Fed Bioequivalence Study of CBZ Formulations

Inclusion criteria

• Non-smoking or smokers of less than 5 cigarettes/day, within the age range of 18 to 50 years.
• Body Mass Index (BMI = weight/height2) greater than or equal to 18.5 kg/m2 and less than or equal to 24.9 kg/m2.
• No clinically significant findings in the physical examination, 12-lead electrocardiogram (ECG) and vital signs (blood pressure between 100-140/58-90 mmHg, heart rate between 50-99 beats/min, temperature between 35.8ºC and 37.6ºC, respiration rate between 12 and 20 breaths/minute)
• No clinical laboratory values outside of the acceptable range as per protocol, unless the Principal Investigator or Sub-investigator decides that they are not clinically significant (NCS).
• Availability of the subject for the entire study period and willingness of the subject to adhere to protocol requirements.
• The subject agrees to abstain from alcohol, coffee and other food and drinks containing methylxanthines (mate, tea, cola, chocolate) for 48hours, and grapefruit containing food and beverages for 72 hours prior study drug administration and during each study period.

Exclusion criteria

• Known history of hypersensitivity to Carbamazepine and/or related drugs.
• Positive test for hepatitis B surface antigen, hepatitis C or HIV.
• Known history of gastrointestinal (e.g: gastritis, inflammatory bowel disease, celiac disease), cardiac, pulmonary, endocrine, musculoskeletal, neurological, hematological, immunological, hepatic or renal disease, or malignancies, unless deemed NCS by the Principal Investigator or Sub-investigator.
• Any history of peptic ulcer disease or gastrointestinal (GI) bleeding.
• Any history of gastrointestinal surgery (except for appendectomy).
• Presence of any significant physical or organ abnormality.
• Any illness during the 4 weeks before this study, unless deemed NCS by the Clinical Investigator or Sub-investigator.
• Any history or evidence of psychiatric or psychological disease, unless deemed NCS by the Clinical Investigator or Sub-investigator.
• Any history of asthma (after 12 years of age).
• Any history of severe allergic reaction (including drugs, food, insect bites, environmental allergens).
• Known history or presence of food allergies, or any condition known to interfere with the absorption, distribution, metabolism or excretion of drugs.
• Any history of drug and psychoactive medicines abuse.
• Any recent history of alcohol abuse (less than 1 year).
• Use of any prescription medication within 14 days preceding this study.
• Use of vaccinations within 30 days preceding this study.
• Use of over-the-counter (OTC) medication within the 7 days preceding this study (except for spermicidal/barrier contraceptive products, sunscreen and sunblock products).
• Participation as a plasma donor in a plasmapheresis program within 7 days preceding this study.
• Blood donations within 60 days preceding and after this study.
• Participation in a clinical trial with an investigational drug within 180 days preceding this study, and agreement not to participate in a clinical trial for 180 days after this study.
• Intolerance to venipuncture.