Plus Therapeutics公司近日公布，其已成功完成与美国食品药品监督管理局（FDA）举行的B类会议。此次会议的核心目标在于推动该公司旗下药物Reyobiq™用于治疗软脑膜转移瘤的加速审批流程。这一关键步骤标志着该疗法在监管路径上取得了重要进展。
Plus Therapeutics公司近日公布，其已成功完成与美国食品药品监督管理局（FDA）举行的B类会议。此次会议的核心目标在于推动该公司旗下药物Reyobiq™用于治疗软脑膜转移瘤的加速审批流程。这一关键步骤标志着该疗法在监管路径上取得了重要进展。
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