新桥生物今日公布了其Givastomig联合疗法在IB期临床试验剂量扩展阶段的最新数据，该研究针对一线治疗转移性胃癌患者。
数据显示，在剂量扩展队列中，Givastomig展现出令人鼓舞的临床活性与可控的安全性特征。这一积极进展为后续临床开发提供了重要依据。
研究采用阶梯式剂量递增方案，逐步探索Givastomig与标准化疗联合使用的最佳治疗窗口。最新分析结果证实了该疗法在肿瘤缩小率和疾病控制率方面的潜在优势。
目前，研究团队正进一步分析生物标志物数据，以识别最可能从该疗法中获益的患者群体。这些发现将为即将开展的注册性临床研究奠定坚实基础。
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