| Eligibility |
Inclusion Criteria:
- All Subjects
1. Able to understand and willing to sign the ICF and able to comply with the study
restrictions
2. Adult male or female subjects age 18 to 75 years, inclusive, at the time of
informed consent
3. BMI 18.0 - 35.0 kg/m2, inclusive, where BMI (kg/m2) = body weight (kg) / height2
(m2) at Screening
4. Female subjects of childbearing potential willing to use an acceptable form of
birth control, as outlined in Section 12.1.9
5. Male subjects with female partners of childbearing potential may be enrolled if
they, use an acceptable form of birth control, as outlined in Section 12.1.9
Hepatically-impaired Subjects (in addition)
1. Diagnosis of cirrhosis due to parenchymal liver disease, which is confirmed and
documented by at least one of the following: medical history, physical examination,
hepatic ultrasound, computed tomography (CT) scan, magnetic resonance imaging (MRI),
and/or liver biopsy
2. Stable hepatic impairment (Child-Pugh score consistent with severe hepatic
impairment), defined as no clinically significant change in disease status, as judged
by the Investigator
Healthy Subjects (in addition)
1. Subjects with normal hepatic function as judged by the Investigator
2. Judged to be in good health in the opinion of the Investigator on the basis of a
medical evaluation that reveals the absence of any clinically relevant abnormality
(including a physical examination, medical history, ECG, vital signs, and the results
of biochemistry, coagulation and hematology tests and urinalysis carried out at
Screening) or Subject has a stable disease (e.g., hypertension, hyperlipidemia,
diabetes mellitus, hyperthyreosis) under medical control (i.e., adequate treatment),
and does not show clinically relevant abnormalities that are not in line with the
underlying disease
Exclusion Criteria:
- All subjects
1. Clinically relevant abnormal medical history, abnormal findings on physical
examination, vital signs, ECG, or laboratory tests at Screening that the
Investigator judges as likely to interfere with the objectives of the trial or
the safety of the volunteer except for conditions associated with hepatic
impairment in subjects with compromised hepatic function (Group 2)
2. Any surgical or medical condition that may significantly alter the absorption,
distribution, metabolism, or excretion of drugs, or which may jeopardize the
subject in case of participation in the study
3. History of or present epileptic episodes or suicidal attempts
4. Documented congenital QT syndrome
5. Corrected QT interval (QTc) using Fridericia correction (QTcF) at Screening or
predose > 450 ms or < 350 ms
6. Unstable ischemic heart disease or severe heart failure (New York Heart
Association Class III or IV)
7. Uncontrolled treated/untreated hypertension (defined as a mean of 3 repeated
measurements for systolic blood pressure = 160 mmHg and/or diastolic blood
pressure = 105 mmHg); current or documented history of repeated clinically
significant hypotension
8. Primary biliary cirrhosis
9. Subject has a history of any serious drug-induced hypersensitivity reaction
(including, but not limited to, Stevens Johnson syndrome, toxic epidermal
necrolysis, or Drug Reaction with Eosinophilia and Systemic Symptoms [DRESS]) or
any drug-related rash requiring hospitalization
10. History of AED-associated rash that involved conjunctiva or mucosae
11. History of more than one non-serious drug-related hypersensitivity reaction that
required discontinuation of the medication
12. Known hypersensitivity or previous intolerance to cenobamate or any of its
excipients
13. History of cancer (judged not to be in full remission) or presence of cancer
(except basal cell skin cancer or squamous cell skin cancer) as judged by the
Investigator
14. Acute illness within 14 days prior to study drug administration unless mild in
severity and approved by the Investigator and Sponsor's medical representative
15. Active infection of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2)
16. Presence of active infection requiring antibiotics
17. Concomitant use of medications known to be linked with DRESS syndrome (including
carbamazepine, lamotrigine, phenytoin, any sulfonamide [e.g., sulfasalazine,
dapsone, sulfamethoxazole], minocycline and nevirapine, abacavir) should be
excluded at least 4 weeks prior to dosing and up to 4 weeks post cenobamate
dosing
18. Use of any prescription or non-prescription drugs, including over-the-counter
medication, non-routine vitamins and herbal products within 2 weeks prior to
study drug administration unless discussed and agreed with the Sponsor's medical
representative in writing (Medication used to treat TEAEs does not lead to a
compulsory exclusion of subjects)
19. Ingestion of alcohol within 72 hours prior to study drug administration and
during inhouse period. Outside the in-house period, regular alcohol consumption
below 24 units for males and 17 units for females per week (1 unit equals 250 mL
of beer, 75 mL of wine or 25 mL of spirits) is allowed
20. Active smokers within the last 6 months
21. Consumption of an average of more than 5 servings (240 mL per serving) per day of
coffee, cola, or other caffeinated beverage before screening. Subjects may not
consume any caffeinated beverages from 48 hours prior to dosing until the end of
the in-house stay on Day 5.
22. Participation in a clinical study involving administration of either an
investigational or a marketed drug within 2 months or 7 half-lives (whichever is
longer) before Screening
23. Donation or loss of more than 450 mL blood during the 3 months before the start
of Screening
24. Female subjects who are pregnant, nursing, or planning to become pregnant during
the study
25. Clinically significant renal disease (creatinine clearance [CLCr] < 60 mL/min as
calculated by the Cockcroft-Gault formula at Screening)
26. Positive serology for human immunodeficiency virus antibodies (anti-HIV-1/2) at
Screening.
27. Positive urine drug screen (if not due to concomitant medication) or alcohol
breath test at Screening and/or Day -1
28. Legal incapacity or limited legal capacity
29. Consumption of grapefruit or grapefruit-containing products within 48 hours
before Study Day 1 and during the PK sampling period.
Hepatically-impaired Subjects (in addition)
1. History of esophageal bleeding within the last 3 months prior to study drug
administration.
2. Severe hepatic encephalopathy (Grade > 2) or degree of central nervous system (CNS)
impairment which the Investigator considers sufficiently serious to interfere with the
informed consent, the conduct, the completion, or the results of this trial, or
constitutes an unacceptable risk to the subject
3. Has had clinical exacerbation of liver disease within 14 days before study drug
administration (e.g., abdominal pain, ascites, nausea, vomiting, anorexia, fever, or
worsening of laboratory results related to hepatic function)
4. Has evidence of acute viral hepatitis within 1 month before Day -1
5. Has evidence of severe or acute renal failure
6. History of drug or alcohol abuse within 3 months prior to dosing
7. Any significant change in chronic treatment medication within 14 days before inclusion
8. Any medical condition other than hepatic impairment which might alter the drug
metabolism
9. Have used any drugs known to significantly affect hepatic metabolism within 28 days,
or is unable or unwilling to forgo the use of such products throughout the study
10. Has evidence of hepato-renal syndrome
11. Have acute, fulminant alcoholic hepatitis, determined either clinically or by
histology, hepatoma or metastatic disease of the liver
12. History of liver transplantation
13. Advanced ascites and ascites which require emptying and albumin supplementation, as
judged by the Investigator
14. Hemoglobin concentration < 105 g/L
Healthy Subjects (in addition)
1. Any clinically unstable, uncontrolled medical condition, which in the opinion of the
Investigator would preclude the subject participation to the study
2. Positive serology for HBsAg or anti-HCV
3. History of any illness or condition that, in the opinion of the Investigator, might
confound the results of the study or pose an additional risk in administering study
drug to the subject
4. Illness within 5 days before the start of study drug dosing ("illness" is defined as
an acute [serious or non-serious] condition [e.g., the flu or the common cold])
5. History of drug abuse within the last 2 years prior to study drug administration
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