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

This study has been completed.
Sponsor:
ClinicalTrials.gov Identifier:
NCT01301066
First Posted: February 23, 2011
Last Update Posted: April 29, 2014
The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our disclaimer for details.
Collaborators:
Kowa Pharmaceuticals America, Inc.
Eli Lilly and Company
Information provided by (Responsible Party):
Kowa Research Institute, Inc.
Results First Submitted: February 10, 2014  
Study Type: Interventional
Study Design: Allocation: Randomized;   Intervention Model: Parallel Assignment;   Masking: Double (Participant, Investigator);   Primary Purpose: Treatment
Condition: Dyslipidemia
Interventions: Drug: Pitavastatin
Drug: Pravastatin

  Participant Flow
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Recruitment Details
Key information relevant to the recruitment process for the overall study, such as dates of the recruitment period and locations
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Pre-Assignment Details
Significant events and approaches for the overall study following participant enrollment, but prior to group assignment
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Reporting Groups
  Description
Pitavastatin 4 mg QD Pitavastatin: Pitavastatin 4 mg QD
Pravastatin 40 mg QD Pravastatin: Pravastatin 40 mg QD

Participant Flow:   Overall Study
    Pitavastatin 4 mg QD   Pravastatin 40 mg QD
STARTED   126   126 
COMPLETED   99   91 
NOT COMPLETED   27   35 
Lost to Follow-up                5                11 
Protocol Violation                8                7 
Withdrawal by Subject                4                9 
Adverse Event                6                6 
Sponsor Decision                2                1 
Physician Decision                0                1 
Other                2                0 



  Baseline Characteristics


  Outcome Measures

1.  Primary:   Change of Fasting Serum Low-density Lipoprotein Cholesterol (LDL-C) at 12 Weeks   [ Time Frame: 12 weeks minus baseline ]


  Serious Adverse Events


  Other Adverse Events


  Limitations and Caveats
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Limitations of the study, such as early termination leading to small numbers of participants analyzed and technical problems with measurement leading to unreliable or uninterpretable data
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  More Information
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Certain Agreements:  
Principal Investigators are NOT employed by the organization sponsoring the study.
There IS an agreement between Principal Investigators and the Sponsor (or its agents) that restricts the PI's rights to discuss or publish trial results after the trial is completed.
The agreement is:
unchecked The only disclosure restriction on the PI is that the sponsor can review results communications prior to public release and can embargo communications regarding trial results for a period that is less than or equal to 60 days. The sponsor cannot require changes to the communication and cannot extend the embargo.
unchecked The only disclosure restriction on the PI is that the sponsor can review results communications prior to public release and can embargo communications regarding trial results for a period that is more than 60 days but less than or equal to 180 days. The sponsor cannot require changes to the communication and cannot extend the embargo.


Results Point of Contact:  
Name/Title: Roger Morgan, MD, FACS
Organization: Kowa Research Institute, Inc.
phone: 919-433-1600
e-mail: RMorgan@kowaus.com



Responsible Party: Kowa Research Institute, Inc.
ClinicalTrials.gov Identifier: NCT01301066     History of Changes
Other Study ID Numbers: NK-104-4.05US
First Submitted: February 18, 2011
First Posted: February 23, 2011
Results First Submitted: February 10, 2014
Results First Posted: April 29, 2014
Last Update Posted: April 29, 2014