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Lilly's Olumiant Gets FDA Approval for Severe Alopecia Areata in Adolescents","url":"https://stock-news.laohu8.com/highlight/detail?id=2670287686","media":"MT Newswires Live","labels":["productRelease"],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2670287686?lang=en_us&edition=fundamental","pubTime":"2026-09-28 16:09","pubTimestamp":1790582940,"startTime":"0","endTime":"0","summary":"Eli Lilly  said Friday the US Food and Drug Administration approved its drug, Olumiant, for patients ages 12 and older with severe alopecia areata, expanding its US approval to adolescents.The approval was based on 36-week data from a Phase 3 trial. The company said the approval was based on a phase 3 trial that showed 42% of patients taking 4 mg and 27% taking 2 mg achieved at least 80% scalp hair coverage, compared with 5% on placebo.The drug carries an FDA boxed warning for serious infections, cancer, major cardiovascular events, blood clots, and death, Lilly 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Pharma ETF Huabao (562050) Rises Against the Market, Livzon Pharmaceutical Group Hits Limit Up! Medical Devices Show Localized Strength, Mindray and United Imaging Advance Together","url":"https://stock-news.laohu8.com/highlight/detail?id=1132272624","media":"Deep News","labels":["dataReport"],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/1132272624?lang=en_us&edition=fundamental","pubTime":"2026-09-28 13:22","pubTimestamp":1790572929,"startTime":"0","endTime":"0","summary":"On the first trading day after the Mid-Autumn Festival (September 28), A-shares underwent a deep correction, with the Shanghai Composite Index falling nearly 2% at one point. Pharmaceutical assets...","market":"hk","thumbnail":"","type":0,"news_type":0,"thumbnails":[],"rights":null,"property":[],"language":"en","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":"dataReport","news_rank":0,"length":0,"strategy_id":0,"source":null,"symbols":["GDOC","09996","BK1100","BK1574","LGHT","LNGR","BK1515","BK0188","BK1161","000513","AGNG","BK0187","HART","BK1583","BK0028","BK0239","562050","PTH","159883","159938","09939","IEIH","MEDX","RSPH","MDEV"],"isVideo":false,"video":null,"gpt_icon":0},{"id":"2670404993","title":"Nektar selloff on trial brings ‘strong entry point,’ says BTIG","url":"https://stock-news.laohu8.com/highlight/detail?id=2670404993","media":"TIPRANKS","labels":[],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2670404993?lang=en_us&edition=fundamental","pubTime":"2026-09-28 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Lilly Gets Expanded Label Approval from FDA for Alopecia Drug","url":"https://stock-news.laohu8.com/highlight/detail?id=2670442248","media":"Dow Jones","labels":["productRelease"],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2670442248?lang=en_us&edition=fundamental","pubTime":"2026-09-26 05:26","pubTimestamp":1790371560,"startTime":"0","endTime":"0","summary":"Eli Lilly received expanded label approval from the Food and Drug Administration for Olumiant, a drug for pediatric patients 12 years of age or older with severe alopecia areata.The company said Friday that the FDA had approved the expanded U.S. label for the drug, known generically as baricitinib, based on the results of a Phase 3 study. Olumiant was previously approved for adults with moderately to severely active rheumatoid arthritis and severe alopecia areata.\"The visible and often extensive hair loss that comes with severe alopecia areata can have a profound impact on anyone, especially adolescents who are at a pivotal stage of life,\" Lilly Immunology president Adrienne Brown said. \"Expanding Olumiant to patients as young as 12 provides them a much-needed treatment choice and reinforces our commitment to advancing care for people living with immune-mediated 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