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    EANS-Adhoc  425  0 Kommentare Marinomed Biotech AG announces top line results of the Phase III study for Budesolv

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    Disclosed inside information pursuant to article 17 Market Abuse Regulation
    (MAR) transmitted by euro adhoc with the aim of a Europe-wide distribution.
    The issuer is responsible for the content of this announcement.
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    Research & Development
    23.04.2019

    Vienna - Marinomed Biotech AG, a globally active biopharmaceutical company with
    headquarters in Vienna, has announced the successful completion of the pivotal
    Phase III study for Budesolv. The top line results are now available and show
    that Budesolv achieves at least the same effect as the product which is
    currently on the market, with a significantly lower dose. The planned primary
    endpoint of the study for the first product of the innovative Marinosolv®
    technology platform has thus been achieved. The approval process can be
    continued as scheduled.

    As announced, the complete Phase III study with detailed results is expected and
    will be published by the end of the second quarter of 2019 at the latest.

    Marinosolv® and the flagship product Budesolv
    Marinomed has succeeded in increasing the bioavailability of hardly soluble
    compounds to treat sensitive tissues such as nose and eyes via the Marinosolv®
    technology platform. The platform's flagship product is Budesolv, a nasal spray
    for the treatment of allergic rhinitis.

    About Marinomed Biotech AG
    Marinomed Biotech AG is a biopharmaceutical company with headquarters in Vienna
    and has been listed in the Prime Market of the Vienna Stock Exchange since
    February 1, 2019. The company focuses on the development of innovative products
    based on patent-protected technology platforms in the field of respiratory and
    ophthalmological diseases. The Marinosolv® technology platform increases the
    efficacy of hardly soluble compounds for the treatment of sensitive tissues such
    as the eyes and nose. The Carragelose® platform comprises innovative patent-
    protected products targeting viral infections of the respiratory tract.
    Carragelose® is used in nasal sprays, throat sprays and lozenges, which are sold
    via international partners in over 30 countries worldwide. Further information
    is available at: www.marinomed.com [http://www.marinomed.com/].





    Further inquiry note:
    Dr. Eva Prieschl-Grassauer
    Chief Scientific Officer, Marinomed
    Veterinärplatz 1, 1210 Wien, Austria
    T +43 (0)1 250 77 446
    E-mail: eva.prieschl@marinomed.com
    http://www.marinomed.com

    Roland Mayrl
    Managing Partner, Metrum Communications
    Prinz-Eugen-Straße 80/16, 1040 Wien, Austria
    T +43 (0) 1 504 69 87 331
    E-mail: r.mayrl@metrum.at
    http://www.metrum.at

    end of announcement euro adhoc
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    issuer: Marinomed Biotech AG
    Veterinärplatz 1
    A-1210 Wien
    phone: 0043250774460
    FAX: 0043250774493
    mail: office@marinomed.com
    WWW: www.marinomed.com
    ISIN: ATMARINOMED6, AT0000A1WD52
    indexes:
    stockmarkets: Wien
    language: English





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    EANS-Adhoc Marinomed Biotech AG announces top line results of the Phase III study for Budesolv - Disclosed inside information pursuant to article 17 Market Abuse Regulation (MAR) transmitted by euro adhoc with the aim of a Europe-wide distribution. The issuer is responsible for the content of this announcement. - Research & Development …

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