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Human fetal ganglionic eminence cells are an experimental cell therapy investigated for the treatment of Huntington's disease. Developed by Assistance Publique - Hôpitaux de Paris (AP-HP), this approach involves the surgical intrastriatal transplantation of primary neurons derived from the fetal ganglionic eminence, which is the developmental precursor to the striatum. The therapeutic goal is to replace degenerated GABAergic medium spiny neurons and restore the functional integrity of the striatal-cortical circuits in patients with early-stage disease. This therapy was evaluated in the Multicentric Intracerebral Grafting in Huntington's Disease (MIG-HD) Phase II trial, a randomized, delayed-start study. However, the trial failed to demonstrate a significant clinical benefit compared to the control group, and some patients experienced graft-related complications such as alloimmunization and rejection.
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