭吸入溶液治療自身免疫性肺泡蛋白沉積症的生物製品許可申請審評周期

BUZZ--美國股票走勢-醫療保險公司、Arista、Savara

BUZZ-英國接受罕見肺病藥物申請，薩瓦拉公司股價上漲

Savara宣佈英國MHRA受理Molgradex治療自身免疫性肺泡蛋白沉積症的上市許可申請

Savara宣佈英國藥品和保健品管理局接受Molgradex上市許可申請用於治療自身免疫性肺泡蛋白沉積症

Savara宣佈歐洲藥品管理局驗證Molbreevi*治療自身免疫性肺泡蛋白沉積症的上市授權申請

Savara, Inc.盤中異動大幅拉升5.16%報5.71美元

Savara收到美國FDA第74日函件顯示該機構無計劃召開諮詢委員會會議

Savara公布Molbreevi*治療自身免疫性肺泡蛋白沉積症研發項目的監管進展

Master Tec集團宣佈Sediacom獲1050萬令吉授標函

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Lowrance將於2026年7月15日卸任","url":"https://stock-news.laohu8.com/highlight/detail?id=1172355328","media":"美股速递","labels":["executive"],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/1172355328?lang=zh_tw&edition=fundamental","pubTime":"2026-06-09 04:06","pubTimestamp":1780949172,"startTime":"0","endTime":"0","summary":"Savara公司宣布，其首席财务及行政官Dave Lowrance将于2026年7月15日正式离职。公司正着手进行继任规划，以确保相关职责的平稳过渡。","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":"executive","news_rank":0,"length":0,"strategy_id":0,"source":null,"symbols":["SVRA","BK4139"],"isVideo":false,"video":null,"gpt_icon":0},{"id":"1144218221","title":"Savara在美國胸科學會2026年國際會議上公布其Molgramostim吸入溶液用於自身免疫性肺泡蛋白沉積症的Impala-2三期臨床試驗新生物標誌物數據","url":"https://stock-news.laohu8.com/highlight/detail?id=1144218221","media":"美股速递","labels":[],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/1144218221?lang=zh_tw&edition=fundamental","pubTime":"2026-05-20 20:15","pubTimestamp":1779279333,"startTime":"0","endTime":"0","summary":"Savara Inc. 在近日举行的美国胸科学会2026年国际会议上，公布了其核心候选药物Molgramostim吸入溶液针对自身免疫性肺泡蛋白沉积症（aPAP）的Impala-2三期临床试验的最新生物标志物数据。\n此次公布的数据进一步揭示了该疗法的潜在作用机制与生物活性。生物标志物的动态变化为评估药物在患者体内的疗效反应提供了关键的科学依据。数据的呈现增强了业界对该疗法临床路径的理解，也标志着Savara在推进这一罕见呼吸疾病治疗方案的进程中取得了新的进展。","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","SVRA"],"isVideo":false,"video":null,"gpt_icon":0},{"id":"1128565481","title":"Savara公布IMPALA-2三期臨床試驗中莫格司亭吸入溶液治療自身免疫性肺泡蛋白沉積症的新運動能力數據","url":"https://stock-news.laohu8.com/highlight/detail?id=1128565481","media":"美股速递","labels":["dataReport"],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/1128565481?lang=zh_tw&edition=fundamental","pubTime":"2026-05-19 02:56","pubTimestamp":1779130579,"startTime":"0","endTime":"0","summary":"Savara公司公布了其IMPALA-2三期临床试验中，关于莫格司亭吸入溶液治疗自身免疫性肺泡蛋白沉积症的新运动能力数据。该试验旨在评估莫格司亭对这一罕见肺部疾病患者的疗效与安全性。","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":"0","news_top_title":null,"news_tag":"dataReport","news_rank":0,"length":0,"strategy_id":0,"source":null,"symbols":["SVRA","BK4139"],"isVideo":false,"video":null,"gpt_icon":0},{"id":"1168628720","title":"Savara Inc：處方藥使用者付費法案目標審評日期延長三個月至2026年11月22日","url":"https://stock-news.laohu8.com/highlight/detail?id=1168628720","media":"美股速递","labels":[],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/1168628720?lang=zh_tw&edition=fundamental","pubTime":"2026-04-16 04:06","pubTimestamp":1776283576,"startTime":"0","endTime":"0","summary":"生物制药公司Savara Inc宣布，美国食品药品监督管理局（FDA）已将其核心在研药物的处方药使用者付费法案（PDUFA）目标审评日期延长三个月。新的最终决定期限设定为2026年11月22日。\n此次延期为FDA完成对该公司新药申请（NDA）的全面审查提供了额外时间。PDUFA日期延后通常意味着监管机构需要更多数据或信息来做出最终批准决定，这在此类审查过程中属于常规程序。