drugset / Trial / NCT06825858

A Phase I, Open-label, Multicenter, Dose-Escalating Study to Evaluate the Safety and Tolerability of KH658 Gene Therapy in Participants With Neovascular Age-related Macular Degeneration

NCT06825858 ↗

Phase 1 Active not recruiting 9 enrolled Chengdu Origen Biotechnology Co., Ltd.
NaSingle-groupOpen-labelTreatment

Summary

VAN-2401 is Phase I clinical trial to assess the safety and tolerability of KH658 in subjects with neovascular AMD. KH658 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 ocular injections.

Timeline

Start
2025-04-07
Primary completion
2027-01
Completion
2027-03

Drugs

EvaluationDrugModalityDoseRoute
Subject KH658 Gene therapy (AAV / viral vector) — Other