Leveraging Directed Evolution to Facilitate Targeted Delivery of an AAV-based Retinal Gene Therapy
Time: 2:30 pm
day: Clinical PM -Day 1
Details:
- Overcoming barriers to efficient intravitreal delivery of AAVbased gene therapy to the retina
- Employing directed evolution in nonhuman primates to discover novel retinotropic AAV vectors for clinical gene therapy
- Exploring key translational research considerations to facilitate clinical trial development