\n该公司表示将继续与FDA密切合作，以推进该药物的审评进程。此次延期不影响公司对其研发管线推进的战略规划。","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":["SVRA","BK4139"],"isVideo":false,"video":null,"gpt_icon":0},{"id":"1106015571","title":"Savara宣佈美國FDA延長莫格司亭吸入溶液治療自身免疫性肺泡蛋白沉積症的生物製品許可申請審評周期","url":"https://stock-news.laohu8.com/highlight/detail?id=1106015571","media":"美股速递","labels":["policyRegulatory"],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/1106015571?lang=zh_tw&edition=fundamental","pubTime":"2026-04-16 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21:08","pubTimestamp":1775567334,"startTime":"0","endTime":"0","summary":".N** 博通公司AVGO.O：BUZZ - 因与谷歌达成开发定制人工智能芯片的长期协议而在盘前上涨  nL4N40Q0HL ** CVS Health Corp CVS.N：** UnitedHealth Group Inc UNH.N：** Elevance Health Inc ELV.N：BUZZ - 美国最终确定将医疗保险优势支付上调 2.48%，医疗保险公司大涨 nL4N40Q0I3 ** Greenwich LifeSciences Inc GLSI.O:BUZZ - 新数据扩大了潜在的乳腺癌药物市场，导致该公司股价上涨。nL4N40Q0PW ** Humana Inc HUM.N:BUZZ - 因医疗保险费率上调而跳涨；富国银行上调评级   nL4N40Q0R7 ** Old Dominion Freight Line Inc ODFL.OODFL.O:BUZZ - 因需求前景强劲，富国银行将其评级上调至 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20:46","pubTimestamp":1775565980,"startTime":"0","endTime":"0","summary":"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:20260407:nL4S40Q0WR: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":["BK4139","SVRA"],"isVideo":false,"video":null,"gpt_icon":0},{"id":"1176735830","title":"Savara宣佈英國MHRA受理Molgradex治療自身免疫性肺泡蛋白沉積症的上市許可申請","url":"https://stock-news.laohu8.com/highlight/detail?id=1176735830","media":"投资观察","labels":["policyRegulatory"],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/1176735830?lang=zh_tw&edition=fundamental","pubTime":"2026-04-07 20:21","pubTimestamp":1775564504,"startTime":"0","endTime":"0","summary":"Savara Inc宣布，英国药品和保健品管理局（MHRA）已正式受理其药物Molgradex用于治疗自身免疫性肺泡蛋白沉积症的上市许可申请。\n根据公司披露的时间表，MHRA对Molgradex上市许可申请的决定预计将在2026年第四季度公布。与此同时，美国食品药品监督管理局（FDA）针对Molgradex生物制品许可申请设定的处方药用户付费法案目标日期为2026年8月22日。此外，欧洲药品管理局人用药品委员会对Molgradex上市许可申请的决定预计将于2027年第一季度作出。\n","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":"policyRegulatory","news_rank":0,"length":0,"strategy_id":0,"source":null,"symbols":["SVRA","BK4139"],"isVideo":false,"video":null,"gpt_icon":0},{"id":"1199822860","title":"Savara宣佈英國藥品和保健品管理局接受Molgradex上市許可申請用於治療自身免疫性肺泡蛋白沉積症","url":"https://stock-news.laohu8.com/highlight/detail?id=1199822860","media":"美股速递","labels":["productRelease"],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/1199822860?lang=zh_tw&edition=fundamental","pubTime":"2026-04-07 20:06","pubTimestamp":1775563586,"startTime":"0","endTime":"0","summary":"Savara Inc. 宣布，英国药品和保健品管理局（MHRA）已正式受理其药物Molgradex®用于治疗自身免疫性肺泡蛋白沉积症（autoimmune PAP）的上市许可申请（MAA）。这一进展标志着该药物在英国监管审批流程中迈出了关键一步。","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":["SVRA","BK4139"],"isVideo":false,"video":null,"gpt_icon":0},{"id":"1115780051","title":"Savara宣佈歐洲藥品管理局驗證Molbreevi*治療自身免疫性肺泡蛋白沉積症的上市授權申請","url":"https://stock-news.laohu8.com/highlight/detail?id=1115780051","media":"美股速递","labels":[],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/1115780051?lang=zh_tw&edition=fundamental","pubTime":"2026-03-30 20:10","pubTimestamp":1774872613,"startTime":"0","endTime":"0","summary":"Savara Inc宣布，其针对自身免疫性肺泡蛋白沉积症（Autoimmune PAP）的治疗药物Molbreevi*的上市授权申请（MAA）已获得欧洲药品管理局（EMA）的正式验证。