drugset / Trial / NCT01285323

A Study to Evaluate the Efficacy and Safety of Reslizumab in Patients With Eosinophilic Asthma

NCT01285323 ↗

Phase 3 Completed 464 enrolled Teva Branded Pharmaceutical Products R&D, Inc.
RandomizedParallel-groupQuadruple-blindTreatment

Summary

The primary objective of this study is to determine whether reslizumab is more effective than placebo in reducing the number of clinical asthma exacerbations (CAEs) in patients with eosinophilic asthma.

Timeline

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

Outcome

Mixed primary results

registry analysis (unspecified test); Placebo vs Reslizumab 3.0 mg/kg; p <0.0001; CAE rate ratio (reslizumab vs placebo) 0.4063 NCT01285323 ↗

registry analysis (unspecified test); Placebo vs Reslizumab 3.0 mg/kg; p = 0.4020; CAE rate ratio 0.6686 NCT01285323 ↗

Publications

Drugs

EvaluationDrugModalityDoseRoute
Subject Reslizumab Monoclonal antibody 3 mg/kg Intravenous

Indications