drugset / Trial / NCT01033643

A Multiple Dose Study of MK-3614 (MK-3614-002)

NCT01033643 ↗

Phase 1 Completed 30 enrolled Merck Sharp & Dohme LLC
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

EvaluationDrugModalityDoseRoute
Subject MK-3614 Unknown 0.25 mg Oral
Subject MK-3614 Unknown 0.5 mg Oral

Indications