drugset / Trial / NCT03607422

A Study to Evaluate Upadacitinib in Adolescents and Adults With Moderate to Severe Atopic Dermatitis (Measure Up 2)

NCT03607422 ↗

Phase 3 Completed 912 enrolled AbbVie
RandomizedParallel-groupQuadruple-blindTreatment

Summary

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

Timeline

Start
2018-07-27
Primary completion
2021-03-11
Completion
2025-11-11

Outcome

Met primary endpoint

registry analysis (superiority test); Placebo vs Upadacitinib 30 mg QD; p <0.001; Adjusted Response Rate Difference 59.6 (95% CI 53.1 to 66.2) NCT03607422 ↗

registry analysis (superiority test); Placebo vs Upadacitinib 30 mg QD; p <0.001; Adjusted Response Rate Difference 47.4 (95% CI 41.0 to 53.7) NCT03607422 ↗

release “monotherapy met both primary and all secondary endpoints in Measure Up 2” abbvie.com ↗

release “Measure Up 1 and Measure Up 2 showing upadacitinib (15 mg or 30 mg) met the co-primary endpoints” abbvie.com ↗

Publications

Drugs

EvaluationDrugModalityDoseRoute
Subject Upadacitinib Small molecule 15 mg Oral
Subject Upadacitinib Small molecule 30 mg Oral

Indications