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Sitosterolemia Extension Study (0653-003)(COMPLETED)

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Organon

Status and phase

Completed
Phase 3

Conditions

Lipid Metabolism, Inborn Errors
Heart Disease

Treatments

Drug: MK0653, ezetimibe
Drug: Comparator: placebo

Study type

Interventional

Funder types

Industry

Identifiers

NCT00092807
2004_032
P02257

Details and patient eligibility

About

This is an extension study for patients having unusually high absorption of non-cholesterol sterols, resulting in heart-related diseases. This study will evaluate the long term safety and the ability to lower cholesterol levels with an investigational drug.

Full description

The duration of treatment is 52 weeks.

Enrollment

37 patients

Sex

All

Ages

10+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Patients with elevated sitosterol levels while taking current medication

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 contacts and locations

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Data sourced from clinicaltrials.gov

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