万达生物制药公司宣布,美国食品药品监督管理局已正式受理其候选药物imsidolimab用于治疗泛发性脓疱型银屑病的生物制品许可申请。
FDA已为该申请设定了目标审评日期为2026年12月12日。
万达生物制药公司宣布,美国食品药品监督管理局已正式受理其候选药物imsidolimab用于治疗泛发性脓疱型银屑病的生物制品许可申请。
FDA已为该申请设定了目标审评日期为2026年12月12日。
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