drugset / Trial / NCT02395133

A Study to Confirm the Efficacy and Safety of Different Dupilumab Dose Regimens in Adults With Atopic Dermatitis (AD)

NCT02395133 ↗

Phase 3 Completed 422 enrolled Regeneron Pharmaceuticals Sanofi · collab
RandomizedParallel-groupTriple-blindTreatment

Summary

The primary objective of the study was to assess the ability of different Dupilumab dose regimens, administered as monotherapy, to maintain the treatment response achieved after 16 weeks of initial treatment with Dupilumab monotherapy compared to placebo.

Timeline

Start
2015-03-25
Primary completion
2016-07
Completion
2016-10-18

Outcome

Met primary endpoint

registry analysis (superiority test); Placebo QW vs Dupilumab 300 mg Q8W; p = 0.0001; Percent Change Difference -14.83 (95% CI -22.34 to -7.33); ANCOVA NCT02395133 ↗

registry analysis (superiority test); Placebo QW vs Dupilumab 300 mg Q8W; p = 0.0040; Percentage difference 24.5 (95% CI 9.70 to 39.29); Cochran-Mantel-Haenszel NCT02395133 ↗

Drugs

EvaluationDrugModalityDoseRoute
Subject Dupilumab Monoclonal antibody 300 mg Subcutaneous

Indications