美股詳情

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AMPLIFY WEIGHT LOSS DRUG & TREATMENT ETF

25.37

-0.0975-0.38%

盤後：25.370.00000.00%16:10 EDT

成交量：860

成交額：2.18萬

市值：583.42萬

市盈率：- -

高：25.72

開：25.72

低：25.29

收：25.46

52周最高：27.94

52周最低：22.63

股本：23.00萬

流通股本：23.00萬

量比：1.35

換手率：0.37%

股息：0.41

股息率：1.63%

淨資產收益率：--

總資產收益率：--

市淨率：--

市盈率(LYR):- -

資料載入中...

總覽公司新聞資訊公告

禮來：Foundayo現已在英國上市，符合資格的成人可通過私人處方獲得

禮來公司在英國推出口服減肥藥Foundayo

市場消息： HIMS 的減重方案因信用卡糾紛遭到處罰。

Scholar Rock撤回了針對肌肉無力藥物的歐洲申報，計劃重新提交

Scholar Rock控股公司獲日本PMDA認可，無需補充臨床研究；計劃2026年底提交Apitegromab上市申請

Scholar Rock Holding公司撤回歐洲上市申請，計劃以替代灌裝生產線重新提交

Scholar Rock Holding Corp：蓄勢待發，靜候FDA批准，Apitegromab擬於2026年9月30日PDUFA日期登陸美國市場

巴克萊預計Hims銷售額將實現增長，但短期內面臨盈利壓力

禮來與Amplitude合作開發反式擴增RNA疫苗

Amplitude Therapeutics：禮來獲獨家靶向權利，推動合作靶點產品開發與商業化

Amplitude：首批項目聚焦高未滿足需求的傳染病領域，禮來保留至多兩個新增靶點選擇權

Amplitude Therapeutics攜手禮來，共研傳染病自擴增RNA疫苗

美股生物醫藥概念持續衝高，Moderna升逾130%，默沙東升逾11%

老虎资讯综合

禮來股價上漲5.3%，報1290美元/股，續刷記錄新高，總市值報1.21萬億美元。

美股深夜創新藥公司大漲，Moderna漲幅超100%，默沙東股價上漲10%，刷新歷史新高

諾和諾德啓動研究，旨在確定Wegovy口服藥的最低有效劑量

Novo啓動研究，旨在確定Wegovy口服藥的最低有效劑量

諾和諾德(NVO.US)啓動低劑量Wegovy口服藥臨床研究瞄準更廣泛減重人群

據媒體消息，諾和諾德(NVO.US)在一項新的肥胖症研究中，開始測試低劑量Wegovy口服藥片。

禮來(LLY)股票8月18日盤中上漲3.19%：釋放什麼信號？

TradingKey中文

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661249567","media":"路透中文","labels":["productRelease"],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2661249567?lang=zh_tw&edition=fundamental","pubTime":"2026-08-24 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Rock表示，公司已将其美国FDA申请中涉及的印第安纳州生产基地移除，并继续预期监管机构将在9月30日的目标行动日期前作出批准决定。","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:20260821:nL4T44I0W4:1","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":["THNR","BK4139","IBRN","SRRK"],"isVideo":false,"video":null,"gpt_icon":0},{"id":"1132368667","title":"Scholar Rock控股公司獲日本PMDA認可，無需補充臨床研究；計劃2026年底提交Apitegromab上市申請","url":"https://stock-news.laohu8.com/highlight/detail?id=1132368667","media":"美股速递","labels":["productRelease"],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/1132368667?lang=zh_tw&edition=fundamental","pubTime":"2026-08-21 21:12","pubTimestamp":1787317946,"startTime":"0","endTime":"0","summary":"Scholar Rock控股公司迎来重大利好——日本药品和医疗器械管理局（PMDA）已明确表态，认为无需再进行额外的临床研究。这一进展为该公司旗下在研药物Apitegromab的日本上市之路扫清了关键障碍。据此，Scholar Rock计划于2026年底前正式向PMDA提交该药物的上市许可申请（JNDA）。此举标志着公司在全球战略布局中迈出了坚实一步，尤其在亚太核心市场的推进节奏上，展现出明确的执行力与前瞻性。","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":"1","news_top_title":null,"news_tag":"productRelease","news_rank":0,"length":0,"strategy_id":0,"source":null,"symbols":["THNR","SRRK","IBRN","BK4139"],"isVideo":false,"video":null,"gpt_icon":0},{"id":"1162355391","title":"Scholar Rock 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Rock管理层在声明中表达了对项目前景的信心，并承诺将与欧洲监管机构保持密切沟通，以确保后续流程高效推进。","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":["SRRK","BK4139","IBRN","THNR"],"isVideo":false,"video":null,"gpt_icon":0},{"id":"1158808120","title":"Scholar