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.
Study Type
INTERVENTIONAL
Allocation
NA
Purpose
TREATMENT
Masking
NONE
Enrollment
9
KH658: AAV vector containing a coding sequence for an anti-VEGF protein
Kanghong Investigative Site
Phoenix, Arizona, United States
Kanghong Investigative Site
Lemont, Illinois, United States
Kanghong Investigative Site
Memphis, Tennessee, United States
Safety
type, severity and incidence of ocular and systemic AEs and SAEs
Time frame: 52 Weeks
Safety
Change in Best Corrected Visual Acuity
Time frame: 52 Weeks
Safety
type, severity and incidence of ocular and systemic AEs and SAEs
Time frame: 24Weeks
Rescue Injections
Mean Number of Rescue Injections
Time frame: 24Weeks
Rescue Injections
Mean Number of Rescue Injections
Time frame: 52Weeks
Safety
Change in Best Corrected Visual Acuity
Time frame: 24 Weeks
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