drugset / Trial / NCT02755649

A Study to Assess the Efficacy and Safety of Dupilumab in Participants With Severe Atopic Dermatitis (AD) That Are Not Controlled With Oral Cyclosporine A (CSA) or for Those Who Cannot Take Oral CSA Because it is Not Medically Advisable

NCT02755649 ↗

Phase 3 Completed 325 enrolled Regeneron Pharmaceuticals Sanofi · collab
RandomizedParallel-groupQuadruple-blindTreatment

Summary

The main objective of the trial is to evaluate the efficacy of 2 dose regimens of dupilumab compared to placebo, administered with concomitant topical corticosteroids (TCS), in adult patients with severe AD who are not adequately controlled with, or are intolerant to, oral Cyclosporine A (CSA), or when this treatment is currently not medically advisable. The secondary objective is to assess the safety and tolerability of 2 dose regimens of dupilumab compared to placebo, administered with concomitant TCS, in adult patients with severe AD who are not adequately controlled with, or are intolerant to, oral CSA, or when this treatment is currently not medically advisable.

Timeline

Start
2016-01-31
Primary completion
2017-01-04
Completion
2017-03-31

Outcome

Met primary endpoint

registry analysis (superiority test); Placebo QW + TCS vs Dupilumab 300 mg QW + TCS; p < 0.0001; Difference in Percentages 29.5 (95% CI 16.87 to 42.05) NCT02755649 ↗

registry analysis (superiority test); Placebo QW + TCS vs Dupilumab 300 mg Q2W + TCS; p < 0.0001; difference in percentages 33 (95% CI 20.41 to 45.57) NCT02755649 ↗

Publications

Drugs

EvaluationDrugModalityDoseRoute
Subject Dupilumab Monoclonal antibody 300 mg Subcutaneous

Indications