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美股
詳情
本頁面由Tiger Trade Technology Pte. Ltd.提供服務
再生元製藥公司
746.00
-7.9300
-1.05%
盤後：
743.00
-3.0000
-0.40%
19:45 EDT
成交量：
50.54萬
成交額：
3.78億
市值：
788.67億
市盈率：
17.94
高：
756.00
開：
749.56
低：
742.69
收：
753.93
52周最高：
821.11
52周最低：
476.49
股本：
1.06億
流通股本：
1.03億
量比：
0.76
換手率：
0.49%
股息：
3.52
股息率：
0.47%
每股收益(TTM):
41.59
每股收益(LYR):
41.48
淨資產收益率：
14.87%
總資產收益率：
5.91%
市淨率：
2.52
市盈率(LYR):
17.98
資料載入中...
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葛兰素史克周二表示，美国卫生监管机构已批准葛兰素史克的GSK.L治疗严重哮喘的附加疗法，提供了一种用药频率较低的选择，但拒绝将其用于另一种疾病。FDA批准Exdensur作为12岁及以上重度嗜酸性粒细胞哮喘患者的附加维持治疗药物，使其成为首个获准一年两次给药的生物制剂。\"葛兰素史克公司发言人告诉路透：\"我们对Exdensur能为CRSwNP患者带来的益处仍充满信心，并将继续与FDA进行讨论。","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:20251217:nL4T3XN006:1","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":["GSK.UK","IE00BFTCPJ56.SGD","LU1261432733.SGD","LU1323610961.USD","LU1267930573.SGD","LU1880407132.USD","REGN","LU0052756011.USD","LU0211331839.USD","LU1267930490.SGD","LU0128525929.USD","IE0009355771.USD","LU1228905540.USD","LU1098665638.USD","LU2468319806.SGD","IE00BWDBJ516.SGD","LU1104425308.USD","LU0496365809.HKD","LU0109981661.USD","LU0310800379.SGD","LU1309081286.SGD","LU2362541273.HKD","03165","LU2242646821.SGD","BK4581","AMGN","LU1078025761.USD","LU2324357040.USD","LU2279689827.SGD","LU1035777561.USD","LU2023251221.USD","LU0976567544.SGD","LU1670756490.USD","LU0827474353.SGD","LU1880407215.USD","AZN.UK","BK4534","LU0047473722.EUR","LU0029864427.USD","LU1084165304.USD","LU0997586432.USD","LU1400636574.HKD","LU1015430645.USD","LU1400636657.SGD","LU1481600234.SGD","LU1119994496.HKD","LU0047473722.SGD","BK4139","IE00B2B36J28.USD","LU0499090636.EUR"],"isVideo":false,"video":null,"gpt_icon":0},{"id":"1164632612","title":"歐洲藥品管理局推薦擴展Arexvy、Aspaveli、Dovprela、Elucirem、Eylea、Nucala、Recarbrio、Simponi、Uplizna、Vueway的適應症","url":"https://stock-news.laohu8.com/highlight/detail?id=1164632612","media":"美股速递","labels":["policyRegulatory"],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/1164632612?lang=zh_tw&edition=fundamental","pubTime":"2025-12-12 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FDA 高層內部推動加快對禮來減肥藥的判決","url":"https://stock-news.laohu8.com/highlight/detail?id=2590508504","media":"路透中文","labels":["policyRegulatory"],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2590508504?lang=zh_tw&edition=fundamental","pubTime":"2025-12-12 19:00","pubTimestamp":1765537207,"startTime":"0","endTime":"0","summary":"独家-美国 FDA 高层内部推动加快对礼来减肥药的判决美国食品及药物管理局局长办公室表示希望将申报审查时间从 60 天缩短至一周该办公室表示，可能会根据复杂程度将审查时间缩短为两到三周如果采用新的时间表，该机构最早可能在 3 月 28 日对礼来的药片做出决定Patrick Wingrove/Dan Levine. 路透12月12日 - 路透看到的文件显示，在礼来公司要求加快时限之后，美国食品和药物管理局的领导在内部要求审查人员加快对礼来LLY.N试验性减肥药的评估。","market":"us","thumbnail":null,"type":0,"news_type":0,"thumbnails":[],"rights":null,"property":[],"language":"zh","translate_title":"","themeId":"88e4ec322662429deaabe33a5ac0ce39","theme_name":"","theme_type":"","isJumpTheme":false,"source_url":"https://api.refinitiv.com/data/news/v1/stories/urn:newsml:reuters.com:20251212:nL4S3XI0RH: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":["LLY","IE0004445015.USD","IE00BJJMRZ35.SGD","LU0882574055.USD","LU2746