Active, not recruitingPHASE1, PHASE2NCT05243017
Safety and Efficacy of AMT-130 in European Adults With Early Manifest Huntington's Disease
Studying Huntington disease
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
- UniQure Biopharma B.V.
- Principal Investigator
- David Margolin, MD, PhDUniQure Biopharma B.V.
- Intervention
- intra-striatal rAAV5-miHTT(genetic)
- Enrollment
- 14 enrolled
- Eligibility
- 25-65 years · All sexes
- Timeline
- 2021 – 2029
Study locations (4)
- Instytut Psychiatrii i Neurologii, Warsaw, Poland
- Interventional Neuro Center, Warsaw, Poland
- Cardiff University, Cardiff, United Kingdom
- National Hospital for Neurology & 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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