Type III Dysbetalipoproteinemia

Study identifier:D3560C00071

ClinicalTrials.gov identifier:N/A

EudraCT identifier:N/A

CTIS identifier:N/A

Study Complete

Official Title

An 18-week, Randomized, Multicenter, Phase 3b, Double-blind, Crossover Study, Followed by an 18-week Open-Label Period to Evaluate the Efficacy & Safety of the Lipid-Regulating Agents, Rosuvastatin & Pravastatin in the Treatment of Subjects with Dysbetalipoproteinemia (Frederickson Type III Hyperlipoproteinemia)

Medical condition

Hyperlipoproteinemia Type III

Phase

Phase 3

Healthy volunteers

No

Study drug

Rosuvastatin, rosuvastatin, pravastatin

Sex

All

Actual Enrollment

30

Study type

Interventional

Age

18 Years +

Date

Study Start Date: 01 Feb 2005
Primary Completion Date: 01 Feb 2007
Study Completion Date: 01 Feb 2007

Study design

Allocation: Randomized
Endpoint Classification: Efficacy Study
Intervention Model: Crossover Assignment
Masking: Double Blind
Primary Purpose: Treatment

Verification:

Verified 01 Nov 2013 by AstraZeneca Pharmaceuticals

Sponsors

AstraZeneca Pharmaceuticals

Collaborators

-

Inclusion and exclusion criteria