Drugs / OTOV101N
last change Jul 2025 re-read 3 minutes ago

OTOV101N

Gene therapy (AAV / viral vector) targets OTOF

Developed for
autosomal recessive nonsyndromic hearing loss 9
Investigated by
Otovia Therapeutics

Trials 1

PhaseRegistry idDatesIndicationSponsorStatusOutcome
— NCT05901480 Jun 2023 → Dec 2024 autosomal recessive nonsyndromic hearing loss 9 Otovia Therapeutics Unknown No outcome recorded

Evidence & citations 4 cited values

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

FieldValueCited text
Known as OTOV101N ClinicalTrials.gov intervention name — accepted as the source's own label NCT05901480 ↗
Modality Gene therapy (AAV / viral vector) “adeno-associated virus (AAV)-OTOF gene therapy” PMID 40603731 ↗ Jul 2025
Route Other “via intracochlear injection” NCT05901480 ↗
Target OTOF “AAV-OTOF gene therapy” PMID 40603731 ↗ Jul 2025