Alzheimer's & dementia : the journal of the Alzheimer's Association
Phase 3 randomized trial of latozinemab in frontotemporal dementia due to GRN mutations
Par Simmons A, Boeve B, Ber IL et 22 autres.
Contenu en anglais
Résumé
Introduction
Heterozygous progranulin gene mutations causing frontotemporal dementia (FTD-GRN) are associated with deficiency in progranulin (PGRN). Latozinemab is a human monoclonal immunoglobulin G1 (IgG1) antibody designed to elevate PGRN levels in people with heterozygous loss-of-function (LOF) GRN mutations.



