drugset / Trial / NCT01185353

A Study in Participants With Rheumatoid Arthritis on Background Methotrexate Therapy

NCT01185353 ↗

Phase 2 Completed 301 enrolled Eli Lilly and Company Incyte Corporation · collab
RandomizedParallel-groupQuadruple-blindTreatment

Summary

The purpose of this trial is to evaluate the safety and efficacy of LY3009104 in participants with Rheumatoid Arthritis (RA).

Timeline

Start
2010-10
Primary completion
2011-12
Completion
2014-03

Outcome

Met primary endpoint

paper Significantly more patients in the combined baricitinib 4 and 8 mg groups compared with placebo achieved an ACR20 response at week 12 (76% vs 41%, p<0.001). PMID 25431052 ↗

Publications

Drugs

EvaluationDrugModalityDoseRoute
Subject Baricitinib Small molecule 1 mg Oral
Subject Baricitinib Small molecule 2 mg Oral
Subject Baricitinib Small molecule 4 mg Oral
Subject Baricitinib Small molecule 8 mg Oral
Background Methotrexate Small molecule — Oral

Indications