Drugs / VG901
last change Apr 2026 re-read 3 minutes ago

VG901

Gene therapy (AAV / viral vector) targets CNGA1

Developed for
retinitis pigmentosa
Investigated by
VeonGen Therapeutics GmbH

Trials 1

202420252026
PhaseRegistry idDatesIndicationSponsorStatusOutcome
Phase 1 NCT06291935 Sep 2023 → Apr 2026 overdue retinitis pigmentosa VeonGen Therapeutics GmbH Recruiting No outcome recorded

News releases announcing trial results or a regulatory action · 3

DateIssuerRelease
2025-01-08 VeonGen Therapeutics GmbH Regulatory ViGeneron Announces FDA Rare Pediatric Disease Designation for VG901 and DSMB Approval to Advance Dose Escalation in Phase 1b Retinitis Pigmentosa Trial veongen.com ↗
2023-08-22 VeonGen Therapeutics GmbH Regulatory ViGeneron announces EMA Approval of Clinical Trial Application for VG901, a gene therapy to treat Retinitis Pigmentosa veongen.com ↗
2022-10-11 VeonGen Therapeutics GmbH Results ViGeneron presents preclinical data on intravitreal gene therapy of Stargardt disease at ESGCT veongen.com ↗
ViGeneron GmbH, a next-generation gene therapy company, today announced the presentation of preclinical data on its program VG801 in ABCA4‐associated Stargardt disease (STGD1).

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 VG901 ClinicalTrials.gov intervention name — accepted as the source's own label NCT06291935 ↗
Modality Gene therapy (AAV / viral vector) “a gene therapy, VG901” NCT06291935 ↗
Route Intravitreal “single intravitreal dose of VG901” NCT06291935 ↗
Target CNGA1 “Recombinant Adeno-associated Virus Vector Expressing CNGA1” NCT06291935 ↗