Drugs / rAAV2/8-hCYP4V2
last change Apr 2024 re-read 3 minutes ago

rAAV2/8-hCYP4V2

Gene therapy (AAV / viral vector)

Developed for
Bietti crystalline corneoretinal dystrophy
Investigated by
Beijing Tongren Hospital

Trials 1

20222023202420252026
PhaseRegistry idDatesIndicationSponsorStatusOutcome
Phase 0 NCT04722107 Apr 2021 → Jan 2024 Bietti crystalline corneoretinal dystrophy Beijing Tongren Hospital Unknown No outcome recorded

Evidence & citations 2 cited values

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

FieldValueCited text
Known as rAAV2/8-hCYP4V2 ClinicalTrials.gov intervention name — accepted as the source's own label NCT04722107 ↗
Modality Gene therapy (AAV / viral vector) “rAAV2/8-hCYP4V2 Gene Replacement Therapy Drug Administered as a Single Subretinal Injection” NCT04722107 ↗