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A Study of MK0653A (Ezetimibe (+) Simvastatin) in Patients With Hypercholesterolemia (0653A-038)

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Organon

Status and phase

Completed
Phase 3

Conditions

Hypercholesterolemia

Treatments

Drug: MK0653A, ezetimibe (+) simvastatin
Drug: Comparators: simvastatin and ezetimibe

Study type

Interventional

Funder types

Industry

Identifiers

NCT00092651
0653A-038
2004_048

Details and patient eligibility

About

The purpose of this study is to evaluate the lipid lowering effects of an investigational drug in patients with hypercholesterolemia (high cholesterol).

Full description

The duration of treatment is 4 months.

Enrollment

1,398 patients

Sex

All

Ages

18 to 80 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • High cholesterol

Exclusion criteria

  • Patient has a condition which, in the opinion of the investigator, might pose a risk to the patient, interfere with participation in the study, or does not meet the additional criteria as required by the study.

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Double Blind

Trial contacts and locations

0

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Data sourced from clinicaltrials.gov

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