drugset / Trial / NCT05657301

Safety and Tolerability of KH631 Gene Therapy in Participants With Neovascular Age-related Macular Degeneration

NCT05657301 ↗

Phase 1 Active not recruiting 25 enrolled Chengdu Origen Biotechnology Co., Ltd.
NaSingle-groupOpen-labelTreatment

Summary

VAN-2201 is Phase I clinical trial to assess the safety and tolerability of KH631 in subjects with neovascular AMD. KH631 is gene therapy designed to deliver a protein which targets and blocks VEGF via an adeno-associated viral vector. The standard of care for patients with neovascular AMD are anti-VEGF treaments, which have demonstrated improvement in vision and reduction in fluid. A one time placement of a product which inhibits VEGF has the potential to reduce the patient burden of regular intraocular injections.

Timeline

Start
2023-10-16
Primary completion
2026-09
Completion
2027-09

Drugs

EvaluationDrugModalityDoseRoute
Subject KH631 Gene therapy (AAV / viral vector) — Other