Humacyte (HUMA) has released an update.
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Humacyte, Inc. has announced that the FDA has granted Priority Review to their Biologics License Application for the use of their human acellular vessel in urgent arterial repairs. This significant step forward is specifically for cases where synthetic grafts are not suitable and using the patient’s own veins is not possible. This development could mark a notable advancement in vascular trauma treatment, potentially impacting the stock’s appeal to investors.
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For a comprehensive understanding of the announcement, you can read the full document here.