drugset / Trial / NCT01854047

An Evaluation of Dupilumab in Patients With Moderate to Severe Uncontrolled Asthma

NCT01854047

Phase 2 Completed 776 enrolled Sanofi Regeneron Pharmaceuticals · collab
RandomizedParallel-groupTriple-blindTreatment

Summary

Primary Objective: To evaluate the efficacy of different doses and regimens of dupilumab in participants with moderate to severe uncontrolled asthma. Secondary Objective: To evaluate different doses and regimens of dupilumab in participants with moderate to severe uncontrolled asthma, with regard to: * Safety and tolerability * Dupilumab systemic exposure and anti-drug antibodies

Timeline

Start
2013-06
Primary completion
2014-11
Completion
2015-04

Publications

Drugs

EvaluationDrugModalityDoseRoute
Subject Dupilumab Monoclonal antibody 200 mg Subcutaneous
Subject Dupilumab Monoclonal antibody 300 mg Subcutaneous
Background Levalbuterol Other / unclassified Inhaled
Background Mometasone furoate /formoterol Unknown Inhaled
Background Salbutamol Unknown Inhaled
Background budesonide / formoterol Unknown Inhaled
Background fluticasone propionate / salmeterol Unknown Inhaled

Indications