drugset / Trial / NCT02286089

Safety and Efficacy Study of OpRegen for Treatment of Advanced Dry-Form Age-Related Macular Degeneration

NCT02286089 ↗

Phase 1/2 Active not recruiting 24 enrolled Hoffmann-La Roche
NaSingle-groupOpen-labelTreatment

Summary

The main objective of the study is evaluation of the safety and tolerability of OpRegen - Human embryonic stem cell-derived retinal pigment epithelial (RPE) cells. The study will also include initial exploration of the ability of transplanted OpRegen cells to engraft, survive, and moderate disease progression.

Timeline

Start
2015-04-01
Primary completion
2021-12-31
Completion
2031-01-31

Drugs

EvaluationDrugModalityDoseRoute
Subject OpRegen Cell therapy — Other