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Eisai Co. is currently focusing on three clinical development programs related to its mainstay product Aricept® (donepezil hydrochloride) to further contribute to patients with Alzheimer’s disease
Tokyo, Japan | July 2, 2009 | Eisai Co., Ltd. (Headquarters: Tokyo, President & CEO: Haruo Naito, “Eisai”) is currently focusing on three clinical development programs related to its mainstay product Aricept® (donepezil hydrochloride) to further contribute to patients with Alzheimer’s disease. As progress in these programs has been made, Eisai announces the current status of each one as follows:
1. Sustained Release Tablets
Eisai has completed a phase III study of 23mg donepezil sustained release (SR) in patients with moderate to severe Alzheimer’s disease. Donepezil SR is being developed to increase clinical benefits compared with currently marketed 10mg donepezil immediate release, raising the blood level of donepezil while maintaining favourable safety profile.
Based on the preliminary review of the data from this phase III study, Eisai plans to submit a New Drug Application (NDA) with the U.S. Food and Drug Administration (FDA) in August or September of this year.
2. Pediatric Use
Eisai filed a Proposed Pediatric Study Request (PPSR), an application that proposes a rationale and study design for pediatric studies, with the U.S. FDA in February of this year to evaluate the clinical benefits of donepezil in children with attention impairment following cancer treatment. Eisai received a notice from the U.S. FDA that there were insufficient grounds to issue a Written Request to obtain pediatric exclusivity. Eisai plans to complete the ongoing studies to provide important information on this therapeutic approach for an underserved patient population currently with limited treatment options.
3. Transdermal Patch Formulation
Clinical trials of a once-a-week transdermal patch formulation of donepezil, which include a bioequivalence study compared to the currently marketed formulation of donepezil, are currently being conducted by Teikoku Pharma USA, Inc. in the United States. An NDA submission to the U.S. FDA is planned for the middle of fiscal year 2009 with the results of the clinical trials. Eisai is working on this new formulation of donepezil based on agreements with Teikoku Seiyaku Co., Ltd. and its U.S. subsidiary, Teikoku Pharma USA, Inc.
SOURCE: Eisai Co., Ltd. |
