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Amprenavir/Ritonavir or Saquinavir/Ritonavir in HIV-Infected Patients Following Failure with Kaletra (lopinavir/ritonavir) as Their Second Protease Inhibitor. Clinical Trials Data presented on Clinical Trials Search is not meant to be a substitute for qualified health advice, visits or treatment with a real mD. We are not doctors. Always consult your doctor about Amprenavir/Ritonavir or Saquinavir/Ritonavir in HIV-Infected Patients Following Failure with Kaletra (lopinavir/ritonavir) as Their Second Protease Inhibitor. conditions. Clinical Trials Search.org is a site devoted to listing clinical research studies in human subjects. Amprenavir/Ritonavir or Saquinavir/Ritonavir in HIV-Infected Patients Following Failure with Kaletra (lopinavir/ritonavir) as Their Second Protease Inhibitor. Clinical research trials and Amprenavir/Ritonavir or Saquinavir/Ritonavir in HIV-Infected Patients Following Failure with Kaletra (lopinavir/ritonavir) as Their Second Protease Inhibitor. healthcare trials happen in many of places across the United States. A clinical trial or clinical study is a research project with human volunteer subjects. Clinical drug trials and pharmaceutical clinical trials generally assess the effectivity of new drugs. The purpose of the studies / projects is to solve particular human medical questions. Clinical trials are a popular way for doctors, government agencies, and private sector companies to discover cures for all varieties of conditions, such as Amprenavir/Ritonavir or Saquinavir/Ritonavir in HIV-Infected Patients Following Failure with Kaletra (lopinavir/ritonavir) as Their Second Protease Inhibitor.. Amprenavir/Ritonavir or Saquinavir/Ritonavir in HIV-Infected Patients Following Failure with Kaletra (lopinavir/ritonavir) as Their Second Protease Inhibitor. Clinical Trials and other clinical trials allow volunteers to have health treatment alternatives before they are available to the masses. Some times the human subjects obtain treatment for without cost, and sometimes they are compensated for their time. Occasionally there is a cost for a Amprenavir/Ritonavir or Saquinavir/Ritonavir in HIV-Infected Patients Following Failure with Kaletra (lopinavir/ritonavir) as Their Second Protease Inhibitor. clinical trial. Test subjects oftentimes receive the most effective healthcare possible for their Amprenavir/Ritonavir or Saquinavir/Ritonavir in HIV-Infected Patients Following Failure with Kaletra (lopinavir/ritonavir) as Their Second Protease Inhibitor. condition. Dangers are a reality, however, and may include extra or frequent physician visits, healthcare dangers (possibly life-jeopardising), and/or the treatment being uneffective. Trials are federally governed with rigorous guidelines to protect clinical trials patients.
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Home > "A" Clinical Trials Conditions > Amprenavir/Ritonavir or Saquinavir/Ritonavir in HIV-Infected Patients Following Failure with Kaletra (lopinavir/ritonavir) as Their Second Protease Inhibitor. Amprenavir/Ritonavir or Saquinavir/Ritonavir in HIV-Infected Patients Following Failure with Kaletra (lopinavir/ritonavir) as Their Second Protease Inhibitor.
Amprenavir/Ritonavir or Saquinavir/Ritonavir in HIV-Infected Patients Following Failure with Kaletra (lopinavir/ritonavir) as Their Second Protease Inhibitor.
For Condition: HIV Infections
Status: Completed
Sponsor(s): Abbott Laboratories ,
Synopsis: 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.
Details:
Eligibility:
Study Type: Interventional, Treatment, Open Label, Uncontrolled, Parallel Assignment, Safety/Efficacy Study
Minimum Age/Maximum Age: 18 Years/
Genders: Both
Protocol Entry Criteria: Inclusion: - Subject must remain on current antiretroviral therapy during screening until a new regimen is initiated. - Subject demonstrates reduced susceptibility to lopinavir. - Subject's two most recent viral loads obtained after at least 16 weeks of lopinavir/ritonavir therapy, and while still on Kaletra therapy must be at least 1,000 copies/mL. - The Kaletra regimen must be the subject's second PI containing regimen and must not contain any other PIs. - Subject is at least 18 years of age. - Subject has not been treated for an active opportunistic infection within 30 days of screening. Exclusion: - Subject has a history of active substance abuse or psychiatric illness that could preclude compliance to the protocol. - Female subject pregnant or lactating. - Use of an Investigational drug within 30 days prior to the initiation of drug dosing. - Subject is receiving systemic chemotherapy. - Subject has a history of acute or chronic pancreatitis.
Total Enrollment: 16
Location and Contact Information:
Hospital Universitario Vergen del Rocio
Sevilla, , 41013
Spain
Hospital do Servidor Publico Estadual de Sao Paulo
Sao Paulo, SP, 04029-000
Brazil
Hospital Carlos III
Madrid, , 28010
Spain
Hospital Yves Le Foll
Saint-Brieuc, , 22023
France
University of Miami School of Medicine
Miami, Florida, 33136
United States
Diversified Medical Practices, P.A.
