drugset / Trial / NCT03800797

Efficacy and Safety of Loxoprofen Hydrogel Patch in Patients With Ankylosing Spondylitis

NCT03800797

Phase 4 Completed 70 enrolled Sun Yat-sen University
RandomizedParallel-groupOpen-labelTreatment

Summary

To assess the efficacy and safety of loxoprofen sodium hydrogel patch (LX-P) versus loxoprofen sodium tablet (LX-T) in patients with active ankylosing spondylitis(AS). The trial includes 70 patients who are randomly assigned to either the LX-P group (LX-P 100 mg per day) or LX-T group (LX-T 60 mg t.i.d.) for 4 weeks.

Timeline

Start
2015-05-25
Primary completion
2015-12-10
Completion
2015-12-10

Drugs

EvaluationDrugModalityDoseRoute
Subject Loxoprofen Small molecule 60 mg
Subject Loxoprofen Small molecule 100 mg