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Amprenavir/Ritonavir, Saquinavir/Ritonavir or Efavirenz in HIV-Infected Patients Following Failure with Kaletra (ABT-378/Ritonavir) as Their First Protease Inhibitor Based HAART Clinical Trials Information presented on Clinical Trials Search is not designed to be a substitute for certified medical advice, trips or professional assistance with a real medical doctor. We aren't docs. Always confer with your doctor about Amprenavir/Ritonavir, Saquinavir/Ritonavir or Efavirenz in HIV-Infected Patients Following Failure with Kaletra (ABT-378/Ritonavir) as Their First Protease Inhibitor Based HAART conditions. Clinical Trials Search.org is a website committed to listing clinical research studies in human subjects. Amprenavir/Ritonavir, Saquinavir/Ritonavir or Efavirenz in HIV-Infected Patients Following Failure with Kaletra (ABT-378/Ritonavir) as Their First Protease Inhibitor Based HAART Clinical research trials and Amprenavir/Ritonavir, Saquinavir/Ritonavir or Efavirenz in HIV-Infected Patients Following Failure with Kaletra (ABT-378/Ritonavir) as Their First Protease Inhibitor Based HAART health trials happen in many of cities across the US. A clinical trial or clinical study is a research project with human volunteer subjects. Clinical drug trials and pharmaceutical clinical trials generally measure the effectualness of new does drugs. The intention of the studies / projects is to figure out particular human healthcare questions. Clinical trials are a popular manner for doctors, government agencies, and private sector corporations to detect cures for all forms of circumstances, like Amprenavir/Ritonavir, Saquinavir/Ritonavir or Efavirenz in HIV-Infected Patients Following Failure with Kaletra (ABT-378/Ritonavir) as Their First Protease Inhibitor Based HAART. Amprenavir/Ritonavir, Saquinavir/Ritonavir or Efavirenz in HIV-Infected Patients Following Failure with Kaletra (ABT-378/Ritonavir) as Their First Protease Inhibitor Based HAART Clinical Trials and other clinical trials allow for volunteers to undergo medical treatment options before they are available to the general public. Most times the subjects get treatment for free of charge, and occasionally they are paid for their time. Occasionally there is a cost for a Amprenavir/Ritonavir, Saquinavir/Ritonavir or Efavirenz in HIV-Infected Patients Following Failure with Kaletra (ABT-378/Ritonavir) as Their First Protease Inhibitor Based HAART clinical trial. Subjects frequently get the best healthcare possible for their Amprenavir/Ritonavir, Saquinavir/Ritonavir or Efavirenz in HIV-Infected Patients Following Failure with Kaletra (ABT-378/Ritonavir) as Their First Protease Inhibitor Based HAART condition. Hazards are a reality, however, and could include more or frequent mD visits, health risks (possibly life-jeopardizing), and/or the treatment being ineffectual. Trials are federally regulated with exacting guidelines to protect clinical trials patients.
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Home > "A" Clinical Trials Conditions > Amprenavir/Ritonavir, Saquinavir/Ritonavir or Efavirenz in HIV-Infected Patients Following Failure with Kaletra (ABT-378/Ritonavir) as Their First Protease Inhibitor Based HAART Amprenavir/Ritonavir, Saquinavir/Ritonavir or Efavirenz in HIV-Infected Patients Following Failure with Kaletra (ABT-378/Ritonavir) as Their First Protease Inhibitor Based HAART
Amprenavir/Ritonavir, Saquinavir/Ritonavir or Efavirenz in HIV-Infected Patients Following Failure with Kaletra (ABT-378/Ritonavir) as Their First Protease Inhibitor Based HAART
For Condition: HIV Infections
Status: Completed
Sponsor(s): Abbott Laboratories ,
Synopsis: The purpose of this study is to study amprenavir/ritonavir, saquinavir/ritonavir or efavirenz in HIV-infected patients following failure with Kaletra (ABT-378/ritonavir as their first protease inhibitor based HAART.
Details:
Eligibility:
Study Type: Interventional, Treatment, Non-Randomized, Open Label, Uncontrolled, Parallel Assignment, Safety/Efficacy Study
Minimum Age/Maximum Age: 18 Years/
Genders: Both
Protocol Entry Criteria: Inclusion: - Remain on present anti-HIV drugs during screening until a new regimen is started. - Have a viral load of at least 1,000 copies/ml on the 2 most recent tests after at least 24 weeks of lopinavir/ritonavir and while still on it. - Have an HIV which shows reduced susceptibility to lopinavir. - Are at least 18 years old. - Are not presently ill. - Have not been treated for an opportunistic infection within 30 days of screening. - Agree not to take certain drugs and agree to inform and get permission from the doctor before taking any medicines, over the counter medicines, herbal medicines, alcohol or recreational drugs. - Agree to use an accepted barrier method of birth control. Exclusion: - Female subject is pregnant or lactating. - Have taken any protease inhibitor other than lopinavir/ritonavir for more that two weeks. - Are taking chemotherapy. - Have a medical problem with their pancreas. - Have been screened for this study within the past 12 weeks. - Appear to be unsuitable in the opinion of the doctor.
Total Enrollment: 24
Location and Contact Information:
AIDS Health Care Foundation - Research Center
Los Angeles, California, 90027
United States
La Seyne sur Mer, Hopital Chalucet
Toulon, , 83056
France
Hospital Heliopolis
Sao Paulo, , 01332-000
Brazil
Gary J. Richmond, M.D.
