Exhibit 99.1
Protalix BioTherapeutics Announces Proposed Public Offering of Common Stock
CARMIEL, Israel, March 17, 2011 /PR Newswire/Protalix BioTherapeutics, Inc. (NYSE-AMEX:PLX,
TASE:PLX) announced today that it intends, subject to market conditions, to offer and sell shares
of its common stock in an underwritten public offering. Citi and Barclays Capital Inc. are acting
as the joint book-running managers for the offering. The offering is subject to market conditions,
and there can be no assurance as to whether or when the offering may be completed, or as to the
actual size or terms of the offering.
The Company expects to use the net proceeds from the sale of the shares for one or more of the
following: to fund clinical trials for the Company’s product candidates; to fund the Company’s
research and development activities; to enhance the Company’s manufacturing capacity; and for
working capital and general corporate purposes.
The offering is being made pursuant to an effective shelf registration statement. Before you
invest, you should read the base prospectus in such shelf registration statement, the preliminary
prospectus supplement, when available, and other documents the Company has filed with the
Securities and Exchange Commission, or SEC, for more complete information about the Company and
this offering. The offering may be made only by means of a prospectus supplement and the
accompanying prospectus, copies of which may be obtained by sending a request to the offices of
Citi at Brooklyn Army Terminal, 140 58th Street, 8th Floor, Brooklyn, NY 11220, telephone number
(800) 831-9146 or to Barclays Capital Inc. at Barclays Capital Inc., c/o Broadridge Financial
Solutions, 1155 Long Island Avenue, Edgewood, New York 11717; Barclaysprospectus@broadridge.com
(phone: 888-603-5847). Alternatively, you may get these documents for free by visiting EDGAR on
the SEC website at www.sec.gov.
This press release shall not constitute an offer to sell, or the solicitation of an offer to buy,
any of the securities, nor shall there be any sale of these securities, in any state or other
jurisdiction in which such offer, solicitation or sale would be unlawful prior to the registration
or qualification under the securities laws of any such state or other jurisdiction.
About Protalix
Protalix is a biopharmaceutical company focused on the development and commercialization of
recombinant therapeutic proteins expressed through its proprietary plant cell based expression
system.
Forward Looking Statements
To the extent that statements in this press release are not strictly historical, all such
statements are forward-looking, and are made pursuant to the safe-harbor provisions of the Private
Securities Litigation Reform Act of 1995. Such statements include, but are not limited to,
statements regarding the Company’s expectations with respect to the completion, timing and size of
its proposed public offering and the use of the net proceeds therefrom. These forward-looking
statements are subject to known and unknown risks and uncertainties that may cause actual future
experience and results to differ materially from the statements made. These statements are
based on the Company’s current beliefs and expectations as to such future outcomes. Drug discovery
and development involve a high degree of risk. Factors that might cause material differences
include, among others, risks relating to: the review process of the U.S. Food and Drug
Administration, or the FDA, the European Medicines Agency, or the EMEA, other foreign regulatory
bodies and other governmental regulatory bodies, including the risk that regulatory authorities may
find that the data from our clinical trials and other studies is insufficient for regulatory
approval; the risk that the FDA may find that the information we provide in a resubmission of the
NDA for taliglucerase alfa in response to the Company’s receipt of a complete response letter from
the FDA in February 2011 is insufficient for regulatory approval; delays in the FDA’s, the EMEA’s
or other health regulatory authorities’ approval of any applications we file or refusals to approve
such filings, including the NDA and the marketing authorization applications (MAAs) we filed with
the FDA, the EMEA and other health regulatory authorities for taliglucerase alfa for the treatment
of Gaucher disease; the successful preclinical development of the Company’s product candidates; the
completion of the Company’s clinical trials; and other factors described in the Company’s filings
with the SEC. The statements in this release are valid only as of the date hereof and the Company
disclaims any obligation to update this information.
Investor Contact
Marcy Nanus
The Trout Group, LLC
Telephone: 646-378-2927
Email: mnanus@troutgroup.com
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