A Pilot Study to Evaluate the Immunologic Consequences of a Highly Active Antiretroviral Therapy Regimen (HAART) Consisting of Ritonavir (ABT-538), Zidovudine (AZT), and Lamivudine (3TC) in Moderately Advanced HIV-1 Disease
Ritonavir
+ Lamivudine
+ Zidovudine
Infections transmises par le sang+14
+ Maladies génito-urinaires
+ Maladies Génitales
Étude thérapeutique
Résumé
Although plasma viral load drops dramatically after initiation of powerful antiretrovirals, it does not drop to zero. It appears that a new steady state is reached, suggesting that a reservoir may exist of virus-producing cells, possibly cells of monocyte/macrophage lineage, that continue to produce a low level of virus despite antiretroviral treatment. Patients undergo 5 weeks of antiretroviral washout before initiating therapy with ritonavir alone for 9 days, followed by combination therapy with ritonavir, zidovudine, and lamivudine from day 10 through week 48. [AS PER AMENDMENT 1/31/97: The availability of the current, open-label study treatment has been extended to allow patients who have completed 48 weeks of therapy to continue protocol therapy until the last enrolled patient completes 48 weeks of study treatment.]
Protocole
Cette section fournit des détails sur le plan de l'étude, y compris la manière dont l'étude est conçue et ce qu'elle évalue.55 participants à inclure
Nombre total de participants que l'essai clinique vise à recruter.Traitement
Éligibilité
Les chercheurs recherchent des patients correspondant à une certaine description appelée critères d'éligibilité : état de santé général ou traitements antérieurs du patient.Tout sexe
Le sexe biologique des participants éligibles à s'inscrire.À partir de 16 ans
Tranche d'âge des participants éligibles à participer.Volontaires sains non autorisés
Indique si les individus en bonne santé et ne présentant pas la condition étudiée peuvent participer.Conditions
Pathologie
Critères
Inclusion Criteria Concurrent Medication: Allowed: Recombinant erythropoietin and/or G-CSF for AZT-related bone marrow suppression. Antibiotics other than metronidazole. PCP prophylaxis. Regularly prescribed medications such as antipyretics, analgesics, allergy medicine, and oral contraceptives. Vitamins and herbal therapies. Concurrent Treatment: Allowed: Acupuncture. Visualization techniques. Patients must have: Documented HIV infection. CD4 count 100-300 cells/mm3. At least 3 consecutive months of prior AZT at a dosage of 500-600 mg bid, but with 5 weeks of antiretroviral washout prior to study entry. Consent of parent or guardian if less than 18 years old. Prior Medication: Required: Prior AZT at 500-600 mg bid at any time. PCP prophylaxis during antiretroviral washout. Allowed: Prior ddI and/or ddC. Prior recombinant erythropoietin and/or G-CSF for AZT-related bone marrow suppression. Exclusion Criteria Co-existing Condition: Patients with the following symptoms or conditions are excluded: Chronic pancreatitis. Psychological conditions that would affect compliance. Intolerance to 500-600 mg/day AZT. Concurrent participation on another antiretroviral research treatment study (study treatment for opportunistic infection or complications of HIV is allowed). Considered likely to be noncompliant on study. Concurrent Medication: Excluded: Immunomodulators such as systemic corticosteroids, thalidomide, or cytokines. Rifabutin. Disulfiram (Antabuse) or other medications with similar effects, including metronidazole. Other drugs contraindicated with ritonavir. [AS PER AMENDMENT 8/27/96: Immunization must be avoided during the antiretroviral washout period.] Patients with the following prior conditions are excluded: Active opportunistic infection or febrile illness with temperature >= 38.5 C within 3 days prior to study entry. History of acute pancreatitis within the past 2 years. Prior Medication: Excluded: Prior 3TC or a protease inhibitor. Experimental drugs except those for HIV-related conditions, within the past 30 days. [AS PER AMENDMENT 8/27/96: Immunization must be avoided prior to the antiretroviral washout period.] Active substance abuse.
Centres d'étude
Ce sont les hôpitaux, cliniques ou centres de recherche où l'essai est conduit. Vous pouvez trouver le site le plus proche de vous ainsi que son statut.Cette étude comporte 3 sites
University of Colorado Hospital CRS
Aurora, United StatesOuvrir University of Colorado Hospital CRS dans Google MapsRush Univ. Med. Ctr. ACTG CRS
Chicago, United StatesCase CRS
Cleveland, United States