Kymera Therapeutics, Inc.（简称Kymera Therapeutics）宣布，其首创口服Stat6降解剂KT-621获得美国食品药品监督管理局（FDA）的快速通道资格，用于治疗中重度哮喘患者。这一重要进展有望加速该创新疗法的临床开发进程。
Kymera Therapeutics, Inc.（简称Kymera Therapeutics）宣布，其首创口服Stat6降解剂KT-621获得美国食品药品监督管理局（FDA）的快速通道资格，用于治疗中重度哮喘患者。这一重要进展有望加速该创新疗法的临床开发进程。
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