Study of Iguratimod in Sjögren's Syndrome

Status Recruiting

Clinical Trial Summary

A single-center, self-control, open-label study of efficacy and safety of Iguratimod in patients with Sjögren's Syndrome

Clinical Trial Description

In this study, patients with Sjögren's Syndrome are enrolled and received Iguratimod 25 mg twice a day for 24 weeks. The differences of ESSPRI (EULAR Sjogren's Syndrome Patient Reported Index) score, ESSPRI(EULAR Sjogren's Syndrome Patient Reported Index) score, unstimulated salivary flow rate, Schirmer's test SF-36 score and HAQ score between baseline and week 24 are evaluated to determine the efficacy of Iguratimod in patients with Sjögren's Syndrome. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details

NCT number	NCT03023592
Study type	Interventional
Source	Peking Union Medical College Hospital
Contact	Hua Chen, Dr.
Phone	86-10-69158797
Email	chenhua@pumch.cn
Status	Recruiting
Phase	Phase 1/Phase 2
Start date	February 2017
Completion date	April 2018

View Details

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