drugset / Trial / NCT03560466

Assessment of the Safety and Efficacy of Dupilumab in Children With Asthma (Liberty Asthma Excursion)

NCT03560466

Phase 3 Completed 378 enrolled Sanofi Regeneron Pharmaceuticals · collab
NaSingle-groupOpen-labelTreatment

Summary

Primary Objective: * To evaluate the long-term safety and tolerability of dupilumab in pediatric patients with asthma who participated in a previous dupilumab asthma clinical study. * To evaluate the efficacy of dupilumab in children of 6 to \<12 years of age with uncontrolled persistent asthma in the Japan sub-study. Secondary Objectives: * To evaluate the long-term efficacy of dupilumab in pediatric patients with asthma who participated in a previous dupilumab asthma clinical study. * To evaluate dupilumab in pediatric patients with asthma who participated in a previous dupilumab asthma clinical study with regard to: * Systemic exposure. * Anti-drug antibodies (ADAs). * Biomarkers. * To evaluate the safety and tolerability of dupilumab in pediatric patients with asthma in the Japan sub-study * To evaluate dupilumab in pediatric patients with asthma in the Japan substudy with regard to: * Systemic exposure, * Anti-drug antibodies (ADAs), * Biomarkers

Timeline

Start
2018-06-21
Primary completion
2025-04-01
Completion
2025-04-01

Drugs

EvaluationDrugModalityDoseRoute
Subject Dupilumab Monoclonal antibody 100 mg Subcutaneous
Subject Dupilumab Monoclonal antibody 200 mg Subcutaneous
Subject Dupilumab Monoclonal antibody 300 mg Subcutaneous
Background Prednisolone Other / unclassified
Background Prednisone Other / unclassified

Indications