MMI wins FDA clearance to expand REMIND Alzheimer’s microsurgery study enrollment to 15 patients

• Fountain Healthcare Partners portfolio company MMI secured FDA clearance to expand enrollment in its REMIND early feasibility study in Alzheimer’s patients.
• The IDE supplement lifts the cap from up to five patients to 15, following review of 30-day safety data from the initial cohort.
• REMIND is evaluating MMI’s Symani surgical system to support microsurgical procedures aimed at restoring lymphatic drainage in deep cervical lymph nodes.
• MMI expects the safety and feasibility dataset to guide future research, including planning for a larger pivotal trial.

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