drugset / Trial / NCT03099187

A Study of Pirfenidone in Patients With Unclassifiable Progressive Fibrosing Interstitial Lung Disease

NCT03099187 ↗

Phase 2 Completed 253 enrolled Hoffmann-La Roche
RandomizedParallel-groupDouble-blindTreatment

Summary

The purpose of this study is to evaluate the efficacy and safety of pirfenidone in participants with fibrosing interstitial lung disease (ILD) who cannot be classified with moderate or high confidence into any other category of fibrosing ILD by multidisciplinary team (MDT) review ("unclassifiable" ILD).

Timeline

Start
2017-05-15
Primary completion
2018-11-21
Completion
2020-01-10

Outcome

Missed primary endpoint

registry analysis (superiority test); Pirfenidone vs Placebo; p = 0.6777; Difference in Group Means -134.6 (95% CI -772.4 to 503.3); t-test, 2 sided; reads as missed primary endpoint NCT03099187 ↗

registry analysis (superiority test); Pirfenidone vs Placebo; p = 0.4682; Difference in Group Means -216.0 (95% CI -803.6 to 371.7); Student's t-test; reads as missed primary endpoint NCT03099187 ↗

release “which prevented application of the prespecified statistical model to the primary endpoint assessment.” reads as unknown gene.com ↗

Publications

Drugs

EvaluationDrugModalityDoseRoute
Subject Pirfenidone Small molecule 801 mg Oral