drugset / Trial / NCT03711162

A Clinical Study to Test How Effective and Safe GLPG1690 is for Subjects With Idiopathic Pulmonary Fibrosis (IPF) When Used Together With Standard of Care

NCT03711162 ↗

Phase 3 Terminated 525 enrolled Lakefront Biotherapeutics NV
RandomizedParallel-groupQuadruple-blindTreatment

Summary

The main purpose of this study was to see how GLPG1690 works together with your current standard treatment on your lung function and IPF disease in general. The study also investigated how well GLPG1690 is tolerated (for example if you got any side effects while on study drug).

Timeline

Start
2018-11-28
Primary completion
2021-03-30
Completion
2021-03-30

Outcome

Missed primary endpoint

Stopped: “The benefit-risk profile no longer supports continuing the study”

registry analysis (superiority test); GLPG1690 600 mg vs Placebo; p = 0.5525; Least square (LS) mean difference 22.7 (95% CI -52.3 to 97.6); NCT03711162 ↗

registry analysis (superiority test); GLPG1690 200 mg vs Placebo; p = 0.4776; LS mean difference -26.7 (95% CI -100.5 to 47.1); NCT03711162 ↗

paper Ziritaxestat did not improve the annual rate of FVC decline vs placebo in either study. PMID 37159034 ↗

Drugs

EvaluationDrugModalityDoseRoute
Subject ZIRITAXESTAT Small molecule 200 mg Oral
Subject ZIRITAXESTAT Small molecule 600 mg Oral