Amgen Board Authorizes $5 Billion Increase in Stock Repurchase Program
08 December 2009 - 1:01AM
PR Newswire (US)
THOUSAND OAKS, Calif., Dec. 7 /PRNewswire-FirstCall/ -- Amgen
(NASDAQ: AMGN) today announced that its board of directors has
authorized repurchases of up to an additional $5 billion in Amgen
common stock. The company currently has approximately $1.2 billion
remaining under its previous stock repurchase authorization. This
new authorization reflects Amgen's confidence in its long-term
prospects. About Amgen Amgen discovers, develops, manufactures, and
delivers innovative human therapeutics. A biotechnology pioneer
since 1980, Amgen was one of the first companies to realize the new
science's promise by bringing safe, effective medicines from lab,
to manufacturing plant, to patient. Amgen therapeutics have changed
the practice of medicine, helping millions of people around the
world in the fight against cancer, kidney disease, rheumatoid
arthritis, and other serious illnesses. With a deep and broad
pipeline of potential new medicines, Amgen remains committed to
advancing science to dramatically improve people's lives. To learn
more about our pioneering science and our vital medicines, visit
http://www.amgen.com/. Forward-Looking Statements This news release
contains forward-looking statements that involve significant risks
and uncertainties, including those discussed below and others that
can be found in our Form 10-K for the year ended Dec. 31, 2008, and
in our periodic reports on Form 10-Q and Form 8-K. Amgen is
providing this information as of the date of this news release and
does not undertake any obligation to update any forward-looking
statements contained in this document as a result of new
information, future events or otherwise. No forward-looking
statement can be guaranteed and actual results may differ
materially from those we project. The Company's results may be
affected by our ability to successfully market both new and
existing products domestically and internationally, clinical and
regulatory developments (domestic or foreign) involving current and
future products, sales growth of recently launched products,
competition from other products (domestic or foreign), difficulties
or delays in manufacturing our products. In addition, sales of our
products are affected by reimbursement policies imposed by
third-party payors, including governments, private insurance plans
and managed care providers and may be affected by regulatory,
clinical and guideline developments and domestic and international
trends toward managed care and health care cost containment as well
as U.S. legislation affecting pharmaceutical pricing and
reimbursement. Government and others' regulations and reimbursement
policies may affect the development, usage and pricing of our
products. Furthermore, our research, testing, pricing, marketing
and other operations are subject to extensive regulation by
domestic and foreign government regulatory authorities. We or
others could identify safety, side effects or manufacturing
problems with our products after they are on the market. Our
business may be impacted by government investigations, litigation
and products liability claims. Further, while we routinely obtain
patents for our products and technology, the protection offered by
our patents and patent applications may be challenged, invalidated
or circumvented by our competitors. We depend on third parties for
a significant portion of our manufacturing capacity for the supply
of certain of our current and future products and limits on supply
may constrain sales of certain of our current products and product
candidate development. In addition, we compete with other companies
with respect to some of our marketed products as well as for the
discovery and development of new products. Discovery or
identification of new product candidates cannot be guaranteed and
movement from concept to product is uncertain; consequently, there
can be no guarantee that any particular product candidate will be
successful and become a commercial product. Further, some raw
materials, medical devices and component parts for our products are
supplied by sole third-party suppliers. CONTACT: Amgen, Thousand
Oaks David Polk, 805-447-4613 (media) Arvind Sood, 805-447-1060
(investors) (Logo:
http://www.newscom.com/cgi-bin/prnh/20081015/AMGENLOGO)
http://www.newscom.com/cgi-bin/prnh/20081015/AMGENLOGO
http://photoarchive.ap.org/ DATASOURCE: Amgen CONTACT: media, David
Polk, +1-805-447-4613, or investors, Arvind Sood, 805-447-1060,
both of Amgen Web Site: http://www.amgen.com/
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