drugset / Trial / NCT01366209

Efficacy and Safety of Pirfenidone in Patients With Idiopathic Pulmonary Fibrosis (IPF)

NCT01366209

Phase 3 Completed 555 enrolled Genentech, Inc.
RandomizedParallel-groupQuadruple-blindTreatment

Summary

PIPF-016 (ASCEND) is a Randomized, Double-Blind, Placebo Controlled, Phase 3 Study of the Efficacy and Safety of Pirfenidone in Patients with Idiopathic Pulmonary Fibrosis. The study objectives are to confirm the treatment effect of pirfenidone compared with placebo on change in percent predicted forced vital capacity (%FVC) in patients with idiopathic pulmonary fibrosis (IPF), and to confirm the safety of treatment with pirfenidone compared with placebo in patients with IPF.

Timeline

Start
2011-06
Primary completion
2014-02
Completion
2014-02

Publications

Drugs

EvaluationDrugModalityDoseRoute
Comparator Pirfenidone Small molecule 2403 mg Oral