单克隆抗体
哮喘
医学
免疫学
相(物质)
抗体
化学
有机化学
作者
Qian Chen,Chen Yu,Yang Zou,Lika Ye,Jun Yang,Zhi Xiang,Zhihua Shi,Min Zhang,Jianlong Wu,Xin Li,Yingqun Zhu,Lihong Wang,Nan Xu,Xing Gao,Hongda Lin,Meng Fu,Kai Sheng,Jinrui Wang,Huize Han,Xiaopeng Wang
出处
期刊:The European respiratory journal
[European Respiratory Society]
日期:2024-09-14
卷期号:: OA1972-OA1972
被引量:1
标识
DOI:10.1183/13993003.congress-2024.oa1972
摘要
Introductions: SHR-1905 is a humanized monoclonal antibody against thymic stromal lymphopoietin (TSLP). We aimed to investigate the safety, tolerability, PK, and PD of SHR-1905 in healthy subjects (HSs) and patients (pts) with asthma. Methods: In this double-blind, single-ascending-dose, phase 1 study in China ( NCT04905602 ), HSs were randomized 4:1 to receive SHR-1905 or placebo (50, 100, 200, 400, and 600 mg; n=10 per dose cohort), and asthma pts were randomized 2:1 to receive SHR-1905 or placebo (mild asthma, 200 mg; moderate-severe asthma, 100 and 600 mg; n=12 per dose cohort). Results: SHR-1905 was safe and well-tolerated, with all treatment-related adverse events being mild to moderate. Peak concentrations were observed 8.5-15.0 days after dosing of 50-600 mg SHR-1905 in HSs, and mean t1/2 was 82.9-106 days. SHR-1905 exposure increased dose-proportionally. PK profiles in asthma pts were similar to those in HSs. Compared to placebo, SHR-1905 significantly reduced the levels of eosinophils, fractional exhaled nitric oxide, thymus and activation-regulated chemokine, and eotaxin-3, while significantly improving level of forced expiratory volume in one second in asthma pts (Fig). Conclusion: SHR-1905 showed favorable safety, tolerability, PK and PD profiles. Its long half-life supported extended dosing intervals (every 24 or 12 weeks) compared with clinically available anti-TSLP antibodies. Supporting information: Figure Mean (SD) change of biomarkers (EOS, FeNO, FEV1) from baseline following a single subcutaneous dose in patients with moderate-to-severe asthma