3
Clinical Trials associated with EXG-202 / Not yet recruitingPhase 1/2 A Phase I/II Clinical Study Evaluating the Safety and Preliminary Efficacy of EXG202 in Patients With Neovascular Age-related Macular Degeneration (nAMD)
VEGF inhibitors (anti-VEGF),such as aflibercept has been shown to be safe and effective for treating nAMD and have demonstrated improvement in vision. However, anti-VEGF therapy is administered frequently via intravitreal injection and can be a significant burden to the patients.
EXG 202 is a recombinant adeno-associated virus (rAAV) gene therapy vector carrying a coding sequence for a soluble anti-VEGF protein. The long-term, stable delivery of this therapeutic protein following a 1 time gene therapy treatment for nAMD could potentially reduce the treatment burden of currently available therapies while maintaining vision with a favorable benefit.
/ Not yet recruitingEarly Phase 1 An Open-label, Dose-escalation Study to Evaluate the Safety and Efficacy of Intravitreal EXG202 Injection in Patients with Wet (neovascular) Age-related Macular Degeneration (wAMD)
The goal of this clinical trial is to evaluate the safety, tolerability and efficacy of intravitreal injection of EXG202 in subjects with neovascular age-related Macular Degeneration (nAMD).
/ Not yet recruitingNot ApplicableIIT An open-label, dose-escalation, and dose-expansion study to evaluate the safety and preliminary efficacy of intravitreal EXG202 injection in patients with wet (neovascular) age-related macular degeneration (wAMD)
100 Clinical Results associated with EXG-202
100 Translational Medicine associated with EXG-202
100 Patents (Medical) associated with EXG-202
100 Deals associated with EXG-202