Drugs / AAV8-hCARp.hCNGB3
last change May 2023 re-read 3 minutes ago

AAV8-hCARp.hCNGB3

Gene therapy (AAV / viral vector)

Developed for
achromatopsia
Investigated by
Janssen Research & Development, LLC · MeiraGTx UK II Ltd

Trials 1

20172018201920202021202220232024202520262027
PhaseRegistry idDatesIndicationSponsorStatusOutcome
Phase 1/2 NCT03001310 Jan 2017 → Oct 2019 achromatopsia MeiraGTx UK II Ltd Completed No outcome recorded

Evidence & citations 3 cited values

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

FieldValueCited text
Known as AAV8-hCARp.hCNGB3 “First-in-Human Gene Therapy Trial of AAV8-hCARp.hCNGB3 in Adults and Children With CNGB3-associated Achromatopsia.” PMID 37172884 ↗ May 2023
Modality Gene therapy (AAV / viral vector) “AAV8-hCARp.hCNGB3 gene therapy” PMID 37172884 ↗ May 2023
Route Other “Subretinal administration of a single low dose of AAV - CNGB3” NCT03001310 ↗