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Completed Phase 4 Interventional Results available

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

ClinicalTrials.gov ID: NCT01301066

Public ClinicalTrials.gov record NCT01301066. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Sep 1, 2026, 5:36 PM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

A 12-Week, Randomized, Double-Blind, Active-Controlled, Parallel-Group Study Comparing Pitavastatin 4 mg vs. Pravastatin 40 mg in HIV-Infected Subjects With Dyslipidemia, Followed by a 40-Week Safety Extension Study

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

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

Study identification

NCT ID
NCT01301066
Recruitment status
Completed
Study type
Interventional
Phase
Phase 4
Lead sponsor
Kowa Research Institute, Inc.
Industry
Enrollment
252 participants

Conditions and interventions

Conditions

Interventions

Drug

Eligibility (public fields only)

Age range
18 Years to 70 Years
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Nov 30, 2010
Primary completion
Feb 28, 2013
Completion
Feb 28, 2013
Last update posted
Apr 28, 2014

2010 – 2013

United States locations

U.S. sites
35
U.S. states
14
U.S. cities
35
Facility City State ZIP Site status
Not listed Phoenix Arizona
Not listed Beverly Hills California
Not listed Costa Mesa California
Not listed Long Beach California
Not listed Los Angeles California
Not listed Newport Beach California
Not listed San Francisco California
Not listed Washington D.C. District of Columbia
Not listed Coral Gables Florida
Not listed Fort Lauderdale Florida
Not listed Ft. Pierce Florida
Not listed Miami Florida
Not listed Miami Beach Florida
Not listed Tampa Florida
Not listed Vero Beach Florida
Not listed Atlanta Georgia
Not listed Decatur Georgia
Not listed Springfield Massachusetts
Not listed Berkley Michigan
Not listed St Louis Missouri
Not listed Hillsborough New Jersey
Not listed Randolph Township New Jersey
Not listed New York New York
Not listed Rochester New York
Not listed Huntersville North Carolina
Not listed Addison Texas
Not listed Austin Texas
Not listed Corpus Christi Texas
Not listed Fort Worth Texas
Not listed Harlingen Texas
Not listed Houston Texas
Not listed Longview Texas
Not listed Annandale Virginia
Not listed Seattle Washington
Not listed Spokane Washington

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT01301066, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Apr 28, 2014 · Synced Sep 1, 2026

Related: full search, browse by condition, browse by drug or therapy, browse by sponsor, browse by U.S. city.

Open the official record

The complete protocol, eligibility criteria, and contact information for NCT01301066 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →