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Completed Phase 2 Interventional

Study on the Safety and Effects on Lipids of FM-VP4 in Subjects With Primary Hypercholesterolemia

ClinicalTrials.gov ID: NCT00293878

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This page only displays public information reproduced from the official ClinicalTrials.gov record NCT00293878. It adds no medical advice, opinions, or eligibility judgments. The official record remains the source of truth for eligibility criteria, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Nov 14, 2026, 8:20 PM EST

All trial information on this site comes from the official ClinicalTrials.gov public API (clinicaltrials.gov/api/v2), run by the U.S. National Library of Medicine. We only display that public information; we do not add opinions, endorsements, or any other intent. Always review the official ClinicalTrials.gov record for the latest information.

Official title

A Phase 2, Randomized, Double-Blind, Placebo-Controlled, Multicenter Study of the Safety and Effects on Lipids of 12 Weeks of 2 Doses of FM-VP4 in Subjects With Primary Hypercholesterolemia

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

The purpose of this study is to evaluate the safety and effects on lipids of FM-VP4 administered for 12 weeks in subjects with mild to moderate primary hypercholesterolemia.

Study identification

NCT ID
NCT00293878
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Lead sponsor
Forbes Medi-Tech
Industry
Enrollment
150 participants

Conditions and interventions

Eligibility (public fields only)

Age range
18 Years to 75 Years
Sex
All
Healthy volunteers
Not listed

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Nov 2005 (Type not available)
Primary completion
Not listed
Completion
Not listed
Last update posted
Feb 26, 2007

Started 2005

United States locations

U.S. sites
14
U.S. states
11
U.S. cities
13
Facility City State ZIP Site status
Coastal Clinical Research Mobile Alabama 36608 —
Radiant Research San Diego California 92123 —
Radiant Research Daytona Beach Florida 32114 —
Radiant Research Gainesville Florida 32605 —
Radiant Research Boise Idaho 83704 —
Radiant Research Chicago Illinois 60610 —
Midwest Institute for Clinical Research Indianapolis Indiana 46260 —
PRA International Pharmacology Center Lenexa Kansas 66219 —
The Center for Pharmaceutical Research Kansas City Missouri 64114 —
Radiant Research Portland Oregon 97201 —
Coastal Carolina Research Center Mt. Pleasant South Carolina 29464 —
Radiant Research Austin Texas 78758 —
Research Across America Dallas Texas 75234 —
Radiant Research Dallas Texas 75235 —

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT00293878, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Feb 26, 2007 · Synced Nov 14, 2026

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