Rock Holding Corp：蓄勢待發，靜候FDA批准，Apitegromab擬於2026年9月30日PDUFA日期登陸美國市場","url":"https://stock-news.laohu8.com/highlight/detail?id=1158808120","media":"美股速递","labels":["productRelease"],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/1158808120?lang=zh_tw&edition=fundamental","pubTime":"2026-08-21 21:10","pubTimestamp":1787317810,"startTime":"0","endTime":"0","summary":"Scholar Rock Holding Corp已经做好全面准备，一旦获得美国食品药品监督管理局的批准，其药物Apitegromab即刻启动在美国市场的上市进程。这一关键节点锁定在2026年9月30日的《处方药使用者付费法案》目标日期。公司上下正厉兵秣马，为这一刻的到来铺平道路。届时，Apitegromab将迅速投放市场，惠及广大患者。这一战略部署彰显了公司对产品获批的坚定信心，也体现了其对市场需求的敏锐把握。随着PDUFA日期的临近，一场精心筹备的市场登陆战即将拉开帷幕。","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":["SRRK","IBRN","BK4139","THNR"],"isVideo":false,"video":null,"gpt_icon":0},{"id":"2660287705","title":"巴克萊預計Hims銷售額將實現增長，但短期內面臨盈利壓力","url":"https://stock-news.laohu8.com/highlight/detail?id=2660287705","media":"路透中文","labels":[],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2660287705?lang=zh_tw&edition=fundamental","pubTime":"2026-08-20 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18:22","pubTimestamp":1787134924,"startTime":"0","endTime":"0","summary":"目前，Wegovy药片的批准长期剂量为25毫克。寻求减重之外的健康益处一些患者已经开始微量服用或使用低于批准剂量的GLP-1类药物，包括Wegovy和礼来公司的Zepbound注射剂。该研究将排除患有糖尿病或近期体重发生重大变化的患者，以及正在接受GLP-1类药物治疗的任何人。诺和诺德尚未明确说明此次测试的新剂量规格。Wegovy口服片剂已获批的剂量包括1.5毫克、4毫克和9毫克。","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:20260819:nL4T44G0SS:1","is_publish_highlight":false,"source_rank":0,"column":"","sentiment":"0","news_top_title":null,"news_tag":"productRelease","news_rank":0,"length":0,"strategy_id":0,"source":null,"symbols":["LLII","LLYZ","LU2491049909.HKD","SG9999001176.SGD","IE0005OL40V9.USD","ELIS","LU0786609619.USD","OZEM","LU0345770993.USD","LU2361044865.SGD","TRUH","LU0787776722.HKD","LU2237443549.SGD","THNR","MEDI","WDNA","AGNG","GDOC","LU1623119135.USD","LLY","IE0001KFT4U8.USD","IYH","PJP","LU1814569148.SGD","XLV","FTXH","CURE","IXJ","LU0820561909.HKD","ILDR","FHLC","HRTS","RXL","LU0114720955.EUR","CANC","PPH","LU1712237335.SGD","VHT","LU0320765059.SGD","LU1023059063.AUD","LU0266013472.USD","LLYX","MEDX","ELIL","TMED","LU1720051108.HKD","MHIP","IE00BFTCPJ56.SGD","IHE","JDOC"],"isVideo":false,"video":null,"gpt_icon":0},{"id":"2660120449","title":"Novo啓動研究，旨在確定Wegovy口服藥的最低有效劑量","url":"https://stock-news.laohu8.com/highlight/detail?id=2660120449","media":"路透中文","labels":["productRelease"],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2660120449?lang=zh_tw&edition=fundamental","pubTime":"2026-08-19 17:27","pubTimestamp":1787131647,"startTime":"0","endTime":"0","summary":"Novo启动研究，旨在确定Wegovy口服药的最低有效剂量路透伦敦8月19日-据美国政府临床试验数据库显示，丹麦制药公司诺和诺德NOVOb.CO正在一项新的晚期临床研究  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