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REGN 再生元制药公司
交易中 01-09 14:58:49 EST
793.90
-7.11
-0.89%
最高
821.11
最低
790.93
成交量
46.48万
今开
802.97
昨收
801.01
日振幅
3.77%
总市值
834.38亿
流通市值
820.12亿
总股本
1.05亿
成交额
3.74亿
换手率
0.45%
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
--
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
再生元制药公司获美银全球研究上调评级至“买入” 盘前股价应声上涨2.3%
美股速递 · 01-07 19:37
再生元制药公司获美银全球研究上调评级至“买入” 盘前股价应声上涨2.3%
美银全球研究上调再生元制药评级至买入 目标价跃升至860美元
美股速递 · 01-07 19:27
美银全球研究上调再生元制药评级至买入 目标价跃升至860美元
新闻发布：赛诺菲与再生元制药公司的Dupixent在日本获得批准，用于6至11岁支气管哮喘儿童的治疗
美股速递 · 2025-12-23
新闻发布：赛诺菲与再生元制药公司的Dupixent在日本获得批准，用于6至11岁支气管哮喘儿童的治疗
默沙东(MRK.US)、施贵宝(BMY.US)等多家药企同意下调美国药价 以换取特朗普政府关税豁免和政策支持
智通财经 · 2025-12-20
默沙东(MRK.US)、施贵宝(BMY.US)等多家药企同意下调美国药价 以换取特朗普政府关税豁免和政策支持
欧洲药品管理局推荐扩展Arexvy、Aspaveli、Dovprela、Elucirem、Eylea、Nucala、Recarbrio、Simponi、Uplizna、Vueway的适应症
美股速递 · 2025-12-12
欧洲药品管理局推荐扩展Arexvy、Aspaveli、Dovprela、Elucirem、Eylea、Nucala、Recarbrio、Simponi、Uplizna、Vueway的适应症
独家：美国FDA促请审评员加快对礼来减肥药的评估 - 内部文件
美股速递 · 2025-12-12
独家：美国FDA促请审评员加快对礼来减肥药的评估 - 内部文件
Lynozyfic™（Linvoseltamab）单药治疗新诊断多发性骨髓瘤（Ndmm）显著反应，支持作为一线治疗潜在基础的合理性
美股速递 · 2025-12-08
Lynozyfic™（Linvoseltamab）单药治疗新诊断多发性骨髓瘤（Ndmm）显著反应，支持作为一线治疗潜在基础的合理性
再生元制药公司：公司将50:50共享全球开发费用和未来利润
美股速递 · 2025-12-01
再生元制药公司：公司将50:50共享全球开发费用和未来利润
再生元制药公司与Tessera Therapeutics联合开发针对α-1抗胰蛋白酶缺乏症的研究性基因编辑治疗Tsra-196
美股速递 · 2025-12-01
再生元制药公司与Tessera Therapeutics联合开发针对α-1抗胰蛋白酶缺乏症的研究性基因编辑治疗Tsra-196
汇丰：首予再生元制药(REGN.US)“买入”评级 看好Eylea HD放量及肿瘤管线多点催化
智通财经 · 2025-11-25
汇丰：首予再生元制药(REGN.US)“买入”评级 看好Eylea HD放量及肿瘤管线多点催化
新闻稿：Dupixent，由赛诺菲和再生元制药公司开发，成为十多年来欧盟首个针对特发性慢性荨麻疹的靶向药物
美股速递 · 2025-11-25
新闻稿：Dupixent，由赛诺菲和再生元制药公司开发，成为十多年来欧盟首个针对特发性慢性荨麻疹的靶向药物
Dupixent®（Dupilumab）成为十多年来欧洲联盟（EU）首个获批的针对慢性自发性荨麻疹（CSU）的靶向药物
美股速递 · 2025-11-25
Dupixent®（Dupilumab）成为十多年来欧洲联盟（EU）首个获批的针对慢性自发性荨麻疹（CSU）的靶向药物
一周美股牛榜 | 再生元上周飙升9%；谷歌和罗斯百货扬8%；美敦力升6%
老虎资讯综合 · 2025-11-24
一周美股牛榜 | 再生元上周飙升9%；谷歌和罗斯百货扬8%；美敦力升6%
再生元制药公司 - 与Catalent Indiana协调解决2025年7月FDA一般现场检查中发现的问题
美股速递 · 2025-11-20
再生元制药公司 - 与Catalent Indiana协调解决2025年7月FDA一般现场检查中发现的问题
Eylea Hd® (Aflibercept) 注射剂 8 毫克通过 FDA 批准用于治疗视网膜静脉阻塞后的黄斑水肿，并可在批准适应症中进行每月给药
美股速递 · 2025-11-20
Eylea Hd® (Aflibercept) 注射剂 8 毫克通过 FDA 批准用于治疗视网膜静脉阻塞后的黄斑水肿，并可在批准适应症中进行每月给药
再生元制药公司杜比尤单抗关键试验达成所有主要和次要终点，显著减轻过敏性真菌性鼻窦炎症状；sBLA获得FDA优先审查
投资观察 · 2025-11-20
再生元制药公司杜比尤单抗关键试验达成所有主要和次要终点，显著减轻过敏性真菌性鼻窦炎症状；sBLA获得FDA优先审查
再生元制药公司Libtayo®（Cemiplimab）在欧盟获得批准，成为首个也是唯一用于高复发风险的皮肤鳞状细胞癌术后及放疗辅助治疗的免疫疗法
美股速递 · 2025-11-19
再生元制药公司Libtayo®（Cemiplimab）在欧盟获得批准，成为首个也是唯一用于高复发风险的皮肤鳞状细胞癌术后及放疗辅助治疗的免疫疗法
赛诺菲与再生元的Dupixent达成关键终点，获FDA优先审查接受
投资观察 · 2025-11-07
赛诺菲与再生元的Dupixent达成关键终点，获FDA优先审查接受
新闻稿：Acaai：由Sanofi和再生元制药公司进行的Dupixent关键研究达成主要和次要评估标准，减轻过敏性真菌性鼻窦炎的症状
美股速递 · 2025-11-07
新闻稿：Acaai：由Sanofi和再生元制药公司进行的Dupixent关键研究达成主要和次要评估标准，减轻过敏性真菌性鼻窦炎的症状
再生元制药公司：Dupixent Sbla获得美国FDA优先审查，目标行动日期为2026年2月28日
美股速递 · 2025-11-07
再生元制药公司：Dupixent Sbla获得美国FDA优先审查，目标行动日期为2026年2月28日
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公司概况
公司名称：
再生元制药公司
所属市场：
NASDAQ
上市日期：
--
主营业务：
