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　　康方生物-B（09926-HK）公布，公司核心自主研发的新药PD-1/VEGF双特异性抗体（研发代号：AK112）Ia期临床研究阶段性数据已在2020中国肿瘤免疫治疗会议上发布。

　　目前AK112已经在澳洲和中国开展Ia期临床研究，最初剂量递增阶段的临床研究结果令人鼓舞。本研究的结果显示，在有至少经历过一次肿瘤评估并对PD-1抑制剂不敏感或接受过PD-1抑制剂治疗的11例晚期实体瘤患者中，共有4例达到了缓解（客观缓解率（ORR）：36 %），共7例肿瘤缩小且疾病稳定（疾病控制率（DCR）：64%）。

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