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Ionis因Angelman综合症药物获得FDA突破性治疗地位
2025-09-09 23:18
- Ionis Pharmaceuticals (NASDAQ:IONS) said on Tuesday that the U.S. FDA has granted breakthrough therapy status to its antisense medicine, ION582, for the treatment of angelman syndrome, a neurological disease.
- This designation is based on results from a trial of ION582 that showed consistent improvement on domains including communication, cognition and motor function, as well as favorable safety and tolerability.
- The breakthrough therapy designation from the FDA is intended to expedite the review of medicines that treat a serious or life-threatening condition.
- The stock is up about 3% today.
More on Ionis Pharmaceuticals
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- Ionis Pharmaceuticals, Inc. (IONS) Presents At Wells Fargo 20th Annual Healthcare Conference 2025 Transcript
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- Ionis upgraded at BMO Capital Markets after data for lipid-lowering agent
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