美股详情

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诺和诺德

40.93

+0.12000.29%

盘后：40.930.00000.00%19:59 EDT

成交量：1,608.38万

成交额：6.56亿

市值：1,816.90亿

市盈率：11.30

高：41.41

开：41.26

低：40.23

收：40.81

52周最高：81.44

52周最低：35.12

股本：44.39亿

流通股本：31.88亿

量比：1.08

换手率：0.50%

股息：1.72

股息率：4.21%

每股收益(TTM):3.62

每股收益(LYR):3.62

净资产收益率：60.70%

总资产收益率：17.43%

市净率：6.36

市盈率(LYR):11.30

数据加载中...

总览公司新闻资讯公告

Hims & Hers Health盘后暴涨，诺和诺德计划在其平台上销售减肥药

老虎资讯综合

Hims & Hers Health盘后股价飙升39%，因报道称礼来与诺和诺德将合作销售减肥药

据彭博新闻社报导，诺和诺德与 Hims 解决纠纷，将共同销售肥胖症药物

Hims & Hers Health美股盘后涨近37%，报道称诺和诺德计划在Hims的平台上销售其减肥药

诺和诺德和HIMS将共同销售减肥药，结束双方的争端。

速递｜一针一周的组合拳：IcoSema在华获批，诺和诺德把胰岛素和GLP-1装进同一支笔

GLP1减重宝典

背景资料-顶级制药公司竞相推出减肥药

全球首个基础胰岛素/GLP-1RA周制剂在中国获批

诺和诺德“依柯胰岛素司美格鲁肽复方”在华获批上市

治疗MASH!“司美格鲁肽”第五项适应症在华申报上市

诺和诺德“司美格鲁肽”治疗MASH拟纳入优先审评，即将惠及国内广大MASH患者

礼来瞄准雇主GLP-1覆盖以与诺和诺德竞争

环球市场播报

正大天晴与赛诺菲达成超15亿独家授权；诺和诺德MASH新适应症拟纳入优先审评；全球首款宫颈癌前病变无创治疗药物获批上市

诺和诺德、武田、默克等齐换帅，中国市场进入战略新周期

大型研究显示，GLP-1 药物可防止出现新的或恶化的成瘾现象

诺和诺德股票3月4日盘中上涨3.81%：真相来了

TradingKey中文

诺和诺德MASH新药获优先审评，礼来IL-13单抗在华申报上市，德琪医药授权优时比

医药经济报

大摩下调诺和诺德目标价至40美元

速递｜FDA重拳出击，30家远程医疗公司因虚假宣传复合GLP-1产品遭警告

GLP1减重宝典

国内外药企共同发力，大批新药、新适应症同日获批 / 申报！

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16:56","pubTimestamp":1772787369,"startTime":"0","endTime":"0","summary":"界面新闻获悉，国家药品监督管理局（NMPA）正式批准了诺和杰®（依柯胰岛素司美格鲁肽注射液）在中国的上市申请，诺和杰®是全球首个且目前唯一获批的基础胰岛素/胰高糖素样肽-1受体激动剂（GLP-1RA）周制剂，由全球首个胰岛素周制剂依柯胰岛素和全球应用广泛的GLP-1RA周制剂司美格鲁肽组成，适用于接受基础胰岛素或GLP-1RA治疗后血糖控制不佳的成人2型糖尿病患者，在饮食和运动基础上联合口服降糖药物进行治疗。","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=nesSN20260306165609a6aa55d0&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, .recom-box, 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15:51","pubTimestamp":1772783477,"startTime":"0","endTime":"0","summary":"3月6日，国家药监局官网显示，诺和诺德的依柯胰岛素司美格鲁肽注射液获批上市，用于治疗2型糖尿病。依柯胰岛素司美格鲁肽注射液是诺和诺德开发的一款复方药物，内含依柯胰岛素和司美格鲁肽两种活性成分。依柯胰岛素是一款超长效胰岛素制剂，人体内半衰期长达196h，已于2024年6月获国家药监局批准上市。诺和诺德已在三项III期研究中验证了IcoSema的降糖效果，包括COMBINE 1、COMBINE 2、COMBINE 3。在COMBINE 1研究中，IcoSema取得了优效于依柯胰岛素的结果。","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=nesSN20260306160639a4533e4c&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, .recom-box, 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07:32","pubTimestamp":1772753532,"startTime":"0","endTime":"0","summary":"自2017年首次获批以来，司美格鲁肽的适应症版图持续扩张。3相关临床研究此次MASH适应症的申报，主要基于III期ESSENCE试验的部分结果。司美格鲁肽获FDA批准治疗MASH），使其成为全球首个获批治疗MASH的GLP-1疗法。然而，司美格鲁肽在中国市场正面临多重挑战。结 语司美格鲁肽MASH适应症在华申报上市，不仅是诺和诺德产品管线的重要拓展，更是中国MASH患者迎来首个有效治疗药物的关键一步。","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=nesSN20260306073939a4518115&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, .recom-box, 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07:28","pubTimestamp":1772753310,"startTime":"0","endTime":"0","summary":"2026年3 月 3 日，CDE 官网显示，诺和诺德“司美格鲁肽注射液”新适应症在国内申报上市，并拟纳入优先审评，适应症为：用于治疗代谢相关脂肪性肝炎伴中重度肝纤维化的非肝硬化成人患者。全球约有2.5亿MASH患者，其中超过三分之一的超重或肥胖人群同时患有MASH，疾病负担日益加重。司美格鲁肽治疗MASH的作用机制司美格鲁肽通过多重直接与间接途径改善MASH病理进程。","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=nesSN20260306074632a4518566&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, .recom-box, 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21:39","pubTimestamp":1772717940,"startTime":"0","endTime":"0","summary":"礼来公司推出“Employer Connect”，为新型多剂量Zepbound提供每月449美元的净价格，并与Teladoc Health和GoodRx等合作伙伴整合，以扩大肥胖药物的可及性；诺和诺德仍是主要竞争对手。\n\n\n海量资讯、精准解读，尽在新浪财经APP\n\n责任编辑：张俊 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15:02","pubTimestamp":1772607756,"startTime":"0","endTime":"0","summary":"整理 | GLP1减重宝典内容团队美国食品药品监督管理局于 3月3日 正式宣布，向30家远程医疗公司发出了警告信，指责这些公司在其官方网站上对复合GLP-1产品存在虚假或误导性宣传。违规行为包括声称复合制剂与FDA批准的原研药“相同”，以及以远程医疗公司名称或商标推广药品，暗示其为合规的配药商。据了解，在过去6个月内，FDA已经向数千家制药公司及远程医疗公司发出警告，要求撤除误导性广告。","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=nesSN20260304154137a44a31f1&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, .recom-box, 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14:33","pubTimestamp":1772606026,"startTime":"0","endTime":"0","summary":"2026年以来，国内已有多款1 类创新药、全球首创产品、新适应症获批上市，同时有多个重磅品种申报上市获受理，覆盖肿瘤、自身免疫、妇科、代谢等核心赛道。如在3月3日，诺和诺德、礼来、亚虹医药等多家药企就相继宣布新药/新适应症在国内申报上市，或获得了《药品注册证书》。截至目前，司美格鲁肽在中国已获批4项适应症。这是吡洛西利继联合氟维司群、单药治疗适应症获批后，在中国获批的第三个适应症。","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=nesSN20260304143745a449f534&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, .recom-box, 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