To Evaluate the Pharmacokinetics and Safety/Tolerability of Lacosamide in 3 Dosages in Healthy Male Korean Subjects

NCT ID: NCT01450111

Last Updated: 2011-10-14

Basic Information

• Recruitment Status: COMPLETED
• Clinical Phase: PHASE1
• Total Enrollment: 51 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2008-11-30
• Study Completion Date: 2009-02-28

Brief Summary

Primary objective of this trial was to investigate the pharmacokinetics of single dose and repeated dose applications of lacosamide in healthy male Korean subjects.

Conditions

Epilepsy

Study Design

• Allocation Method: RANDOMIZED
• Intervention Model: PARALLEL
• Blinding Strategy: DOUBLE

Study Groups

Lacosamide 50 mg group

Lacosamide 50 mg tablet, once a day per os (po)

Group Type: EXPERIMENTAL

Lacosamide

Intervention Type: DRUG

Lacosamide 50 mg, tablet, once in the morning on Day 1

Placebo group matched with lacosamide 50 mg

Placebo matched with lacosamide 50 mg tablet, po

Group Type: PLACEBO_COMPARATOR

Placebo

Intervention Type: OTHER

Placebo matched with Lacosamide 50 mg tablet once in the morning on day 1.

Lacosamide 100 mg group

Lacosamide 100 mg tablet, po

Group Type: EXPERIMENTAL

Lacosamide

Intervention Type: DRUG

Lacosamide 100 mg, tablet, once in the morning on Day 1 Lacosamide 100 mg, tablet, twice daily Day 5 to Day 8 and once in the morning on Day 9

Placebo group matched with lacosamide 100 mg

Placebo matched with lacosamide 100 mg tablet, po

Group Type: PLACEBO_COMPARATOR

Placebo

Intervention Type: OTHER

Placebo matched with Lacosamide 100 mg, tablet, once in the morning on Day 1 Placebo matched with Lacosamode 100 mg, tablet, twice daily Day 5 to Day 8 and once in the morning on Day 9

Lacosamide 200 mg group

Lacosamide 200 mg tablet, po

Group Type: EXPERIMENTAL

Lacosamide

Intervention Type: DRUG

Lacosamide 200 mg, tablet, once in the morning on Day 1 Lacosamide 200 mg, tablet, twice daily Day 5 to Day 8 and once in the morning on Day 9

Placebo group matched with lacosamide 200 mg

Placebo matched with lacosamide 200 mg tablet, po

Group Type: PLACEBO_COMPARATOR

Placebo

Intervention Type: OTHER

Placebo matched with Lacosamide 200 mg, tablet, once in the morning on Day 1 Placebo matched with Lacosamide 200 mg, tablet, twice daily Day 5 to Day 8 and once in the morning on Day 9

Interventions

Lacosamide

Lacosamide 50 mg, tablet, once in the morning on Day 1

Intervention Type: DRUG

Lacosamide

Lacosamide 100 mg, tablet, once in the morning on Day 1 Lacosamide 100 mg, tablet, twice daily Day 5 to Day 8 and once in the morning on Day 9

Intervention Type: DRUG

Lacosamide

Lacosamide 200 mg, tablet, once in the morning on Day 1 Lacosamide 200 mg, tablet, twice daily Day 5 to Day 8 and once in the morning on Day 9

Intervention Type: DRUG

Placebo

Placebo matched with Lacosamide 50 mg tablet once in the morning on day 1.

Intervention Type: OTHER

Placebo

Placebo matched with Lacosamide 100 mg, tablet, once in the morning on Day 1 Placebo matched with Lacosamode 100 mg, tablet, twice daily Day 5 to Day 8 and once in the morning on Day 9

Intervention Type: OTHER

Placebo

Placebo matched with Lacosamide 200 mg, tablet, once in the morning on Day 1 Placebo matched with Lacosamide 200 mg, tablet, twice daily Day 5 to Day 8 and once in the morning on Day 9

