Polaryx Therapeutics公司宣布，其研发的药物Plx-200已获得美国食品药品监督管理局（FDA）授予的快速通道资格，用于治疗晚婴期神经元蜡样脂褐质沉积症（CLN2病）。这一资格将加速该药物的研发和审评进程，为患者带来新的治疗希望。
Polaryx Therapeutics公司宣布，其研发的药物Plx-200已获得美国食品药品监督管理局（FDA）授予的快速通道资格，用于治疗晚婴期神经元蜡样脂褐质沉积症（CLN2病）。这一资格将加速该药物的研发和审评进程，为患者带来新的治疗希望。
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