iScience (Sep 2024)

Stapokibart (CM310) targets IL-4Rα for the treatment of type 2 inflammation

  • Wei Liu,
  • Yan Zhao,
  • Yanyun He,
  • Xinyu Yan,
  • Juntao Yu,
  • Qin Song,
  • Libo Zhang,
  • Bohan Dong,
  • Gang Xu,
  • Changyu Wang,
  • Jianzhong Zhang,
  • Bo Chen

Journal volume & issue
Vol. 27, no. 9
p. 110721

Abstract

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Summary: Stapokibart (CM310) is a humanized IL-4Rα monoclonal antibody currently undergoing phase 3 trials for type 2 inflammatory diseases. In contrast to dupilumab, which bound exclusively to human IL-4Rα, stapokibart demonstrated cross-species reactivity to IL-4Rα from human, cynomolgus monkey, and rat. Stapokibart exhibited comparable blocking activity to dupilumab. Epitope mapping revealed that stapokibart bound to distinct sites on IL-4Rα compared to dupilumab. In vitro assays showed that stapokibart was comparable or numerically superior in blocking IL-4Rα-mediated signaling compared to dupilumab. In vivo studies further demonstrated that stapokibart effectively inhibited the progression of type 2 inflammation. Pharmacokinetic studies revealed a circulating half-life of approximately 298–351 h in cynomolgus monkeys and 55–142 h in rats for stapokibart. Toxicity studies indicated a favorable safety profile in cynomolgus monkeys and rats. The preclinical evaluation of stapokibart supports its clinical development.

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