Intervention Type: OTHER

Other Intervention Names

Vimpat®; Vimpat®; Vimpat®

Eligibility Criteria

Inclusion Criteria

• Subject is healthy male and between 20 and 45 years of age (inclusive)
• Subject has no clinically relevant cardiovascular, renal, gastrointestinal, hepatic, metabolic, endocrine, neurological, or psychiatric abnormalities and is in general good health
• Subject is of normal body weight as determined by a body mass index (BMI) between 19 and 28 kgm^2
• Subject is Korean (both parents are of pure Korean ethnicity)

Exclusion Criteria

• Subject has a history of or present psychiatric or neurological condition that, in the opinion of the Investigator, could jeopardize or would have compromised the subject's ability to participate in this trial
• Subject has a known or suspected drug hypersensitivity, in particular to the trial medication
• Subject consumes more than 40 g alcohol/day (amount corresponds to 1 L beer/day or 0.5 L wine/day or 6 glasses (à 2cL) liquor/day)
• Subject has donated blood or had a comparable blood loss (>400 mL) within the last 3 months prior to Eligibility Assessment (EA)
• Subject smokes more than 5 cigarettes per day or had done so within 6 months prior to EA.
• Subject consumes more than 600 mg caffeine/day (200 mL coffee contain approximately 100 mg caffeine, 200 mL black tea approximately 30 mg, and 200 mL cola approximately 20 mg)
• Subject has a diet which deviates notably from the "normal" amounts of protein, carbohydrate, and fat, as judged by the Investigator (eg, vegetarians or vegans)
• Subject has taken herbal medicine therapy within 2 weeks prior to the first dosing
• Subject has a clinically relevant allergy
• Subject is taking any concomitant medication currently or within 2 weeks prior to the first dosing (with the exception of acetaminophen which is allowed to be taken orally up to 1000 mg per dose up to 48 hours prior to commencement of dosing)
• Subject has positive tests for alcohol and/or drugs (urine test) at EA and at confinement
• Subject has a high risk behavior for the HIV
• Subject is tested to be positive for HIV antibodies (HIV Ab), hepatitis B surface antigen (HBs Ag), or hepatitis C virus antibody (HCV Ab)
• Subject has a history or present condition of hepatic disorders, eg, clinically relevant liver enzyme increase (alanine aminotransferase [ALT], aspartate aminotransferase [AST], alkaline phosphatase [AP], and gamma-glutamyl transpeptidase [GGT])
• Subject has a transaminase (either ALT or AST) more than 2 times of the upper limit of normal range (ULN) at confinement
• Subject has clinically relevant out-of-range values for hematology including coagulation parameters, and clinical chemistry, serology or urinalysis parameters
• Subject has any clinically relevant abnormality in the physical examination or vital signs
• Subject has a pulse rate at rest less than 45 bpm or more than 100 bpm at EA
• Subject has a systolic blood pressure lower than 100 mmHg or higher than 160 mmHg or a diastolic blood pressure higher than 95 mmHg at EA
• Subject has clinically relevant findings in the ECG, such as second or third degree atrioventricular (AV) block or PR interval >220 ms, prolongation of the QRS duration to >110 ms, or a QTcB (Bazett corrected) interval over 450 ms or any other clinically relevant ECG finding at EA
• Subject performed heavy physical exertion 2 days before EA or before confinement
• Subject has a history or present condition of respiratory or cardiovascular disorders, eg, cardiac insufficiency, coronary heart disease, hypertension, arrhythmia, tachyarrhythmia, or status after myocardial infarction
• Subject has a history or present condition of malignancy
• Subject has a history or present condition of seizure disorder
• Subject has atrial fibrillation/flutter, ventricular tachyarrhythmia (eg, ventricular tachycardia, ventricular fibrillation, aborted cardiac arrest), symptomatic heart block at Eligibility Assessment Visit, or is diagnosed with Brugada syndrome (also known as Sudden Unexpected Death Syndrome)

• Minimum Eligible Age: 20 Years
• Maximum Eligible Age: 45 Years
• Eligible Sex: MALE
• Accepts Healthy Volunteers: Yes

Sponsors

UCB Pharma

INDUSTRY

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Principal Investigators

UCB Clinical Trial Call Center

Role: STUDY_DIRECTOR

+1 877 822 9493 (UCB)

Other Identifiers

SP0952

Identifier Type: -

Identifier Source: org_study_id