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Clinical Trial Summary

This surveillance's objectives are 1. Unknown adverse reactions 2. Incidences of adverse drug reaction 3. Efficacy during long-term administration 4. Factors considered to have effect to safety and effectiveness 5. Incidences of status epileptics, skin disorders and hyper sensitivity reaction, and central nervous system-related adverse events(ataxia , somnolence and/or dizzy, etc.)


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT02175173
Study type Observational
Source Eisai Inc.
Contact
Status Completed
Phase
Start date June 13, 2013
Completion date November 2, 2022

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