Kamada Ltd. (NASDAQ:KMDA) (TASE:KMDA), a plasma-derived protein
therapeutics company focused on orphan indications, announces that it
will release financial results for the three months ended March 31, 2015
prior to the market open on Tuesday, May 12, 2015.
Kamada management will host an investment community conference call on
Tuesday, May 12, 2015 at 8:30 a.m. Eastern time to discuss these results
and answer questions. Shareholders and other interested parties may
participate in the conference call by dialing 888-803-5993 (from within
the U.S.), 706-634-5454 (from outside the U.S.) or 1-809-315-362
(toll-free from Israel) and entering the conference identification
number: 44127836.
A replay of the call will be accessible two hours after its completion
through May 18, 2015 by dialing 855-859-2056 (from within the U.S.) or
404-537-3406 (from outside the U.S.) and entering the conference
identification number: 44127836. The call will also be archived for 90
days at www.streetevents.com
and www.kamada.com.
About Kamada
Kamada Ltd. is focused on plasma-derived protein therapeutics for orphan
indications, and has a commercial product portfolio and a robust
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 proteins.
AAT is a protein derived from human plasma with known and
newly-discovered therapeutic roles given its immunomodulatory,
anti-inflammatory, tissue-protective and antimicrobial properties. The
Company’s flagship product is Glassia®, the first and only liquid,
ready-to-use, intravenous plasma-derived AAT product approved by the
U.S. Food and Drug Administration. Kamada markets Glassia in the U.S.
through a strategic partnership with Baxter International. In addition
to Glassia, Kamada has a product line of nine other pharmaceutical
products that are marketed through distributors in more than 15
countries, including Israel, Russia, Brazil, India and other countries
in Latin America, Eastern Europe and Asia. Kamada has five late-stage
plasma-derived protein products in development, including an inhaled
formulation of AAT for the treatment of AAT deficiency that completed a
pivotal Phase 2/3 clinical trials in Europe and has initiated Phase 2
clinical trials in the U.S. Kamada also leverages its expertise and
presence in the plasma-derived protein therapeutics market by
distributing 10 complementary products in Israel that are manufactured
by third parties. For more information, visit www.kamada.com.
Cautionary Note Regarding Forward-Looking Statements
This release includes forward-looking statements within the meaning of
Section 27A of the U.S. Securities Act of 1933, as amended, Section 21E
of the US 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, such as statements regarding assumptions and results
related to financial results forecast, commercial results, clinical
trials, Intellectual Property, the EMA and U.S. FDA filings and
authorizations and timing of clinical trials. 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,
unexpected results of clinical trials, delays or denial in the U.S. FDA
or the EMA approval process, additional competition in the AATD market
or further regulatory delays. 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 by law.
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