A 12-Week Study Comparing Pitavastatin 4 mg vs. Pravastatin 40 mg in HIV-Infected Subjects

Completed · Phase 4

Conditions studied: Dyslipidemia

In brief

A 12-Week, Randomized, Double-Blind, Active-Controlled, Parallel-Group Study.

Key facts

Study ID

NCT01301066

Run by

Kowa Research Institute, Inc.

People needed

252

Starts

2010-12-01

Expected to finish

2013-03-01

Last updated by the study team

2014-04-29

Who can join

Age: 18 and older, up to 70. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• Males and females (non-pregnant, non-lactating females) 18-70 years of age, inclusive, at time of consent.
• Both men and women of child bearing potential (i.e., not surgically sterile or post-menopausal defined as age >40 years without menses for ≥2 years) must agree to use at least 2 reliable forms of contraception
• Documented HIV infection.

You may not qualify if…

• Homozygous familial hypercholesterolemia
• Any conditions that may cause secondary dyslipidemia
• History of coronary artery disease (CAD) or CAD equivalent

Where it is running

• Study site — Phoenix, Arizona, United States
• Study site — Beverly Hills, California, United States
• Study site — Costa Mesa, California, United States
• Study site — Long Beach, California, United States
• Study site — Los Angeles, California, United States
• Study site — Newport Beach, California, United States
• Study site — San Francisco, California, United States
• Study site — Washington D.C., District of Columbia, United States
• Study site — Coral Gables, Florida, United States
• Study site — Fort Lauderdale, Florida, United States
• Study site — Ft. Pierce, Florida, United States
• Study site — Miami, Florida, United States
• Study site — Miami Beach, Florida, United States
• Study site — Tampa, Florida, United States
• Study site — Vero Beach, Florida, United States
• Study site — Atlanta, Georgia, United States
• Study site — Decatur, Georgia, United States
• Study site — Springfield, Massachusetts, United States
• Study site — Berkley, Michigan, United States
• Study site — St Louis, Missouri, United States
• Study site — Hillsborough, New Jersey, United States
• Study site — Randolph Township, New Jersey, United States
• Study site — New York, New York, United States
• Study site — Rochester, New York, United States
• Study site — Huntersville, North Carolina, United States

Full record on ClinicalTrials.gov

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