Drugs / AAV9.SLC6A1
last change May 2026 re-read 3 minutes ago

AAV9.SLC6A1

Gene therapy (AAV / viral vector) targets SLC6A1 via restoration

Developed for
inborn disorder of neurotransmitter metabolism and transport
Investigated by
Emily de los Reyes

Trials 1

202620272028
PhaseRegistry idDatesIndicationSponsorStatusOutcome
Phase 1/2 NCT07173153 Aug 2025 → Aug 2028 expected inborn disorder of neurotransmitter metabolism and transport Emily de los Reyes Enrolling by invitation No outcome recorded

Evidence & citations 5 cited values

Every value below carries the sentence it was read from. 2 sources stand behind the page.

FieldValueCited text
Known as AAV9.SLC6A1 ClinicalTrials.gov intervention name — accepted as the source's own label NCT07173153 ↗
Action Restore “Adeno-associated virus serotype 9-mediated gene replacement normalized electroencephalography abnormalities in preclinical models” PMID 42173049 ↗ May 2026
Modality Gene therapy (AAV / viral vector) “Adeno-associated virus serotype 9-mediated gene replacement” PMID 42173049 ↗ May 2026
Route Intrathecal “delivered one time through an intrathecal injection” NCT07173153 ↗
Target SLC6A1 “Phase I/II Intrathecal Gene Delivery Clinical Trial of scAAV9.P546.SLC6A1 for SLC6A1 Neurodevelopmental Disorder” NCT07173153 ↗