Status:

COMPLETED

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

Lead Sponsor:

Forbes Medi-Tech

Conditions:

Hypercholesterolemia

Eligibility:

All Genders

18-75 years

Phase:

PHASE2

Brief Summary

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.

Eligibility Criteria

Inclusion

  • Mild to moderate primary hypercholesterolemia
  • Able to give informed consent and to comply with study procedures (including diet)

Exclusion

  • Homozygous familial hypercholesterolemia
  • Age \<18 or \>75 years
  • Pregnant women or women of child-bearing potential

Key Trial Info

Start Date :

November 1 2005

Trial Type :

INTERVENTIONAL

End Date :

Estimated Enrollment :

150 Patients enrolled

Trial Details

Trial ID

NCT00293878

Start Date

November 1 2005

Last Update

February 26 2007

Active Locations (14)

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Page 1 of 4 (14 locations)

1

Coastal Clinical Research

Mobile, Alabama, United States, 36608

2

Radiant Research

San Diego, California, United States, 92123

3

Radiant Research

Daytona Beach, Florida, United States, 32114

4

Radiant Research

Gainesville, Florida, United States, 32605

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