This is a Phase 2 study of the efficacy, safety, tolerability and pharmacokinetics of two doses of EXPD-101 in participants with COPD. Study participants will be randomized to receive either study drug or placebo administered once daily for 52 weeks.
Age range
40 Years – 85 Years
Sex
ALL
See this in plain English?
AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.
Bring these to your next appointment. They're a starting point for a shared conversation — not a sign you qualify or a recommendation to enrol.
Generated to help you prepare — always confirm anything about your own eligibility and care with the study team and your doctor.
The trial coordinator is the person who runs the study day to day. These cover the practical side — logistics, costs, and what taking part would actually mean for your life. The study team confirms whether you meet the criteria; these are questions to ask, not a sign you qualify.
A starting point for the conversation — always confirm anything about your own eligibility, costs, and care with the study team and your doctor.
Annualized rate of moderate and severe COPD exacerbations
Timeframe: Over 52 Weeks
The number of participants experiencing an adverse events (AEs)
Timeframe: Over 52 weeks
Changes in vital sign parameters
Timeframe: Over 52 weeks
Changes in electrocardiogram (ECG) parameters
Timeframe: Over 52 weeks
Number of Participants with Clinically Significant Changes in Physical Examination Findings
Timeframe: Over 52 weeks
Number of participants with clinically significant abnormalities
Timeframe: Over 52 weeks
Changes in Physical Exam Parameters - Body Weight
Timeframe: Over 52 weeks