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    Helius Medical Announces Results from a Case Series of Subjects with Advanced MS

    Investing News Network
    Jun. 21, 2016 08:05AM PST
    Medical Device Investing

    NEWTOWN, Pa.–(BUSINESS WIRE)–Helius Medical Technologies, Inc. (TSX: HSM, HSM.S, OTCQB: HSDT) (“Helius” or the “Company”) is pleased to announce the results of a case series of individuals with advanced symptoms of Multiple Sclerosis (MS) treated with PoNS™ Therapy. This study was performed at TCNL1, University of Wisconsin, Madison and the data was presented at the 2016, …

    NEWTOWN, Pa.–(BUSINESS WIRE)–Helius Medical Technologies, Inc. (TSX: HSM, HSM.S, OTCQB: HSDT)
    (“Helius” or the “Company”) is pleased to announce the results of a case
    series of individuals with advanced symptoms of Multiple Sclerosis (MS)
    treated with PoNS™ Therapy.

    This study was performed at TCNL1, University of Wisconsin,
    Madison and the data was presented at the 2016, Annual Meeting of the
    Consortium of Multiple Sclerosis Centers (CMSC).
    Six subjects with advanced MS (Expanded Disability Status Scale (EDSS)2
    scores ranging from 6.5 to 7.5) were enrolled in a six-month pilot
    study. Subjects were trained in PoNS™ Therapy which combines use of the
    prototype PoNS™ device with physical training in balance, gait, movement
    and postural stability. Results demonstrated improvements in physical,
    cognitive and quality of life parameters. The demanding training regimen
    also resulted in significant real life improvements such as re-adopting
    a walker for community mobility, decreased fatigue, increased
    independence with daily activities, overcoming physical obstacles at
    home and increased community access.
    “Those with greater functional ability at the beginning of the study
    (EDSS 6.5-7.0) made the most significant gains but all subjects could be
    qualified as improved. The intervention shows promise to prolong
    functional ambulation and independence with daily activity,” said
    Principal Investigator Mitch Tyler.
    In a separate MS Pilot study, sponsored by Helius (see press release
    November 2, 2015), the average EDSS score of the subjects was 4.5, while
    the average in this subject pool was 7.0. In applauding the efforts of
    the TCNL investigators, Helius CEO Phillippe Deschamps noted, “The
    patients in this study represent a much more challenging cohort and
    received PoNSTM Therapy for a longer period (6-months vs.
    14-weeks), yet compliance remained high. The outcome is very
    encouraging.”

    1)

    The TCNL is the Tactile Communications and Neurorehabilitation
    Laboratory at the University of Wisconsin, Madison. The PoNS™ was
    developed at TCNL and licensed to a Helius subsidiary.

    2)EDSS is a measure of MS disease severity where 0=normal and 10=death.

    About PoNS™ Therapy
    The Portable Neuromodulation Stimulator (PoNS™) is an investigational
    non-invasive device designed to deliver neurostimulation through the
    tongue. PoNS™ Therapy combines the use of the device with physical
    therapy and is currently being evaluated in a multicenter clinical trial
    for the treatment of balance disorder for subjects with mild to moderate
    Traumatic Brain Injury.
    About Helius Medical Technologies, Inc.
    Helius Medical Technologies is a medical technology company focused on
    neurological wellness. Helius seeks to develop, license and acquire
    unique and non-invasive platform technologies that amplify the brain’s
    ability to heal itself. Helius intends to file for FDA clearance for the
    PoNS™ device. For more information, please visit www.heliusmedical.com.
    The Toronto Securities Exchange has not reviewed and does not accept
    responsibility for the adequacy or accuracy of the content of this news
    release.
    Cautionary Disclaimer Statement:
    Certain statements in this news release are not based on historical
    facts and constitute forward-looking statements or forward-looking
    information within the meaning of the U.S. Private Securities Litigation
    Reform Act of 1995 and Canadian securities laws (“forward-looking
    statements”).
    All statements other than statements of historical fact included in this
    news release are forward-looking statements that involve risks and
    uncertainties. Such forward-looking statements include, among others,
    statements regarding ongoing or planned clinical research, expected
    future development timelines, regulatory approvals, business initiatives
    and objectives and use of proceeds from financings or other business
    initiatives.
    Forward-looking statements are often identified by terms such as “will”,
    “may”, “should”, “anticipate”, “expects” and similar expressions.
    There can be no assurance that such statements will prove to be accurate
    and actual results and future events could differ materially from those
    anticipated in such statements. Important factors that could cause
    actual results to differ materially from the Company’s expectations
    include the failure of the Company to achieve its business objectives
    and other risks detailed from time to time in the filings made by the
    Company with securities regulators.
    The reader is cautioned that assumptions used in the preparation of any
    forward-looking statements may prove to be incorrect. Events or
    circumstances may cause actual results to differ materially from those
    predicted, as a result of numerous known and unknown risks,
    uncertainties, and other factors, many of which are beyond the control
    of the Company. The reader is cautioned not to place undue reliance on
    any forward-looking statement. Such information, although considered
    reasonable by management at the time of preparation, may prove to be
    incorrect and actual results may differ materially from those
    anticipated. Forward-looking statements contained in this news release
    are expressly qualified by this cautionary statement. Risks and
    uncertainties about the Company’s business are more fully discussed in
    the Company’s disclosure materials, including the short form prospectus
    filed in connection with the Offering, its Annual Report on Form 10-K
    filed with the United States Securities and Exchange Commission and the
    Canadian securities regulators and which can be obtained from either at www.sec.gov
    or www.sedar.com.
    The forward-looking statements contained in this news release are made
    as of the date of this news release and the Company assumes no
    obligation to update any forward-looking statement or to update the
    reasons why actual results could differ from such statements except to
    the extent required by law.

    fda clearancehelius medical technologiesmultiple sclerosismedical technology companymedical technology
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