Ft. Lauderdale, Florida, 33316
United States
Phoenix Body Positive, Inc.
Phoenix, Arizona, 85006
United States
Klinikum J.W. Goethe Universitat
Frankfurt, , 60596
Germany
University of Miami School of Medicine
Miami, Florida, 33136
United States
Hospital Yves Le Foll
Saint-Brieuc, , 22023
France
Donna E. Sweet, M.D.
Wichita, Kansas, 67214
United States
Hospital Clinic I Provincial
Barcelona, , 08036
Spain
CORE Center
Chicago, Illinois, 60612
United States
Centro Familiar, Inc
Ponce, , 00731
Puerto Rico
Howard A. Grossman, M.D.
New York City, New York, 10011
United States
The Research & Education Group
Portland, Oregon, 97209
United States
Universitatsklinikum
Dusseldorf, , 40225
Germany
Hospital Germans Trias I Pujol
Badalona, , 08916
Spain
David Parks, M.D.
St. Louis, Missouri, 63139
United States
Diversified Medical Practices, P.A.
Houston, Texas, 77027
United States
Infectious Disease Research Institute, Inc.
Tampa, Florida, 33614
United States
David Wright, M.D.
Austin, Texas, 78705
United States
Albrecht Ulmer, M.D.
Stuttgart, , 70197
Germany
Institut fur Immunologie Pathologie und Molekularbiologie
Hamburg, , 20099
Germany
University of Colorado Health Sciences Center
Denver, Colorado, 80262
United States
State University of New York at Stony Brook
Stony Brook, New York, 11794-08153
United States
Associates in Research
Ft. Myers, Florida, 33901
United States
Hospital La Paz
Madrid, , 28046
Spain
Ottawa Hospital General Campus
Ottawa, Ontario, K1H 8L6
Canada
Hospital Carlos III
Madrid, , 28010
Spain
20th Avenue Medical Center Kaiser Permanente
Denver, Colorado, 80205
United States
Fundacion Huesped
Buenos Aires, , 4981-1855
Argentina
University of Texas Medical Branch
Galveston, Texas, 77555-0435
United States
Toronto General Hospital Division of The University Health Network
Toronto, Ontario, M5G-2C4
Canada
Hopital Michalon - C.H.U. de Grenoble
Grenoble, , 38043
France
Hopital Tenon
Paris, , 75970
France
Paul J. Cimoch, M.D.
Fountain Valley, California, 92780
United States
C.H.U. Brabois - Tour Drouet, Rue du Morvan
Vandoeuvre, , 54511
France
Royal Free Hospital
London, , NW3 2QG
United Kingdom
Hospital De La Sta Creu I San Pau
Barcelona, , 08025
Spain
Hospital Muniz - FUNDAI
Buenos Aires, , 4304-2180
Argentina
Wojewodzki Szpital Zakazny
Warszawa, , 01-201
Poland
S. Raffaele Hospital
Milan, , 20127
Italy
New Puerto Rico CONCRA
Rio Piedras, , 00925
Puerto Rico
University of Cincinnati Medical Center
Cincinnati, Ohio, 45267-0405
United States
Hospital Universitario Vergen del Rocio
Sevilla, , 41013
Spain
Tower Infectious Diseases Medical Associates
Los Angeles, California, 90048
United States
Saint Michael's Medical Center
Newark, New Jersey, 07102
United States
IDC Research Initiative
Altamonte Springs, Florida, 32701
United States
CORE Center
Berlin, , 13353
Germany
Hampton Roads Medical Specialists
Hampton, Virginia, 23666
United States
AIDS Research Consortium of Atlanta, Inc.
Atlanta, Georgia, 30308
United States
Groupe Hospitalier Cochin -Saint-Vincent-de-Paul La Roche-Guyon
Paris, , 75679
France
Montreal Chest Institute/Royal Victoria Hospital
Montreal, Quebec, H2X 2PA
Canada
John B. Montana, M.D.
New York City, New York, 10011
United States
Bornemann Internal Medicine
Reading, Pennsylvania, 19601
United States
Additional Information:
Study ID Numbers: M01-287;
Study Start Date: April 2001
Record last reviewed: September 2003
Additional information available at: clinicaltrials.gov
Clinicaltrials.gov Reference link: NCT00038532
Other Hiv Infections Studies:
1. A Compassionate Treatment Protocol for the Use of Trimetrexate Glucuronate (Neutrexin) With Leucovorin Protection for European Adult Patients (>= 13 Years Old) With Pneumocystis carinii Pneumonia
2. A Comparison of Nelfinavir Plus Saquinavir Plus Delavirdine or 3TC/ZDV Versus Nelfinavir Plus 3TC/ZDV in HIV-Infected Patients
3. A Study of Stem Cells and Filgrastim
4. Open label safety study (OLSS) of tipranavir/ritonavir in HIV patients with limited treatment options
5. A Study of DAPD Alone Versus DAPD Plus MMF for Treatment of HIV Infection
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Amprenavir/Ritonavir, Saquinavir/Ritonavir or Efavirenz in HIV-Infected Patients Following Failure with Kaletra (ABT-378/Ritonavir) as Their First Protease Inhibitor Based HAART
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