这一关键进展标志着该药物的审评程序在欧洲市场正式启动，为罕见呼吸系统疾病患者带来新的治疗希望。","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","SVRA"],"isVideo":false,"video":null,"gpt_icon":0},{"id":"2618990263","title":"Savara, Inc.盤中異動 大幅拉升5.16%報5.71美元","url":"https://stock-news.laohu8.com/highlight/detail?id=2618990263","media":"市场透视","labels":[],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2618990263?lang=zh_tw&edition=fundamental","pubTime":"2026-03-10 21:51","pubTimestamp":1773150685,"startTime":"0","endTime":"0","summary":"北京时间2026年03月10日21时51分，Savara, Inc.股票出现波动，股价快速拉升5.16%。截至发稿，该股报5.71美元/股，成交量9.1595万股，换手率0.05%，振幅4.79%。Savara, Inc.股票所在的生物技术行业中，整体涨幅为1.98%。其相关个股中，Longeveron Inc.、Mink Therapeutics, Inc.、Acurx Pharmaceuticals, Inc.涨幅较大，Biorestorative Therapies, Inc.、Mink Therapeutics, Inc.、Scisparc Ltd.较为活跃，换手率分别为576.95%、233.82%、145.88%，振幅较大的相关个股有Longeveron Inc.、Acurx Pharmaceuticals, Inc.、Artelo Biosciences, Inc.，振幅分别为54.24%、28.12%、20.22%。Savara, Inc.公司简介：Savara Inc 是一家生物制药公司。","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=nesSN20260310215125a6b5a7f3&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, 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Inc（纳斯达克代码：SVRA）近日宣布，已收到美国食品药品监督管理局（FDA）发出的第74日函件。该函件明确指出，FDA目前并无召集咨询委员会会议的计划。\n这一进展标志着Savara在监管审批流程中迈出了重要一步。通常情况下，FDA会通过咨询委员会会议对创新疗法进行深入评估，而此次无需召开此类会议的决定，可能预示着审批流程的加速。\n公司表示将继续与FDA保持密切沟通，积极推进相关药物的审评工作。市场关注此举是否意味着Savara的研发项目将获得更快的监管反馈。","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","SVRA"],"isVideo":false,"video":null,"gpt_icon":0},{"id":"1163688181","title":"Savara公布Molbreevi*治療自身免疫性肺泡蛋白沉積症研發項目的監管進展","url":"https://stock-news.laohu8.com/highlight/detail?id=1163688181","media":"美股速递","labels":[],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/1163688181?lang=zh_tw&edition=fundamental","pubTime":"2026-03-07 05:06","pubTimestamp":1772831205,"startTime":"0","endTime":"0","summary":"Savara Inc（简称Savara）近日就其针对自身免疫性肺泡蛋白沉积症（Autoimmune PAP）的Molbreevi*研发项目，发布了最新的监管动态。\n公司方面表示，相关进展将有助于推动该疗法的后续开发进程，为患者带来新的治疗希望。","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","SVRA"],"isVideo":false,"video":null,"gpt_icon":0},{"id":"1100831277","title":"Master Tec集團宣佈Sediacom獲1050萬令吉授標函","url":"https://stock-news.laohu8.com/highlight/detail?id=1100831277","media":"投资观察","labels":[],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/1100831277?lang=zh_tw&edition=fundamental","pubTime":"2026-03-06 18:35","pubTimestamp":1772793354,"startTime":"0","endTime":"0","summary":"3月6日 - Master Tec集团宣布，其子公司Sediacom已正式接受价值1050万令吉的工程、采购、施工和调试（EPCC）合约。该合约内容涵盖275千伏地下电缆项目及国家能源公司（TNB）开关站扩建工程。\n此次中标将进一步巩固Master Tec在能源基建领域的市场地位，为公司未来业绩提供新的增长动力。","market":"hk","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","SVRA"],"isVideo":false,"video":null,"gpt_icon":0}],"pageSize":20,"totalPage":1,"pageCount":1,"totalSize":17,"code":"91000000","status":"200"}]}}