668974.SGD","LU1280957306.USD","LU1061106388.HKD","BK4533","LU0114720955.EUR","LU2360106947.USD","LU0672654240.SGD","LU0320765992.SGD","LU1551013342.USD","LU0053666078.USD","IE00BWXC8680.SGD","LU2237443382.USD","LU2602419157.SGD","LU0058720904.USD","LU2462157665.USD","LU2491050071.SGD","LU0266013472.USD","SG9999017495.SGD","LU0053671581.USD","LU1267930730.SGD","LU2063271972.USD","LU2552382058.USD","LU0787776722.HKD","LU2108987350.USD","LU0316494557.USD","IRON","SG9999013999.USD","LU1988902786.USD","LU1868837136.USD","LU0683600562.USD","LU1232071149.USD","LU1814569148.SGD","LU2491050154.USD","SGXZ81514606.USD","LU1323610961.USD","LU0820561818.USD","LU2324357040.USD","LU1093756325.SGD","LU0354030511.USD","LU1064131342.USD","REGN","LU0432979614.USD","LU2237443895.HKD","IE0004445239.USD","LU1551013425.SGD","SG9999001176.USD"],"isVideo":false,"video":null,"gpt_icon":1},{"id":"2590245510","title":"BUZZ-Biohaven 因癌症治療在早期試驗中顯示出前景而躍升","url":"https://stock-news.laohu8.com/highlight/detail?id=2590245510","media":"路透中文","labels":["dataReport"],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2590245510?lang=zh_tw&edition=fundamental","pubTime":"2025-12-12 00:31","pubTimestamp":1765470714,"startTime":"0","endTime":"0","summary":"BUZZ-Biohaven 因癌症治疗在早期试验中显示出前景而跃升12月11日 - ** 制药商Biohaven BHVN.N股价上涨8.5%至11.50美元 ** 该公司称，其试验性疗法BHV-1510与Regeneron Pharmaceuticals公司>的Libtayo联合使用，在一项早期试验中对多种肿瘤显示出疗效和可控的安全性。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:20251211:nL4S3XH18U:1","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","LU0823434740.USD","BK4585","LU2106854487.HKD","LU0289739699.SGD","LU0058720904.USD","BHVN","BK4588","LU2362541273.HKD","LU2468319806.SGD","REGN","LU1093756325.SGD","LU0109394709.USD","BK4139","LU0823434583.USD","LU2362541513.USD","LU1093756168.USD","LU0114720955.EUR","LU0823416689.USD","LU0889565916.HKD","LU0053666078.USD","LU0882574055.USD","LU1974910355.USD","LU0320765992.SGD","LU2023250504.SGD","LU2237438978.USD","LU2362540622.SGD","LU2089984988.USD"],"isVideo":false,"video":null,"gpt_icon":0},{"id":"2590765329","title":"健康巡講：Regeneron 藥物在小規模試驗中消滅殘留的多發性骨髓瘤細胞","url":"https://stock-news.laohu8.com/highlight/detail?id=2590765329","media":"路透中文","labels":["productRelease"],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2590765329?lang=zh_tw&edition=fundamental","pubTime":"2025-12-10 04:33","pubTimestamp":1765312390,"startTime":"0","endTime":"0","summary":"抗体可消除多发性骨髓瘤的踪迹一项小型中期试验的初步数据显示，Regeneron制药公司REGN.O最近批准的一种抗体药物能消除多发性骨髓瘤在最初治疗后的残留痕迹，从而有可能让患者避免艰苦的骨髓移植。相反，研究中的患者接受的是Regeneron公司的Lynozyfic，该药已于今年7月获得美国食品和药物管理局批准，用于治疗复发性多发性骨髓瘤。","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:20251209:nL4T3XF1OZ: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":["LU1003076772.USD","LU0109394709.USD","LU0640476718.USD","LU1481599808.USD","LU0471298777.SGD","IE00BK4W5M84.HKD","LU2237443895.HKD","LU0997586432.USD","LU1481600234.SGD","LU1104425308.USD","LU2362540622.SGD","LU1061106388.HKD","SGXZ51526630.SGD","IE0005OL40V9.USD","LU0963555726.SGD","LU2361044865.SGD","SGXZ99366536.SGD","LU0784384876.USD","IE00B1XK9C88.USD","IE00BJJMRZ35.SGD","LU1623119135.USD","LU0960981461.USD","LU1974910355.USD","LU2491049909.HKD","