Alvotech (NASDAQ: ALVO), a global biotech company specializing in
the development and manufacture of biosimilar medicines for
patients worldwide, today announced that it has reached settlement
agreements with Johnson & Johnson in Japan, Canada and in the
European Economic Area (EEA) for AVT04, a biosimilar to Stelara®
(ustekinumab). Regulatory approval for AVT04 in these markets has
already been granted. Market applications for AVT04 are currently
pending in additional global markets, including in the U.S.
Market entry of AVT04 in Canada is expected in Q1 2024. Launch
of AVT04 in Japan is anticipated after the upcoming round of
National Health Insurance reimbursement price listings, in May
2024. Entry to the first European markets is expected as soon as
possible after the expiration date of the European Supplementary
Protection Certificate (SPC) for Stelara, which is in late July
2024.
“We look forward to working with our commercial partners in
launching the first biosimilar to Stelara in these global markets,
thereby increasing patient access to a vital biologic,” said Robert
Wessman, Chairman and CEO of Alvotech.
Market authorization for AVT04 in Japan is held by Alvotech’s
commercial partner Fuji Pharma Co. Ltd., where the biosimilar will
be marketed as Ustekinumab BS (F). Alvotech’s commercial partner
and market authorization holder for AVT04 in Canada is JAMP Pharma
Group, where the biosimilar will be marketed as Jamteki®. In the
EEA, Alvotech’s commercial partner and market authorization holder
for AVT04 is STADA Arzneimittel AG, where the trade name for AVT04
will be Uzpruvo®.
In June 2023, Alvotech and Teva, the commercialization partner
for AVT04 in the U.S., reached a settlement and license agreement
with Johnson & Johnson, that grants an entry date for AVT04 in
the U.S. no later than February 21, 2025, pending approval of the
Biologics License Application by the U.S. Food and Drug
Administration, which is expected by the Biosimilar User Fee Act
goal date of April 16, 2024.
About AVT04 (ustekinumab) AVT04
is a monoclonal antibody and a biosimilar of Stelara®
(ustekinumab). Ustekinumab binds to two cytokines, IL-12 and IL-23,
that are involved in inflammatory and immune responses [1]. AVT04
has been approved in Japan, Canada and the EEA, which includes in
the 27 member states of the European Union, as well as Norway,
Iceland and Liechtenstein. Market applications are pending in other
global markets, including the U.S.
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 Statements
Certain 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 and financial performance. 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 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 for AVT04; (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; (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 including AVT04; (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 potential impact of the
ongoing COVID-19 pandemic on the FDA’s review timelines, including
its ability to complete timely inspection of manufacturing sites;
(15) the impact of worsening macroeconomic conditions, including
rising inflation and interest rates and general market conditions,
war in Ukraine and global geopolitical tension, and the ongoing and
evolving COVID-19 pandemic on the Alvotech’s business, financial
position, strategy and anticipated milestones; (16) future
liquidity and financing needs, which may impact the anticipated
utilization of the Yorkville facility or other financing sources;
and (17) 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 OR INVESTOR
RELATIONSBenedikt StefanssonSenior Director of Investor
Relations and Global Communicationalvotech.ir@alvotech.com
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