A Randomized Study of Activity, Safety, and Tolerance of Oral Ro 24-7429 (Tat Antagonist) in Patients With HIV Infection
Ro 24-7429
+ Zidovudine
+ Didanosine
Infections transmises par le sang+14
+ Maladies génito-urinaires
+ Maladies Génitales
Étude thérapeutique
Résumé
The HIV genome contains a number of genes that regulate viral replication. Control of the activity of these genes and their encoded proteins represents a potential target for development of new antiretroviral drugs. The tat (transactivator of transcription of HIV) antagonist Ro 24-7429 is the first compound for clinical testing that utilizes this approach for therapy of HIV infection. Ninety-six patients (four treatment arms of 24 patients each) are randomized to receive oral Ro 24-7429 at 1 of 3 doses or nucleoside control (either zidovudine or didanosine). The study will be blinded only for the arms receiving Ro 24-7429. Treatment continues for 12 weeks. After 12 weeks, patients on the nucleoside control arm receive the highest tolerated dose of Ro 24-7429 in addition to their nucleoside.
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.96 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 12 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: Chemoprophylaxis for P. carinii pneumonia, TB, and mucocutaneous candidiasis. Methadone maintenance. Hormonal contraceptives. Patients must have: HIV-1 seropositivity. CD4 count 50 - 500 cells/mm3. Life expectancy of at least 24 weeks. Stable weight (+/- 2 kg) by 28 days prior to study entry (by history). NOTE: At least 50 percent of patients must be p24 antigen positive (>= 50 pg/ml). Exclusion Criteria Co-existing Condition: Patients with the following symptoms and conditions are excluded: Known or suspected hypersensitivity to benzodiazepines. Presence of any malignancy other than basal cell carcinoma or limited cutaneous Kaposi's sarcoma (defined as no more than five lesions with no mucosal involvement). Ongoing diarrhea, defined as more than 2 liquid stools per day. History, physical exam, or laboratory results consistent with a subclinical AIDS-defining opportunistic infection. Grade 2 or greater signs and symptoms of AIDS Dementia Complex. Evidence of clinically significant cardiac, respiratory, hepatic, gastrointestinal, endocrine, hematologic, psychiatric, neurologic, dermatologic, or allergic disease. Concurrent Medication: Excluded: Chronic suppressive therapy for CMV, MAI, toxoplasmosis, cryptococcosis, cryptosporidiosis, coccidioidomycosis, and histoplasmosis. ddC, ddI, AZT (except for control groups) or other experimental antiretrovirals or immunomodulating agents. Other medications excluded from the study. Patients with the following prior conditions are excluded: History of serious adverse reactions to benzodiazepines. History of intolerance to AZT at 600 mg/day or less or ddI at 400 mg/day or less. History of unexplained fever, defined as a temperature of 38.5 deg C or greater with or without night sweats for more than 7 of the past 28 days. Prior Medication: Excluded: Benzodiazepines within 14 days prior to study entry. Active drug or alcohol abuse that would interfere with study compliance.
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 4 sites
Johns Hopkins Hosp
Baltimore, United StatesHarvard (Massachusetts Gen Hosp)
Boston, United StatesCase Western Reserve Univ
Cleveland, United States