• Cat-intel
  • MedIntelliX
  • Resources
  • About Us
  • Arteriovenous Malformation Companies

    ID: MRFR/LS/3656-HCR
    100 Pages
    Kinjoll Dey
    September 2025

    Arteriovenous malformation (AVM) is an abnormal tangle of blood vessels connecting arteries and veins, which can disrupt normal blood flow and lead to various complications. Companies involved in the medical field may offer products or services related to the diagnosis and treatment of AVM.

    Share:
    Download PDF ×

    We do not share your information with anyone. However, we may send you emails based on your report interest from time to time. You may contact us at any time to opt-out.

    Top Industry Leaders in the Arteriovenous Malformation Market

    Arteriovenous Malformation Key CompaniesLatest Arteriovenous malformation Companies Update

    January 2023: Eisai Co., Ltd. and Biogen Inc. jointly declared that the U.S. Food and Drug Administration (FDA) had granted approval for lecanemab-irmb 100 mg/mL injection for intravenous administration via the Accelerated Approval Pathway. Lecanemab-irmb is a humanized immunoglobulin gamma 1 (IgG1) monoclonal antibody designed to target aggregated soluble and insoluble forms of amyloid beta (Aβ). It is indicated for the treatment of Alzheimer's disease (AD). The approval is predicated on Phase 2 data indicating that LEQEMBI decreased the deposition of Aβ plaque in the brain, which is a characteristic feature of Alzheimer's disease. Eisai will expeditiously employ the data recently disclosed from the expansive worldwide confirmatory Phase 3 clinical trial, Clarity AD, to submit a Supplemental Biologics License Application (sBLA) to the FDA in pursuit of conventional pathway approval.


    August 2022: Vaderis Therapeutics AG emerged from covert mode with a clinical-ready drug candidate and an emphasis on allosteric AKT inhibitors, thanks to financial backing from Medicxi. The nascent biotechnology company intends to initiate a proof-of-concept clinical trial to evaluate its principal compound VAD044 in individuals afflicted with Hereditary Hemorrhagic Telangiectasia (HHT). HHT, which is also referred to as Osler-Weber-Rendu Syndrome, is a hereditary condition characterized by the formation of arteriovenous malformations, which are aberrant connections between veins and arteries. Nose, lung, brain, and liver are the organs most frequently impacted by these malformations. The malformations may eventually induce spontaneous hemorrhage. Anemia, iron deficiency, shortness of breath, and seizures are all symptoms of the disease that can negatively impact quality of life. At this time, no pharmaceuticals have been approved by the FDA for the specific purpose of treating HHT. Vaderis aspires to be the first organization to transport a candidate for this disease through the clinic.


    List of Arteriovenous malformation Key companies in the market

    • Toshiba Medical Systems Corporation (Japan)

    • Fujifilm Holdings (Japan)

    • Carestream Health (U.S.)

    • Electrical Geodesics Inc. (U.S.)

    • Nihon Kohden Corporation (Japan)