CI

At a glance

ClinicalIndex Comparison Record
Phase 3Active· 880 enrolled
Drug / intervention
Dupilumabdrug
Likely dose
Not stated in record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.

Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.

Search/NCT02612454
NCT02612454Phase 3Active

An Open-Label Extension Study to Assess the Long-Term Safety and Efficacy of Dupilumab in Patients ≥6 Months to <18 Years of Age With Atopic Dermatitis

Regeneron Pharmaceuticals·interventional·Posted Nov 23, 2015·Updated May 29, 2026

In Brief

A Phase 3 clinical trial evaluating Dupilumab for Atopic Dermatitis. Active but no longer recruiting, targeting 880 participants across 84 sites in 7 countries.

Detailed Summary

The primary objective of the study is to assess the long-term safety of dupilumab in pediatric participants with AD. The secondary objectives of the study are: * To assess the long-term efficacy of dupilumab in pediatric participants with AD * To assess the trough concentrations of functional dupilumab in serum and the immunogenicity in pediatric participants with AD after re-treatment with dupilumab Optional Pre-filled Pen (PFP) Sub-Study in pediatric patients ≥2 to \<12 years of age with AD Co-Primary Objectives are: * To evaluate the pharmacokinetic (PK) of dupilumab PFPs * To evaluate the safety of dupilumab PFPs Secondary Objective is: \- To evaluate the immunogenicity of dupilumab PFPs

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
CountriesCanada, Czechia, Germany, Hungary, Poland, United Kingdom, United States
CollaboratorsSanofi

Timeline

Phase 3Active
201620172018201920202021202220232024202520262027
First PostedNov 23, 2015
Enrollment StartOct 15, 2015
Primary CompletionOct 7, 2026
TodayJul 2, 2026
Enrollment to primary: 11.0 yearsPosted 10.6 years agoPrimary completion in 3 months

Interventions

Dupilumabdrug

Weight-tiered dosing administered subcutaneous (SC)