| E.1 Medical condition or disease under investigation |
| E.1.1 | Medical condition(s) being investigated |
| Epilepsy, partial onset or generalised tonic-clonic seizures. |
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| MedDRA Classification |
| E.1.2 Medical condition or disease under investigation |
| E.1.2 | Version | 12.1 |
| E.1.2 | Level | LLT |
| E.1.2 | Classification code | 10015037 |
| E.1.2 | Term | Epilepsy |
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| E.1.3 | Condition being studied is a rare disease | No |
| E.2 Objective of the trial |
| E.2.1 | Main objective of the trial |
| The objective of this study is to compare the efficacy and safety of Lacosamide (LCM) (200 to 600mg/day) to Carbamazepine Controlled release CBZ CR (400 to 1200mg/day) used as monotherapy for at least 1 year, efficacy being measured as a primary endpoint by 6 month seizure freedom, in newly or recently diagnosed epilepsy subjects. The study will employ a noninferiority design to show at least a similar benefit risk balance for LCM compared with CBZ CR, using 6-month seizure freedom as primary endpoint. |
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| E.2.2 | Secondary objectives of the trial |
| See protocol sections 4.1.2 and 4.2.2 |
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| E.2.3 | Trial contains a sub-study | No |
| E.3 | Principal inclusion criteria |
Subjects must fulfill the following inclusion criteria to be eligible to participate in this study:
1. An Institutional Review Board (IRB)/Independent Ethics Committee (IEC) approved written Informed Consent form is signed and dated by the subject or by the parent(s) or legal representative. The Consent form or a specific Assent form, where required, will be signed and dated by minors.
2. Subject is willing and able to comply with all study requirements.
3. Subject is male or female and ≥16 years of age. Minors will be included in some countries only if legally permitted.
4. Subject has newly or recently diagnosed epilepsy having experienced unprovoked POS (IA, IB, IC with clear focal origin) or generalized tonic-clonic seizures (without clear focal origin) that are classifiable according to the ILAE Classification of Epileptic Seizures, 1981. The discrimination between IC and IIE is not requested for inclusion.
5. Subject has experienced at least 2 unprovoked seizures (separated by a minimum of 48 hours) in the year preceding randomization out of which at least 1 unprovoked seizure occurred in the 3 months preceding randomization.
6. Subject has had an electroencephalogram (EEG) (that is normal or consistent with the diagnosis of partial-onset epilepsy) and a brain computed tomography (CT) scan or magnetic resonance imaging (MRI) exam of the brain consistent with the diagnosis of partial onset or generalized tonic-clonic seizures (without clear focal origin) within the past year. If the EEG and brain CT scan or MRI exam were not performed prior to Visit 1, they need to be completed and results must be available prior to randomization at Visit 2.
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| E.4 | Principal exclusion criteria |
Subjects are not permitted to enroll in the study if any of the following criteria are met:
1. Subject has previously participated in this study or subject has previously been assigned to treatment in a study of the drugs under investigation in this study.
2. Subject is currently participating or has participated within the last 2 months in any study of an investigational drug or experimental device.
3. Subject has a history or presence of seizures of other types than partial-onset (IA, IB, IC with clear focal origin) and generalized tonic-clonic (without clear focal origin) seizures (eg, myoclonic, absence).
4. Subject has a history or presence of seizures occurring only in clustered patterns, defined as repeated seizures occurring over a short period of time (ie, <20 minutes) with or without function regained between 2 ictal events.
5. Subject has a history, clinical, or EEG finding suggestive of idiopathic generalized epilepsy (IGE) at randomization (according to the ILAE Classification of Epileptic Seizures, 1989).
6. Subject has current or previous diagnosis of pseudoseizures, conversion disorders, or other nonepileptic ictal events which could be confused with seizures.
7. Subject has any medical or psychiatric condition, which in the opinion of the investigator, could jeopardize the subject’s health or would compromise the subject’s ability to participate in this study.
8. Subject has a history of suicide attempt, has received professional counseling for suicidal ideation, or is currently experiencing active suicidal ideation.
9. Subject has a known hypersensitivity to any components of the investigational product(s).
10. Subject has ever been treated (for any indication) with LCM or CBZ in the past.
11. Subject has been treated for epilepsy with any AED (including benzodiazepines) in the last 6 months before Visit 1.
• However, acute and subacute seizure treatment is accepted with a maximum of 2 weeks duration and if treatment was stopped at least 1 week before Visit 1.
• Prior use of felbamate or vigabatrin is not allowed.
• Benzodiazepines as rescue therapy for epilepsy may have been used as needed in this time period, but not more frequently than once per week.
12. Subject has received treatment with phenobarbital or primidone within 28 days prior to Visit 1.
13. Subject is taking benzodiazepines for a nonepilepsy indication.
14. The use of monoamine oxidase inhibitors (MAOIs) is not allowed within 14 days of Visit 1.
15. Subject has experienced seizure(s) while treated with any AED for an indication other than epilepsy.
16. Subject is taking any drug or product (eg, grapefruit) that may influence CBZ metabolism.
17. Subject has a known history of severe anaphylactic reaction, serious blood dyscrasias, or hepatic porphyrias.
18. Subject has an acute or sub-acutely progressive central nervous system disease.
19. Subject has alanine aminotransferase (ALT), aspartate aminotransferase (AST), or total bilirubin levels ≥2× the upper limit of normal (ULN) or has alkaline phosphatase levels ≥3× the ULN.
