诺和诺德(NVO)

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Denmark's 'Novo Town' holds its breath as Wegovy fever fades
Reuters· 2025-09-25 06:09
In Denmark's seaside town of Kalundborg, also known as "Novo Town", therapist Heidi Thron Rune has learnt to live with the noise of building work as new facilities take shape to meet demand for Novo Nordisk's Wegovy weight-loss drug. ...
NOVO DEADLINE ALERT: Bragar Eagel & Squire, P.C. Reminds Investors a Class Action Lawsuit Has Been Filed Against Novo Nordisk A/S and Encourages Investors to Contact the Firm Before September 30th
Globenewswire· 2025-09-24 21:23
Bragar Eagel & Squire, P.C. Litigation Partner Brandon Walker Encourages Investors Who Suffered Losses In Novo (NVO) To Contact Him Directly To Discuss Their Options If you purchased or acquired securities in Novo between May 7, 2025, to July 28, 2025 and would like to discuss your legal rights, call Bragar Eagel & Squire partner Brandon Walker or Marion Passmore directly at (212) 355-4648. Click here to participate in the action. NEW YORK, Sept. 24, 2025 (GLOBE NEWSWIRE) -- What’s Happening: Bragar Eagel ...
Novo Nordisk A/S (NVO) Attracts Park Avenue Securities Investment
Yahoo Finance· 2025-09-24 20:37
Novo Nordisk A/S (NYSE:NVO) is among the best safe stocks to buy now. Park Avenue Securities LLC acquired a new stake in Novo Nordisk A/S (NYSE:NVO) through the purchase of 85,970 shares of the company’s stock during the second quarter. According to the recent filing with the SEC, the firm’s investment in the company amounts to $5,934,000. Despite downgrades in outlook discouraging investors from acquiring the stock, there’s much to like about Novo Nordisk A/S (NYSE:NVO). The company has shown encouraging ...
LLY vs. NVO: Which Obesity Drug Stock Is the Better Buy Now?
ZACKS· 2025-09-24 17:25
Key Takeaways Lilly's Mounjaro and Zepbound now drive about half of its total revenues.Novo Nordisk cut 2025 guidance as Wegovy and Ozempic face supply and pricing pressures.LLY forecasts $60B-$62B revenues in 2025, up over 30% year over year.Novo Nordisk (NVO) and Eli Lilly (LLY) dominate the diabetes and obesity market on the back of the tremendous success of their GLP-1 products. Lilly markets its dual GIP and GLP-1 receptor agonist, tirzepatide, as Mounjaro for type II diabetes and as Zepbound for obes ...
SHAREHOLDER ALERT: Faruqi & Faruqi, LLP Investigates Claims on Behalf of Investors of Novo Nordisk
Prnewswire· 2025-09-24 14:05
If you suffered losses exceeding $100,000 in Novo between May 7, 2025, to July 28, 2025and would like to discuss your legal rights, call Faruqi & Faruqi partner Josh Wilson directly at 877-247-4292 or 212-983- 9330Â (Ext. 1310). [You may also click here for additional information] NEW YORK, Sept. 24, 2025 /PRNewswire/ -- Faruqi & Faruqi, LLP, a leading national securities law firm, is investigating potential claims against Novo Nordisk A/S ("Novo" or the "Company") (NYSE: NVO) and reminds investors of the S ...
司美格鲁肽中国专利即将到期,诺和诺德加速推进口服减重药上市
第一财经· 2025-09-24 12:10
2025.09. 24 本文字数:1531,阅读时长大约3分钟 作者 | 第一财经 钱童心 2026年,丹麦制药巨头诺和诺德的明星减重药司美格鲁肽核心分子在中国的专利即将到期,届时, 该药物将面临大量来自中国仿制药的竞争。在这一背景下,诺和诺德正在积极推动口服版司美格鲁肽 减重药在全球的上市进程。 近日,诺和诺德在《新英格兰医学杂志》(NEJM)上发表一项最新三期临床数据,试验评估了在研 的每日一次口服司美格鲁肽片(25mg片剂)的有效性和安全性。结果显示,在服药64周时,口服司 美格鲁肽片25mg组患者实现了16.6%的平均体重降幅,患者中有1/3以上(34.4%)实现了20% 及以上的体重降幅,减重效果与司美格鲁肽注射液相当。 诺和诺德已于今年2月向美国FDA递交了每日一次司美格鲁肽25mg片剂的新药申请。该公司预计, FDA将于今年年底完成审批,届时该药物也有望成为全球首个获批上市的用于减重的GLP-1口服片 剂。诺和诺德还称,如获FDA批准,司美格鲁肽口服片剂将在美国境内制造。 口服司美格鲁肽上市将有助于诺和诺德占领口服减重药的市场先机。在全球市场上,该公司不仅面临 着主要竞争对手礼来的挑战,还有来自 ...
