Drugs / rAAV-Olig001-ASPA
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rAAV-Olig001-ASPA

Gene therapy (AAV / viral vector)

Developed for
Canavan disease
Investigated by
Myrtelle Inc.

Trials 1 · a red edge is where a trial was stopped

20222023202420252026
PhaseRegistry idDatesIndicationSponsorStatusOutcome
Phase 1/2 NCT04833907 Apr 2021 → Aug 2026 overdue Canavan disease Myrtelle Inc. Enrolling by invitation No outcome recorded

Evidence & citations 3 cited values

Every value below carries the sentence it was read from. 1 source stands behind the page.

FieldValueCited text
Known as rAAV-Olig001-ASPA ClinicalTrials.gov intervention name — accepted as the source's own label NCT04833907
Modality Gene therapy (AAV / viral vector) “The latest generation AAV viral vector (rAAV-Olig001-ASPA) will be administered to patients using neurosurgical procedure which involves direct administration of gene therapy...” NCT04833907
Route Other “delivered intracerebroventricularly” NCT04833907