drugset / Trial / NCT03568318

A Study to Evaluate Upadacitinib in Combination With Topical Corticosteroids in Adolescent and Adult Participants With Moderate to Severe Atopic Dermatitis

NCT03568318 ↗

Phase 3 Active not recruiting 1533 enrolled AbbVie
RandomizedParallel-groupQuadruple-blindTreatment

Summary

The objective of this study is to assess the efficacy and safety of upadacitinib combined with topical corticosteroids (TCS) for the treatment of adolescent and adult participants with moderate to severe atopic dermatitis (AD) who are candidates for systemic therapy.

Timeline

Start
2018-08-09
Primary completion
2021-02-16
Completion
2030-10-23

Outcome

Met primary endpoint

registry analysis (superiority test); Placebo + Topical Corticosteroids vs Upadacitinib 30 mg + Topical Corticosteroids; p <0.001; Adjusted Response Rate Difference 50.6 (95% CI 43.8 to 57.4) NCT03568318 ↗

registry analysis (superiority test); Placebo + Topical Corticosteroids vs Upadacitinib 30 mg + Topical Corticosteroids; p <0.001; Adjusted Response Rate Difference 47.6 (95% CI 41.1 to 54.0) NCT03568318 ↗

release “met the co-primary endpoints and all secondary endpoints in AD Up” abbvie.com ↗

Publications

Drugs

EvaluationDrugModalityDoseRoute
Subject Upadacitinib Small molecule 15 mg Oral
Subject Upadacitinib Small molecule 30 mg Oral
Background Hydrocortisone Other / unclassified 1 % Topical
Background Triamcinolone Acetonide Other / unclassified 0.1 % Topical
Background fluocinolone acetonide Other / unclassified 0.025 % Topical

Indications