A Pilot Pharmacokinetic Phase I Evaluation of BI-RG-587 in HIV-Infected Children
Nevirapine
Infections transmises par le sang+13
+ Maladies génito-urinaires
+ Maladies Génitales
Étude thérapeutique
Résumé
Test tube studies have shown that nevirapine (BI-RG-587) inhibits replication (reproduction) of HIV. Nevirapine works with zidovudine (AZT) and is active against strains of the virus that are resistant to AZT. Studies of the drug in HIV-infected adults showed no serious adverse effects. Two doses, given by mouth, are evaluated: Three patients receive the lower dose, and 7 days after the third patient receives the lower dose, three additional patients receive the higher dose. After dosing, blood is drawn at 1, 2, 4, 8, 24, 48, 96, 168 hours to measure blood levels of the drug.
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.6 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.De 2 mois à 13 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: Intravenous gammaglobulin. Pneumocystis prophylaxis according to published guidelines. Patients must have the following: HIV infection. Parent or guardian must be available to give written informed consent. Exclusion Criteria Concurrent Medication: Excluded: Zidovudine (AZT). Steroid dependency. Excluded within 1 hour before and 4 hours after study drug administration: Drugs that might interfere with the absorption of study drug (H2 blockers, antacids, carafate, cholestyramine). Benzodiazepines. Alcohol-containing substances. Concurrent Treatment: Excluded: Requiring supplemental oxygen. Patients with the following are excluded: Active opportunistic or serious bacterial infection. Lymphoid interstitial pneumonitis (LIP) and steroid dependent or requiring supplemental oxygen or have a pretreatment pa02 < 70 mm Hg. Pre-existing malignancies. Prior Medication: Excluded: Zidovudine (AZT) within 7 days prior to administration of study drug. Excluded for at least 4 weeks prior to drug administration: Other approved or investigational antiretroviral agents. All other investigational agents. Biologic response modifiers (e.g., interferon) or immunomodulators. Immunosuppressive agents (including glucocorticoids). Coumadin and other anticoagulant medications. Prior Treatment: Excluded: Red blood cell transfusion within 4 weeks of study entry. Patients may not have the following: Opportunistic or serious bacterial infection. Zidovudine (AZT) > 7 days prior to administration of study drug. Active alcohol or drug abuse.
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
Univ of Massachusetts Med Ctr / Biotech II
Worcester, United StatesOuvrir Univ of Massachusetts Med Ctr / Biotech II dans Google Maps