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Condition: Frontotemporal Dementia Behavioral Variant Synced from ClinicalTrials.gov · July 28, 2026

Recruiting studies: Frontotemporal Dementia Behavioral Variant

Studies currently listed as recruiting on the public registry for this search term. Each page explains the study in plain language, with locations and the study team's contact details. Clinicians: generate a printable list for your patient →

A Study to Evaluate the Safety and Effect of AVB-101, a Gene Therapy Product, in Subjects With a Genetic Sub-type of Fro
Phase 1/Phase 2 · 19 location(s) · AviadoBio Ltd · NCT06064890
ARTFL LEFFTDS Longitudinal Frontotemporal Lobar Degeneration (ALLFTD)
Phase N/A · 27 location(s) · Mayo Clinic · NCT04363684
Premorbid Personality Profile of Patients With Cognitive and Behavioral Disorders
Phase N/A · 1 location(s) · Nantes University Hospital · NCT06059313
Links Between Self-awareness and Sociocognitive Processes in Neurodegenerative Diseases
Phase N/A · 1 location(s) · Assistance Publique - Hôpitaux de Paris · NCT07531732
A Study of the Behavioral Variant of Frontotemporal Dementia and Bipolar Disorder: a Neuroimaging and Epigenetics Integr
NA · 1 location(s) · Fondazione IRCCS Ca' Granda, Ospedale Maggiore Policlinico · NCT06706687
Social & Affective Cognition in Alzheimer's Disease & Associated Disorders
NA · 1 location(s) · University Hospital, Lille · NCT06338397
Diagnosing Frontotemporal Lobar Degeneration
Phase N/A · 1 location(s) · University Health Network, Toronto · NCT02964637
ECOCAPTURE for the Assessment of Apathy Under Real-life Conditions
Phase N/A · 1 location(s) · Institut National de la Santé Et de la Recherche Médicale, F · NCT04865172
Vortioxetine for the Treatment of Mood and Cognitive Symptoms in Frontotemporal Dementia
Phase 2 · 1 location(s) · Johns Hopkins University · NCT06604520
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This page is independently generated by Eichor from the public ClinicalTrials.gov record and re-synced daily. It is not the sponsor's official website unless claimed. Nothing here is medical advice; eligibility is always determined by the study team — talk to your own doctor first.