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Clinical Trial Details

Trial ID: L3946
Source ID: NCT00618995
Associated Drug: Comparator: Er Niacin (+) Laropiprant
Title: A Study to Evaluate the Effects of ER Niacin/Laropiprant, Laropiprant, ER Niacin, and Placebo on Urinary Prostanoid Metabolites (0524A-079)(COMPLETED)
Acronym:
Status: COMPLETED
Study Results: YES
Results: https://ClinicalTrials.gov/show/NCT00618995/results
Conditions: Type 2 Diabetes Mellitus
Interventions: DRUG: Comparator: ER niacin (+) laropiprant|DRUG: Comparator: ER niacin|DRUG: Comparator: laropiprant|DRUG: Comparator: placebo
Outcome Measures: Primary: Urinary 11-Dehydrothromboxane B2 (11-dTxB2), The creatinine-normalized urine levels of 11-dTxB2 on Day 7 following a 7 day course of daily dosing in the overall 24 hour collection interval, On Day 7 across the 24-hour urinary collection period. | Secondary: Prostaglandin I Metabolite (PGI-M), PGI-M in the Overall 24 Hour Collection Interval Following Administration on Day 7, On Day 7 across the 24-hour urinary collection period.
Sponsor/Collaborators: Sponsor: Merck Sharp & Dohme LLC
Gender: ALL
Age: ADULT, OLDER_ADULT
Phases: PHASE1
Enrollment: 26
Study Type: INTERVENTIONAL
Study Designs: Allocation: RANDOMIZED|Intervention Model: CROSSOVER|Masking: DOUBLE (PARTICIPANT, INVESTIGATOR)|Primary Purpose: TREATMENT
Start Date: 2007-08
Completion Date: 2007-12
Results First Posted: 2009-02-05
Last Update Posted: 2015-09-07
Locations:
URL: https://clinicaltrials.gov/show/NCT00618995