Rehovot, Israel, November 8, 2021 — Kamada Ltd. (NASDAQ & TASE: KMDA), a plasma-derived
biopharmaceutical company, today announced that it will release financial results for the three and nine months
ended September 30, 2021, prior to the open of the U.S. financial markets on Monday, November 22, 2021.
Kamada management will host an investment community conference call on Monday, November 22, at 8:30am
Eastern Time to discuss these results and answer questions. Shareholders and other interested parties may
participate in the conference call by dialing 877-407-0792 (from within the U.S.), 1-809-406-247 (from Israel),
or 201-689-8263 (International) and entering the conference identification number: 13724183. The call will also
be webcast live on the Internet at:
https://78449.themediaframe.com/dataconf/productusers/vvdb/mediaframe/47019/indexl.html.
The call will also be archived for 90 days on the Company’s website at www.kamada.com.
About Kamada
Kamada Ltd. (the “Company”) is a global specialty plasma-derived biopharmaceutical company with a diverse
portfolio of marketed products, a robust development pipeline and industry-leading manufacturing capabilities.
The Company’s strategy is focused on driving profitable growth from its current commercial products, its plasmaderived
development pipeline and its manufacturing expertise, while evolving into a vertically integrated plasmaderived
company. The Company’s two leading commercial products are GLASSIA® and KEDRRAB®.
GLASSIA was the first liquid, ready-to-use, intravenous plasma-derived AAT product approved by the FDA. The
Company markets GLASSIA in the U.S. through a strategic partnership with Takeda Pharmaceuticals Company
Limited (“Takeda”) and in other countries through local distributors. Pursuant to an agreement with Takeda, the
Company will continue to produce GLASSIA for Takeda through 2021 and Takeda will initiate its own
production of GLASSIA for the U.S. market in 2021, at which point Takeda will commence payment of royalties
to the Company until 2040. KEDRAB is an FDA approved anti-rabies immune globulin (Human) for postexposure
prophylaxis treatment. KEDRAB is being marketed in the U.S. through a strategic partnership with
Kedrion S.p.A. The Company has additional four plasma-derived products administered by injection or infusion,
that are marketed through distributors in more than 15 countries, including Israel, Russia, Brazil, Argentina, India
and other countries in Latin America and Asia. The Company has two leading development programs; an inhaled
AAT for the treatment of AAT deficiency for which the Company is currently conducting the InnovAATe clinical
trial, a randomized, double-blind, placebo-controlled, pivotal Phase 3 trial, and a plasma-derived hyperimmune
immunoglobulin (IgG) product as a potential treatment for coronavirus disease (COVID-19). The Company
leverages its expertise and presence in the Israeli pharmaceutical market to distribute in Israel more than 20
products that are manufactured by third parties and have recently added nine biosimilar products to its Israeli
distribution portfolio, which, subject to EMA and the Israeli MOH approvals, are expected to be launched in
Israel between the years 2022 and 2025. FIMI Opportunity Fund, the leading private equity investor in Israel, is
the Company’s lead shareholder, beneficially owning approximately 21% of the outstanding ordinary shares.
CONTACTS:
Chaime Orlev
Chief Financial Officer
IR@kamada.com
Bob Yedid
LifeSci Advisors, LLC
646-597-6989
Bob@LifeSciAdvisors.com