drugset / Trial / NCT01287039

A Study to Evaluate the Efficacy and Safety of Reslizumab (3.0 mg/kg) in the Reduction of Clinical Asthma Exacerbations in Patients (12-75 Years of Age) With Eosinophilic Asthma

NCT01287039 ↗

Phase 3 Completed 489 enrolled Teva Branded Pharmaceutical Products R&D, Inc.
RandomizedParallel-groupQuadruple-blindTreatment

Summary

This is a Phase 3, multicenter, randomized, double-blind, placebo-controlled, parallel-group study to evaluate the efficacy, safety, and immunogenicity of treatment with reslizumab in patients with eosinophilic asthma.

Timeline

Start
2011-04
Primary completion
2013-12
Completion
2014-03

Outcome

Mixed primary results

registry Placebo vs Reslizumab 3.0 mg/kg; p <0.0001; CAE rate ratio (reslizumab vs placebo) 0.5010 (95% CI 0.3726 to 0.6737) NCT01287039 ↗

registry Placebo vs Reslizumab 3.0 mg/kg; p <0.0001; CAE rate ratio (reslizumab vs placebo) 0.4499 (95% CI 0.3255 to 0.6220) NCT01287039 ↗

registry Placebo vs Reslizumab 3.0 mg/kg; p = 0.2572; CAE rate ratio (reslizumab vs placebo) 0.6595 (95% CI 0.3210 to 1.3550) NCT01287039 ↗

Publications

Drugs

EvaluationDrugModalityDoseRoute
Subject Reslizumab Monoclonal antibody 3 mg/kg Intravenous

Indications