Aytu BioScience, Inc. (NASDAQ: AYTU), a specialty pharmaceutical
company focused on commercializing novel products that address
significant patient needs, and Neos Therapeutics, Inc. (NASDAQ:
NEOS), a commercial-stage pharmaceutical company developing and
manufacturing central nervous system-focused products, today
announced that the companies’ respective special meetings of
stockholders related to the proposed merger between Aytu and Neos
have been set for Thursday, March 18, 2021. Stockholders of record
of each company as of February 5, 2021 will be eligible to receive
notice of and to vote at their respective company’s special
meeting.
Following stockholder approval and the satisfaction or waiver of
the other conditions to the closing of the merger, the combined
company will be renamed Aytu Biopharma, Inc., and its common stock
will continue to trade under the symbol “AYTU” on the Nasdaq
Capital Market.
As described in more detail in the definitive joint proxy
statement/prospectus, both companies’ Board of Directors encourage
all stockholders of their respective companies to vote “FOR” all
proposals in advance of the special meetings by telephone, via the
Internet or by signing, dating and returning the proxy cards upon
receipt by following the instructions on the proxy cards. The joint
proxy statement/prospectus, which is publicly available, will first
be mailed to Aytu stockholders and Neos stockholders on or about
February 12, 2021.
If Neos stockholders of record have any questions or need
assistance voting, please contact MacKenzie Partners, Inc., Neos’
proxy solicitor, by calling (800) 322-2885 or by email to
proxy@mackenziepartners.com.
If Aytu stockholders of record have any questions or need
assistance voting, please contact the Proxy Advisory Group, LLC,
Aytu’s proxy solicitor, by calling (212) 616-2181 or by email to
info@proxyadvisory.net.
About Aytu BioScience, Inc.
Aytu BioScience is a commercial-stage specialty pharmaceutical
company focused on commercializing novel products that address
significant patient needs. Aytu currently markets a portfolio of
prescription products addressing large primary care and pediatric
markets. The primary care portfolio includes (i) Natesto®, the only
FDA-approved nasal formulation of testosterone for men with
hypogonadism (low testosterone, or "Low T"), (ii) ZolpiMist®, the
only FDA-approved oral spray prescription sleep aid, and (iii)
Tuzistra® XR, the only FDA-approved 12-hour codeine-based
antitussive syrup. The pediatric portfolio includes (i) Cefaclor, a
second-generation cephalosporin antibiotic suspension; (ii)
Karbinal® ER, an extended-release carbinoxamine (antihistamine)
suspension indicated to treat numerous allergic conditions; and
(iii) Poly-Vi-Flor® and Tri-Vi-Flor®, two complementary
prescription fluoride-based supplement product lines containing
combinations of fluoride and vitamins in various formulations for
infants and children with fluoride deficiency. Aytu also
distributes a COVID-19 IgG/IgM rapid antibody test and rapid
antigen test. These tests are used separately in the rapid,
qualitative diagnostic assessment of the 2019 Novel Coronavirus.
Additionally, Aytu recently licensed worldwide rights to develop
the Healight™ technology platform. Healight is an investigational
medical device being studied as a prospective treatment for
COVID-19 and other respiratory infections.
Aytu operates a consumer health subsidiary, Innovus
Pharmaceuticals, Inc. ("Innovus"), a specialty pharmaceutical
company commercializing, licensing and developing safe and
effective consumer healthcare products designed to improve men's
and women's health and vitality. Innovus commercializes numerous
novel consumer health products competing in large healthcare
categories including diabetes, men's health, sexual wellness,
respiratory health, and general wellness. The Innovus product
portfolio is commercialized through direct-to-consumer marketing
channels utilizing the company's proprietary Beyond Human®
marketing and sales platform.
Aytu's strategy is to continue building its portfolio of
revenue-generating Rx and consumer health products, leveraging its
focused commercial team and expertise to build leading brands
within large therapeutic markets. For more information visit
aytubio.com and visit innovuspharma.com to learn about Aytu's
consumer healthcare products.
About Neos Therapeutics
Neos Therapeutics, Inc. is a commercial-stage pharmaceutical
company developing and manufacturing central nervous system
(CNS)-focused products. Neos markets Adzenys XR-ODT® (amphetamine)
extended-release orally disintegrating tablets (see Full
Prescribing Information, including Boxed WARNING), Cotempla XR-ODT®
(methylphenidate) extended-release orally disintegrating tablets
(see Full Prescribing Information, including Boxed WARNING), and
Adzenys-ER® (amphetamine) extended-release oral suspension (see
Full Prescribing Information, including Boxed WARNING), all for the
treatment of ADHD. Neos also has a development candidate, NT0502,
for the treatment of sialorrhea in patients with neurological
conditions. Additional information about Neos is available at
www.neostx.com.
Forward-Looking Statements
This press release includes forward-looking statements within
the meaning of Section 27A of the Securities Act of 1933, as
amended, and Section 21E of the Securities Exchange Act of 1934, or
the Exchange Act. All statements other than statements of
historical facts contained in this press release, are
forward-looking statements. Forward-looking statements are
generally written in the future tense and/or are preceded by words
such as ''may,'' ''will,'' ''should,'' ''forecast,'' ''could,''
''expect,'' ''suggest,'' ''believe,'' ''estimate,'' ''continue,''
''anticipate,'' ''intend,'' ''plan,'' or similar words, or the
negatives of such terms or other variations on such terms or
comparable terminology. All statements other than statements of
historical facts contained in this presentation, are
forward-looking statements, including but not limited to any
statements regarding the expected timetable for completing the
proposed transaction, the results of the proposed transaction and
any other statements regarding Aytu's or Neos' future expectations,
beliefs, plans, objectives, financial conditions, assumptions or
future events or performance. These statements are just predictions
and are subject to risks and uncertainties that could cause the
actual events or results to differ materially. These risks and
uncertainties include, among others: failure to obtain the required
votes of Neos' stockholders or Aytu's stockholders to approve the
transaction and related matters, the risk that a condition to
closing of the proposed transaction may not be satisfied, that
either party may terminate the merger agreement or that the closing
of the proposed transaction might be delayed or not occur at all.
We also refer you to (i) the risks described in “Risk Factors” in
the definitive joint proxy statement/prospectus filed by Aytu and
dated as of February 9, 2021, (ii) the risks described in ''Risk
Factors'' in Part I, Item 1A of Aytu's Annual Report on Form 10-K
and in the other reports and documents it files with the Securities
and Exchange Commission and (iii) the Risk Factors set forth in
Neos' Annual Report on Form 10-K and Quarterly Reports on Form 10-Q
filed with the SEC and in the other filings Neos makes with the SEC
from time to time.
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