LU0122379950.USD","LU1989772840.SGD","LU1880407215.USD","LU0047473722.EUR","BK5011","LU1019634622.SGD","LU1267930573.SGD","LU0456855351.SGD","IE00B1BXHZ80.USD","LU0949170426.SGD","LU2265009873.SGD","LU0211326755.USD","LU2324357040.USD","LU1496350171.SGD","LU0432979614.USD","LU1301847155.USD","LU1496350502.SGD","LU0097036916.USD","BK4599","LU1015430645.USD","LU0689472784.USD","LU2108987350.USD","LU0708995401.HKD","LU0238689110.USD","LU0096364046.USD","LU0345777659.USD","LU0077335932.USD","LU0471298694.HKD","LU1280957306.USD","LU0784385840.USD","LU1323610961.USD","LU2552382132.HKD","LU0211326839.USD","LU0203347892.USD","LU0784385170.HKD","LU2168563687.JPY","LU1804176565.USD","LU1551013425.SGD","LU2091194634.USD","IE00B3T34201.USD","LU1023059063.AUD","IE00BFTCPJ56.SGD","IE00B7KXQ091.USD","LU2063271972.USD","LU0256863811.USD","LU0316494557.USD","LU2746668461.USD","BK4585","LU1868836591.USD","LU0029864427.USD","LU1267930813.SGD","IE00B775H168.HKD","SG9999013999.USD","LU0882574139.USD","LU0640478417.SGD","SG9999018857.SGD","LU1868837300.USD","IE00B4R5TH58.HKD","LU0158827948.USD","LU0708994859.HKD","LU0053666078.USD","LU0786609619.USD","LU0171293334.USD","LU1551013342.USD","LU2750360997.AUD","LU0957799991.USD","LU0320765992.SGD","LU1720051017.SGD","LU0211327993.USD","LU0972486137.USD","LU1868836757.USD","LU2089284900.SGD","LU2237443978.SGD","LU2539964713.USD","LU2023250504.SGD","LU2168564495.EUR","LU0672654240.SGD","LU1153584641.USD","LU1261432733.SGD","BK4588","IE00B4JS1V06.HKD","LU0011850046.USD","LU0047473722.SGD","LU1119994496.HKD","LU2361045086.USD","SG9999014906.USD","LU2089283258.USD","LU1093756168.USD","LU1814569148.SGD","BK4516","SGXZ31699556.SGD","LU1712237335.SGD","LU2362541513.USD","LU1064131342.USD","LU2456880835.USD","IE00BK4W5L77.USD","LU0058720904.USD","LU1983299246.USD","LU1989771016.USD","LU0784383803.USD","LU0499090636.EUR","LU0354030511.USD","LU0820561909.HKD","LU2293690082.USD","LU0079474960.USD","LU2237443549.SGD","LU0203345920.USD","LU1232071149.USD","LU1267930490.SGD","LU1548497426.USD","LU2491050071.SGD","LU2279689827.SGD","LU2471134523.USD","LU0234572021.USD","LU0823434740.USD","LU1988902786.USD","SG9999017495.SGD","LU2471134879.HKD","IE00BKPKM429.USD","LU0310799852.SGD","LU0385154629.USD","LU2602419157.SGD","LU1051770623.HKD","LU2471134952.CNY","LU0575583348.USD","REGN","LU1057294990.SGD","LU0823434583.USD","BK4534","LU1989772923.USD","SGXZ81514606.USD","LU2168564065.EUR","LU1868837136.USD","IE00BJT1NW94.SGD","LU0203202063.USD","LU0889566641.SGD","LU0964806797.USD","LU1267930227.SGD","IE00BJLML261.HKD","BK4007","LU2461242641.AUD","LU2112291526.USD","LU2491050154.USD","LU1487256676.USD","LU2362541273.HKD","SG9999015986.USD","SG9999015978.USD","IE00BWXC8680.SGD","BK4581","LU2087625088.SGD","LU2089984988.USD","LU2168564149.EUR","LU2236285917.USD","LU2361044949.HKD","LU0496365809.HKD","IE0009355771.USD","LU1868836914.USD","LU0661504455.SGD","SG9999001176.SGD","SG9999014914.USD","LU0820561818.USD","03165","LU1078025761.USD","IE00BKDWB100.SGD","LU0526926950.USD","LU0823399737.USD","LU0094547139.USD","LU0466842654.USD","LU0889565080.SGD","LU1064927863.SGD","BK4533","LU1127390331.HKD","LU0052756011.USD","