drugset / Trial / NCT00769132

A Study to Evaluate the Effects of Extended Release (ER) Niacin/Laropiprant, Laropiprant, ER Niacin, and Placebo on Urinary Prostanoid Metabolites in Subjects With High Cholesterol (0524A-075)(COMPLETED)

NCT00769132

Phase 1 Completed 26 enrolled Merck Sharp & Dohme LLC
RandomizedCrossoverDouble-blindTreatment

Summary

The purpose of this study is to evaluate the potential effects of ER niacin/laropiprant, ER niacin, laropiprant, and placebo over the course of seven days on urinary levels of a metabolite of thromboxane A2 (TxA2), as a marker of in vivo platelet reactivity.

Timeline

Start
2007-08-03
Primary completion
2007-10-13
Completion
2007-11-06

Drugs

EvaluationDrugModalityDoseRoute
Subject Niacin Small molecule 2 g
Subject laropiprant Small molecule 40 mg

Indications