drugset / Trial / NCT00514683

Safety And Efficacy of BIBF 1120 in Idiopathic Pulmonary Fibrosis

NCT00514683 ↗

Phase 2 Completed 432 enrolled Boehringer Ingelheim
RandomizedParallel-groupDouble-blindTreatment

Summary

The general purpose of this trial is to investigate the efficacy and safety of 4 dose strategies of BIBF 1120 treatment for 12 months, compared to placebo in patients with idiopathic pulmonary fibrosis. The primary objective of this study is to demonstrate whether at least one dose strategy is superior to placebo in patients with IPF, in modifying the rate of decline of Forced Vital Capacity (FVC). As a secondary objective, additional parameters will be assessed in order to differentiate between dose strategies on the basis of safety and efficacy

Timeline

Start
2007-08
Primary completion
2010-06
Completion
—

Outcome

Missed primary endpoint

registry analysis (superiority or other test); Placebo vs Nintedanib 150 Bid; p = 0.0639; Mean Difference (Final Values) 0.131 (95% CI 0.027 to 0.235) NCT00514683 ↗

Drugs

EvaluationDrugModalityDoseRoute
Subject Nintedanib Small molecule 50 mg Oral
Subject Nintedanib Small molecule 100 mg Oral
Subject Nintedanib Small molecule 150 mg Oral

Indications