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A Study of MK0859 in Patients With Primary Hypercholesterolemia or Mixed Hyperlipidemia (MK-0859-011)(COMPLETED)

Status
Completed
Phases
Phase 1
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00565292
Enrollment
50
Registered
2007-11-29
Start date
2006-07-31
Completion date
2006-08-31
Last updated
2015-02-25

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Hypercholesterolemia, Hyperlipidemia

Brief 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).

Interventions

DRUGMK0859

Sponsors

Merck Sharp & Dohme LLC
Lead SponsorINDUSTRY

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
DOUBLE

Eligibility

Sex/Gender
ALL
Age
18 Years to 75 Years
Healthy volunteers
No

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

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Apr 6, 2026