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Eisai Resubmits Supplemental New Drug Application for Aricept, Alzheimers Disease Drug, to FDA.


Tokyo, Japan, Dec 21, 2005 - (JCN JCN Japan Corporate News
JCN Journal of Cognitive Neuroscience
JCN Journal of Cardiovascular Nursing
JCN Journal of Christian Nursing
JCN Job Control Number
JCN Journal of Child Neurology
JCN joint communications network (US DoD) 
) - Eisai has announced that its US subsidiary Eisai Medical Research resubmitted a supplemental new drug application (sNDA) for Aricept, the company's proprietary agent for treating severe Alzheimer's disease Alzheimer's disease (ăls`hī'mərz, ôls–), degenerative disease of nerve cells in the cerebral cortex that leads to atrophy of the brain and senile dementia. , to the US Food and Drug Administration (FDA FDA
abbr.
Food and Drug Administration


FDA,
n.pr See Food and Drug Administration.

FDA,
n.pr the abbreviation for the Food and Drug Administration.
) as of December 16.

The US subsidiary first submitted the sNDA on August 31, but the FDA turned down the application on the grounds that the application did not conform to Verb 1. conform to - satisfy a condition or restriction; "Does this paper meet the requirements for the degree?"
fit, meet

coordinate - be co-ordinated; "These activities coordinate well"
 the FDA standard. The resubmitted sNDA is expected to be accepted by the FDA within 60 days.

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No portion of this article can be reproduced without the express written permission from the copyright holder.
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Publication:JCNN News Summaries
Date:Dec 24, 2005
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