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Evaluate the Preliminary Efficacy, Safety, and PK of Subcutaneous JS005 in Chinese Adult Patients With Active Nr-axSpA

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研究单位: [1]Shanghai Junshi Bioscience Co.,Ltd. [2]First Affiliated Hospital of Kunming Medical University Kunming,Yunnan,China,250063 [3]The First Affiliated Hospital of Xiamen University Xiamen,Fujian,China,410011 [4]Sun Yat-sen Memorial Sun Yat-sen University Guangzhou,Guangdong,China,510120 [5]Nanfang Hospital of Nanfang Medical University Guangzhou,Guangdong,China,510515 [6]Shantou University Medical Collge No.1 Affiliated Hospital Shantou,Guangdong,China,515041 [7]Shenzhen People's Hospital Shenzhen,Guangdong,China,518001 [8]Pking University Shenzhen Hospital Shenzhen,Guangdong,China,518036 [9]The First Affiliated Hospital of Zhengzhou University Zhengzhou,Henan,China,361001 [10]Tongji Hospital,Tongji Medical College of HUST Wuhan,Hubei,China,430030

研究目的:
The purpose of this study is to evaluate preliminary efficacy, safety pharmacokinetic (PK) characteristics, pharmacodynamics (PD) haracteristics and immunogenicity of JS005 at different doses in Chinese patients with active non-radiographic axial spondyloarthritis(nr-axSpA). Treatment difference of JS005 150mg,300mg,450mg vs. placebo in Chinese nr-axSpA patients in terms of ASAS 40 response rate at Week 16 as well as safety profile will be provided by the study .

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