再生元制药公司于1988年在纽约州成立。再生元制药公司是一家完全集成的生物技术公司，它发现、发明、开发、制造和商业化治疗严重疾病的药物。其正在开发的商业化药物和候选产品旨在帮助患有眼疾、过敏性和炎症性疾病、癌症、心血管和代谢性疾病、疼痛、传染病和罕见疾病的患者。它的核心业务战略是在基础科学研究和发现启用技术方面保持坚实的基础，并建立在临床开发、制造和商业能力的基础上。其目标是继续成为一家综合性、多产品的生物技术公司，为患者和医疗专业人员提供预防和治疗人类疾病的重要选择。
发行价格：
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HD相关的监管风险有望在短期内得到解决，这将为2026年药物加速普及和渗透率提升奠定基础”。此外，该联合疗法用于黑色素瘤辅助治疗的III期临床数据可能于明年公布。","market":"us","thumbnail":null,"type":0,"news_type":0,"thumbnails":[],"rights":null,"property":["rate"],"language":"zh","translate_title":"","themeId":null,"theme_name":"","theme_type":"","isJumpTheme":false,"source_url":"http://www.zhitongcaijing.com/content/detail/1373216.html","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":"stock_zhitongcaijing","symbols":["REGN","01477","HSBC","HD"],"gpt_icon":0},{"id":"1159316672","title":"新闻稿：Dupixent，由赛诺菲和再生元制药公司开发，成为十多年来欧盟首个针对特发性慢性荨麻疹的靶向药物","url":"https://stock-news.laohu8.com/highlight/detail?id=1159316672","media":"美股速递","labels":[],"top":-1,"itemType":null,"share":"https://www.laohu8.com/m/news/1159316672?lang=zh_cn&edition=full","pubTime":"2025-11-25 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| 再生元上周飙升9%；谷歌和罗斯百货扬8%；美敦力升6%","url":"https://stock-news.laohu8.com/highlight/detail?id=1142970680","media":"老虎资讯综合","labels":[],"top":-1,"itemType":null,"share":"https://www.laohu8.com/m/news/1142970680?lang=zh_cn&edition=full","pubTime":"2025-11-24 10:17","pubTimestamp":1763950659,"startTime":"0","endTime":"0","summary":"Solventum董事会已批准一项 股票回购计划，授权公司回购 最多10亿美元 的普通股。Solventum股价上周上涨 9.6%。谷歌A上周五收涨 3.5%，市值达到 3.62万亿美元，上周股价大涨 8.4%。公司第三季度销售也超出预期，上周股价上涨 8.4%。美敦力上调全年销售增长预期，因心脏设备需求强劲 $美敦力$ 第二财季业绩超出预期，并在上周二上调全年销售增长预期，因心脏设备需求旺盛，股价上周上涨 5.6%。","market":"us","thumbnail":"https://community-static.tradeup.com/news/226b03648204ea05089b5982a628b9f4","type":0,"news_type":0,"thumbnails":["https://community-static.tradeup.com/news/226b03648204ea05089b5982a628b9f4"],"rights":null,"property":[],"language":"zh","translate_title":"","themeId":"","theme_name":"","theme_type":"","isJumpTheme":false,"source_url":"","is_publish_highlight":true,"source_rank":0,"column":"","sentiment":"1","news_top_title":null,"news_tag":"","news_rank":0,"length":0,"strategy_id":0,"source":null,"symbols":["MDT","GOOGL","ROST","REGN"],"gpt_icon":1},{"id":"1140117891","title":"再生元制药公司 - 与Catalent Indiana协调解决2025年7月FDA一般现场检查中发现的问题","url":"https://stock-news.laohu8.com/highlight/detail?id=1140117891","media":"美股速递","labels":["policyRegulatory"],"top":-1,"itemType":null,"share":"https://www.laohu8.com/m/news/1140117891?lang=zh_cn&edition=full","pubTime":"2025-11-20 05:12","pubTimestamp":1763586732,"startTime":"0","endTime":"0","summary":"再生元制药公司 - 与Catalent 