Your browser doesn't support javascript.
loading
Stapokibart (CM310) targets IL-4Rα for the treatment of type 2 inflammation.
Liu, Wei; Zhao, Yan; He, Yanyun; Yan, Xinyu; Yu, Juntao; Song, Qin; Zhang, Libo; Dong, Bohan; Xu, Gang; Wang, Changyu; Zhang, Jianzhong; Chen, Bo.
Affiliation
  • Liu W; Research and Development Department, Keymed Biosciences (Chengdu) Limited, Chengdu 610000, China.
  • Zhao Y; Department of Dermatology, Peking University People's Hospital, Beijing 100044, China.
  • He Y; Research and Development Department, Keymed Biosciences (Chengdu) Limited, Chengdu 610000, China.
  • Yan X; Research and Development Department, Keymed Biosciences (Chengdu) Limited, Chengdu 610000, China.
  • Yu J; Research and Development Department, Keymed Biosciences (Chengdu) Limited, Chengdu 610000, China.
  • Song Q; Research and Development Department, Keymed Biosciences (Chengdu) Limited, Chengdu 610000, China.
  • Zhang L; Research and Development Department, Keymed Biosciences (Chengdu) Limited, Chengdu 610000, China.
  • Dong B; Tallulah Falls School, Georgia, GA 30573, USA.
  • Xu G; Research and Development Department, Keymed Biosciences (Chengdu) Limited, Chengdu 610000, China.
  • Wang C; Research and Development Department, Keymed Biosciences (Chengdu) Limited, Chengdu 610000, China.
  • Zhang J; Department of Dermatology, Peking University People's Hospital, Beijing 100044, China.
  • Chen B; Research and Development Department, Keymed Biosciences (Chengdu) Limited, Chengdu 610000, China.
iScience ; 27(9): 110721, 2024 Sep 20.
Article in En | MEDLINE | ID: mdl-39262798
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. 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.
Key words

Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: IScience Year: 2024 Document type: Article Affiliation country: China Country of publication: United States

Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: IScience Year: 2024 Document type: Article Affiliation country: China Country of publication: United States