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UnknownNCT00176020

Nicotinic Acid - Pharmacokinetics, Pharmacodynamics, Receptor Expression

Double-Blind, Randomized, Placebo-Controlled, Single-Center, 2 Treatment, 3-Way Crossover Study to Investigate the Pharmacodynamics, Pharmacokinetics and Safety of a Single Oral Repeated Dose of 500 Mg Nicotinic Acid as Tablets in Healthy Subjects

Status
Unknown
Phase
Phase 1
Study type
Interventional
Enrollment
18 (planned)
Sponsor
Heidelberg University · Academic / Other
Sex
All
Age
18 Years – 45 Years
Healthy volunteers
Accepted

Summary

The study will be a double-blind, randomized, placebo-controlled, single-center, 2 treatment, 3--way crossover. Subjects will be randomly allocated to a treatment sequence - AAB, ABA or BAA. The two treatments will be: * Treatment A: 500 mg nicotinic acid (Niacor(R)) * Treatment B: Niacor(R) Placebo Each trial period will last one day, there will be a wash-out period of at least 2 days between each trial period. Five to seven days after study day 1 of trial period 3 there will be a final safety examination.

Conditions

Interventions

TypeNameDescription
DRUGnicotinic acid

Timeline

First posted
2005-09-15
Last updated
2006-03-15

Source: ClinicalTrials.gov record NCT00176020. Inclusion in this directory is not an endorsement.

Nicotinic Acid - Pharmacokinetics, Pharmacodynamics, Receptor Expression (NCT00176020) · Clinical Trials Directory