Recruitment

Recruitment Status
Active, not recruiting
Estimated Enrollment
600

Summary

Conditions
Asthma
Type
Interventional
Phase
Phase 3
Design
Allocation: N/AIntervention Model: Single Group AssignmentIntervention Model Description: Open labelMasking: None (Open Label)Primary Purpose: Treatment

Participation Requirements

Age
Between 18 years and 130 years
Gender
Both males and females

Description

This is an open-label, multicenter study designed to evaluate efficacy and safety of reducing daily oral corticosteroid (OCS) use after initiation of 30 mg dose of benralizumab administered subcutaneously (SC) in patients with severe eosinophilic asthma receiving high-dose inhaled corticosteroid (IC...

This is an open-label, multicenter study designed to evaluate efficacy and safety of reducing daily oral corticosteroid (OCS) use after initiation of 30 mg dose of benralizumab administered subcutaneously (SC) in patients with severe eosinophilic asthma receiving high-dose inhaled corticosteroid (ICS)/long-acting ?2 agonist (LABA) and OCS with or without additional asthma controller(s).

Tracking Information

NCT #
NCT03557307
Collaborators
Not Provided
Investigators
Not Provided