drugset / Trial / NCT02252328
Use of Simvastatin as a Steroid Sparing Agent for Uveitis Patients
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
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Subject | Simvastatin | Small molecule | 80 mg | — |