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Clinical Trial Summary

This is a multi-center, prospective, randomized controlled non-inferior clinical study. A total of 120 subjects with non-infectious intermediate, posterior, or panuveitis were enrolled in Zhongshan Ophthalmic Center and three other centers. They were randomly assigned to the experimental group and the control group according to ( 1 : 1 ). We hypothesized that adalimumab biosimilars combined with immunosuppressive agents in the treatment of non-infectious uveitis is not inferior to glucocorticoids combined with immunosuppressive agents, and there are no additional adverse events and safety issues.


Clinical Trial Description

The study will be followed up in the screening-baseline period and at 4,8,12,18,24,36, and 48 weeks after the start of the study drug. The ETDRS letter number change of the best corrected visual acuity ( BCVA ) at 24 weeks compared with the baseline was used as the main indicator. The last follow-up was performed at 48 weeks. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT06310837
Study type Interventional
Source Zhongshan Ophthalmic Center, Sun Yat-sen University
Contact Wei Chi
Phone 13710616456
Email dr_chiwei@163.com
Status Recruiting
Phase N/A
Start date March 27, 2024
Completion date September 27, 2025

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