Drugs / ACDN-01
last change Jun 2024 re-read 3 minutes ago

ACDN-01

Gene therapy (AAV / viral vector) targets ABCA4

Developed for
cone-rod dystrophy · macular degeneration, early-onset · Stargardt disease
Investigated by
Ascidian Therapeutics, Inc

Trials 1

202520262027202820292030
PhaseRegistry idDatesIndicationSponsorStatusOutcome
Phase 1/2 NCT06467344 Jun 2024 → Aug 2030 expected Stargardt disease, cone-rod dystrophy, macular degeneration, early-onset Ascidian Therapeutics, Inc Recruiting No outcome recorded

Evidence & citations 4 cited values

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

FieldValueCited text
Known as ACDN-01 ClinicalTrials.gov intervention name — accepted as the source's own label NCT06467344 ↗
Modality Gene therapy (AAV / viral vector) “ACDN-01 is an AAV-based vector” NCT06467344 ↗
Route Other “via subretinal injection” NCT06467344 ↗
Target ABCA4 “an ABCA4 RNA exon editor” NCT06467344 ↗