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  3. Assessing the effect of dexpramipexole in people with eosinophilic asthma
Research Study

A Randomized, Double-blind, Placebo-controlled, Parallel-group Study to Assess the Efficacy, Safety, and Tolerability of Dexpramipexole Administered Orally for 24 Weeks in Participants With Eosinophilic Asthma (EXHALE-4)

Principal Investigator
Céline Bergeron

Overview

Body Locations and Systems
Lungs and Breathing
Asthma
ClinicalTrials.gov#
NCT05748600
Status
Closed for Recruitment
Start/End Dates
Jun 1, 2024
Locations
Gordon and Leslie Diamond Health Care Centre
Name/Title
Maria Naval, Study Coordinator
Phone
604-875-5697
Email Address
maria.naval@vch.ca
Purpose of Study

The purpose of this study is to evaluate dexpramipexole as an add-on therapy in participants with inadequately controlled eosinophilic asthma, on Global Initiative for Asthma (GINA) 2021 Step 3, 4 or 5 therapy (or GINA 2021 Step 4 or 5 therapy in Poland) to confirm improvements in lung function, asthma control and quality of life.

Eligibility

Visit ClinicalTrials.gov for more information.

Disclaimer

Study Coordinators and Research Nurses cannot give medical advice over the phone. Telephone numbers and email addresses are provided for obtaining additional information on specific research studies only. If you have specific questions which require clinical expertise, please call your primary care physician.

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