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Human Pharmacology Study (Keppra Dry Syrup Bioequivalence Study)

2014-08-27 03:19:03 | BioPortfolio

Summary

To demonstrate the bioequivalence of a Levetiracetam dry syrup (50% (500mg/1000mg)versus Levetiracetam 500 mg oral tablet, used as reference, after single dose administration in healthy Japanese subjects.

Study Design

Allocation: Randomized, Endpoint Classification: Bio-equivalence Study, Intervention Model: Crossover Assignment, Masking: Open Label

Conditions

Healthy

Intervention

Levetiracetam (Keppra)

Location

London
United Kingdom

Status

Completed

Source

UCB, Inc.

Results (where available)

View Results

Links

Published on BioPortfolio: 2014-08-27T03:19:03-0400

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