Alvotech (NASDAQ: ALVO), a global biotech company specializing in
the development and manufacture of biosimilar medicines for
patients worldwide, today announced that the reinspection of
Alvotech’s facility in Iceland by the U.S. Food and Drug
Administration (FDA) which started on January 10, 2024, has been
concluded. Following the FDA inspection, Alvotech received a form
483 with one observation. Alvotech expects to provide the FDA with
a response in the following days.
“We believe that the observation is readily addressable, and we
intend to respond as quickly as possible,” said Robert Wessman,
Chairman and CEO of Alvotech.
Based on the conclusion of the facility reinspection, Alvotech
believes it is in a position to receive approval in the U.S. for
AVT02 and AVT04 by February 24, 2024, and April 16, 2024, their
respective goal dates.
About AlvotechAlvotech is a biotech company,
founded by Robert Wessman, focused solely on the development and
manufacture of biosimilar medicines for patients worldwide.
Alvotech seeks to be a global leader in the biosimilar space by
delivering high quality, cost-effective products, and services,
enabled by a fully integrated approach and broad in-house
capabilities. Alvotech’s current pipeline includes eight disclosed
biosimilar candidates aimed at treating autoimmune disorders, eye
disorders, osteoporosis, respiratory disease, and cancer. Alvotech
has formed a network of strategic commercial partnerships to
provide global reach and leverage local expertise in markets that
include the United States, Europe, Japan, China, and other Asian
countries and large parts of South America, Africa and the Middle
East. Alvotech’s commercial partners include Teva Pharmaceuticals,
a US affiliate of Teva Pharmaceutical Industries Ltd. (US), STADA
Arzneimittel AG (EU), Fuji Pharma Co., Ltd (Japan), Advanz Pharma
(EEA, UK, Switzerland, Canada, Australia and New Zealand),
Cipla/Cipla Gulf/Cipla Med Pro (Australia, New Zealand, South
Africa/Africa), JAMP Pharma Corporation (Canada), Yangtze River
Pharmaceutical (Group) Co., Ltd. (China), DKSH (Taiwan, Hong Kong,
Cambodia, Malaysia, Singapore, Indonesia, India, Bangladesh and
Pakistan), YAS Holding LLC (Middle East and North Africa), Abdi
Ibrahim (Turkey), Kamada Ltd. (Israel), Mega Labs, Stein, Libbs,
Tuteur and Saval (Latin America) and Lotus Pharmaceuticals Co.,
Ltd. (Thailand, Vietnam, Philippines, and South Korea). Each
commercial partnership covers a unique set of product(s) and
territories. Except as specifically set forth therein, Alvotech
disclaims responsibility for the content of periodic filings,
disclosures and other reports made available by its partners. For
more information, please visit www.alvotech.com. None of the
information on the Alvotech website shall be deemed part of this
press release.
Forward Looking StatementsCertain statements in
this communication may be considered “forward-looking statements”
within the meaning of the Private Securities Litigation Reform Act
of 1995, as amended. Forward-looking statements generally relate to
future events or the future financial operating performance of
Alvotech and may include, for example, Alvotech’s expectations
regarding its expected future business, financial performance, and
the use of proceeds from private placements. In some cases, you can
identify forward-looking statements by terminology such as “may”,
“should”, “expect”, “intend”, “will”, “estimate”, “anticipate”,
“believe”, “predict”, “potential”, “aim” or “continue”, or the
negatives of these terms or variations of them or similar
terminology. Such forward-looking statements are subject to risks,
uncertainties, and other factors which could cause actual results
to differ materially from those expressed or implied by such
forward-looking statements. These forward-looking statements are
based upon estimates and assumptions that, while considered
reasonable by Alvotech and its management, are inherently uncertain
and are inherently subject to risks, variability, and
contingencies, many of which are beyond Alvotech’s control. Factors
that may cause actual results to differ materially from current
expectations include, but are not limited to: (1) the outcome of
any legal proceedings that may be instituted against Alvotech or
others following the business combination between Alvotech Holdings
S.A., Oaktree Acquisition Corp. II and Alvotech; (2) changes in
applicable laws or regulations; (3) the possibility that Alvotech
may be adversely affected by other economic, business, and/or
competitive factors; (4) Alvotech’s estimates of expenses and
profitability; (5) Alvotech’s ability to develop, manufacture and
commercialize the products and product candidates in its pipeline
including AVT02 and AVT04; (6) actions of regulatory authorities,
which may affect the initiation, timing and progress of clinical
studies or future regulatory approvals or marketing authorizations
including the approval of AVT02 and AVT04 in the U.S. or other
countries; (7) the ability of Alvotech or its partners to gain
approval from regulators for planned clinical studies, study plans
or sites; (8) the ability of Alvotech’s partners to conduct,
supervise and monitor existing and potential future clinical
studies, which may impact development timelines and plans; (9)
Alvotech’s ability to obtain and maintain regulatory approval or
authorizations of its products, including the timing or likelihood
of expansion into additional markets or geographies such as the
U.S.; (10) the success of Alvotech’s current and future
collaborations, joint ventures, partnerships or licensing
arrangements; (11) Alvotech’s ability, and that of its commercial
partners, to execute their commercialization strategy for approved
products; (12) Alvotech’s ability to manufacture sufficient
commercial supply of its approved products; (13) the outcome of
ongoing and future litigation regarding Alvotech’s products and
product candidates; (14) the impact of worsening macroeconomic
conditions, including rising inflation and interest rates and
general market conditions, war in Ukraine and global geopolitical
tension, on Alvotech’s business, financial position, strategy and
anticipated milestones; (15) future liquidity and financing needs,
which may impact the anticipated utilization of the Yorkville
facility or other financing sources; and (16) other risks and
uncertainties set forth in the sections entitled “Risk Factors” and
“Cautionary Note Regarding Forward-Looking Statements” in documents
that Alvotech may from time to time file or furnish with the SEC.
There may be additional risks that Alvotech does not presently know
or that Alvotech currently believes are immaterial that could also
cause actual results to differ from those contained in the
forward-looking statements. Nothing in this communication should be
regarded as a representation by any person that the forward-looking
statements set forth herein will be achieved or that any of the
contemplated results of such forward-looking statements will be
achieved. You should not place undue reliance on forward-looking
statements, which speak only as of the date they are made. Alvotech
does not undertake any duty to update these forward-looking
statements or to inform the recipient of any matters of which any
of them becomes aware of which may affect any matter referred to in
this communication. Alvotech disclaims any and all liability for
any loss or damage (whether foreseeable or not) suffered or
incurred by any person or entity as a result of anything contained
or omitted from this communication and such liability is expressly
disclaimed. The recipient agrees that it shall not seek to sue or
otherwise hold Alvotech or any of its directors, officers,
employees, affiliates, agents, advisors, or representatives liable
in any respect for the provision of this communication, the
information contained in this communication, or the omission of any
information from this communication.
CONTACTS FOR THE MEDIA AND IRAlvotech
Investor Relations and Global CommunicationsBenedikt
Stefansson, Senior Directoralvotech.ir@alvotech.com
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