Eisai Co., Ltd. Annual Report 2001 - Eisai GmbH
Eisai Co., Ltd. Annual Report 2001 - Eisai GmbH
Eisai Co., Ltd. Annual Report 2001 - Eisai GmbH
Create successful ePaper yourself
Turn your PDF publications into a flip-book with our unique Google optimized e-Paper software.
2<br />
TO OUR SHAREHOLDERS<br />
In fiscal 2000, which ended March 31, <strong>2001</strong>, <strong>Eisai</strong> achieved record<br />
consolidated results, due to the continued sales growth in global<br />
markets of the Alzheimer’s disease treatment Aricept, and the proton<br />
pump inhibitor Aciphex/Pariet. This achievement reflects the ongoing<br />
support of shareholders and other stakeholders in the <strong>Co</strong>mpany. On<br />
behalf of everyone at <strong>Eisai</strong>, we would like to express our sincerest<br />
appreciation.<br />
<strong>Eisai</strong> sees our ultimate goal as satisfying customers—the patients<br />
using our products—and our fundamental mission as determining<br />
effective ways and allocating management resources effectively to<br />
achieve this goal. Accordingly, we focus on developing pharmaceuticals<br />
that satisfy unmet medical needs and enhance the quality of life<br />
of patients worldwide. We also observe the highest standards of<br />
quality and aim to provide information in easily accessible formats.<br />
With Aricept, we have established a safe and effective course of<br />
treatment for Alzheimer’s disease. Aricept has received approval in<br />
78 countries and is playing a crucial role in efforts to treat patients<br />
with mild to moderate Alzheimer's disease. We are also developing an<br />
agent for treating sepsis, E5564, which is produced using proprietary<br />
synthesis technologies. In the area of cancer research, we are pursuing<br />
the development of substances with various mechanisms—such as<br />
E7070 that affects the cell cycle at the G1 stage, tubulin antagonists<br />
and antiangiogenics, which inhibit blood vessel formation—that offer<br />
new hope for treating this disease. In the field of neurology, which we<br />
have positioned as our most important strategic therapeutic area, we<br />
are working toward the development of effective treatments for<br />
neurogenerative disorders including multiple sclerosis and other<br />
illnesses. Substances currently in development include the serotonin<br />
receptor antagonist E2101, and the amino-3-hydroxy-5-methyl-4isoxazolepropionate<br />
(AMPA) type glutamate receptor antagonist<br />
E2007, for which we have received a concept patent for the inhibition<br />
of neural dysfunction associated with multiple selerosis. Our research<br />
in the neurology area also includes the development of additional<br />
indications for Aricept.<br />
<strong>Eisai</strong> <strong>Annual</strong> <strong>Report</strong> <strong>2001</strong>