THINK … EFFICACY, TOLERABILITY & LONG TERM

LONG-TERM EFFICACY, RETENTION AND SAFETY of CENOBAMATE

Epilepsy is one of the most common neurological disorders worldwide, with a prevalence estimated to be between 4 and 10 per 1000 people. Most of the people diagnosed with epilepsy are treated with antiepileptic drugs, and approximately 70% can become seizure-free once the most effective regimen is followed. However, non-adherence to medication is a prevalent and persistent healthcare problem and evidence indicates that poor adherence to medication is common among epilepsy-patients.²

Poor adherence to anti-epileptic drugs is associated with:²

Reasons for poor adherence are varied but may include:^3,4

It is not easy to accurately measure adherence⁴ but the rate of non-adherence in adults with epilepsy is estimated to be between 29-66%.^3,*

Retention rates for anti-seizure medications (ASMs) provide a composite measure of efficacy, tolerability, safety and adherence over a defined time period,⁵ and their use as an outcome measure is recommended by the European Medicines Agency (EMA) as a global indicator of a drug's clinical effectiveness.⁵

Data from retention studies may also provide benchmarks for interpreting and comparing clinical efficacy of ASMs, as well as evaluating long-term efficacy and tolerability beyond controlled clinical trials.⁵

High rates of retention on ONTOZRY^® were observed during the clinical development programme⁵  

Retention rates on ONTOZRY^® appear to be comparable to or better than rates reported for ASMs in pre-marketing open-label extension studies conducted as part of respective clinical development programmes.⁵

• High long-term retention rates with ONTOZRY^® suggests sustained clinical efficacy and tolerability.⁵
• Concomitant anti-seizure medications did not impact retention.⁵
• These retention rates support the acceptability of the titration schedule and compliance with ONTOZRY⁶

Some aspects of safety

The most common TEAEs (treatment-emergent adverse event) across all three studies included (C013, C017 and C021) in analysis by Sander et al. were central nervous system related. Most TEAEs were mild or moderate in severity (75.8%)⁵

Cognitive and psychiatric side effects of ASMs can have importance in affecting treatment adherence and patient quality of life, so there is a need to understand the safety profile of treatments in terms of those adverse events.⁷

Recently published study by Krauss et al (2024), based on data from two phase 2 randomized, double-blind clinical trials, their open-label extensions, and a phase 3 long-term open-label safety study^†, found that the occurrence of cognitive and psychiatric treatment-emergent adverse events (TEAEs) was low in patients receiving adjunctive cenobamate for up to 7 years, with fewer than 2% of patients discontinuing treatment due to these adverse events. This indicates a potentially good tolerability of cenobamate in regards of psychiatric and cognitive adverse events.⁷

Abbreviations:
AED = Anti-epileptic drug; ASM = anti-seizure medication; OLE = open-label extension; TEAE = treatment-emergent adverse event

*Data from a systematic review of adherence studies in adults with epilepsy who were prescribed AEDs.³

^† C013,  C013 OLE,  C017,  C017 OLE,  C021

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Ontozry® (cenobamat) 12,5 mg odragerad tablett samt 25 mg, 50 mg, 100 mg, 150 mg och 200 mg filmdragerade tabletter. Rx F. ATC-kod: N03AX25 - antiepileptika, övriga antiepileptika. Indikation: Ontozry är indicerat som tilläggsbehandling av fokala anfall, med eller utan sekundär generalisering hos vuxna patienter med epilepsi, som inte kontrollerats tillräckligt trots tidigare behandling med minst två antiepileptika. Kontraindikationer: Överkänslighet mot den aktiva substansen eller mot något hjälpämne, ärftligt kort QT-syndrom. Varningar: Patienter ska instrueras att uppsöka läkare om tecken på självmordstankar/självmordsbeteende uppstår, samt om tecken och symptom på läkemedelsreaktion med eosinofili och systemiska symtom (DRESS) inträffar. Innehåller laktos. Cenobamat kan minska exponeringen av substanser som metaboliseras via CYP3A4, CYP2B6 samt öka exponeringen av substanser som metaboliseras via CYP2C19. Cenobamat rekommenderas inte till fertila kvinnor som inte använder preventivmedel eller vid amning. MAH: Angelini Pharma S.p.A.  Lokal kontakt: Angelini Pharma Nordics, nordic.medinfo@angelinipharma.com. Datum för senaste översyn av SPC: 2/2025. För pris och ytterligare information, se www.fass.se.

MAT-DK-0021-P Apr 2025