drugset / Trial / NCT02951429

Efficacy, Safety, and Tolerability Study of Pirfenidone in Combination With Sildenafil in Participants With Advanced Idiopathic Pulmonary Fibrosis (IPF) and Intermediate or High Probability of Group 3 Pulmonary Hypertension

NCT02951429

Phase 2 Completed 177 enrolled Hoffmann-La Roche
RandomizedParallel-groupDouble-blindTreatment

Summary

This Phase IIb, randomized, placebo-controlled, multicenter, international study will evaluate the efficacy, safety, and tolerability of sildenafil or placebo added to pirfenidone (Esbriet) treatment in participants with advanced IPF and intermediate or high probability of Group 3 pulmonary hypertension (PH) who are on a stable dose of pirfenidone with demonstrated tolerability. Participants will be randomized to receive 1 year of treatment with either oral sildenafil or matching placebo while continuing to take pirfenidone.

Timeline

Start
2016-12-31
Primary completion
2019-09-26
Completion
2020-08-22

Drugs

EvaluationDrugModalityDoseRoute
Subject Sildenafil Unknown 20 mg Oral
Background Pirfenidone Small molecule 1602 mg Oral
Background Pirfenidone Small molecule 2403 mg Oral