Two Doses of 3TC (Lamivudine; GR109714X) for Patients 12 Years and Older
Collecte de données
Infections transmises par le sang+14
+ Maladies génito-urinaires
+ Maladies Génitales
Étude thérapeutique
Résumé
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.
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 3 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
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.
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 1 site
Kern - McNeill International
Morristown, United StatesOuvrir Kern - McNeill International dans Google Maps