Full Press Release Details
Nutriband Inc. receives patent protection from Australia,
ORLANDO, Fla., March 18, 2020 - Nutriband Inc.
(OTCQB: NTRB), a Nevada corporation (the "Company") has received a notice of grant from patent offices in Australia
and Russia and a notice of allowance from Mexico's patent office for the Abuse and Misuse Deterrent Transdermal Systems'
patent application filed by its clinical subsidiary 4P Therapeutics
The patent underpins 4p Therapeutics' abuse deterrent
fentanyl transdermal system. which uses Taste aversion to addresses the primary routes of abuse for opioid based transdermal patches.
About Nutriband Inc.
The Company is primarily
engaged in the development of a portfolio of transdermal pharmaceutical products. Its lead product under development is its abuse
deterrent fentanyl transdermal system which the Company is developing to provide clinicians and patients with an extended-release
transdermal fentanyl product for use in managing chronic pain requiring around the clock opioid therapy combined with properties
designed to help combat the opioid crisis by deterring the abuse and misuse of fentanyl patches.
The Company's website
is www.nutriband.com and 4P's website is www.4PTherapeutics.com. Any material
contained in or derived from the Company's or 4P's websites or any other website is not part of this press release.
About Our Forward-Looking Statements
Certain statements contained in this press release, including,
without limitation, statements containing the words "believes," "anticipates," "expects" and
words of similar import, constitute "forward-looking statements" within the meaning of the Private Securities Litigation
Reform Act of 1995. Such forward-looking statements involve both known and unknown risks and uncertainties. The Company's
actual results may differ materially from those anticipated in its forward-looking statements as a result of a number of factors,
including those including the Company's ability to develop its proposed abuse deterrent fentanyl transdermal system and other
proposed products, its ability to obtain patent protection for its abuse technology, its ability to obtain the necessary financing
to develop products and conduct the necessary clinical testing, its ability obtain Federal Food and Drug Administration approval
to market any product it may develop in the United States and to obtain any other regulatory approval necessary to market any product
in other countries, including countries in Europe, its ability to market any product it may develop, its ability to create, sustain,
manage or forecast its growth; its ability to attract and retain key personnel; changes in the Company's business strategy
or development plans; competition; business disruptions; adverse publicity and international, national and local general economic
and market conditions and risks generally associated with an undercapitalized development stage company that does not have a product
that can be marketed and the risks contained under "Risk Factors" and "Management's Discussion and Analysis
of Financial Condition and Results of Operations" in the Company's Form 10-K for the year ended January 31, 2018 and
under "Management's Discussion and Analysis of Financial Conditions and Results of Operations" in the Company's
Form 10-Q for the nine months ended October 31, 2018, and the Company's other filings with the Securities and Exchange Commission.
Except as required by applicable law, we undertake no obligation to revise or update any forward-looking statements in order to
reflect any event or circumstance that may arise after the date hereof.
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