drugset / Trial / NCT02808871

Phase ll Study of Pirfenidone in Patients With RAILD (TRAIL1)

NCT02808871

Phase 2 Completed 123 enrolled Brigham and Women's Hospital
RandomizedParallel-groupTriple-blindTreatment

Summary

The purpose of this study is to to assess the safety and tolerability of pirfenidone 2403 mg/day for the treatment of RA-associated interstitial lung disease.

Timeline

Start
2017-04-07
Primary completion
2021-04-07
Completion
2021-04-07

Drugs

EvaluationDrugModalityDoseRoute
Subject Pirfenidone Small molecule 2403 mg Oral