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DOI 10.1038/s41467-025-63682-x

Медицинская библиотека · Nature communications · 2025

An anti-TSLP monoclonal antibody for uncontrolled CRSwNP: the DUBHE randomized clinical trial.

Xian Mu, Lan Feng, Yan Bing, Shen Shen, Liu Shixi, Wan Lijia, Song Xicheng, Jiang Luyun, Jiang Yan, Xue Jinmei, Chen Jianjun, Su Lizhong, Ye Jing, Yang Yucheng, Fang Hongyan, Tan Guolin, Zhang Qinna, Qu Shenhong, Wei Xin, Luo Xianyang, Xu Yu, Yu Shaoqing, Xiao Zian, Liu Feng, Li Qin, Zhang Yu, Xie Yan, Wang Lin, Yang Guoping, Yan Hongyue, Zhao Guoqing, Chen Bo, Wang Chengshuo, Zhang Luo

СтатьяРандомизированное исследованиеКлиническое исследование II фазыКлиническое исследование I фазыПеревод в очереди

Аннотация

To explore the therapeutic potential of blocking thymic stromal lymphopoietin (TSLP) in patients with chronic rhinosinusitis with nasal polyps (CRSwNP), we conducted a phase 1b/2a, randomized, double-blind, placebo-controlled trial to assess the safety and efficacy of CM326, a monoclonal antibody against TSLP. We enrolled 84 eligible patients with uncontrolled CRSwNP and stratified them based on baseline tissue eosinophil count. Patients are assigned to receive CM326 220 mg (n = 40) or placebo (n = 20) every 2 weeks (Q2W) and CM326 220 mg (n = 20) or placebo (n = 4) every 4 weeks (Q4W) for 16 weeks. Subsequently, all patients continue on CM326 220 mg Q2W or Q4W for an additional 36 weeks, followed by a 12-week follow up. Primary endpoints are safety of CM326 and change from baseline in NPS at week 16 in patients with eosinophilic CRSwNP (ECRSwNP). Main secondary endpoints include the change from baseline in NPS at week 16 in non-eosinophilic CRSwNP (nonECRwNP) and pharmacodynamic markers. Throughout the 64-week study, all treatment-emergent adverse events (TEAEs) are mild or moderate. CM326 Q2W improves NPS in patients with ECRSwNP compared with placebo at week 16 (mean difference [95% CI], -1.2 [-2.3 to -0.1], P = 0.04), with sustained benefits during the open-label and follow-up periods. Notably, peripheral blood and tissue eosinophil counts and concentrations of plasma IL-13 and IL-5 are reduced by week 16 with the treatment of CM326 Q2W versus placebo. A post-hoc analysis demonstrates that all participants with baseline TSLP > 330 fg/mL achieve a substantial reduction in NPS by week 16 with the treatment of CM326 Q2W (mean difference vs. placebo: -1.75 [95%CI, -3.06 to -0.44], P = 0.01). Overall, CM326 is well tolerated and effective in patients with uncontrolled ECRSwNP. A baseline plasma TSLP level of 330 fg/mL may serve as a predictive marker for treatment efficacy of CM326. ClinicalTrials.gov Identifier: NCT05324137.

Для цитирования: Xian Mu, Lan Feng, Yan Bing, Shen Shen, Liu Shixi, Wan Lijia, Song Xicheng, Jiang Luyun, Jiang Yan, Xue Jinmei, Chen Jianjun, Su Lizhong, Ye Jing, Yang Yucheng, Fang Hongyan, Tan Guolin, Zhang Qinna, Qu Shenhong, Wei Xin, Luo Xianyang, Xu Yu, Yu Shaoqing, Xiao Zian, Liu Feng, Li Qin, Zhang Yu, Xie Yan, Wang Lin, Yang Guoping, Yan Hongyue, Zhao Guoqing, Chen Bo, Wang Chengshuo, Zhang Luo. An anti-TSLP monoclonal antibody for uncontrolled CRSwNP: the DUBHE randomized clinical trial.. Nature communications. 2025. DOI: 10.1038/s41467-025-63682-x.

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