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Miromatrix Medical announces FDA clinical hold on miroliverELAP IND application

Miromatrix Medical announced that it was informed via e-mail from the FDA that the miroliverELAP Investigational New Drug, or IND, application for the treatment of acute liver failure has been placed on clinical hold. The miroliverELAP IND application was submitted in mid-November. The FDA indicated they will provide an official clinical hold letter to Miromatrix within 30 days. Miromatrix plans to provide additional updates pending communication with the FDA.

Published first on TheFly

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