drugset / Trial / NCT01920893

An Evaluation of Dupilumab in Patients With Nasal Polyposis And Chronic Symptoms Of Sinusitis

NCT01920893 ↗

Phase 2 Completed 60 enrolled Sanofi Regeneron Pharmaceuticals · collab
RandomizedParallel-groupTriple-blindTreatment

Summary

Primary Objective: To evaluate the efficacy of dupilumab (SAR231893/REGN668) in the treatment of bilateral Nasal Polyposis (NP) by assessment of the endoscopic nasal polyp score (NPS) in comparison to placebo. Secondary Objectives: To evaluate effect of dupilumab with regards to: * symptoms of sinusitis, * sinus computed tomography (CT) scan, * NPS in the sub-group of participants with co-morbid asthma, * Safety and tolerability.

Timeline

Start
2013-08
Primary completion
2014-11
Completion
2014-11

Outcome

Met primary endpoint

registry analysis (superiority test); Placebo vs Dupilumab 300 mg QW; p = 0.0009; Least Square (LS) mean difference -1.55 (95% CI -2.43 to -0.67) NCT01920893 ↗

Publications

Drugs

EvaluationDrugModalityDoseRoute
Subject Dupilumab Monoclonal antibody 300 mg Subcutaneous
Background Mometasone furoate nasal spray Unknown — Intranasal

Indications