drugset / Trial / NCT02252328

Use of Simvastatin as a Steroid Sparing Agent for Uveitis Patients

NCT02252328

Phase 2/3 Unknown 50 enrolled University College, London
RandomizedParallel-groupQuadruple-blindTreatment

Summary

The trial will compare the effect on disease control and immunosuppression treatment of adding simvastatin 80mg once daily, over a follow-up and treatment period of 2 years. Patients will be randomised in a 1:1 fashion to standard treatment with placebo or standard treatment with the addition of simvastatin (80mg daily). They will be followed at 3 months intervals for 2 years with a primary end point of mean reduction in corticosteroid dosage at the 12 month follow-up visit.

Timeline

Start
2015-09
Primary completion
2018-08
Completion
2019-08

Drugs

EvaluationDrugModalityDoseRoute
Subject Simvastatin Small molecule 80 mg

Indications