再生元制药公司(REGN)_个股概要_股票价格_最新资讯_行情走势_历史数据 - 老虎社区

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REGN 再生元制药公司

耶稣受难日休市 04-02 16:00:00 EDT

761.85

-15.40

-1.98%

盘后761.54

-0.31-0.04%

19:34 EDT

最高770.11	最低745.00	成交量100.07万
今开767.04	昨收777.25	日振幅3.23%
总市值805.43亿	流通市值787.01亿	总股本1.06亿
成交额7.57亿	换手率0.97%	流通股本1.03亿
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--

数据加载中...

北京优虎网络科技有限公司

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Pharmaceuticals）宣布建立合作关系，将获取多达3亿患者的去标识化电子健康记录。这一战略性合作旨在加速生命科学领域的研究进程，并推动数字健康解决方案的产品开发。","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":"corporation","news_rank":0,"length":0,"strategy_id":0,"source":null,"symbols":["LU0823416689.USD","LU0053666078.USD","LU1917777945.USD","LU2089984988.USD","LU0823434583.USD","LU0823434740.USD","LU0889565916.HKD","LU2362540622.SGD","LU2362541273.HKD","LU0320765992.SGD","REGN","LU2362541513.USD","LU1974910355.USD","LU2468319806.SGD","LU2237438978.USD","LU0058720904.USD","LU0882574055.USD","BK4585","BK4588","LU2023250504.SGD","LU0289739699.SGD","LU0114720955.EUR","BK4139","LU2106854487.HKD","LU0109394709.USD"],"isVideo":false,"video":null,"gpt_icon":0},{"id":"1155662129","title":"再生元Eylea 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14:01","pubTimestamp":1774332107,"startTime":"0","endTime":"0","summary":"Dupixent®（Dupilumab）近日在日本获得监管批准，这是该国首个用于治疗成人天疱疮（BP）的靶向药物。这一里程碑式的批准为患有这种罕见且严重的自身免疫性皮肤病的成年患者提供了新的治疗选择。","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":"productRelease","news_rank":0,"length":0,"strategy_id":0,"source":null,"symbols":["LU1917777945.USD","LU2089984988.USD","LU0889565916.HKD","LU2237438978.USD","BK4588","LU2362540622.SGD","LU0114720955.EUR","LU0823434583.USD","LU0823434740.USD","LU2023250504.SGD","LU2362541513.USD","BK4585","LU2468319806.SGD","LU0053666078.USD","LU0058720904.USD","LU2106854487.HKD","LU0289739699.SGD","LU0823416689.USD","LU2362541273.HKD","LU1974910355.USD","LU0109394709.USD","REGN","LU0882574055.USD","LU0320765992.SGD","BK4139"],"isVideo":false,"video":null,"gpt_icon":0},{"id":"1121226589","title":"FDA确认2025年11月19日获批的Eylea Hd补充申请符合优先审评券兑换标准","url":"https://stock-news.laohu8.com/highlight/detail?id=1121226589","media":"美股速递","labels":["productRelease"],"top":-1,"itemType":null,"share":"https://www.laohu8.com/m/news/1121226589?lang=zh_cn&edition=full","pubTime":"2026-03-12 21:06","pubTimestamp":1773320790,"startTime":"0","endTime":"0","summary":"美国食品药品监督管理局（FDA）近日裁定，针对再生元制药公司Eylea Hd药品的补充申请——该申请已于2025年11月19日获得批准——完全符合兑换优先审评券的资格条件。这一决定意味着再生元公司可凭借此次获批的补充申请，行使优先审评券赋予的加速审评权益。\n优先审评券制度旨在激励药企研发针对特定疾病的创新疗法，允许企业将券用于其他在研药物的审评流程，从而显著缩短审批时间。