drugset / Trial / NCT02528214

Evaluation of Dupilumab in Patients With Severe Steroid Dependent Asthma

NCT02528214 ↗

Phase 3 Completed 210 enrolled Sanofi Regeneron Pharmaceuticals · collab
RandomizedParallel-groupTriple-blindTreatment

Summary

Primary Objective: To evaluate the efficacy of dupilumab, compared with placebo, for reducing the use of maintenance oral corticosteroids (OCS) in participants with severe steroid-dependent asthma. Secondary Objectives: * To evaluate the safety and tolerability of dupilumab. * To evaluate the effect of dupilumab in improving participants-reported outcomes. * To evaluate dupilumab systemic exposure and the incidence of treatment-emergent antidrug antibodies.

Timeline

Start
2015-10-15
Primary completion
2017-09-20
Completion
2017-11-13

Outcome

Met primary endpoint

registry analysis (superiority test); Placebo q2w vs Dupilumab 300 mg q2w; p < 0.0001; Least Square (LS) Mean Difference 28.24 (95% CI 15.81 to 40.67); NCT02528214 ↗

release “the Phase 3 investigational study evaluating dupilumab in adults and adolescents with severe, steroid-dependent asthma met its primary endpoint and key secondary endpoints.” regeneron.com ↗

release “In the Phase 3 VENTURE trial, a majority of patients treated with DUPIXENT and standard therapies significantly reduced their use of oral steroids” regeneron.com ↗

Publications

Drugs

EvaluationDrugModalityDoseRoute
Subject Dupilumab Monoclonal antibody 300 mg Subcutaneous
Background Levalbuterol Other / unclassified — Inhaled
Background Prednisolone Other / unclassified — Oral
Background Prednisone Other / unclassified — Oral
Background Salbutamol Unknown — Inhaled

Indications