drugset / Trial / NCT03117270

A Study to Assess Efficacy and Safety of Filgotinib in Ankylosing Spondylitis

NCT03117270 ↗

Phase 2 Completed 116 enrolled Lakefront Biotherapeutics NV
RandomizedParallel-groupQuadruple-blindTreatment

Summary

This is a multicenter, Phase 2, double-blind, placebo-controlled study in subjects with active Ankylosing Spondylitis (AS). A total of approximately 100 subjects will be randomized to one of 2 treatment arms in a 1:1 ratio: oral filgotinib tablets q.d. or matching placebo q.d. Treatment duration will be 12 weeks. Each subject will stay in the study for a maximum of 20 weeks (from Screening visit to Follow-up visit).

Timeline

Start
2017-03-07
Primary completion
2018-07-02
Completion
2018-07-02

Outcome

Met primary endpoint

paper The mean ASDAS change from baseline to week 12 was -1·47 (SD 1·04) in the filgotinib group and -0·57 (0·82) in the placebo group PMID 30360970 ↗

paper with a least squares mean difference between groups of -0·85 (95% CI -1·17 to -0·53; p<0·0001). PMID 30360970 ↗

Drugs

EvaluationDrugModalityDoseRoute
Subject Filgotinib Small molecule 200 mg Oral