drugset / Trial / NCT01721044

A Moderate to Severe Rheumatoid Arthritis Study

NCT01721044 ↗

Phase 3 Completed 527 enrolled Eli Lilly and Company
RandomizedParallel-groupQuadruple-blindTreatment

Summary

The purpose of this study is to determine whether baricitinib 4 milligram (mg) once daily is superior to placebo in the treatment of participants with moderately to severely active Rheumatoid Arthritis (RA) who have had an inadequate response to a tumor necrosis factor (TNF) inhibitor, despite ongoing treatment with conventional disease-modifying antirheumatic drugs (cDMARDs).

Timeline

Start
2013-01
Primary completion
2014-06
Completion
2014-09

Outcome

Met primary endpoint

paper Significantly more patients receiving baricitinib at the 4-mg dose than those receiving placebo had an ACR20 response at week 12 (55% vs. 27%, P<0.001). PMID 27028914 ↗

Publications

Drugs

EvaluationDrugModalityDoseRoute
Subject Baricitinib Small molecule 2 mg —
Subject Baricitinib Small molecule 4 mg —

Indications