RecruitingPHASE1, PHASE2NCT06064890
A Study to Evaluate the Safety and Effect of AVB-101, a Gene Therapy Product, in Subjects With a Genetic Sub-type of Frontotemporal Dementia (FTD-GRN)
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
- AviadoBio Ltd
- Intervention
- Intrathalamic AAV.PGRN administration(procedure)
- Enrollment
- 18 enrolled
- Eligibility
- 30-75 years · All sexes
- Timeline
- 2023 – 2030
Study locations (19)
- The Ohio State University (OSU) Wexner Medical Center, Columbus, Ohio, United States
- Vanderbilt University Medical Centre, Nashville, Tennessee, United States
- Houston Methodist Hospital, Houston, Texas, United States
- UZ Leuven, Leuven, Belgium
- Sunnybrook Health Sciences Centre, Toronto, Ontario, Canada
- Fondazione IRCCS Istituto Neurologico Carlo Besta, Milan, Italy
- Amsterdam UMC, Amsterdam, Netherlands
- NEURO-CARE Sp. z o.o. Sp. Komandytowa, Katowice, Poland
- Neurologia Slaska Centrum Medyczne, Katowice, Poland
- Uniwersyteckie Centrum Kliniczne, SUM w Katowicach, Katowice, Poland
- Euromedis Sp. z o.o., Szczecin, Poland
- Centrum Medyczne NeuroProtect Sp z o.o., Warsaw, Poland
- Mazowiecki Szpital Brodnowski Sp. z o. o., Warsaw, Poland
- Hospital Clinic Barcelona, Barcelona, Spain
- Hospital Universitari i Politecnic La Fe, Valencia, Spain
- +4 more locations on ClinicalTrials.gov
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.
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