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A Phase I, Single Centre, Open, Randomised, Parallel Study to Evaluate the Pharmacokinetics and Tolerability of Multiple Doses of Eslicarbazepine Acetate and Oxcarbazepine in Healthy Subject
This purpose of this study is to measure the concentrations of two anti-epileptic drugs (Eslicarbazepine acetate and oxcarbazepine) and their metabolites in the cerebrospinal fluid and blood plasma of healthy subjects and also to assess how these drugs are tolerated.
Age
18 - 55 years
Sex
ALL
Healthy Volunteers
Yes
SGS LSS Clinical Pharmacology Unit Antwerpen
Antwerp, Belgium
Start Date
November 1, 2008
Primary Completion Date
December 1, 2008
Completion Date
February 1, 2009
Last Updated
December 19, 2014
14
ACTUAL participants
Eslicarbazepine acetate
DRUG
Oxcarbazepine
DRUG
Lead Sponsor
Bial - Portela C S.A.
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 ConditionsNCT00465517