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Encorium Group, Inc. Acquires Progenitor International Research, a Vaccine Focused Emerging Market CRO
Wayne
Jul 19, 2010
The acquisition gives Encorium capabilities to run
clinical trials in South America, India and Asia Pacific
Encorium Group, Inc. (Nasdaq: ENCO), (the "Company") a full service
multinational clinical research organization (CRO) conducting studies in
over 30 countries for many of the world's leading pharmaceutical and
biotechnology companies, today announced that it has acquired
Progenitor Holdings AG, a corporation organized in Switzerland and
its wholly-owned subsidiaries organized in Mexico, Panama, Argentina,
Chile, Switzerland, India and Hong Kong for cash and stock valued at
EURO 1.7 million, plus earn-out consideration of cash and stock with a
value of up to EURO 1.5 million.
Progenitor is a European headquartered emerging market clinical
research organization providing international drug development services
in emerging market regions. Progenitor brings value and quality to its
clients' clinical trial programs by offering emerging market geography
together with experienced clinical staff in those regions.
Executive Officer, Dr. Kai Lindevall said, "We are very pleased
and proud to announce this transaction. Progenitor is a prestigious
emerging market company in the field of clinical research. The
acquisition of Progenitor will allow us to offer our clients access to
the value of conducting clinical trials in emerging markets such as
Latin America, India and Asia Pacific while providing excellent trial
management and flexible study delivery. The acquisition provides a key
advancement of our strategic goal of becoming the world's leading
vaccine clinical research organization. We believe our combined
experience in the vaccine field is the most impressive amongst medium
sized CROs and that the potential of the combined organizations is
substantial. We are also happy to broaden our executive team with two
experienced and successful entrepreneurial leaders, Dr. Renee E. Moore
and Mr. Klaus D. Albrecht, the founders of Progenitor. Renee and Klaus
will play significant roles in the combined business and are expected to
contribute significantly to the management of Encorium."
Renee E. Moore, President and CEO of Progenitor said, "The
strategic combination of the teams at Encorium and Progenitor is an
exciting step in the creation of a vaccine focused CRO that can meet
clients' needs internationally. Together the organizations have been
involved in over 70 vaccine and infectious disease trials with over
50,000 patients recruited in recent years. We believe both entities
commitment and focus on excellence in vaccine trial delivery will result
in a value added solution for our customers desiring to run trials
throughout Europe and the emerging markets.
"We are truly inspired by the momentum that exists due to the
complementary list of customers of the two organizations, which already
includes many important pharmaceutical and biotechnology companies
specializing in vaccine drug development. Furthermore, we are excited
by the opportunity to work with the exceptional leadership team at
Encorium, including Dr. Kai Lindevall and his executive team."
About Encorium Group, Inc.
Encorium Group, Inc. is a global clinical research organization
specializing in the design and management of complex clinical trials and
Patient Registries for the pharmaceutical, biotechnology and medical
device industries. The Company's mission is to provide its clients with
high quality, full-service support for their biopharmaceutical and
medical device development programs. Encorium offers therapeutic
expertise, experienced team management and advanced technologies. The
Company has drug and biologics development as well as clinical trial
experience across a wide variety of therapeutic areas such as infectious
diseases, cardiovascular, vaccines, oncology, diabetes
endocrinology/metabolism, gene therapy, immunology, neurology,
gastroenterology, dermatology, hepatology, women's health and
respiratory medicine. Encorium believes that its expertise in the design
of complex clinical trials, its therapeutic experience and commitment
to excellence, and its application of innovative technologies, offer its
clients a means to more quickly and cost effectively move products
through the clinical development process.
This press release contains forward-looking statements identified by
words such as "estimate," "project," "expect," "intend," "believe,"
"anticipate" and similar expressions. Those statements involve risks
and uncertainties, and actual results could differ materially from those
discussed. Factors that could cause or contribute to such differences
include, but are not limited to: (i) our success in attracting new
business and retaining existing clients and projects; (ii) the size,
duration and timing of clinical trials we are currently managing may
change unexpectedly; (iii) the termination, delay or cancellation of
clinical trials we are currently managing could cause revenues and
cash-on-hand to decline unexpectedly; (iv) the timing difference between
our receipt of contract milestone or scheduled payments and our
incurring costs to manage these trials; (v) outsourcing trends in the
pharmaceutical, biotechnology and medical device industries; (vi) the
ability to maintain profit margins in a competitive marketplace; (vii)
our ability to attract and retain qualified personnel; (viii) the
sensitivity of our business to general economic conditions; (ix) other
economic, competitive, governmental and technological factors affecting
our operations, markets, products, services and prices; (x) announced
awards received from existing and potential customers are not definitive
until fully negotiated contracts are executed by the parties; (xi) our
backlog may not be indicative of future results and may not generate the
revenues expected; (xii) uncertainties regarding the availability of
additional capital; (xiii) uncertainties regarding the execution of
change orders by our clients for work already performed; (xiv)
uncertainties regarding continued listing of our common stock on Nasdaq;
(xv) our ability to successfully integrate Encorium and Progenitor, and
(xvi) the risk that we may not have sufficient funds to operate our
business. You should not place undue reliance on any forward-looking
statement. We undertake no obligation to publicly release the result of
any revision of these forward-looking statements to reflect events or
circumstances after the date they are made or to reflect the occurrence
of unanticipated events. Please refer to the section entitled "Risk
Factors" in the Company Annual Report on Form 10-K for the year ended
December 31, 2009 and the Company's Quarterly Report on Form 10-Q for
the quarter ended March 31, 2010.
Source: Encorium Group, Inc.
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