drugset / Trial / NCT03435081

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

NCT03435081 ↗

Phase 3 Completed 440 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 in adult participants with moderate to severe atopic dermatitis.

Timeline

Start
2018-02-20
Primary completion
2019-12-09
Completion
2021-08-16

Outcome

Met primary endpoint

registry NUMBER Placebo: 8.2 (4.7 to 13.7) percentage of participants NUMBER 2 mg Baricitinib: 29.5 (22.7 to 37.3) percentage of participants NCT03435081 ↗

registry analysis (superiority test); Placebo vs 2 mg Baricitinib; p <0.001; Odds Ratio (OR) 4.60 (95% CI 2.31 to 9.15); Regression, Logistic NCT03435081 ↗

Publications

Drugs

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

Indications