Intellipharmaceutics Receives Extension from Nasdaq Hearings
Panel
Toronto, Ontario January 28,
2019 Intellipharmaceutics International Inc. (Nasdaq and
TSX: IPCI) (“Intellipharmaceutics” or the “Company”), a pharmaceutical company
specializing in the research, development and manufacture of novel
and generic controlled-release and targeted-release oral solid
dosage drugs, today announced that it has received notice from the
Nasdaq Hearings Panel (the “Panel”) extending the
continued listing of the Company’s common shares until March
7, 2019, subject to certain conditions, while the Company works to
regain compliance with Nasdaq’s requirements.
At a
hearing held on January 10, 2019, the Company presented its plan to
regain and maintain compliance with Nasdaq’s continued listing requirements.
Following the March 7, 2019 deadline, the Panel will determine
whether a further extension period is warranted in the event the
Company has not regained compliance. However, there can be no
assurance that the Panel will grant such an extension. Moreover,
there can be no assurance that the Company will be able to regain
compliance with Nasdaq’s requirements or, if it does, that it
will be able to maintain compliance with all applicable
requirements for continued listing on Nasdaq over the long term.
The Panel’s determination requires the Company to promptly
notify Nasdaq of any significant events that occur during the
extension period that may affect the Company’s compliance
with Nasdaq requirements.
About Intellipharmaceutics
Intellipharmaceutics
International Inc. is a pharmaceutical company specializing in the
research, development and manufacture of novel and generic
controlled-release and targeted-release oral solid dosage drugs.
The Company's patented Hypermatrix™ technology is a multidimensional
controlled-release drug delivery platform that can be applied to a
wide range of existing and new pharmaceuticals.
Intellipharmaceutics has developed several drug delivery systems
based on this technology platform, with a pipeline of products
(some of which have received U.S. Food and Drug Administration
(“FDA”) approval) in various stages of development. The
Company has abbreviated new drug application (“ANDA”) and new drug application
(“NDA”) 505(b)(2) drug product candidates in its
development pipeline. These include the Company’s abuse- deterrent oxycodone
hydrochloride extended release formulation (“Oxycodone ER”) based on its proprietary
nPODDDS™ novel Point Of
Divergence Drug Delivery System (for which an NDA has been filed
with the FDA), and Regabatin™ XR (pregabalin extended-release
capsules).
Cautionary Statement Regarding Forward-Looking
Information
Certain statements in this
document constitute “forward-looking statements” within
the meaning of the United States Private Securities Litigation
Reform Act of 1995 and/or “forward-looking information”
under the Securities Act (Ontario). These statements include,
without limitation, statements expressed or implied regarding our
expectations regarding our plans, goals and milestones, status of
developments or expenditures relating to our business, plans to
fund our current activities, and statements concerning our
partnering activities, health regulatory submissions, strategy,
future operations, future financial position, future sales,
revenues and profitability, projected costs and market penetration
and risks or uncertainties related to our ability to comply with
the Nasdaq and TSX continued listing standards and our ability to
develop and implement a plan of compliance with the Nasdaq
continued listing standards acceptable to the Nasdaq Panel. In some
cases, you can identify forward-looking statements by terminology
such as “appear”, “unlikely”,
“target”, "may", "will", "should", "expects", "plans",
"plans to", "anticipates", "believes", "estimates", "predicts",
"confident", "prospects", "potential", "continue", "intends", "look
forward", "could", “would”, “projected”,
“goals”, “set to”, “seeking” or
the negative of such terms or other comparable terminology. We made
a number of assumptions in the preparation of our forward-looking
statements. You should not place undue reliance on our
forward-looking statements, which are subject to a multitude of
known and unknown risks and uncertainties that could cause actual
results, future circumstances or events to differ materially from
those stated in or implied by the forward-looking statements. Risks
and uncertainties relating to us and our business can be found in
the "Risk Factors" section of our latest annual information form,
our latest Form 20-F, and our latest Form F-1 and Form F-3
(including any documents forming a part thereof or incorporated by
reference therein), as
amended, as well as in our reports, public disclosure documents and
other filings with the securities commissions and other regulatory
bodies in Canada and the U.S., which are available on www.sedar.com
and www.sec.gov. The forward-looking statements reflect our current
views with respect to future events and are based on what we
believe are reasonable assumptions as of the date of this document
and we disclaim any intention and have no obligation or
responsibility, except as required by law, to update or revise any
forward-looking statements, whether as a result of new information,
future events or otherwise.
Trademarks used herein are the property of their respective
holders.
Unless the context otherwise requires, all references to "we,"
"us," "our," "Intellipharmaceutics," and the "Company" refer to
Intellipharmaceutics International Inc. and its
subsidiaries.
CONTACT INFORMATION
Company
Contact:
Intellipharmaceutics
International Inc.
Isa
Odidi
Chief
Executive Officer
416.798.3001 ext.
102
investors@intellipharmaceutics.com
Investor
Contact:
ProActive
Capital
Kirin
Smith
646.863.6519
ksmith@pcgadvisors.com