Drug: Keppra (Levetiracetam - USB SA Pharma Sector)
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Full eligibility criteria for NCT00926302
Ages eligible for Study
20 Years to 40 Years
Genders eligible for Study
Accepts Healthy Volunteers
Provision of signed written informed consent before enrollment into the study, ability to communicate with the investigators, and to understand and comply with the requirements of the study.
Healthy adult male, aged between 20 and 40 years old.
Body Mass Index between 18.5 and 25 (inclusive).
Physically and mentally healthy subjects as confirmed by an interview, medical history, clinical examination, chest x-ray and electrocardiogram.
No significant deviation from normal biochemistry examination.
No significant deviation from normal hematology examination.
No significant deviation from normal urinalysis examination.
History of drug or alcohol abuse within the past year.
Medical history of severe drug allergy or sensitivity to analogous drug.
Evidence of acute or chronic disease or having undergone surgery from 4 weeks prior to Period I dosing.
Evidence of any clinical significant renal, cardiovascular, hepatic, hematopoietic, neurological, pulmonary or gastrointestinal pathology.
Ongoing peptic ulcer and constipation.
Planned vaccination during the time course of the study.
Taking any clinical investigation drug from 2 months prior to Period I dosing.
Use of any medication, including herb medicine or vitamins from 4 weeks before the study.
Blood donation of more than 500 mL within the past 3 months.
A positive Hepatitis B surface antigen or positive Hepatitis C antibody result.
A positive test for HIV antibody.
All locations for NCT00926302
View full eligibility
Tris trial is registered with FDA with number: NCT00926302. The sponsor of the trial is Tri-Service General Hospital and it is looking for 26 volunteers for the current phase.
Official trial title: A Randomized, Single, Two-Way Crossover Pivotal Study to Assess the Bioequivalence Study of Levetiracetam vs. Keppra Administered Under Fasting Conditions to Healthy Adult Subject
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