2011 Milestones 1Q • Designation for hESC-derived RPE Cells for Stargardt’s Disease
2Q • Sign clinical trial agreements for SMD and Dry AMD sites • Commence patient selection • Treat first patients for SMD and Dry AMD Phase I/II clinical trials • Secure European EMA “Orphan” approval for SMD program • File with European Medicines Agency (EMA) for RPE program
2ndHalf of 2011 • Treat additional cohorts of patients in RPE Phase I/II trials • Early look at data from first cohort of patients in RPE Phase I/II trials • Secure approval from EMA for RPE Program • Continue partnering and licensing discussions • Advance toward IND filing for hemangioblast program
Register for free to join our community of investors and share your ideas. You will also get access to streaming quotes, interactive charts, trades, portfolio, live options flow and more tools.