Efficacy and Safety of GSK3196165 Versus Placebo and Tofacitinib in Participants With Moderately to Severely Active Rheumatoid Arthritis Who Have an Inadequate Response to Conventional Synthetic (cs)/Biologic (b) Disease Modifying Anti-rheumatic Drugs (DMARDs)

NCT03970837 · clinicaltrials.gov ↗
PHASE3
Phase
TERMINATED
Status
1764
Enrollment
INDUSTRY
Sponsor class

Stopped Only Asia cohort is early terminated.Limited efficacy demonstrated in the contRAst program does not support a suitable benefit/risk profile for otilimab as a potential treatment for RA. GSK has decided not to progress with regulatory submissions.

Conditions

Interventions

Sponsor

GlaxoSmithKline

Collaborators