An investigational therapy for retinitis pigmentosa has demonstrated a favorable safety and tolerability profile in an ongoing Phase I/II clinical trial.

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An investigational cell-based therapy for retinitis pigmentosa has demonstrated a favorable safety and tolerability profile in an ongoing Phase I/II clinical trial.
"We are pleased with the results," said jCyte co-founder Henry Klassen, an associate professor of ophthalmology at UCI and a member of the Sue & Bill Gross Stem Cell Research Center, where much of the pre-clinical work took place. "This is an important milestone in our effort to treat these patients."
The cell-based approach taken by jCyte is intended to rescue sick and dying retinal photoreceptor cells (rods, cones) in the diseased retina. Nonclinical studies have shown that transplanted retinal progenitor cells tend not to provoke an immunological rejection response, even when sourced from unrelated donors. Because of this, patients in the study are not immunosuppressed, as is often done in traditional organ transplantation. In addition, the procedure is relatively simple to perform and can be completed in an office setting.
The ongoing Phase I/IIa safety trial is being conducted at the Gavin Herbert Eye Institute at UCI and at Retina Vitreous Associates in Los Angeles.
Based on the interim results from the current trial, further clinical studies are being planned.
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