Valeritas Announces Poster Presentation of Preclinical h-Patch™ Apomorphine Study at the World Congress of Neurology (WCN 2...
08 Octobre 2019 - 1:00PM
Valeritas Holdings, Inc. (NASDAQ: VLRX), a medical technology
company and maker of the V-Go® Wearable Insulin Delivery device,
which uses its proprietary h-Patch™ technology, announced today a
poster presentation at the 24th World Congress of Neurology held
in Dubai, UAE, on October 27-31, 2019. The World Congress
of Neurology is a five-day international event, which brings
together the world’s scientific experts to catalyze and advance
scientific knowledge about neurology, present the most recent
research findings, and promote and enhance scientific
collaborations around the world.
On August 5th, Valeritas announced positive results from a
preclinical pharmacokinetic (PK) study of continuous subcutaneous
infusion of apomorphine (Apo) delivered via its
proprietary h-Patch™ wearable drug delivery device. The
wearable h-Patch™ represents a patient-friendly subcutaneous
delivery mechanism for Apo providing the benefits of a full 24-hour
infusion of low dose Apo to eliminate “off” periods and improve
motor status without tolerability issues seen with subcutaneous
injections.
Valeritas’ h-Patch™ is a drug delivery technology that can
facilitate the simple and effective subcutaneous delivery of
injectable medicines to patients across a broad range of
therapeutic areas. The company’s V-Go is the first FDA-approved
product that utilizes the h-Patch™ technology. To date, more
than 20 million V-Go insulin delivery devices have been sold in the
United States.
Treatment of advanced Parkinson’s disease (PD) remains
challenging, with fluctuations in motor status often resulting in
patients becoming severely handicapped. The magnitude and pattern
of the motor response to a single dose of subcutaneously
administered Apo are qualitatively comparable to that of oral
levodopa; however, side effects of oral dosing (nausea, vomiting,
etc.) can be problematic. Close to a dozen clinical studies have
shown subcutaneous Apo infusions are successful in aborting “off”
periods, reducing dyskinesias, and improving PD motor scores with
the added benefit of a substantial levodopa-sparing effect.
However, bulky infusion pumps requiring delivery of relatively
large volumes of therapeutics remain a barrier to the development
of therapeutic products that are patient and caregiver
friendly.
About Valeritas Holdings, Inc.
Valeritas is a commercial-stage medical technology company
focused on improving health and simplifying life for people with
diabetes by developing and commercializing innovative technologies.
Valeritas’ flagship product, V-Go® Wearable Insulin Delivery
device, is a simple, affordable, all-in-one basal-bolus insulin
delivery option for patients with type 2 diabetes that is worn like
a patch and can eliminate the need for taking multiple daily shots.
V-Go administers a continuous preset basal rate of insulin over 24
hours, and it provides discreet on-demand bolus dosing at
mealtimes. It is the only basal-bolus insulin delivery device
on the market today specifically designed keeping in mind the needs
of type 2 diabetes patients. Headquartered in Bridgewater, New
Jersey, Valeritas operates its R&D functions in Marlborough,
Massachusetts.
More information is available at www.valeritas.com and our
Twitter feed @Valeritas_US, twitter.com/Valeritas_US.
Forward-Looking Statements
This press release may contain forward-looking statements.
Statements in this press release that are not purely historical are
forward-looking statements. Such forward-looking statements
include, among other things, references to Valeritas technologies,
business and product development plans and market information.
Actual results could differ from those projected in any
forward-looking statements due to numerous factors. Such factors
include, among others: the ability to raise the additional funding
needed to continue to pursue Valeritas’ business and product
development plans; Valeritas' expected cash burn rate and its
ability to continue to increase new and total prescription growth;
the expected benefits of the debt exchange on Valeritas’ cash
runway and its anticipated operating costs following the debt
exchange (the $2 million minimum debt covenant remains in place
following the debt exchange, which will continue to limit
Valeritas’ ability to finance its operations); the effects of both
the new issuance of Series B Convertible Preferred Stock and the
May 2019 reverse stock split on the trading price of Valeritas’
common stock, in both the short and long-term; the ability to
continue to commercialize the V-Go® Wearable Insulin Delivery
device with limited resources, competition in the industry in which
Valeritas operates and overall market conditions; the inherent
uncertainties associated with developing new products or
technologies; the potential commercial use of the h-Patch™
technology for subcutaneous delivery of Apo or CBD is dependent on
Valeritas’ ability to identify one or more potential collaboration
partners and enter into mutually agreeable collaboration agreements
(neither the delivery of Apo or CBD by h-Patch™ is currently
cleared for use by the FDA); our statements that (i) subcutaneous
Apo infusions appears to offer qualitatively comparable benefits to
that of oral levodopa and (ii) based on initial studies,
subcutaneous infusion of CBD appears to offer several distinct
advantages over oral dosing of CBD, and other potential benefits of
the h-Patch™ technology to deliver Apo or CBD is based on
third-party clinical studies not conducted by Valeritas; however,
additional studies or research may be needed by our potential
partners to demonstrate to the U.S. Food and Drug Administration
(“FDA”) that delivery of Apo or CBD via the h-Patch™ technology
will offer consistent results to the initial Valeritas study; and
the FDA or other regulatory agencies may require
Valeritas’ collaboration partners to demonstrate the safety or
effectiveness of subcutaneous infusion of Apo or CBD through the
h-Patch™ technology before either of those products can be
commercialized, which can be a lengthy, and uncertain process, and
the FDA may delay or require additional information to provide
clearance for use with our RHI or our V-Go SIM product. Statements
or claims made by third parties regarding the efficacy or
functionality of V-Go as compared to other products are statements
made by such individual and should not be taken as evidence of
clinical trial results supporting such statements or claims. Any
forward-looking statements are made as of the date of this press
release, and Valeritas assumes no obligation to update the
forward-looking statements or to update the reasons why actual
results could differ from those projected in the forward-looking
statements, except as required by law. Investors should
consult all of the information set forth herein and should also
refer to the risk factor disclosure set forth in the reports and
other documents Valeritas files with the SEC available at
www.sec.gov.
Investor Contacts:Lynn Pieper Lewis or Greg ChodaczekGilmartin
Group646-924-1769ir@valeritas.com
Media Contact:Kevin KnightKnight Marketing Communications,
Ltd.206-451-4823pr@valeritas.com
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