drugset / Trial / NCT00849485

Levetiracetam 750 mg Tablets Under Non-Fasting Conditions

NCT00849485

Phase 1 Completed 22 enrolled Teva Pharmaceuticals USA
RandomizedCrossoverOpen-label

Summary

The objective of this study is to compare the rate and extent of absorption of a test formulation of Levetiracetam tablets versus the reference Keppra® administered as a 1 x 750 mg tablet under fed conditions.

Timeline

Start
2005-11
Primary completion
2005-11
Completion
2005-11

Drugs

EvaluationDrugModalityDoseRoute
Subject Levetiracetam Other / unclassified 750 mg

Indications

No indication recorded.