Aquestive Therapeutics to Present at 2020 RBC Capital Markets Global Healthcare Conference
May 07 2020 - 2:00PM
Aquestive Therapeutics, Inc. (NASDAQ:AQST), a pharmaceutical
company focused on developing and commercializing differentiated
products that address patients’ unmet needs and solve therapeutic
problems, today announced that management will present at the 2020
RBC Capital Markets Global Healthcare Conference to be held
virtually on May 19-20. Aquestive is scheduled to present on
Wednesday, May 20th at 1:55 pm ET.
A webcast of the presentation will be available
on the "Events and Presentation" page of the Investors section of
the Company's website. A replay of each webcast will be available
for 90 days following the event. For more information, please visit
investors.aquestive.com.
About Aquestive TherapeuticsAquestive
Therapeutics is a pharmaceutical company that applies innovative
technology to solve therapeutic problems and improve medicines for
patients. Aquestive is advancing a late-stage proprietary product
pipeline to treat CNS conditions and provide alternatives to
invasively administered standard of care therapies. The Company
also collaborates with other pharmaceutical companies to bring new
molecules to market using proprietary, best-in-class technologies,
like PharmFilm®, and has proven capabilities for drug development
and commercialization.
Forward-Looking StatementThis press release
includes forward-looking statements within the meaning of the
Private Securities Litigation Reform Act of 1995. Words such as
“believe,” “anticipate,” “plan,” “expect,” “estimate,” “intend,”
“may,” “will,” or the negative of those terms, and similar
expressions, are intended to identify forward-looking statements.
These forward-looking statements include, but are not limited to,
statements regarding therapeutic benefits and plans and objectives
for regulatory approvals of AQST-108, LibervantTM and our other
product candidates; ability to obtain FDA approval and advance
AQST-108, Libervant and our other product candidates to the market,
statements about our growth and future financial and operating
results and financial position, regulatory approval and pathways,
clinical trial timing and plans, our and our competitors’ orphan
drug approval and resulting drug exclusivity for our products or
products of our competitors, short-term and long-term liquidity and
cash requirements, cash funding and cash burn, business strategies,
market opportunities, and other statements that are not historical
facts. These forward-looking statements also are subject to
the uncertain impact of the COVID-19 global pandemic on our
business including with respect to our clinical trials including
site initiation, patient enrollment and timing and adequacy of
clinical trials; on regulatory submissions and regulatory reviews
and approvals of our product candidates; pharmaceutical
ingredient and other raw materials supply chain, manufacture, and
distribution; sale of and demand of our products; our liquidity and
availability of capital resources; customer demand for our products
and services; customers’ ability to pay for goods and services; and
ongoing availability of an appropriate labor force and skilled
professionals.
These forward-looking statements are based on
our current expectations and beliefs and are subject to a number of
risks and uncertainties that could cause actual results to differ
materially from those described in the forward-looking statements.
Such risks and uncertainties include, but are not limited to, risks
associated with the Company's development work, including any
delays or changes to the timing, cost and success of our product
development activities and clinical trials and plans; risk of
delays in FDA approval of Libervant and our other drug candidates
or failure to receive approval; risk of our ability to demonstrate
to the FDA “clinical superiority” within the meaning of the FDA
regulations of our drug candidate Libervant relative to
FDA-approved diazepam rectal gel and nasal spray products including
by establishing a major contribution to patient care within the
meaning of FDA regulations relative to the approval of products and
there can be no assurance that we will be successful; risk that a
competitor obtains FDA orphan drug exclusivity for a product with
the same active moiety as any of our other drug products for which
we are seeking FDA approval and that such earlier approved
competitor orphan drug blocks such other product candidates in the
U.S. for seven years for the same indication; risk inherent in
commercializing a new product (including technology risks,
financial risks, market risks and implementation risks and
regulatory limitations); risk of development of our sales and
marketing capabilities; risk of legal costs associated with and the
outcome of our patent litigation challenging third party at risk
generic sale of our proprietary products; risk of sufficient
capital and cash resources, including access to available debt and
equity financing and revenues from operations, to satisfy all of
our short-term and longer term cash requirements and other cash
needs, at the times and in the amounts needed; risk of failure to
satisfy all financial and other debt covenants and of any default;
risk related to government claims against Indivior for which we
license, manufacture and sell Suboxone® and which accounts for the
substantial part of our current operating revenues; risk associated
with Indivior’s cessation of production of its authorized generic
buprenorphine naloxone film product, including the impact from loss
of orders for the authorized generic product and risk of eroding
market share for Suboxone and risk of sunsetting product; risks
related to the outsourcing of certain sales, marketing and other
operational and staff functions to third parties; risk of the rate
and degree of market acceptance of our product and product
candidates; the success of any competing products, including
generics; risk of the size and growth of our product markets; risks
of compliance with all FDA and other governmental and customer
requirements for our manufacturing facilities; risks associated
with intellectual property rights and infringement claims relating
to the Company's products; risk of unexpected patent developments;
the impact of existing and future legislation and regulatory
provisions on product exclusivity; legislation or regulatory
actions affecting pharmaceutical product pricing, reimbursement or
access; claims and risks that may arise regarding the safety or
efficacy of the Company's products and product candidates; risk of
loss of significant customers; risks related to legal proceedings,
including patent infringement, investigative and antitrust
litigation matters; changes in government laws and regulations;
risk of product recalls and withdrawals; uncertainties related to
general economic, political, business, industry, regulatory and
market conditions and other unusual items; and other uncertainties
affecting the Company described in the “Risk Factors” section and
in other sections included in our Annual Report on Form 10‑K , in
our Quarterly Reports on Form 10-Q, and in our Current Reports on
Form 8-K filed with the Securities Exchange Commission (SEC). Given
those uncertainties, you should not place undue reliance on these
forward-looking statements, which speak only as of the date made.
All subsequent forward-looking statements attributable to us or any
person acting on our behalf are expressly qualified in their
entirety by this cautionary statement. The Company assumes no
obligation to update forward-looking statements or outlook or
guidance after the date of this press release whether as a result
of new information, future events or otherwise, except as may be
required by applicable law.
PharmFilm® and the Aquestive logo are registered
trademarks of Aquestive Therapeutics, Inc. All other
registered trademarks referenced herein are the property of their
respective owners.
Investor inquiries:Stephanie Carrington
stephanie.carrington@icrinc.com 646-277-1282
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