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Clinical Trial Summary

To demonstrate the relative bioavailability of Sandoz Inc. and UCB Pharma, Inc (Keppra) 750 mg Levetiracetam tablets in healthy adult volunteers under fasting conditions.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT00946751
Study type Interventional
Source Sandoz
Contact
Status Completed
Phase Phase 1
Start date March 2004
Completion date March 2004

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