A Study to Evaluate the Effect of VX-548 on the QT/QTc Interval in Healthy Participants
Completed · Phase 1 · Has a placebo group
Conditions studied: Pain
In brief
The purpose of the study is to evaluate the effects of clinical and high clinical exposures of VX-548 and its metabolite on QTcF, and the safety, tolerability, pharmacokinetics (PK), and pharmacodynamics (PD) of VX-548 and its metabolite.
Key facts
- Study ID
- NCT05818852
- Run by
- Vertex Pharmaceuticals Incorporated
- People needed
- 72
- Starts
- 2023-04-12
- Expected to finish
- 2023-06-28
- Last updated by the study team
- 2024-03-20
Who can join
Age: 18 and older, up to 55. Sex: any. Healthy volunteers: accepted.
Where it is running
- ICON Lenexa — Lenexa, Kansas, United States
- ICON Salt Lake City — Salt Lake City, Utah, United States
Full record on ClinicalTrials.gov
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