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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT00565292
Other study ID # 0859-011
Secondary ID 2007_655
Status Completed
Phase Phase 1
First received November 27, 2007
Last updated February 24, 2015
Start date July 2006
Est. completion date August 2006

Study information

Verified date February 2015
Source Merck Sharp & Dohme Corp.
Contact n/a
Is FDA regulated No
Health authority United States: Food and Drug Administration
Study type Interventional

Clinical Trial Summary

This is a study to assess the safety, efficacy, and tolerability of MK0859 in patients with primary hypercholesterolemia (large amounts of cholesterol in the blood) or mixed hyperlipidemia (high levels of LDL cholesterol, triglycerides, and low levels of HDL cholesterol in blood) This is an early phase trial and some specific protocol information is in progress and not publicly available at this time. (Full information is available to trial participants).


Recruitment information / eligibility

Status Completed
Enrollment 50
Est. completion date August 2006
Est. primary completion date August 2006
Accepts healthy volunteers No
Gender Both
Age group 18 Years to 75 Years
Eligibility Inclusion Criteria:

- Patient is between 18 and 75 years of age

- Patient can be on a stable diet for the study

- Patient has a stable weight for more then 6 weeks before the study and has not participated in a weight loss program

Exclusion Criteria:

- Patient has chronic heart failure or a history of heart disease

- Patient has blood, digestive, or central nervous system disorders

- Patient is pregnant or nursing

- Patient is HIV positive

Study Design

Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Double-Blind, Primary Purpose: Treatment


Related Conditions & MeSH terms


Intervention

Drug:
MK0859


Locations

Country Name City State
n/a

Sponsors (1)

Lead Sponsor Collaborator
Merck Sharp & Dohme Corp.
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