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

Outcome

Met primary endpoint

registry analysis (superiority test); Placebo q2w vs Dupilumab 300 mg q2w; p = 0.0063; Least Square (LS) Mean Difference 0.21 (95% CI 0.06 to 0.36); NCT01854047 ↗

registry analysis (superiority test); Placebo q2w vs Dupilumab 300 mg q2w; p = 0.0002; LS Mean Difference 0.16 (95% CI 0.08 to 0.25); NCT01854047 ↗

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