Clinical Trials Directory

Trials / Completed

CompletedNCT01728467

The Effects of RVX000222 on Glucose Metabolism in Individuals With Pre-diabetes

Phase 2 Randomised, Double-blind, Placebo-controlled, Cross-over Study for the Assessment of Glucose Metabolism Changes With RVX000222 in Individuals With Pre-diabetes

Status
Completed
Phase
Phase 2
Study type
Interventional
Enrollment
20 (actual)
Sponsor
Resverlogix Corp · Industry
Sex
Male
Age
18 Years – 70 Years
Healthy volunteers
Not accepted

Summary

This study builds on data that high-density lipoprotein (HDL) has a number of potentially beneficial effects including directly modulating glucose metabolism through multiple mechanisms. The primary objective of this study is to determine the effects of RVX000222 on postprandial plasma glucose in male individuals with impaired fasting glucose (IFG) or impaired glucose tolerance (IGT), during a frequently sampled oral glucose tolerance test (OGTT).

Conditions

Interventions

TypeNameDescription
DRUGRVX000222capsule, 200 mg, administer with food, 100 mg twice daily 10-12 hrs apart, 31-35 days
DRUGPlacebo, RVX000222capsule, administer with food, twice daily 10-12 hrs apart, 31-35 days

Timeline

Start date
2012-11-01
Primary completion
2014-03-01
Completion
2014-03-01
First posted
2012-11-19
Last updated
2014-04-02

Locations

1 site across 1 country: Australia

Source: ClinicalTrials.gov record NCT01728467. Inclusion in this directory is not an endorsement.

The Effects of RVX000222 on Glucose Metabolism in Individuals With Pre-diabetes (NCT01728467) · Clinical Trials Directory