Amprenavir/Ritonavir or Saquinavir/Ritonavir in HIV-Infected Subjects Following Failure With Kaletra as Their Second Protease Inhibitor

Study Identifier
M00-261
CT.gov Identifier
EudraCT Identifier
Not available
EUCTIS ID
Not available
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Study Complete

Results Available

Scientific Result Summary
Available Language(s): English

Study Details

Medical Condition
  • Human Immunodeficiency Virus (HIV)
  • Study Drug
  • Amprenavir/ritonavir
  • Saquinavir/ritonavir
  • Phase
    CSR.ORG
    Sex
    Female & Male
    Age
    18+ years

    Protocol Summary

    The purpose of this study is to study the safety and efficacy of Amprenavir/ritonavir or

    saquinavir/ritonavir in HIV infected patients that have failed Kaletra as their second

    protease inhibitor based HAART.

    Study Locations

    Location
    Status
    Location
    Phoenix Body Positive, Inc.
    Phoenix,, Arizona, United States, 85006
    Status
    Not applicable
    Location
    AIDS Health Care Foundation - Research Center
    Los Angeles, California, United States, 90027
    Status
    Not applicable
    Location
    20th Avenue Medical Center Kaiser Permanente
    Denver, Colorado, United States, 80205
    Status
    Not applicable
    Location
    University of Colorado Health Sciences Center
    Denver, Colorado, United States, 80262
    Status
    Not applicable
    Location
    IDC Research Initiative
    Altamonte Springs, Florida, United States, 32701
    Status
    Not applicable
    Location
    Associates in Research
    Fort Myers, Florida, United States, 33901
    Status
    Not applicable
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