CompletedPhase 1NCT06705192
Study in Asymptomatic GRN-FTD Patients to Investigate the Safety, Tolerability, Pharmacokinetics, and Pharmacodynamics of VES001
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
- Mads Kjolby
- Principal Investigator
- Mads Kjoelby, MD, PhDVesper Bio
- Intervention
- VES001(drug)
- Enrollment
- 6 enrolled
- Eligibility
- 18-75 years · All sexes
- Timeline
- 2024 – 2025
Study locations (2)
- Erasmus University Medical Center, Rotterdam, Netherlands
- Leonard Wolfson Experimental Neurology Centre CRF National Hospital for Neurology and Neurosurgery, 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.
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