drugset / Trial / NCT05704556
Evaluation of the Pharmacokinetics and Safety of VX-548 in Participants With Renal Impairment
Non-randomizedParallel-groupOpen-labelTreatment
Summary
The purpose of this study is to evaluate the pharmacokinetics (PK), safety, and tolerability of VX-548 and its metabolite in participants with severe or moderate renal impairment and healthy participants.
Timeline
- Start
- 2023-02-27
- Primary completion
- 2024-03-30
- Completion
- 2024-03-30
Drugs
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Subject | Suzetrigine | Small molecule | — | Oral |
Indications
No indication recorded.