A Study to Investigate the Efficacy and Safety of GSK5784283 (Felcorekibart) Compared With Placebo in Participants With Moderate to Very Severe COPD (PERSIST COPD-1)
Part of paid clinical trials in Doral, Florida.
- Sponsor
- GlaxoSmithKline
- Study ID
- NCT07780669
- Phase
- PHASE3
- Status
- Recruiting
Conditions
Eligibility Criteria
- Sex
- ALL
- Age
- 40 Years - 80 Years
- Healthy Volunteers
- Not accepted
Interventions
- GSK5784283 — DRUGGSK5784283 will be administered.
- Placebo — DRUGPlacebo will be administered.
- Standard of care — DRUGStandard of care will be administered.
Study Details
The study primarily aims to demonstrate the superiority of GSK5784283 as an add-on therapy compared to placebo in reducing the annualized rate of moderate and severe chronic obstructive pulmonary disease (COPD) exacerbations.
Key Dates
- First listed
- Aug 21, 2026
- Start date
- Aug 27, 2026
- Status verified
- Sep 2026
- Primary completion
- Jul 20, 2029
- Completion
- Mar 15, 2030
Study Design
- Enrollment
- 624 participants (estimated)
- Allocation
- RANDOMIZED
- Intervention model
- PARALLEL
- Primary purpose
- TREATMENT
Arms
- Experimental: Participants receiving GSK5784283 plus standard of care
- Placebo Comparator: Participants receiving matching placebo plus standard of care
Primary Outcome Measure
Annualized rate of moderate or severe COPD Exacerbations [ Time Frame: Up to Week 78 ]
Central Contacts
- US GSK Clinical Trials Call Center877-379-3718
- EU GSK Clinical Trials Call Center+44 (0) 20 89904466
Locations (2)
| Facility | City | State | ZIP | Site coordinators |
|---|---|---|---|---|
| GSK Investigational Site | Doral | Florida | 33172 | Alan Kaufman (PRINCIPAL_INVESTIGATOR) |
| GSK Investigational Site | Lake Charles | Louisiana | 70605 | Jason Langhofer (PRINCIPAL_INVESTIGATOR) |
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