drugset / Trial / NCT01033643
A Multiple Dose Study of MK-3614 (MK-3614-002)
RandomizedParallel-groupDouble-blindTreatment
Summary
This study will evaluate the safety, tolerability, pharmacokinetics and pharmacodynamics of multiple doses of MK-3614 in male participants with mild to moderate hypertension. The primary hypotheses are: 1) Multiple oral doses of MK-3614 are sufficiently safe and well tolerated to permit continued clinical investigation 2) Aortic Augmentation Index (Aix) is reduced 24 hours post the last dose of MK-3614 administered compared to placebo and 3) Increase in the 12-hour weighted averages (TWA 0-12hours) of the heart rate is within 15 beats per minute (bpm) of baseline on first day of multiple dosing of MK-3614 and within 10 bpm of baseline on last day of multiple dosing of MK-3614.
Timeline
- Start
- 2009-05-27
- Primary completion
- 2009-12-09
- Completion
- 2009-12-09
Drugs
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Subject | MK-3614 | Unknown | 0.25 mg | Oral |
| Subject | MK-3614 | Unknown | 0.5 mg | Oral |