drugset / Trial / NCT02852213
A Single-Stage, Adaptive, Open-label, Dose Escalation Safety and Efficacy Study of AADC Deficiency in Pediatric Patients
Phase 1
Recruiting
42 enrolled
Krzysztof Bankiewicz
National Institute of Neurological Disorders and Stroke (NINDS) · collabUniversity of California, San Francisco · collab
NaSingle-groupOpen-labelTreatment
Summary
The overall objective of this study is to determine the safety and efficacy of AAV2-hAADC delivered to the substantia nigra pars compacta (SNc) and ventral tegmental area (VTA) in children with aromatic L-amino acid decarboxylase (AADC) deficiency.
Timeline
- Start
- 2016-07-01
- Primary completion
- 2029-03
- Completion
- 2037-03
Outcome
Met primary endpoint
paper Both the primary and secondary endpoints of the study were met. PMID 34253733 ↗
Publications
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Drugs
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Subject | Eladocagene Exuparvovec | Gene therapy (AAV / viral vector) | 1.3e+11 vg | Other |
| Subject | Eladocagene Exuparvovec | Gene therapy (AAV / viral vector) | 4.2e+11 vg | Other |
| Subject | Eladocagene Exuparvovec | Gene therapy (AAV / viral vector) | 1.3e+12 vg | Other |
| Subject | Eladocagene Exuparvovec | Gene therapy (AAV / viral vector) | 1.6e+12 vg | Other |