Eylea Hd作为再生元旗下的重要眼科治疗产品，此次补充申请的获批及符合兑换标准，不仅强化了该产品的市场地位，也为企业后续产品线的加速推进创造了有利条件。","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":"productRelease","news_rank":0,"length":0,"strategy_id":0,"source":null,"symbols":["LU0823434583.USD","LU1917777945.USD","LU2089984988.USD","BK4588","LU2362540622.SGD","LU0114720955.EUR","LU2362541273.HKD","LU2468319806.SGD","LU0823416689.USD","BK4139","LU0289739699.SGD","LU0053666078.USD","LU0109394709.USD","REGN","LU2237438978.USD","LU0889565916.HKD","LU0320765992.SGD","LU0823434740.USD","LU1974910355.USD","LU2023250504.SGD","LU2362541513.USD","LU0058720904.USD","BK4585","LU0882574055.USD","LU2106854487.HKD"],"isVideo":false,"video":null,"gpt_icon":0},{"id":"1160965279","title":"FDA批准Eylea Hd治疗罕见儿科疾病 兑现优先审评券","url":"https://stock-news.laohu8.com/highlight/detail?id=1160965279","media":"美股速递","labels":["productRelease"],"top":-1,"itemType":null,"share":"https://www.laohu8.com/m/news/1160965279?lang=zh_cn&edition=full","pubTime":"2026-03-12 21:06","pubTimestamp":1773320784,"startTime":"0","endTime":"0","summary":"美国食品药品监督管理局（FDA）已正式批准再生元制药公司（Regeneron Pharmaceuticals）的Eylea Hd用于治疗一种罕见儿科疾病。作为此次批准的一部分，再生元制药公司成功兑现了其持有的优先审评券，该举措旨在加速创新疗法的审评流程。\n此次批准标志着Eylea Hd在罕见儿科疾病治疗领域迈出了重要一步。优先审评券的兑现进一步凸显了该疗法在满足未竟医疗需求方面的潜力，为相关患者群体带来了新的希望。","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":["LU0289739699.SGD","LU2089984988.USD","BK4588","LU0320765992.SGD","LU2023250504.SGD","LU0109394709.USD","LU2106854487.HKD","LU0823434583.USD","LU2362541273.HKD","LU0114720955.EUR","BK4139","LU0882574055.USD","LU1974910355.USD","REGN","LU2468319806.SGD","LU2237438978.USD","LU0823434740.USD","LU0053666078.USD","BK4585","LU2362540622.SGD","LU1917777945.USD","LU0889565916.HKD","LU2362541513.USD","LU0058720904.USD","LU0823416689.USD"],"isVideo":false,"video":null,"gpt_icon":0},{"id":"2618157119","title":"FDA 连发多份 CRL，开年大批新药上市申请已遭拒","url":"https://stock-news.laohu8.com/highlight/detail?id=2618157119","media":"制药网","labels":["policyRegulatory"],"top":-1,"itemType":null,"share":"https://www.laohu8.com/m/news/2618157119?lang=zh_cn&edition=full","pubTime":"2026-03-11 14:39","pubTimestamp":1773211194,"startTime":"0","endTime":"0","summary":"2026年以来，全球医药企业就遭遇了FDA的CRL风暴。2月14日消息，Disc Medicine备受瞩目的候选药物Bitopertin用于治疗罕见血液病红细胞生成性卟啉症的上市申请遭到FDA拒绝。2月3日，阿斯利康公告称，美国FDA就Saphnelo用于成人系统性红斑狼疮患者皮下给药的生物制品许可申请发出完整答复函，驳回了其狼疮治疗药物的自行注射剂型上市申请。总的来说，2026 年 开年以来，已有众多新药上市申请被拒。","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=nesSN20260311144149a6b747a8&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, 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19:03","pubTimestamp":1773054229,"startTime":"0","endTime":"0","summary":"再生元制药公司公布的最新数据显示，接受Olatorepatide治疗的患者在第48周时体重减轻幅度最高达到19%。这一结果凸显了该药物在体重管理领域的显著疗效。","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":"productRelease","news_rank":0,"length":0,"strategy_id":0,"source":null,"symbols":["LU0320765992.SGD","LU0823434740.USD","LU0053666078.USD","LU2023250504.SGD","LU0114720955.EUR","LU1974910355.USD","LU0109394709.USD","LU2362540622.SGD","BK4139","REGN","LU2468319806.SGD","LU1917777945.USD","LU2362541513.USD","LU0823416689.USD","LU0289739699.SGD","LU2362541273.HKD","LU2106854487.HKD","LU2237438978.USD","LU0882574055.USD","LU0058720904.USD","LU2089984988.USD","LU0823434583.USD","BK4588","BK4585","LU0889565916.HKD"],"isVideo":false,"video":null,"gpt_icon":0},{"id":"1148298032","title":"再生元制药公司计划今年晚些时候启动Olatorepatide全球三期注册项目","url":"https://stock-news.laohu8.com/highlight/detail?id=1148298032","media":"美股速递","labels":["productRelease"],"top":-1,"itemType":null,"share":"https://www.laohu8.com/m/news/1148298032?lang=zh_cn&edition=full","pubTime":"2026-03-09 19:02","pubTimestamp":1773054148,"startTime":"0","endTime":"0","summary":"再生元制药公司宣布，将于今年晚些时候正式启动其候选药物Olatorepatide的全球三期注册临床试验项目。