mburse for the use of Soliris at
acceptable rates or at all, 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, 2008, and in Alexion's 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.
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(3) Levey AS, Coresh J, Balk E, et al. National Kidney Foundation
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his
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Page: 1 2 3 4 5 6 7 8 Related medicine technology :1.
Alexion Secures U.S. Patent for ALXN6000, a First-In-Class Anti-CD200 Monoclonal Antibody2.
Alexion Completes Enrollment in AEGIS Registration Study of Soliris(R) (eculizumab) in Patients with PNH in Japan3.
Alexion Commences Dosing in AEGIS Registration Study of Soliris(R) (eculizumab) in Patients with PNH in Japan4.
Rib-X Pharmaceuticals Reports Positive Top-Line Results from Phase 2 Study of Delafloxacin5.
GSK Reports PROMACTA(R) (eltrombopag) Significantly Increased Platelet Counts and Reduced Bleeding in Long-Term Study of Patients With Chronic ITP6.
Schering-Plough Reports Preladenant Meets Primary Endpoint in Phase II Dose-Finding Trial for Parkinsons Disease7.
GEN Reports on the Trend Toward Predictive Toxicogenomics8.
Vical Completes Enrollment and Reports Positive Interim Data in CMV Vaccine Phase 2 Trial9.
SCOLR Pharma, Inc. Reports Third Quarter 2008 Financial Results10.
Cadence Pharmaceuticals Reports Third Quarter 2008 Financial Results and Provides Clinical Development Programs Update11.
Bavarian Nordic Reports Successful Safety Data From Phase II Study With IMVAMUNE(R)