Webinars and Presentations

Introduction to Odylia’s RPGRIP1 Gene Therapy Program

Odylia Therapeutics CSO, Ashley Winslow, and Director of Development, Heather Greene, discuss Odylia’s RPGRIP1 Gene Therapy program to treat vision loss in patients diagnosed with Leber Congenital Amaurosis 6 (LCA6). Follow the link to view a recording of the webinar.

Recent Conference Presentations

The challenges of bringing gene therapy treatments for rare disease to clinical trial, World Orphan Drug Congress Europe 2020, Scott Dorfman, CEO

Exploring Innovative Partnerships to Enable Gene Therapy Manufacturing for Rare Ocular Disorders, Gene Therapy for Ophthalmic Disorders 2020- Ashley Winslow, CSO

PANEL DISCUSSION: Evaluating the Current Commercial Landscape in Light of a Recent Ophthalmic Approval, Gene Therapy for Ophthalmic Disorders 2020- Ashley Winslow, CSO

Sharing Insight for Gene Therapy Manufacturing, The NIH and FDA Workshop on Expanding AAV Manufacturing Capacity for Rare Disease Gene Therapies, Scott Dorfman, CEO

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