这一关键性研究旨在评估该药物在目标适应症中的疗效与安全性，标志着Olatorepatide的研发进程迈入商业化前的最终阶段。","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":"productRelease","news_rank":0,"length":0,"strategy_id":0,"source":null,"symbols":["LU0823416689.USD","LU2237438978.USD","LU0053666078.USD","LU0882574055.USD","LU2468319806.SGD","LU2106854487.HKD","REGN","BK4139","LU2362541513.USD","LU0058720904.USD","LU0823434740.USD","BK4585","LU2362541273.HKD","LU1917777945.USD","LU2362540622.SGD","LU2089984988.USD","LU2023250504.SGD","BK4588","LU0823434583.USD","LU1974910355.USD","LU0109394709.USD","LU0114720955.EUR","LU0289739699.SGD","LU0320765992.SGD","LU0889565916.HKD"],"isVideo":false,"video":null,"gpt_icon":0},{"id":"1197814779","title":"再生元制药公司：Olatorepatide展现良好胃肠道耐受性，不良事件发生率更低","url":"https://stock-news.laohu8.com/highlight/detail?id=1197814779","media":"美股速递","labels":["dataReport"],"top":-1,"itemType":null,"share":"https://www.laohu8.com/m/news/1197814779?lang=zh_cn&edition=full","pubTime":"2026-03-09 19:01","pubTimestamp":1773054106,"startTime":"0","endTime":"0","summary":"再生元制药公司近日公布的研究数据显示，其研发的Olatorepatide在临床试验中表现出优异的胃肠道耐受特性，且不良事件发生率显著低于预期。\n该药物在安全性方面的积极结果为其后续开发奠定了良好基础，有望为相关疾病治疗提供新的选择。","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":"dataReport","news_rank":0,"length":0,"strategy_id":0,"source":null,"symbols":["LU1917777945.USD","LU2089984988.USD","LU0889565916.HKD","LU2237438978.USD","BK4588","LU2362540622.SGD","LU0114720955.EUR","LU0823434583.USD","LU0823434740.USD","LU2023250504.SGD","LU2362541513.USD","BK4585","LU2468319806.SGD","LU0053666078.USD","LU0058720904.USD","LU2106854487.HKD","LU0289739699.SGD","LU0823416689.USD","LU2362541273.HKD","LU1974910355.USD","LU0109394709.USD","REGN","LU0882574055.USD","LU0320765992.SGD","BK4139"],"isVideo":false,"video":null,"gpt_icon":0},{"id":"1194637037","title":"再生元高管预期将肥胖症药物定价合理贴近无降胆固醇功效疗法水平——TD 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Cowen会议上，再生元制药公司高管表示，公司计划将其肥胖症药物的定价设定在合理范围内，与那些不具备降低胆固醇功效的疗法保持相近水平。","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":["LU0823434583.USD","LU1917777945.USD","LU2089984988.USD","BK4588","LU2362540622.SGD","LU0114720955.EUR","LU2362541273.HKD","LU2468319806.SGD","LU0823416689.USD","BK4139","LU0289739699.SGD","LU0053666078.USD","LU0109394709.USD","REGN","LU2237438978.USD","LU0889565916.HKD","LU0320765992.SGD","LU0823434740.USD","LU1974910355.USD","LU2023250504.SGD","LU2362541513.USD","LU0058720904.USD","BK4585","LU0882574055.USD","LU2106854487.HKD"],"isVideo":false,"video":null,"gpt_icon":0},{"id":"1105620090","title":"再生元制药公司获CHMP建议：扩展Dupixent适用年龄至2-11岁中重度CSU患儿","url":"https://stock-news.laohu8.com/highlight/detail?id=1105620090","media":"美股速递","labels":[],"top":-1,"itemType":null,"share":"https://www.laohu8.com/m/news/1105620090?lang=zh_cn&edition=full","pubTime":"2026-02-27 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18:56","pubTimestamp":1772189798,"startTime":"0","endTime":"0","summary":"欧洲药品管理局人用医药产品委员会（CHMP）近日提出重要建议，支持将Dupixent（dupilumab）的治疗范围扩展至2至11岁儿童群体的慢性自发性荨麻疹。