ImmunityBio, Inc.宣布，其关键性随机BCG初治非肌层浸润性膀胱癌（NMIBC）试验已证实具备足够的统计学效力，能够检测出Anktiva®联合BCG治疗方案与单用BCG方案之间存在的临床意义差异。
该公司同时确认，针对该疗法的补充生物制剂许可申请（BLA）提交工作正按计划推进，目标在2026年完成。
ImmunityBio, Inc.宣布，其关键性随机BCG初治非肌层浸润性膀胱癌（NMIBC）试验已证实具备足够的统计学效力，能够检测出Anktiva®联合BCG治疗方案与单用BCG方案之间存在的临床意义差异。
该公司同时确认，针对该疗法的补充生物制剂许可申请（BLA）提交工作正按计划推进，目标在2026年完成。
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