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Humacyte Receives FDA Approval for SYMVESS Launch
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Humacyte Receives FDA Approval for SYMVESS Launch

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Humacyte ( (HUMA) ) has issued an update.

Humacyte announced that the FDA has granted full approval for SYMVESS, an acellular tissue-engineered vessel, for use in adults with extremity arterial injuries where autologous vein grafts are not feasible. This approval marks a significant advancement in regenerative medicine, offering a new treatment option that promises to improve trauma care by reducing amputation rates and infection risks. The company is poised for a commercial launch, having prepared an experienced sales team, and anticipates SYMVESS will become the preferred choice for complex vascular injuries, both civilian and military.

More about Humacyte

Humacyte, Inc. is a biotechnology platform company focused on developing universally implantable, bioengineered human tissues at commercial scale. Their primary product, SYMVESS, is a first-in-class bioengineered human tissue designed to be a universally implantable vascular conduit for arterial replacement and repair.

YTD Price Performance: 21.83%

Average Trading Volume: 3,114,708

Technical Sentiment Consensus Rating: Buy

Current Market Cap: $445.2M

Learn more about HUMA stock on TipRanks’ Stock Analysis page.

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