Resumen

The main aim of this study is to learn about the safety profile of lanadelumab in teenagers and adults with hereditary angioedema (HAE) in Argentina as part of routine routine practice. This study is about collecting data only. The study sponsor will not be involved in how participants are treated but will provide instructions on how the clinics will record what happens during the study. The study will collect data from the participant's medical records. Participants do not need to visit their doctor in addition to their normal visits.

Elegibilidad

Edad mínima: 12 YearsSexo: ALL

Criterios de inclusión

Participants (\>=12 years) with investigator confirmed diagnosis of HAE.
Have received at least one dose of lanadelumab according to approved indications.
Signed the mandatory consent that has been agreed with national regulatory authorities (ANMAT) as applicable.

Criterios de exclusión

\- Hypersensitivity to the active substance or to any of the excipients.

Ubicaciones

Ic Projects Srl

Ciudad Autónoma de Buenos Aires, Buenos Aires, Argentina

Patrocinadores

PrincipalTakeda

Post Authorization Study to Monitor Efficacy, Effectiveness and Safety of Lanadelumab (Takhzyro®) in Patients Aged 12 Years and Older With Hereditary Angioedema (HAE) in Argentina