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


Disclaimer: This news brief was created by Public Technologies (PUBT) using generative artificial intelligence. While PUBT strives to provide accurate and timely information, this AI-generated content is for informational purposes only and should not be interpreted as financial, investment, or legal advice. Fountain Healthcare Partners Ltd published the original content used to generate this news brief on July 30, 2026, and is solely responsible for the information contained therein.

Disclaimer:This article represents the opinion of the author only. It does not represent the opinion of Webull, nor should it be viewed as an indication that Webull either agrees with or confirms the truthfulness or accuracy of the information. It should not be considered as investment advice from Webull or anyone else, nor should it be used as the basis of any investment decision.
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