drugset / Trial / NCT02638896

Dose Reduction of Etanercept in Patients With Ankylosing Spondylitis

NCT02638896

Phase 4 Unknown 100 enrolled Zhixiang Huang
RandomizedParallel-groupOpen-labelTreatment

Summary

The primary objective of this study is to evaluate the efficacy of safety of etanercept dose reduction combined with sulfasalazine in ankylosing spondylitis (AS) patients who have achieved a significant clinical response.

Timeline

Start
2016-01
Primary completion
2017-02
Completion
2017-04

Drugs

EvaluationDrugModalityDoseRoute
Subject Etanercept Protein / enzyme biologic 50 mg Subcutaneous
Background Celecoxib Other / unclassified 0.4 g
Background Sulfasalazine Small molecule 2 g Oral