# Adjunctive Use of Cenobamate in Paediatric Drug-Resistant Epilepsy: A Real-World, Single-Centre Experience

**Authors:** Barbara Oleksy, Agata Lipiec, Alicja Goszczańska-Ciuchta, Joanna Żebrowska, Magdalena Bosak, Aleksandra Kuźniar-Pałka, Hanna Mazurkiewicz, Elżbieta Lipińska, Tomasz Mazurczak, Elżbieta Stawicka

PMC · DOI: 10.3390/jcm15031218 · Journal of Clinical Medicine · 2026-02-04

## TL;DR

This study examines cenobamate's use in children with drug-resistant epilepsy, finding some seizure improvement and acceptable tolerability.

## Contribution

The study provides real-world evidence of cenobamate's off-label use in pediatric drug-resistant epilepsy patients.

## Key findings

- 39% of patients achieved complete seizure freedom after cenobamate treatment.
- 78% of patients experienced adverse events, primarily somnolence, but these were generally manageable.
- Some patients reduced or discontinued other antiseizure medications during treatment.

## Abstract

Background/Objectives: Epilepsy represents one of the most common chronic neurological disorders in children, with a considerable proportion of patients exhibiting resistance to pharmacotherapy despite the advent of novel antiseizure medications (ASMs) in recent decades. This retrospective study assesses the off-label administration of cenobamate—a newly approved antiseizure medication (ASM) for focal seizures in adults—in a cohort of paediatric patients with drug-resistant epilepsy at a single neurology centre. Methods: Clinical outcomes were reviewed retrospectively for 18 children who received cenobamate for at least 6 months. Results: Eighteen paediatric patients with drug-resistant epilepsy received cenobamate therapy at a neurology centre. The mean age was 164.6 months, and each patient had previously trialled an average of 8.7 antiseizure medications. During a follow-up period of up to 29 months, 39% of participants achieved complete seizure freedom, while five additional patients experienced a seizure reduction exceeding 80%. Concomitant clobazam use was common among the cohort. Adverse events were reported in 78% of patients, predominantly somnolence, though these were generally transient or manageable. One patient developed a temporary exacerbation of seizures, which resolved following a dosage adjustment. Many patients were able to reduce or discontinue other ASMs during the observation period. Conclusions: Cenobamate demonstrated acceptable tolerability in this paediatric cohort, and seizure improvements were observed in a subset of patients. Further clinical trials are warranted to comprehensively evaluate the efficacy and safety profile of cenobamate in this patient population.

## Linked entities

- **Chemicals:** cenobamate (PubChem CID 11962412), clobazam (PubChem CID 2789)
- **Diseases:** epilepsy (MONDO:0005027)

## Full-text entities

- **Diseases:** focal seizures (MESH:D012640), Epilepsy (MESH:D004827), somnolence (MESH:D006970), Drug-Resistant Epilepsy (MESH:D000069279), neurological disorders (MESH:D009461)
- **Chemicals:** ASM (-), Cenobamate (MESH:C000654784), clobazam (MESH:D000078306)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## References

17 references — full list in the complete paper: https://tomesphere.com/paper/PMC12897677/full.md

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Source: https://tomesphere.com/paper/PMC12897677