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The company said Friday that its phase 3 clinical trial of aficamten in symptomatic non-obstructive hypertrophic cardiomyopathy met both primary endpoints.Hutchmed's  stock was up 1% after the company said a new drug application for fanregratinib to treat liver cancer has been granted conditional approval by China's National Medical Products Administration.Eli Lilly  stock was up 0.5% after the company said the US Food and Drug Administration approved Mounjaro to lower the risk of major adverse cardiovascular events in adults with type 2 diabetes who are at high risk for those 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Nordisk Share Price Already Reflects Plenty of Pessimism","url":"https://stock-news.laohu8.com/highlight/detail?id=2662006493","media":"Dow Jones","labels":[],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2662006493?lang=en_us&edition=fundamental","pubTime":"2026-08-28 18:39","pubTimestamp":1787913540,"startTime":"0","endTime":"0","summary":"1039 GMT - Novo Nordisk has faced immense pricing and competitive pressures, but the share price has baked in more than its fair share of pessimism, AlphaValue analyst Abhishek Raval writes. Oral weight-loss options are likely to be the key vehicles of market expansion, and the Danish drug maker still maintains a massive lead with its Wegovy pill versus Eli Lilly's Foundayo, he says. Novo Nordisk's CagriSema, a next generation obesity/diabetes injection, is expected to launch in 2027, and potential game changer Zenagamtide, an obesity/diabetes drug in both pill and injection form, could launch in 2029. These should fortify Novo Nordisk's already dominant position in the coming years, Raval says. AlphaValue retains its buy rating on the stock and lifts its target price to 466 Danish kroner from 458 kroner. 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Nike Cl B                    NKE    36,364,288     38.44    -0.15     -0.39","market":"other","thumbnail":null,"type":0,"news_type":0,"thumbnails":[],"rights":null,"property":[],"language":"en","translate_title":"","themeId":null,"theme_name":"","theme_type":"","isJumpTheme":false,"source_url":"https://dowjonesnews.com/newdjn/logon.aspx?AL=N","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":["FTXO","PFE","LU0170899867.USD","BK4533","FNCL","PATH","LU0320765489.SGD","LU2265009873.SGD","OZEM","LU0417517546.SGD","LU1989771016.USD","VFH","PATX","BK4543","TFNS","BK4599","UYG","LU0321505868.SGD","IE00BLSP4452.SGD","LU0683600562.USD","LU2129689605.HKD","BK4585","BAC","IE00B19Z3B42.SGD","XLF","BK4592","IE0034235188.USD","IE00B19Z3581.USD","LU0477156953.USD","LU0787776722.HKD","LU1074936037.SGD","BK4568","LU1069347547.HKD","LU0456855351.SGD","LU0234572021.USD","LU1496350171.SGD","KBWB","IYF","LU0053666078.USD","LU0130102774.USD","BK4504","LU0070302665.USD","LU0234570918.USD","BK4207","IYG","IE00B3T34201.USD","LU0320765646.SGD","SG9999003800.SGD","BK4561","LU1057294990.SGD"],"isVideo":false,"video":null,"gpt_icon":0},{"id":"2662035516","title":"FDA Approves Seasonal Covid-19 Vaccines from Moderna, Pfizer, BioNTech","url":"https://stock-news.laohu8.com/highlight/detail?id=2662035516","media":"Dow Jones","labels":["productRelease"],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2662035516?lang=en_us&edition=fundamental","pubTime":"2026-08-28 05:04","pubTimestamp":1787864640,"startTime":"0","endTime":"0","summary":"The Food and Drug Administration approved new seasonal Covid-19 vaccine formulas made by Moderna, Pfizer and BioNTech.The agency gave a green light to supplemental biologics license applications for the 2026-2027 formulas to the Comirnaty vaccine, made by Pfizer and BioNTech, and Moderna's mNexspike and Spikevax shots. The new formulas are designed to target the XFG variant of Covid-19.Pfizer and BioNTech said the new formulation of its vaccine would begin shipping immediately for use beginning in the fall. Moderna said its updated vaccines will be available in the coming days.All three vaccines were approved for adults 65 years of age and older. The FDA also approved the shots for individuals younger than 65 whose underlying conditions put them at high risk for severe outcomes from Covid-19. 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