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This investigational autologous cell therapy consists of CD34+ stem cells isolated from a patient's own bone marrow for the treatment of vision loss associated with central retinal vein occlusion (CRVO). The therapy involves harvesting bone marrow aspirate, isolating the CD34+ progenitor cells using the Miltenyi CliniMACS system under Good Manufacturing Practice (GMP) conditions, and administering them via a single intravitreal injection. These stem cells are naturally occurring repair cells that migrate to sites of injury; in the context of CRVO, they are intended to home to the ischemic retina to promote vascular regeneration and provide paracrine trophic support to damaged retinal tissue. The therapy is currently being evaluated in a Phase I/II clinical trial (NCT02912403) sponsored by the National Eye Institute and coordinated by The Emmes Company, LLC in collaboration with the UC Davis Eye Center.
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