Author
Listed:
- Mu Xian
(Capital Medical University
Capital Medical University
Chinese Academy of Medical Sciences)
- Feng Lan
(Capital Medical University
Capital Medical University
Chinese Academy of Medical Sciences)
- Bing Yan
(Capital Medical University
Capital Medical University
Chinese Academy of Medical Sciences)
- Shen Shen
(Capital Medical University
Capital Medical University
Chinese Academy of Medical Sciences)
- Shixi Liu
(West China Hospital Sichuan University)
- Lijia Wan
(Jingzhou Hospital Affiliated to Yangtze University)
- Xicheng Song
(Qingdao University
Shandong Provincial Clinical Research Centre for Otorhinolaryngologic Diseases)
- Luyun Jiang
(Hospital of Chengdu University of Traditional Chinese Medicine)
- Yan Jiang
(the Affiliated Hospital of Qingdao University)
- Jinmei Xue
(the Second Hospital of Shanxi Medical University)
- Jianjun Chen
(Huazhong University of Science and Technology)
- Lizhong Su
(People’s Hospital of Hangzhou Medical College
People’s Hospital of Hangzhou Medical College)
- Jing Ye
(the First Affiliated Hospital of Nanchang University)
- Yucheng Yang
(the First Affiliated Hospital of Chongqing Medical University)
- Hongyan Fang
(Chongqing General Hospital)
- Guolin Tan
(the Third Xiangya Hospital of Central South University)
- Qinna Zhang
(the First Hospital of Shanxi Medical University)
- Shenhong Qu
(The People’s Hospital of Guangxi Zhuang Autonomous Region)
- Xin Wei
(Hainan Affiliated Hospital of Hainan Medical University)
- Xianyang Luo
(The First Affiliated Hospital of Xiamen University)
- Yu Xu
(Renmin Hospital of Wuhan University
Renmin Hospital of Wuhan University)
- Shaoqing Yu
(Tongji University
Tongji University)
- Zian Xiao
(the Second Xiangya Hospital of Central South University)
- Feng Liu
(West China Hospital Sichuan University)
- Qin Li
(Jingzhou Hospital Affiliated to Yangtze University)
- Yu Zhang
(Qingdao University
Shandong Provincial Clinical Research Centre for Otorhinolaryngologic Diseases)
- Yan Xie
(Hospital of Chengdu University of Traditional Chinese Medicine)
- Lin Wang
(the Affiliated Hospital of Qingdao University)
- Guoping Yang
(Central South University)
- Hongyue Yan
(Ltd)
- Guoqing Zhao
(Ltd)
- Bo Chen
(Ltd)
- Chengshuo Wang
(Capital Medical University
Capital Medical University
Chinese Academy of Medical Sciences)
- Luo Zhang
(Capital Medical University
Capital Medical University
Chinese Academy of Medical Sciences
Capital Medical University)
Abstract
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.
Suggested Citation
Mu Xian & Feng Lan & Bing Yan & Shen Shen & Shixi Liu & Lijia Wan & Xicheng Song & Luyun Jiang & Yan Jiang & Jinmei Xue & Jianjun Chen & Lizhong Su & Jing Ye & Yucheng Yang & Hongyan Fang & Guolin Tan, 2025.
"An anti-TSLP monoclonal antibody for uncontrolled CRSwNP: the DUBHE randomized clinical trial,"
Nature Communications, Nature, vol. 16(1), pages 1-10, December.
Handle:
RePEc:nat:natcom:v:16:y:2025:i:1:d:10.1038_s41467-025-63682-x
DOI: 10.1038/s41467-025-63682-x
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