drugset / Trial / NCT00080223

Safety Study of Oral Pirfenidone in Patients With Pulmonary Fibrosis/Idiopathic Pulmonary Fibrosis

NCT00080223

Phase 2 Completed 83 enrolled Genentech, Inc.
NaSingle-groupOpen-labelOther

Summary

To assess the safety of treatment with pirfenidone (up to 3600 mg/d) in patients with pulmonary fibrosis/idiopathic pulmonary fibrosis (PF/IPF).

Timeline

Start
2003-08-31
Primary completion
2015-04-30
Completion
2015-04-30

Drugs

EvaluationDrugModalityDoseRoute
Subject Pirfenidone Small molecule 3600 mg Oral