drugset / Trial / NCT00287716

Three-Arm Study of the Safety and Efficacy of Pirfenidone in Patients With Idiopathic Pulmonary Fibrosis

NCT00287716

Phase 3 Completed 435 enrolled Genentech, Inc.
RandomizedParallel-groupQuadruple-blindTreatment

Summary

The objectives of this study are to assess the safety and efficacy of treatment with pirfenidone 2403 milligrams per day (mg/d) compared with placebo in patients with idiopathic pulmonary fibrosis (IPF), to assess the safety and efficacy of treatment with pirfenidone 1197 mg/d in patients with idiopathic pulmonary fibrosis and to characterize the pharmacokinetic disposition of pirfenidone in patients with idiopathic pulmonary fibrosis.

Timeline

Start
2006-07-14
Primary completion
2008-11-10
Completion
2008-11-10

Publications

Drugs

EvaluationDrugModalityDoseRoute
Comparator Pirfenidone Small molecule 1197 mg Oral
Comparator Pirfenidone Small molecule 2403 mg Oral