A Randomized, Double-Blind Study of the Antiviral Activity of Once-Daily and Twice-Daily Dosing of Didanosine in Combination With Twice-Daily Dosing of Stavudine in HIV-Infected Subjects
Stavudine
+ Didanosine
Infections transmises par le sang+11
+ Maladies génito-urinaires
+ Maladies Génitales
Étude thérapeutique
Résumé
Date de début de l'étude : 1 février 2004
Date à laquelle le premier participant a commencé l'étude.Patients are randomized to receive ddI given either qd or bid in combination with d4T given bid (no doses specified).
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.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 18 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 Patients must have: Documented HIV infection. CD4 cell count of at least 100 cells/mm3. Plasma HIV RNA count of 10,000 copies/ml or more within 14 days prior to study entry. Exclusion Criteria Co-existing Condition: Patients with the following conditions and symptoms are excluded: Presence of a newly diagnosed AIDS-defining opportunistic infection requiring acute therapy at the time of enrollment. Bilateral peripheral neuropathy or signs and symptoms of bilateral peripheral neuropathy greater than or equal to Grade 2 at the time of screening. Inability to tolerate oral medication. Any other clinical condition that would preclude compliance with dosing requirements. Patients with the following prior conditions are excluded: History of acute or chronic pancreatitis. Intractable diarrhea (6 or more loose stools/day for more than 7 consecutive days) within 30 days prior to study entry. Proven or suspected acute hepatitis within 30 days prior to study entry. 1. Potent neurotoxic drugs, such as vincristine and thalidomide. Other anti-HIV therapy. 1. Prophylaxis for pneumocystis carinii pneumonia (PCP) is strongly recommended for patients with CD4 cell counts less than or equal to 200/mm3 or who have had a prior episode of PCP. Immunizations recommended by ACIP for routine practice. Erythropoietin and G-CSF are allowed if myelosuppression emerges on study. 1. Any antiretroviral therapy. Agents with significant systemic myelosuppressive, neurotoxic, pancreatotoxic, hepatotoxic, or cytotoxic potential within 3 months of study entry. 1. Any prior antiretroviral therapy. Agents with significant systemic myelosuppressive, neurotoxic, pancreatotoxic, hepatotoxic, or cytotoxic potential within 3 months of study entry. Active alcohol or substance abuse that would prevent adequate compliance or would increase the risk of pancreatitis.
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 13 sites
Clinsites / Sorra Research Ctr
Birmingham, United StatesOuvrir Clinsites / Sorra Research Ctr dans Google MapsShared Med Research Foundation
Tarzana, United StatesIndiana Univ School of Medicine / Dept of Infect Dis
Indianapolis, United StatesMedicine Faculty Associates
Ypsilanti, United States