drugset / Trial / NCT01710358

A Study in Moderate to Severe Rheumatoid Arthritis

NCT01710358 ↗

Phase 3 Completed 1307 enrolled Eli Lilly and Company
RandomizedParallel-groupQuadruple-blindTreatment

Summary

The purpose of this study is to determine whether baricitinib is superior to placebo in the treatment of participants with moderately to severely active Rheumatoid Arthritis (RA) who have had an inadequate response to methotrexate (MTX) treatment.

Timeline

Start
2012-10
Primary completion
2015-03
Completion
2015-09

Outcome

Met primary endpoint

paper More patients had an ACR20 response at week 12 with baricitinib than with placebo (primary end point, 70% vs. 40%, P<0.001). PMID 28199814 ↗

Publications

Drugs

EvaluationDrugModalityDoseRoute
Comparator Adalimumab Monoclonal antibody 40 mg Subcutaneous
Subject Baricitinib Small molecule 4 mg Oral
Background Methotrexate Small molecule — Oral

Indications