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

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. <i>In vitro</i> assays showed that stapokibart was comparable or numerically superior in blocking IL-4Rα-mediated signaling compared to dupilumab. <i>In vivo</i> 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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Publication Details

Journal
iScience
Published
2024-08-13
DOI
https://doi.org/10.1016/j.isci.2024.110721
Citations
25
Primary Topic
Asthma and respiratory diseases
Type
article
Field-Weighted Citation Impact
8.16
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article

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

Bohan Dong, Changyu Wang, Gang Xu, Yanyun He et al.
25 citations
iScience
Asthma and respiratory diseases
8.16
article

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

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

Abstract

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. <i>In vitro</i> assays showed that stapokibart was comparable or numerically superior in blocking IL-4Rα-mediated signaling compared to dupilumab. <i>In vivo</i> 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.

iScienceVol. 27(9)
Peking University (CN), Bioscience (China) (CN), Peking University People's Hospital (CN)
Good health and well-being
Openalex Percentile: Top 2%
Asthma and respiratory diseases
8.16
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Stapokibart (CM310) targets IL-4Rα for the treatment of type 2 inflammation — Bohan Dong, Changyu Wang, et al. · iScience (2024) | TGRS Research Map | TGRS