drugset / Trial / NCT01721057

A Study in Moderate to Severe Rheumatoid Arthritis Participants

NCT01721057 ↗

Phase 3 Completed 684 enrolled Eli Lilly and Company
RandomizedParallel-groupQuadruple-blindTreatment

Summary

The purpose of this study is to determine whether baricitinib 4 milligram (mg) once daily (QD) is superior to placebo in the treatment of participants with moderately to severely active Rheumatoid Arthritis (RA) who have had inadequate response to or are intolerant to at least 1 conventional disease-modifying antirheumatic drug (cDMARD)(cDMARD-IR \[inadequate response\] participants) and who have not received a biologic disease-modifying antirheumatic drug (DMARD).

Timeline

Start
2012-12
Primary completion
2014-09
Completion
2014-12

Outcome

Met primary endpoint

paper More patients achieved ACR20 response at week 12 with baricitinib 4 mg than with placebo (62% vs 39%, p≤0.001). PMID 27689735 ↗

registry analysis (unspecified test); Placebo vs Baricitinib 4 mg; p = 0.001; Regression, Logistic NCT01721057 ↗

Publications

Drugs

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

Indications