Houston, Texas, 77027
United States
Infectious Disease Research Institute, Inc.
Tampa, Florida, 33614
United States
Phillip Sestak, M.D
Vancouver, British Columbia, V6Z 3T1
Canada
John B. Montana, M.D.
New York City, New York, 10011
United States
Bornemann Internal Medicine
Reading, Pennsylvania, 19601
United States
Hampton Roads Medical Specialists
Hampton, Virginia, 23666
United States
Wojewodzki Szpital Zakazny
Warszawa, , 01-201
Poland
IRCCS "L. Spallanzani"
Rome, , 00149
Italy
S. Raffaele Hospital
Milan, , 20127
Italy
Royal Free Hospital
London, , NW3 2QG
United Kingdom
Ottawa Hospital General Campus
Ottawa, Ontario, K1H 8L6
Canada
Saint Michael's Medical Center
Newark, New Jersey, 07102
United States
20th Avenue Medical Center Kaiser Permanente
Denver, Colorado, 80205
United States
IDC Research Initiative
Altamonte Springs, Florida, 32701
United States
The Research & Education Group
Portland, Oregon, 97209
United States
Service du C.I.S.I.H. - C.H.U. de Grenoble
La Tronche, , 38700
France
Associates in Research
Ft. Myers, Florida, 33901
United States
CORE Center
Chicago, Illinois, 60612
United States
Hospital Germans Trias I Pujol
Badalona, , 08916
Spain
Donna E. Sweet, M.D.
Wichita, Kansas, 67214
United States
State University of New York at Stony Brook
Stony Brook, New York, 11794-08153
United States
Hospital Evandro Chagas - Fiocryz
Rio de Janeiro, , 21045-900
Brazil
AIDS Health Care Foundation - Research Center
Los Angeles, California, 90027
United States
AIDS Research Consortium of Atlanta, Inc.
Atlanta, Georgia, 30308
United States
Tour Drouet - C.H.U. Brabois
Vandoeuvre, Cedex, 54511
France
Hospital Muniz - FUNDAI
Buenos Aires, , 4304-2180
Argentina
Hospital Tenon
Paris, , 75020
France
La Seyne sur Mer, Hopital Chalucet
Toulon, , 83056
France
III Infectious Diseases Division IRCCS "L. Spallanzani"
Rome, , 00149
Italy
David Parks, M.D.
St. Louis, Missouri, 63139
United States
David Wright, M.D.
Austin, Texas, 78705
United States
Hospital Heliopolis
Sao Paulo, , 01332-000
Brazil
Montreal Chest Institute/Royal Victoria Hospital
Montreal, Quebec, H2X 2PA
Canada
Fundacion Huesped
Buenos Aires, , 4981-1855
Argentina
Groupe Hospitalier Cochin -Saint-Vincent-de-Paul La Roche-Guyon
Paris, , 75679
France
Hospital De La Sta Creu I San Pau
Barcelona, , 08025
Spain
University of Cincinnati Medical Center
Cincinnati, Ohio, 45267-0405
United States
Centro Familiar, Inc
Ponce, , 00731
Puerto Rico
New Puerto Rico CONCRA
Rio Piedras, , 00925
Puerto Rico
University of Colorado Health Sciences Center
Denver, Colorado, 80262
United States
Hospital Clinic I Provincial
Barcelona, , 08036
Spain
Hospital La Paz
Madrid, , 28046
Spain
Gary J. Richmond, M.D.
Ft. Lauderdale, Florida, 33316
United States
Toronto General Hospital Division of The University Health Network
Toronto, Ontario, M5G-2C4
Canada
Phoenix Body Positive, Inc.
Phoenix, Arizona, 85006
United States
Howard A. Grossman, M.D.
New York City, New York, 10011
United States
Hospital "Amedeo di Savoia"
Torino, , 10149
Italy
Additional Information:
Study ID Numbers: M00-261;
Study Start Date: April 2001
Record last reviewed: September 2003
Additional information available at: clinicaltrials.gov
Clinicaltrials.gov Reference link: NCT00038519
Other Hiv Infections Studies:
1. A Phase I, Multicenter, Randomized, Double-Blind, Placebo-Controlled HIV-1 Vaccine Trial to Evaluate the Safety and Immunogenicity of Low Dose MN rsgp120/HIV-1 (Genentech) in Combination with QS21 Adjuvant or Alum in Healthy Adults
2. A Long-Term, Follow-On Safety Study of Four Doses of OPC-8212 (Vesnarinone) in HIV-Infected Persons
3. Subcutaneously Administered Aldesleukin ( Interleukin-2; IL-2 ) Therapy in HIV-Infected Patients
4. Comparing the Safety, Effectiveness, and Tolerability of Three Anti-HIV Drug Regimens for Treatment-Naive Patients
5. A Multicenter Study To Determine Foscarnet Dose Response in HIV Infected Patients with PGL and/or Constitutional Disease
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Amprenavir/Ritonavir or Saquinavir/Ritonavir in HIV-Infected Patients Following Failure with Kaletra (lopinavir/ritonavir) as Their Second Protease Inhibitor.
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