CompletedPhase 1NCT03636204
A First in Human Study in Healthy Volunteers and in Participants With Frontotemporal Dementia With Granulin (GRN) Mutation
Studying Frontotemporal dementia
Last synced from ClinicalTrials.gov
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Clinical trial records are synced from ClinicalTrials.gov through automated extraction.
Report missing dataKey facts
- Sponsor
- Alector Inc.
- Principal Investigator
- George Stoica, M.DBioclinica Research
- Intervention
- AL001(biological)
- Enrollment
- 64 enrolled
- Eligibility
- 18-80 years · All sexes
- Timeline
- 2018 – 2019
Study locations (8)
- University of Alabama, Birmingham, Alabama, United States
- UCSF, San Francisco, California, United States
- Study site, Orlando, Florida, United States
- Mayo Clinic, Rochester, Minnesota, United States
- University of Pennsylvania, Philadelphia, Pennsylvania, United States
- Lawson Health Research Institute, St. Joseph's, London, Ontario, Canada
- Sunnybrook Health Sciences Centre, Toronto, Canada
- University College London, London, United Kingdom
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 NCT03636204 on ClinicalTrials.govOther trials for Frontotemporal dementia
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