20. Subject has a medical condition that could reasonably be expected to interfere with drug absorption, distribution, metabolism, or excretion.
21. Subject has a history of alcohol or drug abuse within the previous 2 years.
22. Subject is of Asian ancestry and tests positive for HLA-B*1502 allele.
23. Subject has impaired renal function, ie, creatinine clearance (CLcr) is lower than 30mL/min at Visit 1. Creatinine clearance will be estimated as follows:
Adult males: CLcr=(140-age)×weight in kg/(72×serum creatinine in mg/dL)
Adult females: CLcr=[(140-age)×weight in kg/(72×serum creatinine in mg/dL)]×0.85
24. Subject has sick sinus syndrome without a pacemaker, or second- or third-degree atrioventricular (AV) block, or subject has any other clinically significant ECG abnormalities.
25. Subject has experienced a myocardial infarction in the last 3 months.
26. Subject has New York Heart Association Class III or Class IV heart failure.
27. Female subject who is pregnant or nursing and/or a woman of childbearing potential who is not surgically sterile, not at least 2 years postmenopausal, or does not practice 2 combined methods of contraception (unless sexually abstinent) for the duration of the study. If oral contraceptives are used, the ethinylestradiol dosage should be at least 50µg per intake.
28. Subject has a history of status epilepticus.
29. Subject has a known sodium channelopathy, such as Brugada syndrome.
30. Male subject who does not agree to practice 2 combined methods of contraception (eg, condom, spermicide), unless sexually abstinent, for the duration of the study.
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| E.5 End points |
| E.5.1 | Primary end point(s) |
1. Primary efficacy variable
The primary efficacy variable is as follows:
•Proportion of subjects remaining seizure free for 6 consecutive months (26 consecutive weeks) of treatment following stabilization at the last evaluated dose for each subject
2.The primary safety variables are as follows:
• AEs reported spontaneously by the subject and/or caregiver or observed by the investigator
• Subject withdrawals due to AEs
• Serious AEs (SAEs)
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| E.6 and E.7 Scope of the trial |
| E.6 | Scope of the trial |
| E.6.1 | Diagnosis | No |
| E.6.2 | Prophylaxis | No |
| E.6.3 | Therapy | Yes |
| E.6.4 | Safety | Yes |
| E.6.5 | Efficacy | Yes |
| E.6.6 | Pharmacokinetic | Yes |
| E.6.7 | Pharmacodynamic | Yes |
| E.6.8 | Bioequivalence | No |
| E.6.9 | Dose response | No |
| E.6.10 | Pharmacogenetic | No |
| E.6.11 | Pharmacogenomic | No |
| E.6.12 | Pharmacoeconomic | Yes |
| E.6.13 | Others | No |
| E.7 | Trial type and phase |
| E.7.1 | Human pharmacology (Phase I) | No |
| E.7.1.1 | First administration to humans | No |
| E.7.1.2 | Bioequivalence study | No |
| E.7.1.3 | Other | No |
| E.7.1.3.1 | Other trial type description | |
| E.7.2 | Therapeutic exploratory (Phase II) | No |
| E.7.3 | Therapeutic confirmatory (Phase III) | Yes |
| E.7.4 | Therapeutic use (Phase IV) | No |
| E.8 Design of the trial |
| E.8.1 | Controlled | Yes |
| E.8.1.1 | Randomised | Yes |
| E.8.1.2 | Open | No |
| E.8.1.3 | Single blind | No |
| E.8.1.4 | Double blind | Yes |
| E.8.1.5 | Parallel group | Yes |
| E.8.1.6 | Cross over | No |
| E.8.1.7 | Other | Yes |
| E.8.1.7.1 | Other trial design description |
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| E.8.2 | Comparator of controlled trial |
| E.8.2.1 | Other medicinal product(s) | Yes |
| E.8.2.2 | Placebo | No |
| E.8.2.3 | Other | No |
| E.8.3 |
The trial involves single site in the Member State concerned
| No |
| E.8.4 | The trial involves multiple sites in the Member State concerned | Yes |
| E.8.4.1 | Number of sites anticipated in Member State concerned | 6 |
| E.8.5 | The trial involves multiple Member States | Yes |
| E.8.5.1 | Number of sites anticipated in the EEA | 100 |
| E.8.6 Trial involving sites outside the EEA |
| E.8.6.1 | Trial being conducted both within and outside the EEA | Yes |
| E.8.6.2 | Trial being conducted completely outside of the EEA | Information not present in EudraCT |
| E.8.6.3 | If E.8.6.1 or E.8.6.2 are Yes, specify the regions in which trial sites are planned |
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| E.8.7 | Trial has a data monitoring committee | No |
| E.8.8 |
Definition of the end of the trial and justification where it is not the last
visit of the last subject undergoing the trial
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| The end of the study is defined as the date of the last visit of the last subject in the study. |
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| E.8.9 Initial estimate of the duration of the trial |
| E.8.9.1 | In the Member State concerned years | 3 |
| E.8.9.1 | In the Member State concerned months | 3 |
| E.8.9.1 | In the Member State concerned days | 0 |
| E.8.9.2 | In all countries concerned by the trial years | 3 |
| E.8.9.2 | In all countries concerned by the trial months | 3 |
| E.8.9.2 | In all countries concerned by the trial days | 0 |
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