LU1291159041.SGD","SG9999015952.SGD","SG9999018865.SGD","IE0034235188.USD","LU2168564222.USD","LU1003077747.HKD","SGXZ57979304.SGD","LU0128525929.USD","LU0792757196.USD","LU2211815571.USD","IE00BJJMRX11.SGD","LU0106261372.USD","IE00BFSS8Q28.SGD","LU0198837287.USD","LU2552382058.USD","LU1153585028.USD","LU0203201768.USD","SG9999015945.SGD","LU2106854487.HKD","LU2133065610.SGD","LU0211328371.USD","LU0969580561.USD","IE00BJJMRY28.SGD","LU0266013472.USD","LU2746668974.SGD","LU0943347566.SGD","SG9999001176.USD","LU1917777945.USD","SG9999014880.SGD","SG9999014898.SGD","LU2357305700.SGD","LU0757432116.USD","LU0882574055.USD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Therapeutix 因計劃快速向 FDA 申請眼疾藥物而上漲","url":"https://stock-news.laohu8.com/highlight/detail?id=2589330263","media":"路透中文","labels":["productRelease"],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2589330263?lang=zh_tw&edition=fundamental","pubTime":"2025-12-08 20:26","pubTimestamp":1765196776,"startTime":"0","endTime":"0","summary":"BUZZ-Ocular Therapeutix 因计划快速向 FDA 申请眼疾药物而上涨12月8日 - ** Ocular Therapeutix OCUL.O 的股票在盘前交易中上涨 13.5% 至 14.28 美元** OCUL 表示，公司计划在目前正在进行的晚期试验取得一年的数据后，为其治疗湿性年龄相关性黄斑变性的实验性眼病药物 Axpaxli 提交上市申请，预计时间为 2026 年第一季度。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:20251208:nL4T3XE0V6:1","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":["LU0823434583.USD","LU2362540622.SGD","LU0058720904.USD","LU2362541273.HKD","LU2468319806.SGD","LU0823434740.USD","LU1917777945.USD","LU2362541513.USD","BK4139","LU0114720955.EUR","OCUL","LU0109394709.USD","REGN","BK4007","LU0889565916.HKD","LU0823416689.USD","LU0320765992.SGD","LU1974910355.USD","LU0053666078.USD","LU2023250504.SGD","LU2089984988.USD","LU0882574055.USD","BK4588","LU2106854487.HKD","LU2237438978.USD","LU0289739699.SGD","BK4585"],"isVideo":false,"video":null,"gpt_icon":0},{"id":"1123079494","title":"Lynozyfic™（Linvoseltamab）單藥治療新診斷多發性骨髓瘤（Ndmm）顯著反應，支持作為一線治療潛在基礎的合理性","url":"https://stock-news.laohu8.com/highlight/detail?id=1123079494","media":"美股速递","labels":["productRelease"],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/1123079494?lang=zh_tw&edition=fundamental","pubTime":"2025-12-08 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的實驗性療法組合對未經治療的癌症患者有效","url":"https://stock-news.laohu8.com/highlight/detail?id=2589269868","media":"路透中文","labels":["productRelease"],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2589269868?lang=zh_tw&edition=fundamental","pubTime":"2025-12-06 22:30","pubTimestamp":1765031407,"startTime":"0","endTime":"0","summary":"Regeneron 的实验性疗法组合对未经治疗的癌症患者有效Sriparna Roy路透12月6日 - Regeneron公司REGN.O周六表示，其实验性癌症联合疗法是有效的，在一项晚期试验的第一部分显示，以前未接受过治疗的一种血癌患者的疾病消失了。该试验有22名患者参加，研究了该公司的疗法odronextamab与化疗联合治疗弥漫性大B细胞淋巴瘤患者的安全性和初步疗效。