Kamada to Announce Fourth Quarter and Fiscal Year Ended

Kamada to Announce Fourth Quarter and

Fiscal Year Ended December 31, 2020 Financial Results, and Host Conference Call on February 10, 2021

Rehovot, Israel, February 3, 2021 --

Kamada Ltd. (NASDAQ & TASE: KMDA), plasma-derived biopharmaceutical company, today announced that it will release financial

results for the fourth quarter and fiscal year ended December 31, 2020, prior to the open of the U.S. financial markets on Wednesday,

Kamada management will host an investment

community conference call on Wednesday, February 10, at 8:00am 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.), or 201-689-8263

(International) and entering the conference identification number: 13715277. The call will also be webcast live on the Internet

on the Company's website at www.kamada.com.

call will also be archived for 90 days on the Company's website at www.kamada.com.

Kamada Ltd. ("the Company")

is a commercial stage plasma-derived biopharmaceutical company focused on orphan indications, with an existing marketed product

portfolio and a late-stage product pipeline. The Company uses its proprietary platform technology and know-how for the extraction

and purification of proteins from human plasma to produce Alpha-1 Antitrypsin (AAT) in a highly-purified, liquid form, as well

as other plasma-derived immune globulins. The Company's flagship product is GLASSIA , the first liquid, ready-to-use,

intravenous plasma-derived AAT product approved by the U.S. FDA. The Company markets GLASSIA in the U.S. through a strategic partnership

with Takeda Pharmaceuticals Company Limited 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 is planning to 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. The Company's second

leading product is KamRab , a rabies immune globulin (Human) for post-exposure prophylaxis against rabies infection. KamRab

is FDA approved and is being marketed in the U.S. under the brand name KEDRAB through a strategic partnership with Kedrion

S.p.A. In addition to Glassia and KEDRAB, the Company has a product line of four other plasma-derived pharmaceutical products administered

by injection or infusion, that are marketed through distributors in more than 15 countries, including Israel, Russia, Brazil, India

and other countries in Latin America and Asia. The Company has late-stage products in development, including an inhaled formulation

of AAT for the treatment of AAT deficiency. In addition, the Company's intravenous AAT is in development for other indications,

such as GvHD and prevention of lung transplant rejection, and during 2020, the Company initiated the development of 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 plasma-derived protein therapeutics market by distributing more than 20 complementary products in

Israel that are manufactured by third parties. 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.

Chief Financial Officer

LifeSci Advisors, LLC