Full Press Release Details
Announces Kedrion Exercised its Option for Two-Year Extension of KEDRAB Distribution Agreement in the U.S.
Israel, and Hoboken, NJ - July 12, 2023 -- Kamada Ltd. (NASDAQ: KMDA; TASE: KMDA.TA) ("Kamada" or the "Company"),
a commercial stage global biopharmaceutical company with a portfolio of marketed products indicated for rare and serious conditions
and a leader in the specialty plasma-derived field, today announced that Kedrion has exercised its option to extend the distribution
agreement between the parties in the U.S. for KEDRAB (Rabies Immune Globulin [Human]), which
is indicated for passive, transient post-exposure prophylaxis (PEP) of rabies infection to persons of all ages when given immediately
after contact with a rabid or possibly rabid animal. The current agreement now extends through March 2026, and the companies are
in discussions to potentially further expand the scope of the collaboration.
"We are pleased that Kedrion has exercised
its option to extend this important distribution agreement for an additional two years," said Amir London, CEO of Kamada. "Rabies
is still present in the U.S and is transmitted by wild animals. Our collaboration with Kedrion contributed to the promotion of KEDRAB
and, through disease awareness campaigns, we achieved substantial growth and gained share in the U.S. market, which is estimated to be
over $150 million annually. During 2022, we generated approximately $16 million in revenues from sales of KEDRAB to Kedrion for further
distribution in the U.S. market and we anticipate a significant increase in sales of the product this year."
Kamada Ltd. (the "Company") is a commercial
stage global biopharmaceutical company with a portfolio of marketed products indicated for rare and serious conditions and a leader in
the specialty plasma-derived field, focused on diseases of limited treatment alternatives. The Company is also advancing an innovative
development pipeline targeting areas of significant unmet medical need. The Company's strategy is focused on driving profitable
growth from its significant commercial catalysts as well as its manufacturing and development expertise in the plasma-derived and biopharmaceutical
fields. The Company's commercial products portfolio includes six FDA approved plasma-derived biopharmaceutical products: CYTOGAM ,
KEDRAB , WINRHO SDF , VARIZIG , HEPAGAM B and GLASSIA , as well as KAMRAB , KAMRHO (D) and two types of
equine-based anti-snake venom (ASV) products. The Company distributes its commercial products portfolio directly, and through strategic
partners or third-party distributors in more than 30 countries, including the U.S., Canada, Israel, Russia, Argentina, Brazil, India,
Australia and other countries in Latin America, Europe, Middle East, and Asia. The Company leverages its expertise and presence in the
Israeli market to distribute, for use in Israel, more than 25 pharmaceutical products that are supplied by international manufacturers.
During recent years the Company added eleven biosimilar products to its Israeli distribution portfolio, which, subject to the European
Medicines Agency (EMA) and the Israeli Ministry of Health approvals, are expected to be launched in Israel through 2028. The Company owns
an FDA licensed plasma collection center in Beaumont, Texas, which currently specializes in the collection of hyper-immune plasma used
in the manufacture of KAMRHO (D). In addition to the Company's commercial operation, it invests in research and development of new
product candidates. The Company's leading investigational product is an inhaled AAT for the treatment of AAT deficiency, for which
it is continuing to progress the InnovAATe clinical trial, a randomized, double-blind, placebo-controlled, pivotal Phase 3 trial. FIMI
Opportunity Funds, the leading private equity firm in Israel, is the Company's lead shareholder, beneficially owning approximately
21% of the outstanding ordinary shares.
Cautionary Note Regarding Forward-Looking Statements
This release includes forward-looking statements
within the meaning of Section 21E of the U.S. Securities Exchange Act of 1934, as amended, and the safe harbor provisions of the U.S.
Private Securities Litigation Reform Act of 1995. Forward-looking statements are statements that are not historical facts, including statements
regarding: (1) potential expansion of the scope of the collaboration between Kamada and Kedrion, (2) an anticipation of a significant
increase in sales of the product to Kedrion in 2023 compared to 2022, and (3) the anti-rabies IgG market, which is estimated to be over
$150 million annually. Forward-looking statements are based on Kamada's current knowledge and its present beliefs and expectations
regarding possible future events and are subject to risks, uncertainties and assumptions. Actual results and the timing of events could
differ materially from those anticipated in these forward-looking statements as a result of several factors including, but not limited
to the continued success of KEDRAB, competition to KEDRAB and market conditions relating to KEDRAB, as well as risks detailed in Kamada's
filings with the U.S. Securities and Exchange Commission (the "SEC") including those discussed in its most recent Annual Report
on Form 20-F and in any subsequent reports on Form 6-K, each of which is on file or furnished with the SEC and available at the SEC's
website at www.sec.gov. The forward-looking statements made herein speak only as of the date of this announcement and Kamada undertakes
no obligation to update publicly such forward-looking statements to reflect subsequent events or circumstances, except as otherwise required
Chief Financial Officer
LifeSci Advisors, LLC