drugset / Trial / NCT02265705

A Study of Baricitinib (LY3009104) in Participants With Rheumatoid Arthritis (RA)

NCT02265705 ↗

Phase 3 Completed 290 enrolled Eli Lilly and Company
RandomizedParallel-groupDouble-blindTreatment

Summary

The main purpose of this study is to evaluate the safety and effectiveness of the study drug known as baricitinib in participants with moderately to severely active rheumatoid arthritis who have had an inadequate response to methotrexate therapy.

Timeline

Start
2014-10
Primary completion
2017-05
Completion
2017-05

Outcome

Met primary endpoint

paper Statistically significant improvement in ACR20 response was achieved with baricitinib at week 12 (53.4 vs. 22.6%, p = 0.001) in Chinese patients, compared to placebo. PMID 32876903 ↗

registry NUMBER Placebo: 28.3 percentage of participants NUMBER Baricitinib: 58.6 percentage of participants analysis (superiority test); Placebo vs Baricitinib; p = 0.001; Odds Ratio (OR) 4.1 (95% CI 2.5 to 6.9); Regression, Logistic NCT02265705 ↗

Publications

Drugs

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

Indications