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TrialConditionsStatusPhaseUpdatedMore infoNCT ID
A Study of PBFT02 in Participants With FTD and Mutations in the Granulin Precursor (GRN) or C9ORF72 GenesFrontotemporal Lobar Degeneration, Nutritional and Metabolic Diseases, Pick disease, TDP-43 proteinopathy, brain disorder, central nervous system disorder, cognitive disorder, dementia, frontotemporal dementia, frontotemporal dementia with motor neuron disease, metabolic disease, nervous system disorder, neurodegenerative disease, proteostasis deficiencies, psychiatric disorderActive, not recruitingPhase 1 / Phase 22026-05-15NCT04747431