XCOPRI TITRATION

Flexible, once-daily XCOPRI dosing as monotherapy and adjunctive therapy1

XCOPRI IS TITRATED AT 2-WEEK INTERVALS. TITRATION PACKS ARE AVAILABLE TO SIMPLIFY TITRATION.

START

Begin with the initial
12.5 mg/25 mg titration pack

Weeks 1-4

CONTINUE

Titrate using the
50 mg/100 mg titration pack

Weeks 5-8

IF ADDITIONAL SEIZURE
REDUCTION IS NEEDED

For patients who require more than 100 mg, dosage may be increased by 50 mg/day every two weeks to a maximum of 400 mg/day*

Effective dosage range
100 mg ‑ 400 mg

XCOPRI may be taken any time, whole or crushed, with or without food.

Patients with mild or moderate hepatic impairment: 200 mg/day is the maximum dosage. XCOPRI is not recommended for use in patients with severe hepatic impairment.

See Full Prescribing Information for additional Dosage and Administration instructions.

*Additional blister packs and bottles available.
Reference: 1. XCOPRI [package insert]. Paramus, NJ: SK Life Science, Inc.
Download Additional Dosing InformationExplore Resources

XCOPRI ONCE-DAILY DOSING

Flexibility for a personal approach—from titration to maintenance dosing

XCOPRI Titration Blister Packs

Designed to simplify the titration schedule of XCOPRI. At-a-glance instructions have been included to assist you and your patients as XCOPRI dosages are increased over time.1

XCOPRI HCP Cenobamate Tablets Titration Blister Packs 12.5 | 25 mg

12.5 mg/25 mg (28-day supply)

XCOPRI Cenobamate Epilepsy Medication Tablets 50 mg & 100 mg Titration Blister Packs

50 mg/100 mg (28-day supply)

XCOPRI Cenobamate Epilepsy Medication Tablets 150 mg & 200 mg Titration Blister Packs

150 mg/200 mg (28-day supply)

XCOPRI Bottles

Designed to give you the flexibility to find the dosage that is right for your individual patients.1

XCOPRI Cenobamate Epilepsy Medication Tablet Bottle 25mg, 50mg, 100mg, 150mg & 200mg

Maintenance bottles available:

• 25 mg (30-count bottle)
• 50 mg (30-count bottle)
• 100 mg (30-count bottle)
• 150 mg (30-count bottle)
• 200 mg (30-count bottle)

XCOPRI Maintenance Blister Packs

Designed to give you the flexibility to find the dosage that is right for your individual patients.1

XCOPRI Cenobamate Epilepsy Medication 250mg & 350mg Maintenance Blister Packs

Maintenance blister
packs available:

• 250 mg [28-day supply]
• 350 mg [28-day supply]

Request Samples From a Rep
Reference: 1. XCOPRI [package insert]. Paramus, NJ: SK Life Science, Inc.

ANTI-SEIZURE MEDICATION (ASM) DOSING CONSIDERATIONS

Using XCOPRI with other ASMs

Decreasing ASM Downward Arrow Icon

XCOPRI makes the concentration of some drugs go up. Consider decreasing the dosage of clobazam, phenytoin, and phenobarbital early in XCOPRI titration.1,2

(anti-seizure medication)

If a patient experiences common adverse events, consider decreasing the dosage of other ASMs.1,2

XCOPRI can be used as monotherapy and adjunctive therapy

XCOPRI Icon

Watch this video to learn more about ASM dosing considerations when adding XCOPRI to a patient’s treatment regimen

In this interactive video, watch as Lawrence Seiden, MD, and Barry Gidal, PharmD, discuss anti-seizure medication (ASM) dosing considerations to be aware of when adding XCOPRI to a patient’s treatment regimen. Discover essential information regarding the optimization of XCOPRI’s efficacy, plus potential ways to minimize side effects—and be sure to bookmark for reference.

Find more information for prescribing XCOPRI with concomitant medications

Dosing ToolDiscuss With a Representative
References: 1. XCOPRI (package insert). Paramus, NJ: SK Life Science, Inc. 2. Rosenfeld WE, Abou-Khalil B, Aboumatar S, et al. Post hoc analysis of a phase 3, multicenter, open-label study of cenobamate for treatment of uncontrolled focal seizures: effects of dose adjustments of concomitant antiseizure medications. Epilepsia. 2021;62(12):3016-3028.
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INDICATION

XCOPRI® (cenobamate tablets) CV is indicated for the treatment of partial‑onset seizures in adult patients.

