drugset / Trial / NCT03334396

A Study of Baricitinib (LY3009104) in Patients With Moderate to Severe Atopic Dermatitis

NCT03334396 ↗

Phase 3 Completed 660 enrolled Eli Lilly and Company Incyte Corporation · collab
RandomizedParallel-groupDouble-blindTreatment

Summary

The purpose of this study is to evaluate the efficacy and safety of baricitinib as monotherapy in participants with moderate to severe atopic dermatitis.

Timeline

Start
2017-11-23
Primary completion
2018-12-06
Completion
2019-08-16

Outcome

Met primary endpoint

registry analysis (superiority test); Placebo vs 2 mg Baricitinib; p = 0.020; Odds Ratio (OR) 2.61 (95% CI 1.17 to 5.84); Regression, Logistic NCT03334396 ↗

registry analysis (superiority test); Placebo vs 4 mg Baricitinib; p <0.001; Odds Ratio (OR) 4.10 (95% CI 1.93 to 8.70); Regression, Logistic NCT03334396 ↗

Publications

Drugs

EvaluationDrugModalityDoseRoute
Subject Baricitinib Small molecule 1 mg Oral
Subject Baricitinib Small molecule 2 mg Oral
Subject Baricitinib Small molecule 4 mg Oral

Indications