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FDA Approves lew Treatment iegimenjor Multiple Sclerosis

机译:FDA批准治疗小儿多发性硬化症

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摘要

Millions of patients with relapsing forms of multiple sclerosis (MS) will not have to endure daily injections any longer, thanks to a new drug application approved by the FDA.The FDA gave the green light to a new treatment regimen that calls for a higher dose of copaxone (glatiramer acetate injection, Teva Pharmaceuticals) fewer times per week for patients with relapsing forms of MS.As a daily injectable at the 20 mg/mL dose, the drug has been a mainstay in MS treatment for nearly 2 decades and ranks as the most prescribed treatment for MS.
机译:由于FDA批准了新药的应用,数百万患有复发性多发性硬化症(MS)的患者将不再需要忍受每日注射.FDA批准了新的治疗方案,该方案要求更高的剂量复发型MS患者每周减少copaxone(醋酸格拉替雷注射液,Teva Pharmaceuticals)的治疗次数。作为每日注射剂量为20 mg / mL的药物,该药物在MS治疗中已占了近20年的主要时间,排名为最处方的MS治疗。

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