Clinical Trial: Sitosterolemia Extension Study (0653-004)(COMPLETED)

Study Status: Completed
Recruit Status: Completed
Study Type: Interventional

Official Title: A Multicenter, Randomized, Double-Blind, Placebo-Controlled Study to Evaluate the Safety and Efficacy of MK0653 When Added to Current Regimen in Patients With Homozygous Sitosterolemia

Brief Summary: 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.

Detailed Summary: The duration of treatment is 52 weeks.
Sponsor: Merck Sharp & Dohme Corp.

Current Primary Outcome: Plasma sitosterol levels after 52 weeks.

Original Primary Outcome:

Current Secondary Outcome: Plasma LDL-C and plasma campesterol. Safety and tolerability.

Original Secondary Outcome:

Information By: Merck Sharp & Dohme Corp.

Dates:
Date Received: September 23, 2004
Date Started: February 12, 2001
Date Completion:
Last Updated: May 10, 2017
Last Verified: May 2017