Ocugen Discloses Data And Safety Monitoring Board Approves Enrollment In High Dose Cohort 3 In Gardian Study For Stargardt Disease; Company Says It Established Medium Dose As Safe And Tolerable Dose In Current OCU410ST Clinical Trial

Six patients with Stargardt disease have been dosed in the Phase 1/2 clinical trial to date in the low dose cohort and medium dose cohort. An additional three patients will be dosed with the high dose in cohort 3.

"The DSMB has recommended moving forward to dose subsequent subjects with Stargardt disease at the targeted high dose," said Dr. Peter Y. Chang, MD, FACS, DSMB Chair for the OCU410ST clinical trial. "No serious adverse events (SAEs) related to OCU410ST have been reported to date. This is an important next step in the clinical progress for OCU410ST and encouraging for patients living with this most common form of inherited retinal disease."