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
Infecciones Transmitidas por la Sangre+13
+ Enfermedades Urogenitales
+ Enfermedades Genitales
Estudio de Tratamiento
Resumen
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.
Protocolo
Esta sección proporciona detalles del plan del estudio, incluyendo cómo está diseñado y qué se está evaluando.Se reclutarán 96 pacientes
Número total de participantes que el ensayo clínico espera reclutar.Estudio de Tratamiento
Elegibilidad
Los investigadores buscan pacientes que cumplan ciertos criterios, conocidos como criterios de elegibilidad: estado general de salud o tratamientos previos.Cualquier sexo
Sexo biológico de los participantes elegibles para inscribirse.A partir de 12 años
Rango de edades de los participantes que pueden unirse al estudio.Voluntarios sanos no permitidos
Indica si personas sanas, sin la condición que se estudia, pueden participar.Condiciones
Patología
Criterios
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.
Centros del Estudio
Estos son los hospitales, clínicas o centros de investigación donde se lleva a cabo el estudio. Puedes encontrar la ubicación más cercana a ti y su estado de reclutamiento.Este estudio tiene 4 ubicaciones
Johns Hopkins Hosp
Baltimore, United StatesHarvard (Massachusetts Gen Hosp)
Boston, United StatesCase Western Reserve Univ
Cleveland, United States