• Humacyte to Present Second Quarter Financial Results and Provide Corporate Update on August 13, 2024

    Source: Nasdaq GlobeNewswire / 12 Aug 2024 07:00:00   America/Chicago

    DURHAM, N.C., Aug. 12, 2024 (GLOBE NEWSWIRE) -- Humacyte, Inc. (Nasdaq: HUMA), a clinical-stage biotechnology platform company developing universally implantable, bioengineered human tissue at commercial scale, will release its financial results for the second quarter ended June 30, 2024, on Tuesday, August 13, 2024. Management will host a webcast and conference call at 8:30 a.m. ET to discuss recent corporate updates from its acellular tissue engineered vessel (ATEV) programs.

    Title:Humacyte Second Quarter 2024 Financial Results and Corporate Update
    Date:August 13, 2024
    Time:8:30 AM Eastern Time
    Conference Call Details:1-877-704-4453 (U.S. Investors Dial)
    1-201-389-0920 (International Investors Dial)
    13747913 (Conference ID)
    Call me™ Feature: Click Here
    Webcast:Webcast Link - Click Here

    The webcast should be accessible 15 minutes prior to the conference call’s start time. A replay of the webcast will be available following the conclusion of the live broadcast and will be accessible on the investors section of the Company’s website for at least 30 days.

    About Humacyte

    Humacyte, Inc. (Nasdaq: HUMA) is developing a disruptive biotechnology platform to deliver universally implantable bioengineered human tissues, advanced tissue constructs, and organ systems designed to improve the lives of patients and transform the practice of medicine. The Company develops and manufactures acellular tissues to treat a wide range of diseases, injuries, and chronic conditions. Humacyte’s initial product candidates, a portfolio of ATEVs, are currently in late-stage clinical trials targeting multiple vascular applications, including vascular trauma repair, arteriovenous (AV) access for hemodialysis, and peripheral artery disease. A Biologics License Application for the ATEV in the vascular trauma indication is currently under review by the FDA and was granted Priority Review with a PDUFA date of August 10, 2024. Preclinical development is also underway in coronary artery bypass grafts, pediatric heart surgery, treatment of type 1 diabetes, and multiple novel cell and tissue applications. Humacyte’s 6mm ATEV for AV access in hemodialysis was the first product candidate to receive the FDA’s Regenerative Medicine Advanced Therapy (RMAT) designation and has also received FDA Fast Track designation. Humacyte’s 6mm ATEV for urgent arterial repair following extremity vascular trauma and for advanced PAD also have received an RMAT designations. The ATEV received priority designation for the treatment of vascular trauma by the U.S. Secretary of Defense. For more information, visit www.Humacyte.com.

    Humacyte Investor Contact:
    Joyce Allaire
    LifeSci Advisors LLC
    +1-617-435-6602
    jallaire@lifesciadvisors.com
    investors@humacyte.com

    Humacyte Media Contact:
    Rich Luchette
    Precision Strategies
    +1-202-845-3924
    rich@precisionstrategies.com
    media@humacyte.com


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