NEJM:口服版司美格鲁肽,减肥新选择
生物世界· 2025-09-24 08:30
撰文丨王聪 编辑丨王多鱼 排版丨水成文 在全世界范围内,肥胖率正不断上升,这会增加 2 型糖尿病和心血管疾病等多种疾病的风险。近几年,以 司美格鲁肽 为代表的 GLP-1 类减肥药正迅速流行起 来,彻底改变了肥胖治疗格局。 司美格鲁肽 是一种胰高血糖素样肽-1 (GLP-1) 受体激动剂,其注射制剂已获批用于 2 型糖尿病以及肥胖的治疗,此外,其口服制剂已获批用于 2 型糖尿病的 治疗。 之前的研究显示,口服版司美格鲁肽可减轻体重,在未患糖尿病的肥胖患者中,每天一次 50 毫克剂量的口服版司美格鲁肽可使体重减轻 15.1%,同时还 改善了多个心血管代谢风险。 2025 年 9 月 17 日,国际顶尖医学期刊《 新英格兰医学杂志 》 (NEJM) 发表了题为: Oral Semaglutide at a Dose of 25 mg in Adults with Overweight or Obesity 的临床研究论文。 这项为期 71 周的双盲、随机、安慰剂对照临床试验,评估了每天一次 25 毫克 剂量 的 口服版司美格鲁肽 作为生活方式干预辅助手段,对未患糖尿病的超重或 肥胖成年人体重减轻的疗效和安全性。 ...
司美格鲁肽中国专利即将到期,诺和诺德加速推进口服减重药上市
第一财经· 2025-09-24 08:05
诺和诺德口服司美格鲁肽进展 - 诺和诺德口服司美格鲁肽25mg片剂在64周临床试验中实现16.6%平均体重降幅 其中34.4%患者达到20%及以上体重降幅 [1] - 公司已于2024年2月向美国FDA提交新药申请 预计2024年底完成审批 可能成为全球首款GLP-1减重口服片剂 [1] - 如获批准 该药物将在美国境内制造 [1] 中国减重药市场竞争格局 - 诺和诺德司美格鲁肽中国专利将于2026年到期 届时将面临中国仿制药竞争 [1][3] - 石药集团和杭州九源基因等公司正在开发司美格鲁肽仿制药 [3] - 中国减重药市场价值预计将达到数十亿美元 [2] 信达生物玛仕度肽商业化进展 - 信达生物正大力推动GLP-1减重药玛仕度肽的商业化 [2] - 晨星预测玛仕度肽2024年销售额将超6亿元人民币(约8440万美元) 2029年达35亿元人民币峰值 占公司总收入的20% [2] - 公司积极拓展线上平台、零售药店、私立医院和诊所等销售渠道 [3] 跨国药企减重药布局 - 罗氏计划在2030年前推动多款减重药上市 预测三款产品年销售额超10亿美元 [2] - 诺和诺德面临礼来等主要竞争对手的挑战 [2] - 晨星预测诺和诺德司美格鲁肽2024年中国销售额约22亿丹麦克朗(约3.46亿美元) 2026年预计增长30% [3] 中国市场定价与销售情况 - 中国减重药目前为自费处方药 未纳入医保范围 [3] - 诺和诺德司美格鲁肽月治疗费用约400美元 礼来替尔泊肽约900美元 信达生物玛仕度肽月治疗费用2920元(约411美元) [3] - 处方量与药物上市时间相关 专家认为随着更多药物上市价格将下降 [3] 资本市场表现 - 信达生物股价自2024年初上涨约155% [2] - 诺和诺德股价同期下跌38% 礼来股价下跌近3% [2]
NVO DEADLINE: ROSEN, LEADING INVESTOR COUNSEL, Encourages Novo Nordisk A/S Investors to Secure Counsel Before Important September 30 Deadline in Securities Class Action - NVO
Globenewswire· 2025-09-23 17:57
NEW YORK, Sept. 23, 2025 (GLOBE NEWSWIRE) -- WHY: Rosen Law Firm, a global investor rights law firm, reminds purchasers of securities of Novo Nordisk A/S (NYSE: NVO) between May 7, 2025 and July 28, 2025, both dates inclusive (the “Class Period”), of the important September 30, 2025 lead plaintiff deadline. SO WHAT: If you purchased Novo Nordisk securities during the Class Period you may be entitled to compensation without payment of any out of pocket fees or costs through a contingency fee arrangement. WH ...
减重药对垒升级:辉瑞拟73亿美元收购一长效制剂 诺和诺德口服减重药平均减重16.6%
每日经济新闻· 2025-09-23 16:03
每经记者|陈星 每经编辑|张海妮 减重药物赛道的较量越来越激烈。 首先是在药物数据上"你来我往"——今年8月,礼来公布ATTAIN-1研究数据,在第72周,礼来在研口服 小分子GLP-1 RA(胰高血糖素样肽-1受体激动剂)药物Orforglipron最高剂量组平均减重12.4kg(降幅 12.4%)。 近期,诺和诺德方面公布了发表在《新英格兰医学杂志》上的口服司美格鲁肽片Ⅲ期试验OASIS 4的结 果。试验结果显示,在64周时,在所有患者依从治疗的情况下,口服司美格鲁肽片25mg组患者实现了 16.6%的平均体重降幅。 其次,MNC(跨国制药企业)也在不断"扫货"GLP-1,随着近日辉瑞宣布以73亿美元收购Metsera,这 一市场的BD(商务拓展)预期和商业化预期都正在被逐步透支。 礼来、诺和诺德"你来我往" 礼来、诺和诺德在GLP-1赛道的竞争愈演愈烈。 礼来公布Orforglipron的Ⅲ期临床研究"ACHIEVE-3"的顶线结果,该结果优于口服司美格鲁肽的结果 后,诺和诺德公布了Ⅲ期试验OASIS 4的结果。在此项为期64周的试验中,口服司美格鲁肽片25mg联合 生活方式干预,在307名肥胖或超重且 ...