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MK0653A (Ezetimibe (+) Simvastatin) Compared to an Approved Drug (Atorvastatin) for the Treatment of High Cholesterol (0653A-051)(COMPLETED)

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Organon

Status and phase

Completed
Phase 3

Conditions

Hypercholesterolemia

Treatments

Drug: Comparator: atorvastatin
Drug: MK0653A, ezetimibe (+) simvastatin

Study type

Interventional

Funder types

Industry

Identifiers

NCT00092690
2004_051
0653A-051

Details and patient eligibility

About

This study is to assess the safety and efficacy of an investigational drug as compared to an approved drug to reduce specific cholesterol levels.

Full description

The duration of treatment is 6 weeks.

Enrollment

1,902 patients

Sex

All

Ages

18 to 79 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Elevated cholesterol

Exclusion criteria

  • Unstable medical conditions or significant heart problems within 3 months prior to first study visit.

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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