CompletedPhase 2NCT03987295

A Phase 2 Study to Evaluate Safety of Long-term AL001 Dosing in Frontotemporal Dementia (FTD) Patients (INFRONT-2)

Studying Frontotemporal dementia

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Key facts

Sponsor
Alector Inc.
Principal Investigator
Peter Ljubenkov, MD, M.D
University of California, San Francisco
Intervention
AL001(drug)
Enrollment
33 enrolled
Eligibility
18-85 years · All sexes
Timeline
20192024

Study locations (12)

Collaborators

GlaxoSmithKline

Primary source

Recruitment status, site addresses, contacts, and full eligibility criteria can change between syncs. Always verify with the trial team before planning travel or treatment.

Open NCT03987295 on ClinicalTrials.gov

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