drugset / Trial / NCT01628042
A Single Dose Study of the Pharmacokinetics of Vibegron (MK-4618) in Participants With Renal Insufficiency (MK-4618-014)
Non-randomizedParallel-groupOpen-labelTreatment
Summary
This study will investigate the impact of impaired renal function on the plasma pharmacokinetics of vibegron (MK-4618) to guide use of vibegron in clinical trials in participants with overactive bladder and to guide recommendations on potential dosing adjustments for individuals with varying degrees of renal impairment.
Timeline
- Start
- 2012-07-16
- Primary completion
- 2013-01-25
- Completion
- 2013-01-25
Drugs
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Subject | Vibegron | Unknown | 100 mg | Oral |