数据还表明，将奥德诺单抗与被称为CHOP的化疗方案联合使用时，无需使用利妥昔单抗就能获得深入而持久的反应。","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:20251206:nL4S3XC045:1","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":["LU0882574055.USD","LU0109394709.USD","REGN","BK4585","LU2468319806.SGD","LU2362540622.SGD","LU0823434583.USD","LU0823416689.USD","LU0289739699.SGD","LU0053666078.USD","LU2362541273.HKD","LU1974910355.USD","LU0320765992.SGD","LU2089984988.USD","BK4139","LU2023250504.SGD","LU0889565916.HKD","BK4588","LU2362541513.USD","LU0058720904.USD","LU0114720955.EUR","LU0823434740.USD","LU2106854487.HKD","LU2237438978.USD","LU1917777945.USD"],"isVideo":false,"video":null,"gpt_icon":0},{"id":"1185904287","title":"再生元製藥公司：公司將50:50共享全球開發費用和未來利潤","url":"https://stock-news.laohu8.com/highlight/detail?id=1185904287","media":"美股速递","labels":[],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/1185904287?lang=zh_tw&edition=fundamental","pubTime":"2025-12-01 20:01","pubTimestamp":1764590487,"startTime":"0","endTime":"0","summary":"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","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":["LU0053666078.USD","LU2362540622.SGD","REGN","LU2468319806.SGD","LU0109394709.USD","LU2362541273.HKD","BK4585","LU0058720904.USD","LU2089984988.USD","BK4588","LU0320765992.SGD","LU0289739699.SGD","LU0882574055.USD","LU0823434583.USD","LU0823416689.USD","LU2023250504.SGD","LU1974910355.USD","BK4139","LU0823434740.USD","LU2106854487.HKD","LU0889565916.HKD","LU1917777945.USD","LU2362541513.USD","LU2237438978.USD","LU0114720955.EUR"],"isVideo":false,"video":null,"gpt_icon":0},{"id":"1199264050","title":"再生元製藥公司與Tessera Therapeutics聯合開發針對α-1抗胰蛋白酶缺乏症的研究性基因編輯治療Tsra-196","url":"https://stock-news.laohu8.com/highlight/detail?id=1199264050","media":"美股速递","labels":["corporation"],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/1199264050?lang=zh_tw&edition=fundamental","pubTime":"2025-12-01 20:01","pubTimestamp":1764590470,"startTime":"0","endTime":"0","summary":"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。","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":["LU1917777945.USD","LU0823434740.USD","BK4585","LU2106854487.HKD","LU0289739699.SGD","LU0058720904.USD","BK4588","LU2362541273.HKD","LU2468319806.SGD","REGN","LU0109394709.USD","BK4139","LU0823434583.USD","LU2362541513.USD","LU0114720955.EUR","LU0823416689.USD","LU0889565916.HKD","LU0053666078.USD","LU0882574055.USD","LU1974910355.USD","LU0320765992.SGD","LU2023250504.SGD","LU2237438978.USD","LU2362540622.SGD","LU2089984988.USD"],"isVideo":false,"video":null,"gpt_icon":0},{"id":"2586442054","title":"滙豐：首予再生元製藥(REGN.US)「買入」評級 看好Eylea HD放量及腫瘤管線多點催化","url":"https://stock-news.laohu8.com/highlight/detail?id=2586442054","media":"智通财经","labels":["productRelease"],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2586442054?lang=zh_tw&edition=fundamental","pubTime":"2025-11-25 15:32","pubTimestamp":1764055926,"startTime":"0","endTime":"0","summary":"智通财经APP获悉，汇丰银行发表研报，首次覆盖再生元制药，并给予 “买入” 评级，目标价为890美元，核心依据包括其药物Eylea HD明年销售额的增长潜力，以及研发管线中多项癌症疗法的积极催化。分析师Yifeng Liu指出，尽管Eylea HD目前的市场渗透速度未达预期，但“与Eylea 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":["HSBC","REGN","HD","01477"],"isVideo":false,"video":null,"gpt_icon":0},{"id":"1159316672","title":"新聞稿：Dupixent，由賽諾菲和再生元製藥公司開發，成為十多年來歐盟首個針對特發性慢性蕁麻疹的靶向藥物","url":"https://stock-news.laohu8.com/highlight/detail?id=1159316672","media":"美股速递","labels":[],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/1159316672?lang=zh_tw&edition=fundamental","pubTime":"2025-11-25 