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    Hansa Medical Treats First Patient with IdeS in Phase II Study

    Chelsea Pratt
    Oct. 11, 2016 01:15AM PST
    Biotech Investing

    Hansa Medical today announced that the firstpatient has been recruited and treated in a Phase II clinical study with IdeS in the acute autoimmune disease acquired Thrombotic Thrombocytopenic Purpura (TTP).

    Hansa Medical AB (publ) (STO:HMED) today announced that the firstpatient has been recruited and treated in a Phase II clinical study with IdeS in the acute autoimmune disease acquired Thrombotic Thrombocytopenic Purpura (TTP) at University College Hospital in London.
    Acquired TTP is a severe and acute autoimmune blood disorder in which
    the presence of autoantibodies can result in systemic life threatening
    micro-clotting in vital organs. The Hansa Medical-sponsored study with
    IdeS in TTP is an open-label study to evaluate the safety, tolerability,
    efficacy, pharmacodynamics and pharmacokinetics of IdeS in asymptomatic
    patients with acquired TTP.
    The patients in the study will have low ADAMTS13 activity. ADAMTS13 is a
    significant component in the coagulation system. An important goal of
    the study is to investigate if one dose of IdeS results in increased
    ADAMTS13 activity by cleaving ADAMTS13 autoantibodies. The Clinical
    Investigator, Dr. Marie Scully, consultant haematologist at UCLH, is a
    leading expert in patient care and clinical research in TTP.
    The study will include up to six patients with acquired TTP and low
    ADAMTS13 activity who are asymptomatic at the time of enrolment into
    this study. The study is expected to be completed during 2017.
    “This novel therapy, initially investigated to determine safety and
    efficacy, could provide an innovative treatment for acute TTP, clearing
    the antibodies against ADAMTS 13, aiding response to remission and
    reducing morbidity and mortality”, says Dr. Scully, who is supported by
    the National Institute for Health Research University College London
    Hospitals Biomedical Research Centre.
    “We are happy to now announce our progress into the autoimmune space
    through the initiation of this explorative Phase II trial with IdeS in
    acquired TTP. The effective and fast IgG-cleaving mode-of-action of IdeS
    makes it highly relevant to evaluate the efficacy and safety of IdeS in
    this potentially devastating acute condition“, says Göran Arvidson, CEO
    of Hansa Medical AB.
    The information in this press release is disclosed pursuant to the EU
    Market Abuse Regulation. The information was released for public
    disclosure through the agency of Göran Arvidson stated below on October
    11, 2016 at 08.30 CET.
    About acquired TTP
    Acquired TTP is an ultra-rare, acute, auto-immune blood clotting
    disorder, affecting 1/100,000 inhabitants. It has a sudden onset caused
    by impaired activity of the ADAMTS13 enzyme (typically <10% of that in
    plasma of healthy individuals), leaving ultra-large Von Willebrand
    Factor (vWF) molecules un-cleaved (vWF is an essential protein involved
    in the blood clotting process). These ultra-large vWF molecules bind to
    blood platelets, resulting in severe thrombocytopenia (very low platelet
    counts) and formation of micro-clots in small blood vessels throughout
    the body. Acquired TTP is associated with severe morbidities of the
    brain, heart and kidney and affects life expectancy and quality of life.
    Mortality is high at 10-15% within 2 weeks after initial diagnosis.
    Moreover, the risk of recurrences is high in patients with persistently
    low levels of ADAMTS13 after treatment with the current standard of
    care, which consists of daily plasma exchange and immune-suppressants.
    About IdeS
    IdeS, a unique molecule with a novel mechanism, is an enzyme that
    specifically cleaves human IgG antibodies. IdeS has been evaluated in a
    Phase I study in healthy subjects and in a Phase II study in sensitized
    patients awaiting kidney transplantation demonstrating that IdeS is
    highly effective in reducing anti-HLA antibodies to levels acceptable
    for transplantation with a favorable safety profile. The efficacy and
    safety of IdeS in transplantation are currently investigated in three
    on-going Phase II studies in sensitized kidney patients in Sweden and
    the US. In addition to transplantation, IdeS has potential applications
    in a variety of rare autoimmune diseases and currently, the efficacy and
    safety of IdeS are investigated in a Phase II study in acquired
    Thrombotic Thrombocytopenic Purpura.
    About Hansa Medical AB (publ)
    Hansa Medical is a biopharmaceutical company focusing on novel
    immunomodulatory enzymes. The lead project IdeS is an antibody-degrading
    enzyme in clinical development, with potential use in transplantation,
    rare autoimmune diseases and oncology. Additional projects focus on
    development of new antibody modulating enzymes, as well as HBP, a
    diagnostic biomarker for prediction of severe sepsis at emergency
    departments that is already introduced on the market. The company is
    based in Lund, Sweden. Hansa Medical’s share (ticker: HMED) is listed on
    Nasdaq Stockholm.
    About UCLH
    UCLH (University College London Hospitals NHS Foundation Trust),
    situated in the West End of London, is one of the largest NHS trusts in
    the United Kingdom and provides first-class acute and specialist
    services. The state-of-the-art University College Hospital which opened
    in 2005, is the focal point of UCLH alongside four cutting-edge
    specialist hospitals. UCLH is committed to research and development and
    forms part of UCL Partners which in March 2009 was officially designated
    as one of the UK’s first academic health science centres by the
    Department of Health. UCLH works closely with UCL, translating research
    into treatments for patients. For more information, visit: www.uclh.nhs.uk,
    Facebook (UCLHNHS), Twitter (@UCLH) or Youtube (UCLHvideo).
    This information was brought to you by Cision https://news.cision.com

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