Eosinophilic Asthma Research Study
Official Title
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
Study Details
The purpose of this study is to evaluate the safety and tolerability of an oral medication in participants with severe asthma while using their regular inhalers.
Principal Investigator
Dr. James Krings
IRB Number
202303199
Eligibility
1. Participants must be at least 18 years old
2. Participants must have asthma and take daily inhaled corticosteroid for at least 3 months
3. Participants must not currently smoke
Compensation is provided (contact the study team for compensation amount).
Volunteer Information
For more information about this study, contact Volunteer for Health at:
- 314.362.1000
- rprstaff@wustl.edu