欧盟批准皮下注射版Rybrevant®▼（Amivantamab）用于晚期EGFR突变非小细胞肺癌患者的每三周及每四周给药方案

美股速递02-24

欧盟委员会已正式批准强生公司旗下皮下注射制剂Rybrevant®▼（Amivantamab）用于治疗晚期EGFR突变非小细胞肺癌患者，新增每三周一次和每四周一次的给药方案。这一决定为患者提供了更为灵活的治疗选择，有望改善治疗便利性与生活质量。

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