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Comparative, Randomized, Single-Dose, 2-way Crossover Bioavailability Study of Sandoz Inc. and UCB Pharma, Inc (Keppra) 750 mg Levetiracetam Tablets In Healthy Adults Volunteers Under Fasting Conditions
To demonstrate the relative bioavailability of Sandoz Inc. and UCB Pharma, Inc (Keppra) 750 mg Levetiracetam tablets in healthy adult volunteers under fasting conditions.
Age
18 - 55 years
Sex
ALL
Healthy Volunteers
Yes
Start Date
March 1, 2004
Primary Completion Date
March 1, 2004
Completion Date
March 1, 2004
Last Updated
March 28, 2017
20
ACTUAL participants
Levetiracetam Tablets, 750 mg (Sandoz Inc.)
DRUG
Keppra (Levetiracetam) Tablets, 750 mg (UCB Pharma, Inc)
DRUG
Lead Sponsor
Sandoz
NCT06700356
NCT05077904
Data Source & Attribution
This clinical trial information is sourced from ClinicalTrials.gov, a service of the U.S. National Institutes of Health.
Modifications: This data has been reformatted for display purposes. Eligibility criteria have been parsed into inclusion/exclusion sections. Location data has been geocoded to enable distance-based search. For the authoritative and most current information, please visit ClinicalTrials.gov.
Neither the United States Government nor Clareo Health make any warranties regarding the data. Check ClinicalTrials.gov frequently for updates.
View ClinicalTrials.gov Terms and ConditionsNCT05667142