Estudio post-autorización para monitorear la eficacia, efectividad y seguridad de maribavir (LIVTENCITY®) en pacientes con infección por citomegalovirus (CMV) post-trasplante en Argentina

Criterios de inclusión

• Adult participants (18 years or older) and pediatric participants (12 years of age and older and weighing at least 35 kilogram \[kg\]) with post-transplant CMV infection/disease that is refractory to treatment (with or without genotypic resistance) with ganciclovir, valganciclovir, cidofovir or foscarnet in the real-world setting of common clinical practice in Argentina.
• Have received at least one dose of maribavir according to approved indications.
• Have signed the mandatory informed consent/assent that has been agreed with national regulatory authorities (ANMAT) as applicable.