Español24/7 enrollment line386-218-5911

At a glance

ConditionCOPD
Therapeutic areaPulmonology
Principal investigatorKristyna D. Paradis, DO
DurationOpening soon — join the interest list
CompensationDetails available once enrollment opens
Trial registryNCT07684820

This study is registered on ClinicalTrials.gov, the U.S. National Library of Medicine's public trial registry. You can independently verify its details, sponsor, and status under identifier NCT07684820.

Who may qualify

The screening call takes about 5 minutes. Coordinators will walk you through the full eligibility criteria; the items below are the most common gates.

  • Adults with COPD
  • Respiratory medication and exacerbation history reviewed at pre-screening
  • Able to attend scheduled site visits in Orange City

What you receive

Tap any item for details.

Investigational treatment at no cost

The investigational treatment is provided at no cost throughout the study.

Pulmonology care

Ongoing care and monitoring from the site’s pulmonology team during the study.

Travel reimbursement

You are reimbursed for travel and mileage to and from your study visits.

How to enroll

The fastest path is to submit the pre-qualification form on this page or call the enrollment line at 386-218-5911. A study coordinator will review your information and call you within one business day to schedule a free screening visit.

You are never obligated to continue. You can stop at any step — before signing consent, during screening, or at any point after enrollment.

About the site

This study is conducted at Optimal Research Sites, an independent clinical trial facility in Orange City, Florida. We've conducted Phase I–IV trials since 1994, with a dedicated 9-bed Phase I inpatient unit, certified sample processing laboratory, and a bilingual study team. Every trial runs under IRB oversight and ICH Good Clinical Practice standards.