drugset / Trial / NCT01888874

Dose-finding Study of GLPG0634 as add-on to Methotrexate in Active Rheumatoid Arthritis Participants (DARWIN1)

NCT01888874 ↗

Phase 2 Completed 599 enrolled Lakefront Biotherapeutics NV
RandomizedParallel-groupQuadruple-blindTreatment

Summary

Participants suffering from active rheumatoid arthritis despite continued treatment with methotrexate were evaluated for improvement of disease activity (efficacy) when taking GLPG0634 (3 different doses - 50 milligram \[mg\], 100 mg and 200 mg daily -, each evaluated as once daily \[QD\] and twice daily \[BID\] regimen) or matching placebo for 24 weeks. •During the course of the study, patients were also examined for any side effects that could occur (safety and tolerability), and the amount of GLPG0634 present in the blood (Pharmacokinetics) as well as the effects of GLPG0634 on disease- and mechanism of action-related parameters in the blood (Pharmacodynamics) were determined. Also, the effects of different doses and dose regiments of GLPG0634 administration on participants' disability, fatigue, and quality of life were evaluated.

Timeline

Start
2013-07-17
Primary completion
2015-02-18
Completion
2015-05-14

Outcome

Met primary endpoint

paper At week 12, significantly more patients receiving filgotinib 100 mg once daily or 200 mg daily (both regimens) achieved an ACR20 response versus placebo. PMID 27993829 ↗

registry analysis (superiority test); Placebo vs GLPG0634 100 mg QD; p = 0.0435; Difference in percentage rates 19.3 (95% CI 4.7 to 34); Regression, Logistic NCT01888874 ↗

Drugs

EvaluationDrugModalityDoseRoute
Subject Filgotinib Small molecule 25 mg Oral
Subject Filgotinib Small molecule 50 mg Oral
Subject Filgotinib Small molecule 100 mg Oral
Subject Filgotinib Small molecule 200 mg Oral

Indications