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Humacyte Reports Q3 2024 Results Amid FDA Review
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Humacyte Reports Q3 2024 Results Amid FDA Review

Humacyte ( (HUMA) ) has released its Q3 earnings. Here is a breakdown of the information Humacyte presented to its investors.

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Humacyte, Inc., a clinical-stage biotechnology company, is pioneering the development of universally implantable bioengineered human tissues for use in various medical conditions, particularly in the vascular sector with its acellular tissue engineered vessel (ATEV) technology. In its recent earnings report, Humacyte highlighted ongoing FDA review of its Biologics License Application for ATEV in vascular trauma, along with significant clinical trial results presented at major medical conferences. The company reported a net loss of $39.2 million for the third quarter of 2024, reflecting an increase from the previous year primarily due to operating expenses and adjustments related to a contingent earnout liability. Humacyte has made strategic advancements, notably in its investigational indications for ATEV, including hemodialysis access and peripheral artery disease, and has expanded its intellectual property portfolio. Looking ahead, Humacyte remains optimistic about the potential FDA approval of its ATEV product and continues to advance its pipeline and prepare for commercialization, despite the current absence of revenue and ongoing financial challenges.

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