drugset / Trial / NCT01385657

Safety and Tolerability of Dupilumab in Participants With Moderate to Severe Atopic Dermatitis

NCT01385657

Phase 1 Completed 37 enrolled Regeneron Pharmaceuticals Sanofi · collab
RandomizedParallel-groupTriple-blindTreatment

Summary

The purpose of this study is to assess the safety and tolerability of repeated subcutaneous (SC) doses of Dupilumab in participants with moderate-to-severe atopic dermatitis (AD).

Timeline

Start
2011-07-31
Primary completion
2012-03-31
Completion
2012-03-31

Drugs

EvaluationDrugModalityDoseRoute
Subject Dupilumab Monoclonal antibody 150 mg Subcutaneous
Subject Dupilumab Monoclonal antibody 300 mg Subcutaneous

Indications