这一突破性进展意味着该药物有望为更广泛的患者提供新的治疗选择。","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":"productRelease","news_rank":0,"length":0,"strategy_id":0,"source":null,"symbols":["BK4588","LU0889565916.HKD","LU2106854487.HKD","LU2362541513.USD","LU2023250504.SGD","LU0823434583.USD","LU0058720904.USD","LU0109394709.USD","LU1974910355.USD","LU1917777945.USD","LU0882574055.USD","BK4585","BK4139","LU0114720955.EUR","LU2362541273.HKD","LU0320765992.SGD","LU0823416689.USD","REGN","LU0053666078.USD","LU2089984988.USD","LU0289739699.SGD","LU0823434740.USD","LU2362540622.SGD","LU2237438978.USD","LU2468319806.SGD"],"isVideo":false,"video":null,"gpt_icon":0},{"id":"1153462180","title":"赛诺菲新适应症获批 鼻科疾病版图再拓展：新增过敏性真菌性鼻窦炎 与伴鼻息肉慢性鼻窦炎形成互补","url":"https://stock-news.laohu8.com/highlight/detail?id=1153462180","media":"美股速递","labels":["productRelease"],"top":-1,"itemType":null,"share":"https://www.laohu8.com/m/news/1153462180?lang=zh_cn&edition=full","pubTime":"2026-02-24 22:35","pubTimestamp":1771943715,"startTime":"0","endTime":"0","summary":"赛诺菲宣布其鼻科疾病治疗领域迎来重要突破——新适应症获得监管批准，使得公司现有治疗范围扩展至过敏性真菌性鼻窦炎（AFRS）。此次获批标志着赛诺菲在鼻科疾病领域的治疗版图实现战略性延伸，与已获批的伴鼻息肉慢性鼻窦炎（CRSwNP）适应症形成协同效应。\n新适应症的纳入不仅丰富了赛诺菲在呼吸道疾病领域的管线布局，更凸显了公司针对复杂鼻科炎症疾病的综合解决方案能力。这一进展将有望为更广泛的患者群体提供新的治疗选择，进一步巩固企业在专科治疗领域的市场地位。","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":"productRelease","news_rank":0,"length":0,"strategy_id":0,"source":null,"symbols":["LU0823434740.USD","LU0823416689.USD","LU0114720955.EUR","LU2237438978.USD","LU2468319806.SGD","LU2023250504.SGD","LU0320765992.SGD","LU0889565916.HKD","LU2106854487.HKD","LU0289739699.SGD","LU2362540622.SGD","LU1974910355.USD","BK4139","BK4585","LU2362541513.USD","LU0058720904.USD","REGN","LU2089984988.USD","LU2362541273.HKD","LU0053666078.USD","LU0882574055.USD","BK4588","LU0109394709.USD","LU0823434583.USD","LU1917777945.USD"],"isVideo":false,"video":null,"gpt_icon":0},{"id":"1185973301","title":"再生元制药garetosmab生物制剂许可申请获FDA优先审评资格","url":"https://stock-news.laohu8.com/highlight/detail?id=1185973301","media":"投资观察","labels":["productRelease"],"top":-1,"itemType":null,"share":"https://www.laohu8.com/m/news/1185973301?lang=zh_cn&edition=full","pubTime":"2026-02-19 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用于治疗进行性骨化性纤维发育不良(FOP)","url":"https://stock-news.laohu8.com/highlight/detail?id=1139723161","media":"美股速递","labels":["productRelease"],"top":-1,"itemType":null,"share":"https://www.laohu8.com/m/news/1139723161?lang=zh_cn&edition=full","pubTime":"2026-02-19 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