None listed
Conditions
Interventions
Intervention1: Test product (T): Lacosamide Sustained Release Tablets 200 mg, oral dosage form total intervention of study is 10 days
: Subjects will fast overnight from at least 10.00 hrs. before con
Sponsors
Eris Lifesciences Ltd
Eligibility
Inclusion criteria
Inclusion criteria: 1. Healthy human subjects, age in the range of 18 - 45 years both inclusive. 2. Body Mass Index between 18.5-30.0 Kg/m2 extremes included with minimum of 48 kg weight. 3. Subjects with normal findings as determined by baseline history, physical examination and vital sign examination. 4. Subjects with clinically acceptable findings as determined by haemogram, biochemistry, urinalysis, 12 lead ECG and chest X-ray (if done). 5. Willingness to follow the protocol requirements especially abstaining from xanthine containing food or beverages (chocolates, tea, coffee or cola drinks) or grapefruit juice, any alcoholic products, the use of cigarettes and the use of tobacco products for 48.00 hours prior to dosing until the last blood sample collection in each study period and adherence to all study restrictions. 6. No history of significant alcoholism. 7. No history of drug abuse (benzodiazepines and barbiturates) for the last one month and other illegal drugs for the last 06 months. 8. Non-smokers as evident from the history obtained. 9. Willing to provide written informed consent to participate in the study.
Exclusion criteria
Exclusion criteria: 1. Known history of hypersensitivity to Lacosamide or related drugs or any of the excipients. 2. Requiring medication for any ailment having enzyme-modifying activity in the previous 28 days, prior to dosing day. 3. Subjects who have taken prescription medications or over-the-counter products (including vitamins and minerals) within 14 days prior to administration of IP. 4. Any medical or surgical conditions, which might significantly interfere with the functioning of gastrointestinal tract, blood-forming organs etc. 5. History of cardiovascular, renal, hepatic, ophthalmic, pulmonary, neurological, metabolic, hematological, gastrointestinal, endocrine, immunological or psychiatric diseases. 6. Not eligible as per OVIS. 7. Volunteer who have donated blood or loss of blood up to 150 ml within 30 days or more than 150 ml to 250 ml within 60 days or more than 250 ml within 90 days (exclude blood loss for screening) prior to first dose of study medication 8. Smokers, or who have smoked within last six months prior to start of the study. 9. History of malignancy or other serious diseases. 10. Subjects with positive result of HIV tests or HBsAg or Hepatitis-C tests during screening. 11. Found positive in breath alcohol test and/or urine test for drug abuse. 12. History of problem in swallowing of tablet/capsule. 13. Any contraindication to blood sampling.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Cmax, AUC(0-t) and AUC(0-inf)Timepoint: Total number of blood samples: 25 samples per period. Sampling hrs: Pre dose [(5 mL) collected within 01.00 hour prior to dosing] and post dose of 3 mL at 01.00, 02.00, 03.00, 04.00, 04.50, 05.00, 05.50, 06.00, 06.50, 07.00, 07.50, 08.00, 09.00, 10.00, 11.00, 12.00, 13.00, 14.00, 16.00, 18.00, 20.00, 24.00, 36.00 and 48.00 hrs. Post-dose. | — |
Secondary
| Measure | Time frame |
|---|---|
| Tmax, Kel, tÃ?½ and AUCExtrapolated%Timepoint: Total number of blood samples: 25 samples per period. Sampling hrs: Pre dose [(5 mL) collected within 01.00 hour prior to dosing] and post dose of 3 mL at 01.00, 02.00, 03.00, 04.00, 04.50, 05.00, 05.50, 06.00, 06.50, 07.00, 07.50, 08.00, 09.00, 10.00, 11.00, 12.00, 13.00, 14.00, 16.00, 18.00, 20.00, 24.00, 36.00 and 48.00 hrs. Post-dose. | — |
Countries
India
Contacts
Public ContactMr Ganesh Boddu
Eris Lifesciences Limited
Outcome results
None listed