14:00","pubTimestamp":1764050418,"startTime":"0","endTime":"0","summary":"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","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","BK4139","BK4585","LU2468319806.SGD","LU0823416689.USD","LU0053666078.USD","LU0058720904.USD","LU0823434740.USD","LU2237438978.USD","REGN","LU2023250504.SGD","LU2362540622.SGD","LU0320765992.SGD","LU0882574055.USD","LU2106854487.HKD","LU1974910355.USD","BK4588","LU2089984988.USD","LU0289739699.SGD","LU0109394709.USD","LU2362541513.USD","LU0889565916.HKD","LU1917777945.USD","LU2362541273.HKD","LU0114720955.EUR"],"isVideo":false,"video":null,"gpt_icon":0},{"id":"1145897938","title":"Dupixent®（Dupilumab）成為十多年來歐洲聯盟（EU）首個獲批的針對慢性自發性蕁麻疹（CSU）的靶向藥物","url":"https://stock-news.laohu8.com/highlight/detail?id=1145897938","media":"美股速递","labels":[],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/1145897938?lang=zh_tw&edition=fundamental","pubTime":"2025-11-25 14:00","pubTimestamp":1764050415,"startTime":"0","endTime":"0","summary":"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","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":["LU2468319806.SGD","LU2089984988.USD","LU2106854487.HKD","BK4585","LU0823434583.USD","LU0053666078.USD","LU0114720955.EUR","LU2237438978.USD","LU1917777945.USD","BK4588","LU0289739699.SGD","LU0889565916.HKD","LU0109394709.USD","LU2362541273.HKD","BK4139","LU2023250504.SGD","LU2362541513.USD","LU0823434740.USD","LU0058720904.USD","LU0320765992.SGD","LU0823416689.USD","LU0882574055.USD","LU2362540622.SGD","LU1974910355.USD","REGN"],"isVideo":false,"video":null,"gpt_icon":0},{"id":"1142970680","title":"一周美股牛榜 | 再生元上周飆升9%；谷歌和羅斯百貨揚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://ttm.financial/m/news/1142970680?lang=zh_tw&edition=fundamental","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"],"isVideo":false,"video":null,"gpt_icon":1},{"id":"2584979764","title":"BUZZ-Regeneron 因 FDA 擴大眼疾藥物批准範圍而獲益","url":"https://stock-news.laohu8.com/highlight/detail?id=2584979764","media":"路透中文","labels":[],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2584979764?lang=zh_tw&edition=fundamental","pubTime":"2025-11-20 06:20","pubTimestamp":1763590806,"startTime":"0","endTime":"0","summary":"11月19日 - ** RegeneronREGN.O股价盘后上涨5.30%至740美元** 美国食品和药物管理局批准其眼病药物Eylea的更高剂量版本，用于治疗视网膜静脉闭塞后黄斑水肿的患者，视网膜静脉闭塞是导致视力丧失的常见原因之一。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:20251119:nL4S3WV1WA:1","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":["BK4585","LU0882574055.USD","LU2381873111.SGD","IE00B3S45H60.SGD","LU0267386448.USD","LU0889565916.HKD","LU1551013342.USD","LU0320765646.SGD","LU1032466523.USD","LU2456880835.USD","LU0211331839.USD","IE0034235295.USD","IE0034235188.USD","LU2237443465.HKD","LU2592432038.USD","LU2237438978.USD","LU1668664300.SGD","LU2552382215.SGD","LU1988902786.USD","LU0215105999.USD","BK4550","IE00BKDWB100.SGD","LU1116320901.HKD","LU0820561818.USD","LU2023250843.SGD","IE00BJLML261.HKD","LU1145028129.USD","IE00BDCRKT87.USD","LU2505996509.AUD","LU2236285917.USD","LU2552382132.HKD","IE00BJTD4V19.USD","LU1914381329.SGD","LU0203345920.USD","LU0208291251.USD","LU0203347892.USD","LU1280957306.USD","IE00BJTD4N35.SGD","LU1894683264.USD","LU1496350171.SGD","LU1064131342.USD","LU2505996681.GBP","LU0942090050.USD","LU2552382058.USD","LU0345769128.USD","LU1496350502.SGD","REGN","IE00B1BXHZ80.USD","BK4588","LU1261432733.SGD"],"isVideo":false,"video":null,"gpt_icon":0},{"id":"1140117891","title":"再生元製藥公司 - 與Catalent Indiana協調解決2025年7月FDA一般現場檢查中發現的問題","url":"https://stock-news.laohu8.com/highlight/detail?id=1140117891","media":"美股速递","labels":["policyRegulatory"],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/1140117891?lang=zh_tw&edition=fundamental","pubTime":"2025-11-20 05:12","pubTimestamp":1763586732,"startTime":"0","endTime":"0","summary":"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","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":"policyRegulatory","news_rank":0,"length":0,"strategy_id":0,"source":null,"symbols":["REGN","LU0889565916.HKD","LU0823416689.USD","LU2106854487.HKD","LU0114720955.EUR","LU0882574055.USD","BK4588","LU2362541513.USD","LU0289739699.SGD","LU1917777945.USD","BK4585","LU0058720904.USD","LU2362540622.SGD","LU0823434583.USD","LU1974910355.USD","LU2362541273.HKD","LU0109394709.USD","LU2468319806.SGD","LU2089984988.USD","LU0823434740.USD","LU0320765992.SGD","LU2237438978.USD","LU0053666078.USD","LU2023250504.SGD","BK4139"],"isVideo":false,"video":null,"gpt_icon":0},{"id":"1132722384","title":"Eylea Hd® (Aflibercept) 注射劑 8 毫克通過 FDA 批准用於治療視網膜靜脈阻塞後的黃斑水腫，並可在批准適應症中進行每月給藥","url":"https://stock-news.laohu8.com/highlight/detail?id=1132722384","media":"美股速递","labels":["productRelease"],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/1132722384?lang=zh_tw&edition=fundamental","pubTime":"2025-11-20 05:11","pubTimestamp":1763586676,"startTime":"0","endTime":"0","summary":"Eylea Hd® (Aflibercept) 注射剂 8 毫克已获 FDA 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":["LU0109394709.USD","LU0823416689.USD","LU2089984988.USD","LU2362541513.USD","LU0889565916.HKD","LU2237438978.USD","LU2362541273.HKD","REGN","LU1917777945.USD","LU0058720904.USD","BK4585","LU2023250504.SGD","LU0320765992.SGD","LU0289739699.SGD","LU2106854487.HKD","BK4588","LU2468319806.SGD","BK4139","LU0882574055.USD","LU0114720955.EUR","LU2362540622.SGD","LU0823434740.USD","LU0823434583.USD","LU1974910355.USD","LU0053666078.USD"],"isVideo":false,"video":null,"gpt_icon":0},{"id":"1158394635","title":"再生元製藥公司杜比尤單抗關鍵試驗達成所有主要和次要終點，顯著減輕過敏性真菌性鼻竇炎症狀；sBLA獲得FDA優先審查","url":"https://stock-news.laohu8.com/highlight/detail?id=1158394635","media":"投资观察","labels":["policyRegulatory","dataReport"],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/1158394635?lang=zh_tw&edition=fundamental","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":["LU2023250504.SGD","LU2089984988.USD","LU0109394709.USD","LU0889565916.HKD","BK4588","LU1974910355.USD","LU0289739699.SGD","LU0823434740.USD","LU0823434583.USD","REGN","LU0114720955.EUR","BK4585","BK4139","LU0823416689.USD","LU2362540622.SGD","LU1917777945.USD","LU2106854487.HKD","LU2362541513.USD","LU2237438978.USD","LU2468319806.SGD","LU0882574055.USD","LU2362541273.HKD","LU0320765992.SGD","LU0053666078.USD","LU0058720904.USD"],"isVideo":false,"video":null,"gpt_icon":0}],"pageSize":20,"totalPage":5,"pageCount":4,"totalSize":96,"code":"91000000","status":"200"}]}}