Cenobamate

Cenobamate

Clinical data
Trade names	Xcopri, Ontozry
Other names	YKP3089
AHFS/Drugs.com	Monograph
MedlinePlus	a620021
License data	US DailyMed: Cenobamate
Routes of administration	By mouth
ATC code	N03AX25 (WHO)
Legal status
Legal status	CA: ℞-only[1][2] UK: POM (Prescription only) US: Schedule V[3][4] EU: Rx-only[5][6]
Pharmacokinetic data
Bioavailability	≥88%
Protein binding	60%
Metabolism	Mainly glucuronidation via UGT2B7
Elimination half-life	50–60 hours
Excretion	Mainly via urine
Identifiers
IUPAC name [(1R)-1-(2-chlorophenyl)-2-(tetrazol-2-yl)ethyl] carbamate
CAS Number	913088-80-9
PubChem CID	11962412
DrugBank	DB06119
ChemSpider	10136642
UNII	P85X70RZWS
KEGG	D11150
ChEMBL	ChEMBL3989949
CompTox Dashboard (EPA)	DTXSID001027948
Chemical and physical data
Formula	C10H10ClN5O2
Molar mass	267.67 g·mol−1
3D model (JSmol)	Interactive image
SMILES C1=CC=C(C(=C1)C(CN2N=CN=N2)OC(=O)N)Cl
InChI InChI=1S/C10H10ClN5O2/c11-8-4-2-1-3-7(8)9(18-10(12)17)5-16-14-6-13-15-16/h1-4,6,9H,5H2,(H2,12,17)/t9-/m0/s1 Key:GFHAXPJGXSQLPT-VIFPVBQESA-N

Cenobamate, sold under the brand names Xcopri (US) and Ontozry (EU), is a medication used for the treatment of partial-onset seizures, a kind of epilepsy, in adults.^[3][7][8] It is taken by mouth.^[3]

Cenobamate was approved for medical use in the United States in November 2019,^[3][7][8][9] and placed in Schedule V of the Controlled Substances Act in March 2020.^[10] Cenobamate was approved for medical use in the European Union in March 2021,^[5] approved for use in the UK in December 2021,^[11] and approved for use in Canada in June 2023.^[12]

In the United States, cenobamate is indicated for the treatment of partial-onset seizures in adults.^[3]

In the European Union, it is indicated for the adjunctive treatment of focal-onset seizures with or without secondary generalization in adults with epilepsy who have not been adequately controlled despite a history of treatment with at least two anti-epileptic medications.^[5]

In the UK, it is used as an add-on treatment, after at least 1 other add-on treatment has not controlled seizures and only when treatment is started in a specialised epilepsy service (tertiary care).^[11]

Cenobamate shortens the QT interval of the heart rhythm. It is therefore contraindicated in people with familial short QT syndrome, a very rare disease of the electrical system of the heart.^[13][14]

The most common side effects are drowsiness (in 37% of people taking the drug), dizziness (33%), and fatigue (24%). Sight disorders, headache and elevated potassium levels in the blood (over 5 mmol/L) are also common.^[13] Hypersensitivity occurs in fewer than 1% of patients, drug reaction with eosinophilia and systemic symptoms (DRESS) in fewer than 0.1%.^[14]

There are few data regarding cenobamate overdose. It is expected that the described adverse effects such as drowsiness, dizziness and fatigue would occur, as well as possibly problems with the heart rhythm. No specific antidote exists.^[13][14]

Using cenobamate together with other central nervous system depressants such as barbiturates, benzodiazepines or alcohol may result in increased drowsiness and other central nervous system symptoms.^[13][14]

Cenobamate induces the enzymes CYP3A4 and CYP2B6 and can therefore decrease blood concentrations of drugs that are metabolized by these enzymes (for example midazolam and bupropion, respectively). Conversely, it inhibits the enzyme CYP2C19, potentially increasing concentrations of drugs metabolized by this enzyme (for example omeprazole).^[13][14]

Cenobamate is a voltage-gated sodium channel (VGSC) blocker.^[15] It is a selective blocker of the inactivated state of VGSCs, preferentially inhibiting persistent sodium current.^[15] It has been proposed that cenobamate additionally enhances presynaptic release of γ-aminobutyric acid (GABA), thereby increasing inhibitory GABAergic neurotransmission.^[15]

Cenobamate is absorbed from the gut to at least 88% and reaches highest concentrations in the blood plasma after one to four hours. When in the bloodstream, 60% of the substance are bound to plasma proteins, mostly to albumin. Cenobamate is inactivated mainly by glucuronidation via the enzyme UGT2B7 and to a lesser extent UGT2B4. The enzymes CYP2E1, CYP2A6, CYP2B6, CYP2C19 and CYP3A4 play smaller roles in the drug's metabolism.^[14]

Steady state conditions are reached after 14 days. Cenobamate and its metabolites are mostly eliminated via the urine and only to 5.2% via the faeces. The terminal half-life is 50 to 60 hours.^[14]

The safety and efficacy of cenobamate to treat partial-onset seizures was established in two randomized, double-blind, placebo-controlled studies that enrolled 655 adults. In these studies, patients had partial-onset seizures with or without secondary generalization for an average of approximately 24 years and median seizure frequency of 8.5 seizures per 28 days during an 8-week baseline period. During the trials, doses of 100, 200, and 400 milligrams (mg) daily reduced the number of seizures per 28 days compared with the placebo group.^[7]

The US Food and Drug Administration (FDA) approved cenobamate in November 2019, and granted the application for Xcopri to SK Life Science Inc.^{[7][8][9][16]}

In January 2021, the Committee for Medicinal Products for Human Use of the European Medicines Agency adopted a positive opinion, recommending the granting of a marketing authorization.^[17] The applicant for this medicinal product is Arvelle Therapeutics Netherlands B.V.^[17] Ontozry was approved on 26 March 2021.^[5][18]