Important Safety Information
and indication

CONTRAINDICATIONS
XCOPRI® is contraindicated in any patients with known hypersensitivity to the compound or any of the components of the drug product.
XCOPRI is contraindicated in patients with Familial Short QT syndrome.

Close IMPORTANT SAFETY INFORMATION

IMPORTANT SAFETY INFORMATION and INDICATION for XCOPRI® (cenobamate tablets) CV

CONTRAINDICATIONS

XCOPRI is contraindicated in any patients with known hypersensitivity to the compound or any of the components of the drug product.

XCOPRI is contraindicated in patients with Familial Short QT syndrome.

WARNINGS AND PRECAUTIONS

Drug Reaction with Eosinophilia and Systemic Symptoms (DRESS): Also known as Multiorgan hypersensitivity, has been reported in patients taking antiepileptic drugs, including XCOPRI. DRESS has been reported, including one fatality, when XCOPRI is titrated rapidly (weekly or faster titration). No cases of DRESS were reported in an open-label safety study of 1339 partial-onset seizure patients when XCOPRI was initiated at 12.5 mg/day and titrated every two weeks. This finding does not establish that the risk of DRESS is prevented by a slower titration; however, XCOPRI should be initiated at 12.5 mg once daily and titrated every two weeks. DRESS typically, although not exclusively, presents with fever, rash, and/or lymphadenopathy, in association with other organ system involvement. Eosinophilia is often present. If such signs or symptoms are present, the patient should be evaluated immediately. XCOPRI should be discontinued immediately and not restarted if an alternative etiology for the signs or symptoms cannot be established.

QT Shortening: XCOPRI can cause shortening of the QT interval. Caution should be used when administering XCOPRI and other drugs that shorten the QT interval as there may be a synergistic effect on the QT interval that would increase the QT shortening risk.

Suicidal Behavior and Ideation: Antiepileptic drugs (AEDs), including XCOPRI, increase the risk of suicidal thoughts or behavior in patients taking these drugs for any indication. Patients treated with any AED for any indication should be monitored for the emergence or worsening of depression, suicidal thoughts or behavior, and/or any unusual changes in mood or behavior. Advise patients, their caregivers, and/or families to be alert for these behavioral changes and report them immediately to a healthcare provider.

Neurological Adverse Reactions: XCOPRI causes dose-dependent increases in the neurologic adverse reactions including, dizziness, diplopia, disturbance in gait and coordination, somnolence, and fatigue.

Prescribers should advise patients against engaging in hazardous activities requiring mental alertness, such as operating motor vehicles or dangerous machinery, until the effect of XCOPRI is known.

Withdrawal of AEDs: As with all antiepileptic drugs, XCOPRI should generally be withdrawn gradually because of the risk of increased seizure frequency and status epilepticus. But if withdrawal is needed because of a serious adverse event, rapid discontinuation can be considered.

MOST COMMON ADVERSE REACTIONS

In adult adjunctive therapy placebo-controlled clinical studies, the most common adverse reactions that occurred in XCOPRI-treated patients (incidence at least 10% and greater than placebo) were somnolence, dizziness, fatigue, diplopia, headache.

DOSING CONSIDERATIONS

Dosage adjustment of XCOPRI or other concomitant medications may be necessary.

  • Consider gradually reducing phenytoin dosages by up to 50% during initial titration.
  • Consider reducing dosages of phenobarbital and clobazam as needed when used concomitantly with XCOPRI. When XCOPRI and carbamazepine or lamotrigine are taken concomitantly, consider increasing dosages as needed of carbamazepine or lamotrigine.
  • Consider increasing dosages as needed of drugs which are CYP2B6 and CYP3A substrates and decreasing dosages as needed of drugs which are CYP2C19 substrates.
  • Effectiveness of hormonal oral contraceptives may be reduced when administered concomitantly with XCOPRI. Women should use additional or alternative non-hormonal birth control.

Dosage reduction of XCOPRI may be considered in patients with mild to moderate and severe renal impairment. XCOPRI use is not recommended in end‑stage renal disease.

The maximum recommended daily dose is 200 mg for patients with mild or moderate hepatic impairment. XCOPRI use is not recommended in patients with severe hepatic impairment

DRUG ABUSE

XCOPRI is a Schedule V controlled substance.

INDICATION

XCOPRI is indicated for the treatment of partial-onset seizures in adult patients.

Please see full Prescribing Information.