Cenobamate for Epilepsy

(CENOBITE Trial)

MC
JW
Overseen ByJong Woo Lee, MD, PhD
Age: 18+
Sex: Any
Trial Phase: Phase < 1
Sponsor: Brigham and Women's Hospital
Must be taking: Antiseizure medications
No Placebo GroupAll trial participants will receive the active study treatment (no placebo)
Approved in 4 JurisdictionsThis treatment is already approved in other countries

What You Need to Know Before You Apply

What is the purpose of this trial?

This trial tests a new epilepsy medication called cenobamate. Researchers aim to evaluate its effectiveness and monitor for serious side effects, such as DRESS syndrome, which can cause skin rashes and fever. Participants will receive the medication under close supervision to ensure safety. This trial may suit individuals with frequent or continuous seizures who are already undergoing EEG monitoring. As an Early Phase 1 trial, participants will be among the first to receive this treatment, aiding researchers in understanding its effects in people.

Will I have to stop taking my current medications?

The trial does not specify if you need to stop your current medications, but it requires that you continue taking conventional antiseizure medication alongside the trial drug. If you are on medications affecting absorption, like phenobarbital, you may need to stop those.

Is there any evidence suggesting that this treatment is likely to be safe for humans?

Research has shown that cenobamate may effectively treat epilepsy, particularly for those who haven't succeeded with other treatments. In previous studies, most patients tolerated cenobamate well. For example, one study found that cenobamate reduced seizures without causing serious side effects. However, some patients experienced minor side effects, which are common with many medications.

A key concern with cenobamate is the potential risk of a rare but serious reaction called DRESS syndrome, which can involve a rash, fever, and organ problems. Regular check-ups during treatment help manage this risk.

While researchers continue to study cenobamate, current evidence suggests it is safe for many people. Always consult a healthcare professional about any concerns before joining a trial.12345

Why do researchers think this study treatment might be promising?

Unlike the standard epilepsy treatments, which often include medications like levetiracetam, valproic acid, or lamotrigine, cenobamate stands out with its unique mechanism of action. Most treatments work by modulating neurotransmitter levels or blocking sodium channels, but cenobamate targets both sodium channels and GABA receptors, which may help stabilize brain activity more effectively. Researchers are excited because this dual action could potentially bring faster and more significant relief for patients who haven't responded well to existing therapies. Additionally, cenobamate's loading phase and short treatment duration offer a promising option for rapid intervention, a notable advantage over the typical long-term medication regimens.

What evidence suggests that cenobamate might be an effective treatment for epilepsy?

Research shows that cenobamate, which participants in this trial will receive, effectively treats seizures, particularly in people with epilepsy unresponsive to other medications. In previous studies, more than 20% of participants stopped having seizures completely, and over half experienced at least a 50% reduction in seizures. Another study found that patients taking cenobamate had up to twice the reduction in seizures compared to those on a placebo. Long-term evidence supports these results, with nearly 50% of patients experiencing a significant decrease in seizures. These findings suggest that cenobamate could be a promising option for managing epilepsy.26789

Who Is on the Research Team?

JW

Jong Woo Lee, MD, PhD

Principal Investigator

Brigham and Women's Hospital

Are You a Good Fit for This Trial?

This trial is for patients with nervous system disorders, epilepsy, or other neurological conditions who require intensive care. Participants will be closely monitored in a multi-center study involving leading critical care EEG monitoring sites.

Inclusion Criteria

Undergoing EEG monitoring
I experience more than one seizure per hour or have had a long seizure lasting more than 5 minutes.
I am taking medication for seizures.

Exclusion Criteria

History of medication-related rash
I am taking medication that affects how my body absorbs food or drugs.
I cannot take cenobamate due to health reasons.

Timeline for a Trial Participant

Screening

Participants are screened for eligibility to participate in the trial

2-4 weeks

Treatment

Participants receive a 400mg load of Cenobamate plus 100mg daily for a maximum of 14 days, with regular monitoring for DRESS syndrome and other adverse reactions

Up to 14 days
Daily monitoring

Follow-up

Participants are monitored for safety and effectiveness after treatment, including seizure cessation and maintenance of therapeutic levels

4 weeks

What Are the Treatments Tested in This Trial?

