Bioequivalence study Bioequivalence study Levetiracetam
Conditions
Interventions
and not chew or crush the tablet. A single dose of Levetiracetam film-
coated tablets (500 mg) will be given with 250 mL of water. Investigational product will be administered directly from the unit dose-
the subject’s oral cavity will be checked by using flashlight to confirm complete medication and fluid consumption by pharmacists.
,The marketed original products which were already available in th
the subject’s oral cavity will be checked by using flashlight to confirm complete medication and fluid consumption by pharmacists.
Experimental Drug,Active Comparator Drug
Levetiracetam film-
coated tablets (500 mg),KEPPRA® 500 MG (FILM-
Sponsors
Bio-innova and Synchron.Co.,Ltd
Eligibility
Sex/Gender
All
Age
18 Years to 55 Years
Inclusion criteria
Inclusion criteria: 1. Willingness to provide written informed consent prior to participate in the study. 2. Healthy Thai subjects are between 18 to 55 years of age. 3. The Body Mass Index (BMI) ranges from 18.5 to 30 kg/m2. 4. Comprehensive of the nature and purpose of the study and compliance with the requirement of the entire protocol and allow investigators to draw 7 mL of blood for monitoring subjects’ safety after the completion of the study. 5. Negative urine pregnancy test for women and no breast-feeding. 6. Absence of significant diseases or clinically significant abnormal laboratory values on the laboratory evaluations, medical history or surgery during the screening. Some of the laboratory values e.g. Complete blood count etc. that out of the normal range will be carefully considered by physician.
Exclusion criteria
Exclusion criteria: 1. History or evidence of allergy or hypersensitivity to Levetiracetam or Antiepileptic Drugs (AEDs) or any related drugs or any of the excipients of this product. 2. Subject with B.P. is Systolic B.P 100 beats per minute. 3. Serum bilirubin greater than 1.5 times the upper limit of reference range (ULRR).* 4. Serum creatinine greater than 1.5 times the upper limit of reference range (ULRR).* 5. Alanine amino transferase (ALT) or aspartate amino transferase (AST) greater than 2 times the upper limit of reference range (ULRR).* 6. Positive of hepatitis B or C virus. 7. Have more than one abnormal EKG, which is considered as clinically significant. * 8. History or evidence of heart, renal, hepatic disease, pulmonary obstructive disease, bronchial asthma, hypertension, glaucoma, or epilepsy. 9. History or evidence of gastrointestinal disorder likely to influence drug absorption or previous GI surgery other than appendectomy. 10. Any major illness in the past 3 months or any significant ongoing chronic medical illness. 11. History of psychiatric disorder or suicidal attempt. 12. History of regular alcohol consumption exceeding 7 drinks/week for females or 14 drinks/week for males (1 drink = 5 ounces (150 mL) of wine or 12 ounces (360 mL) of beer or 1.5 ounces (45 mL) of hard liquor) and cannot stop at least 2 days before the study drug administration and until the completion of each period of the study. 13. History of usually smoking (more than 10 cigarettes per day within past 1 year), if moderate smokers (less than 10 cigarettes per day) cannot stop at least 7 days before the study drug administration and until the completion of the study. 14. High caffeine consumption (more than 5 cups of coffee or tea per day) and cannot stop at least 2 days before the study drug administration and until the completion of each period of the study. 15. Positive drug abused test in urine (Benzodiazepines, Marijuana (THC), Methamphetamine, Cocaine and Opioids). 16. Receipt of any prescription drug therapy within 14 days or 5 half-lives (whichever longer) preceding the first dose of study medication or over-the-counter (OTC) drugs or herbal medicines/food supplement within 7 days or hormonal methods of contraception within 28 days (Depo-Provera® must be discontinued at least 6 months) prior to receiving the first dose of study medication. 17. History of difficulty in accessibility of veins in left and right arm. 18. Blood donation (one unit or 450 mL) within the past 3 months before the study. 19. Participation in any clinical study within the past 3 months before the study. 20. Subjects who are unwilling or unable to comply with the lifestyle guidelines described in this protocol. (* Depend on decision of principal investigator and/or clinical investigator)
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Cmax, AUC0→ t, AUC0→∞ 0, 0.167, 0.33, 0.5, 0.67, 0.83, 1, 1.25, 1.5, 1.75, 2, 2.5, 3, 4, 6, 8, 10, 12, 24, 36, 48 hr. Pharmacokinetic parameters | — |
Secondary
| Measure | Time frame |
|---|---|
| Safety; Adverse events 0, 1.0, 2.0, 4.0, 12.0, 24.0, 36.0 and 48.0 hr. Safety monitoring, vital sign,Safety; assess the suicidal thought at check-in, 1.0, 12.0, 24.0, 36.0 and 48.0 hours questions to assess the suicidal thought | — |
Countries
Thailand
Contacts
Public ContactSasitorn Kittivoravitkul
Bio-innova and Synchron.Co.,Ltd
Outcome results
None listed