Alvotech (NASDAQ: ALVO), a global biotech company specializing in
the development and manufacture of biosimilar medicines for
patients worldwide, and the JAMP Pharma Group (JAMP Pharma), a
Canadian owned pharmaceutical company headquartered in the Montreal
area, announced today that the companies have expanded their
exclusive partnership to commercialize biosimilars developed and
manufactured by Alvotech, by adding two biosimilar candidates from
Alvotech’s pipeline: AVT16 a biosimilar for an immunology product
and AVT33, a biosimilar for an oncology product.
“We are very pleased to be expanding our partnership with
Alvotech, in order to bring more affordable biologics to patients
in Canada,” said Louis Pilon, President and CEO of the JAMP Pharma
Group. “Having already launched Simlandi™, a biosimilar of Humira,
we will continue to leverage our BIOJAMP™ and JAMP Care™ platforms
for the benefit of patients and caregivers.”
“The partnership with JAMP Pharma will allow us to accelerate
towards establishing a leadership position in the Canadian
biosimilars market,” said Robert Wessman, Founder and Executive
Chairman of Alvotech. “Our mission is to broaden and simplify
access to new biosimilars for patients around the world."
Alvotech will be responsible for the development and commercial
supply of the biosimilar candidates. In exchange for milestone
payments and future sales royalties, JAMP Pharma will receive
exclusive rights to commercialize Alvotech’s biosimilars in Canada,
leveraging JAMP Pharma’s strong sales, marketing capabilities and
experience in successfully commercializing new biosimilars in the
fast-growing Canadian market.
In February 2022, JAMP Pharma announced the creation of BIOJAMP™
as part of its goal to establish itself as a leader in the Canadian
biosimilars market. BIOJAMP™ and the JAMP Care™ patient support
program, are both designed to simplify the process for patients and
caregivers of transitioning to lower-cost biosimilar medicines.
About Simlandi™ (adalimumab)
Simlandi™ is a recombinant fully human immunoglobulin G1 (IgG1)
kappa monoclonal antibody (mAb) that specifically binds to tumour
necrosis factor-α (TNF) and blocks its interaction with the p55
(TNFR1) and p75 (TNFR2) cell surface TNF receptors, thereby
neutralizing the effect of TNF in inflammatory conditions.
Simlandi™ is an approved high-concentration, low-volume and
citrate-free biosimilar to Humira® (adalimumab). The same
biosimilar has also been approved in the EU, Norway, Iceland,
Lichtenstein, the UK and Switzerland as Hukyndra®. Dossiers are
under review in multiple countries, including in the United States.
JAMP Pharma launched Alvotech’s Simlandi™ in Canada in April
2022.
About Alvotech
Alvotech 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 contains eight 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), 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.
About JAMP Pharma Group
Founded 34 years ago, the JAMP Pharma Group is a privately-owned
Canadian company headquartered in the Montreal area. The Group is
active in all sectors of the pharmaceutical industry with its
generic products (JAMP Pharma), branded products (Orimed Pharma),
natural health products (Wampole and Laboratoire Suisse), and
beauty and personal care products (Cosmetic Import Ltd). Having
experienced remarkable growth over the past 10 years, the JAMP
Pharma Group has a broad and diversified portfolio with over 300
molecules and 180 supplements and beauty products. JAMP Pharma is
among the industry leaders in terms of annual prescription volume1
and is the Canadian leader in product launches2. Recently, the
Group has made a major investment in biosimilars with the launch of
its BIOJAMPTM division. For more information, please visit
www.jamppharma.ca/en/
(1) Pharmaceutical manufacturers with the
highest reported prescription volume in Canada from August 2018 to
August 2021. Based in part on data obtained under licence from
IQVIA Solutions Canada Inc. on the following information service:
CompuScript, August 2018 to August 2021. All rights reserved. This
statement is not necessarily that of IQVIA Solutions Canada Inc. or
any of its affiliates or subsidiaries.
(2) Total number of notices of compliance
(NOC), Health Canada, from April 1, 2020, to March 31, 2021.
(Public information available at
https://www.canada.ca/en/health-canada/services/drugs-health-products/drug-products/notice-compliance.html)
Alvotech 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 1955, as amended.
Forward-looking statements generally relate to future events or the
future financial operating performance of Alvotech. For example,
Alvotech’s expectations regarding partnerships, future milestone
and royalty payments, product launches, future growth, results of
operations, performance, future capital and other expenditures
including the development of critical infrastructure for the global
healthcare market, competitive advantages, business prospects and
opportunities including pipeline product development, future plans
and intentions, results, level of activities, performance, goals or
achievements or other future events, regulatory review and
interactions, the success of its commercial partnerships, including
its partnership with JAMP Pharma, the potential approval and
commercial launch of its product candidates, the timing of
regulatory approvals and market launches, the estimated size of the
total addressable market of Alvotech’s pipeline products, and the
commercial success of Simlandi, AVT16 and AVT33, subject to
regulatory approvals, in Canada and other countries. 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) the ability to
maintain stock exchange listing standards; (3) changes in
applicable laws or regulations; (4) the possibility that Alvotech
may be adversely affected by other economic, business, and/or
competitive factors; (5) Alvotech’s estimates of expenses and
profitability; (6) Alvotech’s ability to develop, manufacture and
commercialize the products and product candidates in its pipeline,
including AVT16 and AVT33; (7) actions of regulatory authorities,
which may affect the initiation, timing and progress of clinical
studies or future regulatory approvals or marketing authorizations;
(8) the ability of Alvotech or its partners to enroll and retain
patients in clinical studies; (9) the ability of Alvotech or its
partners to gain approval from regulators for planned clinical
studies, study plans or sites; (10) the ability of Alvotech’s
partners to conduct, supervise and monitor existing and potential
future clinical studies, which may impact development timelines and
plans; (11) Alvotech’s ability to obtain and maintain regulatory
approval or authorizations of its products, including AVT16 and
AVT33, including the timing or likelihood of expansion into
additional markets or geographies; (12) the success of Alvotech’s
current and future collaborations, joint ventures, partnerships or
licensing arrangements, including the partnership with JAMP Pharma;
(13) Alvotech’s ability, and that of its commercial partners, to
execute their commercialization strategy for approved products,
including Simlandi™; (14) Alvotech’s ability to manufacture
sufficient commercial supply of its approved products, including
Simlandi™; (15) the outcome of ongoing and future litigation
regarding Alvotech’s products and product candidates; (16) 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; 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
Alvotech Investor Relations and Global
CommunicationBenedikt Stefansson
alvotech.ir@alvotech.com
JAMP Pharma Media RelationsAlexandra
LewickiJAMP Pharma Group Communicationalewicki@jamppharma.com
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