al trials are not
predictive of safety and efficacy results of Soliris in broader patient
populations, the possibility that initial results of commercialization are
not predictive of future rates of adoption of Soliris, the risk that third
parties won't agree to license any necessary intellectual property to us on
reasonable terms or at all, the risk that third party payors will not
reimburse for the use of Soliris at acceptable rates or at all, the risk
that Soliris will not generate interest among physicians, the risk that
estimates regarding the number of PNH patients are inaccurate, the risk
that pending litigation may be resolved adversely, and a variety of other
risks set forth from time to time in Alexion's filings with the Securities
and Exchange Commission, including but not limited to the risks discussed
in Alexion's Quarterly Report on Form 10-Q for the period ended September
30, 2007 and in our other filings with the Securities and Exchange
Commission. Alexion does not intend to update any of these forward- looking
statements to reflect events or circumstances after the date hereof, except
when a duty arises under law.
----------
(1) Bessler M, Schrezenmeier H, Maciejewski JP, et al. Significant
Disease Burden in Paroxysmal Nocturnal Hemoglobinuria Patients with
Lower Levels of Hemolysis, Mild Anemia and Minimal Transfusion:
Clinical Improvement with Eculizumab Therapy. Presented during oral
sessions at the 49th Annual Meeting of the American Society of
Hematology Meeting. December 11, 2007.
(2) Rother RP, Bell L, Hillmen P, et al. The clinical sequelae of
intravascular hemolysis and extracellular plasma hemoglobin: a novel
mechanism of human disease. JAMA. 2005;293:1653-1662.
(3) Hillmen P, Lewis SM, Bessler M, Luzzatto L, Dacie JV. Natural history
of paroxysmal nocturnal hemoglobinuria. N Engl J Med 1995; 333:1253-
1258.
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SOURCE Alexion Pharmaceuticals, Inc. Copyright©2007 PR Newswire. All rights reserved | |
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