Two Doses of 3TC (Lamivudine; GR109714X) for Patients 12 Years and Older
Colección de datos
Complejo Relacionado con el SIDA+13
+ Enfermedades Transmisibles
+ Enfermedades Urogenitales
Estudio de Tratamiento
Resumen
This study focuses on a medication called 3TC, or Lamivudine, for individuals aged 12 and above. The main goal is to evaluate the effectiveness of two different doses of 3TC, with the duration of treatment decided by the patient's doctor or until the program ends. For those under 12, a lower dose of 3TC is provided. The study is particularly important as it aims to improve treatment options for the condition, offering valuable insights into the use of 3TC. During the study, participants are monitored monthly. In some selected locations, blood samples are collected every three months from patients who test positive for HBsAg. An amendment made on 02/28/95 allows patients enrolled before 03/01/95 to either continue with their current dose of 3TC or switch to a combination therapy involving 3TC and another medication, zidovudine.
Protocolo
Esta sección proporciona detalles del plan del estudio, incluyendo cómo está diseñado y qué se está evaluando.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 3 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
Patients must: * Have progressive, symptomatic HIV disease. * Have a mean CD4 count \<= 99 cells/mm3 for adults and \<= 300 cells/mm3 for children (original design was CD4 count \<= 300 cells/mm3 for both adults and children). * Be unable to participate in a controlled trial. * Be refractory to or unable to tolerate other therapies. * Be able to attend clinic on a monthly schedule. * Have consent of parent or guardian if under the age of consent. NOTE: * If a pregnant or breast-feeding woman requests enrollment, her physician should contact Glaxo staff directly to discuss the case. Practice of unsafe sex.
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 una ubicación
Kern - McNeill International
Morristown, United StatesAbrir Kern - McNeill International en Google Maps