drugset / Trial / NCT03570749

A Study of Baricitinib (LY3009104) in Participants With Severe or Very Severe Alopecia Areata

NCT03570749 ↗

Phase 2/3 Completed 784 enrolled Eli Lilly and Company Incyte Corporation · collab
RandomizedParallel-groupDouble-blindTreatment

Summary

This study is designed to select up to two doses of baricitinib (referred to as low dose and high dose) and assess their efficacy and safety for the treatment of severe or very severe alopecia areata. An additional subpopulation of 60 participants in the US will enroll in the open-label addenda.

Timeline

Start
2018-09-24
Primary completion
2021-02-02
Completion
2025-01-29

Outcome

Met primary endpoint

registry analysis (superiority test); Placebo Phase 3 vs 2 mg Baricitinib Phase 3; p <0.001; Odds Ratio (OR) 5.75 (95% CI 2.75 to 12.02); Regression, Logistic NCT03570749 ↗

registry analysis (superiority test); Placebo Phase 3 vs 4 mg Baricitinib Phase 3; p <0.001; Odds Ratio (OR) 11.80 (95% CI 5.89 to 23.62); Regression, Logistic NCT03570749 ↗

paper In two phase 3 trials involving patients with severe alopecia areata, oral baricitinib was superior to placebo with respect to hair regrowth at 36 weeks. PMID 35334197 ↗

Publications

Drugs

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

Indications