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Clinical Trial Summary

Rheumatoid arthritis (RA) is a chronic progressive autoimmune disease with predominantly joint involvement. To compare the efficacy and difference between elamod and tofacitib in the treatment of rheumatoid factor-positive and negative rheumatoid arthritis in RA patients with poor outcome after csDMARDs dosing, in order to better inform the clinical management.


Clinical Trial Description

This is an open, controlled, interventional clinical study enrolling patients with active RA who meet the following entry row criteria, and treating patients with IGU 25 mg bid + tofacitinib 5 mg bid for the intervention. The screening period was defined as the screening visit was conducted within 1 month prior to the baseline visit, and efficacy and safety assessments were performed at time points 0, 4, 12, 18, and 24 weeks from the time the subject was treated with the study protocol (see efficacy and safety endpoints for details), and study subjects were asked to come to the hospital for follow-up within ±3 days of the corresponding follow-up point. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT06146972
Study type Interventional
Source Qianfoshan Hospital
Contact Yanfeng Hou, Dr.
Phone 15168888165
Email yfhou1016@163.com
Status Recruiting
Phase Phase 4
Start date June 1, 2021
Completion date May 31, 2024

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