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Clinical trial

A Randomized, Double-blind, Placebo-controlled, Multicenter, Phase 3 Study to Assess the Efficacy and Safety of Filgotinib Administered for 24 Weeks in Combination With Conventional Synthetic Disease-modifying Anti-rheumatic Drug(s) (csDMARDs) to Subjects With Moderately to Severely Active Rheumatoid Arthritis Who Have an Inadequate Response to Biologic DMARD(s) Treatment

NCT02873936 is registered in ClinicalTrials.gov with Gilead Sciences as lead sponsor.

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Registry record

As filed in ClinicalTrials.gov.

Title
A Randomized, Double-blind, Placebo-controlled, Multicenter, Phase 3 Study to Assess the Efficacy and Safety of Filgotinib Administered for 24 Weeks in Combination With Conventional Synthetic Disease-modifying Anti-rheumatic Drug(s) (csDMARDs) to Subjects With Moderately to Severely Active Rheumatoid Arthritis Who Have an Inadequate Response to Biologic DMARD(s) Treatment
Lead sponsor
Gilead Sciences
Phase
Phase 3
Overall status
Completed
Start date
July 27, 2016
Completion date
June 26, 2018
Enrollment
449 (actual)
Sites
104

Conditions

As the registry lists them; a condition with its own page is linked.

rheumatoid arthritis