美国FDA批准渤健高剂量Spinraza用于治疗脊髓性肌肉萎缩症

格隆汇03-31

美国食品药品监督管理局(FDA)周一批准了渤健脊髓性肌萎缩症(SMA)药物Spinraza的更高剂量版本。此次获批对于这家美国制药商而言无疑是一剂强心针，该公司正面临着来自罗氏的口服药物Evrysdi以及诺华的基因疗法Zolgensma和Itvisma的日益激烈的竞争。新的治疗方案将在未来几周内在美国上市。28毫克规格的Spinraza定价约为15.2万美元，与12毫克规格的定价相同，50毫克规格...

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