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
For general inquiries, please contact
Study Complete
Results Available
Scientific Result Summary
Available Language(s): English
Study Details
Medical Condition
Study Drug
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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