Interventions

  • Cenobamate
Trial Overview The CENOBITE study tests the drug Cenobamate on a small group of 10 patients to see how it affects those with severe neurological issues. Patients' reactions are tracked using advanced tools like EEG and regular lab tests.
How Is the Trial Designed?
1Treatment groups
Experimental Treatment
Group I: CenobamateExperimental Treatment1 Intervention

Cenobamate is already approved in United States, European Union, United Kingdom, Canada for the following indications:

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Approved in United States as Xcopri for:
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Approved in European Union as Ontozry for:
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Approved in United Kingdom as Ontozry for:
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Approved in Canada as Ontozry for:

Find a Clinic Near You

Who Is Running the Clinical Trial?

Brigham and Women's Hospital

Lead Sponsor

Trials
1,694
Recruited
14,790,000+

Published Research Related to This Trial

Cenobamate (XCOPRI®) is a newly approved oral medication for treating partial-onset seizures in adults, developed by SK Life Science Inc. and Arvelle Therapeutics.
The approval was based on positive results from two pivotal phase 2 trials, highlighting its efficacy as a neurotherapeutic option for epilepsy.
Cenobamate: First Approval.Keam, SJ.[2020]
Cenobamate, an antiepileptic drug approved for focal seizures, demonstrated a favorable safety profile in a study involving 210 healthy subjects, with most treatment-emergent adverse events being mild and no deaths reported.
The pharmacokinetics of cenobamate support once-daily dosing, as it showed dose-proportional increases in plasma concentration and a long half-life of 30 to 76 hours, making it a convenient option for managing seizures.
Pharmacokinetics of Cenobamate: Results From Single and Multiple Oral Ascending-Dose Studies in Healthy Subjects.Vernillet, L., Greene, SA., Kamin, M.[2021]
Cenobamate (CNB) demonstrated long-term efficacy in reducing seizure frequency, with a median reduction of 76.1% at 43-48 months, and 16.4% of patients achieving complete seizure freedom during this period.
The treatment was well-tolerated over the long term, with retention rates of 71% at 24 months and no new safety issues identified, although common adverse events included dizziness and fatigue.
Long-Term Efficacy and Safety From an Open-Label Extension of Adjunctive Cenobamate in Patients With Uncontrolled Focal Seizures.Klein, P., Aboumatar, S., Brandt, C., et al.[2022]

Citations

1.pubmed.ncbi.nlm.nih.govpubmed.ncbi.nlm.nih.gov/40119878/
Real-world effectiveness and tolerability of cenobamate in ...The primary effectiveness endpoint was the 50% responder rate, defined as the reduction in seizure frequency ≥50%. Results: Data were collected ...
Cenobamate (YKP3089) and Drug-Resistant EpilepsyCNB is a highly effective drug in managing focal onset seizures, with more than twenty percent of individuals with drug-resistant epilepsy achieving seizure ...
Efficacy and safety of Cenobamate: a multicenter ...In the group of patients who had epilepsy surgery in the past, 28 of 47 (59.6 %) had ≥50 % reduction in seizure frequency, including 11 (23.4 %) ...
XCOPRI® (cenobamate tablets) CV EfficacyPrimary outcome: Patients taking XCOPRI experienced up to 2x greater seizure reduction compared with placebo (55% XCOPRI 400 mg, 55% XCOPRI 200 mg, ...
Long-Term, Real-World Study Results Show Xcopri Is Highly ...Long-Term, Real-World Study Results Show Xcopri Is Highly Effective as a Treatment for Reducing Seizures · 37.3% were 100% responders · 49.2% were ...
Clinical Review - Cenobamate (Xcopri) - NCBI - NIHDespite the availability of several ASMs, there has been no meaningful improvement in epilepsy treatment-related outcomes and no significant increase in seizure ...
Post-hoc analysis of YKP3089C017 randomized clinical trialCenobamate significantly reduced the seizure frequency by 55.6 % compared to 21.5 % with placebo; the percentage of seizure-free patients was 28.3 % in the ...
NCT04903314 | Dose-Escalation Study of Cenobamate ...The secondary objective of this study is to evaluate the safety and tolerability of cenobamate (YKP3089) following single and multiple dosing. Official ...
Evidence from the First Interim Analysis of the BLESS StudyIn adults with uncontrolled focal seizures, the treatment with adjunctive cenobamate was well tolerated and was associated with improved seizure control.
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