万达生物制药（Vanda Pharmaceuticals）用于治疗泛发性脓疱型银屑病（GPP）的候选药物Imsidolimab的生物制品许可申请（BLA），目前正处于美国食品药品监督管理局（FDA）的审评流程中。FDA已为该申请设定了目标审评日期，定为2026年12月12日。
万达生物制药（Vanda Pharmaceuticals）用于治疗泛发性脓疱型银屑病（GPP）的候选药物Imsidolimab的生物制品许可申请（BLA），目前正处于美国食品药品监督管理局（FDA）的审评流程中。FDA已为该申请设定了目标审评日期，定为2026年12月12日。
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