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News & World Report.’ Initiated in July of last year, the Phase I/II trial is designed to determine the protection and tolerability of hESC-derived RPE cells pursuing sub-retinal transplantation in sufferers with SMD at 12 months, the study’s main endpoint. It shall involve a total of 12 patients, with cohorts of three individuals each in an ascending dosage format. As part of its RPE clinical system, the company is certainly concurrently conducting a medical trial for dried out age-related macular degeneration and second trial for SMD in the United Kingdom.