12月8日（路透社） - BioNTech表示，*BIONTECH与ONCOC4宣布选择性Treg调节剂GOTISTOBART在既往治疗的鳞状非小细胞肺癌患者中显示出临床上有意义的总体生存益处*GOTISTOBART在降低死亡风险方面超过标准化疗超过一半*GOTISTOBART已获得美国食品药品监督管理局（“FDA”）的快速通道认证*在GOTISTOBART治疗组中，报告的≥3级治疗相关不良事件（“AE”）为19/45（42.2%），而多西他赛治疗组为20/41（48.8%）。
12月8日（路透社） - BioNTech表示，*BIONTECH与ONCOC4宣布选择性Treg调节剂GOTISTOBART在既往治疗的鳞状非小细胞肺癌患者中显示出临床上有意义的总体生存益处*GOTISTOBART在降低死亡风险方面超过标准化疗超过一半*GOTISTOBART已获得美国食品药品监督管理局（“FDA”）的快速通道认证*在GOTISTOBART治疗组中，报告的≥3级治疗相关不良事件（“AE”）为19/45（42.2%），而多西他赛治疗组为20/41（48.8%）。
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