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批准，用于治疗视网膜静脉阻塞（Rvo）导致的黄斑水肿，并可在所有批准的适应症中进行每月给药。","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":["LU2468319806.SGD","LU2362541273.HKD","LU0320765992.SGD","LU0109394709.USD","LU2362540622.SGD","LU2237438978.USD","LU0889565916.HKD","BK4588","LU1974910355.USD","LU0053666078.USD","BK4139","REGN","LU0289739699.SGD","LU0114720955.EUR","LU0058720904.USD","LU0823434583.USD","LU1917777945.USD","LU0823434740.USD","LU0882574055.USD","LU2362541513.USD","BK4585","LU2106854487.HKD","LU2089984988.USD","LU2023250504.SGD","LU0823416689.USD"],"gpt_icon":0},{"id":"1158394635","title":"再生元制药公司杜比尤单抗关键试验达成所有主要和次要终点，显著减轻过敏性真菌性鼻窦炎症状；sBLA获得FDA优先审查","url":"https://stock-news.laohu8.com/highlight/detail?id=1158394635","media":"投资观察","labels":["policyRegulatory","dataReport"],"top":-1,"itemType":null,"share":"https://www.laohu8.com/m/news/1158394635?lang=zh_cn&edition=full","pubTime":"2025-11-20 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再生元制药公司宣布：*杜比尤单抗（DUPIXENT®）关键试验达成所有主要和次要终点，显著减轻过敏性真菌性鼻窦炎（AFRS）的体征和症状；sBLA获得FDA优先审查*再生元制药公司：杜比尤单抗的sBLA已被美国FDA接受优先审查，目标行动日期为2026年2月28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":"2","news_top_title":null,"news_tag":"policyRegulatory,dataReport","news_rank":0,"length":0,"strategy_id":0,"source":null,"symbols":["LU2362541273.HKD","LU0289739699.SGD","LU2362541513.USD","LU2106854487.HKD","BK4585","BK4588","LU0889565916.HKD","LU0823434740.USD","LU0114720955.EUR","LU2362540622.SGD","LU0823416689.USD","LU0882574055.USD","LU0058720904.USD","BK4139","LU1974910355.USD","LU0053666078.USD","LU1917777945.USD","LU2089984988.USD","LU0320765992.SGD","REGN","LU2468319806.SGD","LU0109394709.USD","LU0823434583.USD","LU2237438978.USD","LU2023250504.SGD"],"gpt_icon":0},{"id":"1196287619","title":"再生元制药公司Libtayo®（Cemiplimab）在欧盟获得批准，成为首个也是唯一用于高复发风险的皮肤鳞状细胞癌术后及放疗辅助治疗的免疫疗法","url":"https://stock-news.laohu8.com/highlight/detail?id=1196287619","media":"美股速递","labels":[],"top":-1,"itemType":null,"share":"https://www.laohu8.com/m/news/1196287619?lang=zh_cn&edition=full","pubTime":"2025-11-19 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赛诺菲公司：赛诺菲与再生元的Dupixent关键研究满足所有主要和次要终点，减少了过敏性真菌性鼻窦炎的症状和体征；申请已被FDA接受为优先审查。三期研究数据显示，Dupixent减少了鼻部症状和体征。该药物已获得美国FDA的优先审查，目标决定日期为2026年2月28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":"productRelease,policyRegulatory","news_rank":0,"length":0,"strategy_id":0,"source":null,"symbols":["LU0889565916.HKD","LU2089984988.USD","LU2362541513.USD","LU2106854487.HKD","LU0823434740.USD","REGN","LU0823416689.USD","LU2362541273.HKD","BK4585","LU0109394709.USD","LU0823434583.USD","LU0053666078.USD","BK4588","LU2468319806.SGD","LU2023250504.SGD","LU0289739699.SGD","LU2237438978.USD","LU0058720904.USD","LU0320765992.SGD","LU0114720955.EUR","LU1917777945.USD","LU0882574055.USD","LU1974910355.USD","LU2362540622.SGD","BK4139"],"gpt_icon":0},{"id":"1124155673","title":"新闻稿：Acaai：由Sanofi和再生元制药公司进行的Dupixent关键研究达成主要和次要评估标准，减轻过敏性真菌性鼻窦炎的症状","url":"https://stock-news.laohu8.com/highlight/detail?id=1124155673","media":"美股速递","labels":["productRelease"],"top":-1,"itemType":null,"share":"https://www.laohu8.com/m/news/1124155673?lang=zh_cn&edition=full","pubTime":"2025-11-07 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