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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.

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

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