A Comparative Study to Investigate the Difference in Blood Levels of Two Different Formulations of GSK5784283
Part of paid clinical trials in Austin, Texas.
- Sponsor
- GlaxoSmithKline
- Study ID
- NCT07712393
- Phase
- PHASE1
- Status
- Recruiting
Conditions
Eligibility Criteria
- Sex
- ALL
- Age
- 18 Years - 60 Years
- Healthy Volunteers
- Accepted
Interventions
- GSK5784283 — DRUGGSK5784283 will be administered.
Study Details
The purpose of this study is to compare how two different formulations of the study medicine (GSK5784283) move through the body over time (pharmacokinetic \[PK\] study) in healthy adults. The aim of the study is to see how the body processes GSK5784283 and determine if the study medicine is safe, how well it is tolerated by the body and if the study medicines being tested work in the body in the same way.
Key Dates
- First listed
- Jul 17, 2026
- Start date
- Jul 17, 2026
- Status verified
- Jul 2026
- Primary completion
- Apr 13, 2027
- Completion
- Apr 26, 2027
Study Design
- Enrollment
- 24 participants (estimated)
- Allocation
- RANDOMIZED
- Intervention model
- PARALLEL
- Primary purpose
- TREATMENT
Arms
- Experimental: GSK5784283 Test Formulation
- Experimental: GSK5784283 Reference Formulation
Primary Outcome Measure
Maximum Observed Concentration (Cmax) of GSK5784283 Serum Samples [ Time Frame: Pre-dose and up to 253 days post dose ]
Central Contacts
- US GSK Clinical Trials Call Center877-379-3718
- EU GSK Clinical Trials Call Center+44 (0) 20 89904466
Locations (1)
| Facility | City | State | ZIP | Site coordinators |
|---|---|---|---|---|
| GSK Investigational Site | Austin | Texas | 78744 | Sean Gilbey (PRINCIPAL_INVESTIGATOR) |
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