Efficacy and tolerability of adjunctive lacosamide in patients aged <4 years with focal seizures

Author:

Makedonska Iryna1,Ng Yu‐Tze2,Beller Cynthia3,Bozorg Ali3,Csikós János4,McClung Carrie3,Moeltgen Holger4,Farkas Mark Kristof5,

Affiliation:

1. Municipal Non‐profit Enterprise City Children's Clinical Hospital #6 of Dnipro City Council Dnipro Ukraine

2. Baylor College of Medicine/The Children's Hospital of San Antonio San Antonio Texas USA

3. UCB Pharma Morrisville North Carolina USA

4. UCB Pharma Monheim am Rhein Germany

5. Pediatric Center, MTA Center of Excellence Semmelweis University Budapest Hungary

Abstract

AbstractObjectivePrimary objective was to evaluate efficacy of lacosamide administered concomitantly with 1–3 antiseizure medications in young children with uncontrolled focal (partial‐onset) seizures.MethodsDouble‐blind, parallel‐group trial (SP0967: NCT02477839/2013‐000717‐20) conducted between June 2015 and May 2020 at hospitals and clinics in 25 countries. Patients (aged ≥1 month to <4 years) with uncontrolled focal seizures were randomized 1:1 to adjunctive lacosamide or placebo using an interactive voice/web response system and stratified by age. After a 20‐day titration period, patients who reached target‐dose range (8–12 mg/kg/day) entered a 7‐day maintenance period. Region‐specific primary efficacy variables were based on ≤72‐h video‐electroencephalograms: change in average daily frequency (ADF) of electrographic focal seizures as measured on end‐of‐maintenance video‐electroencephalogram versus end‐of‐baseline video‐electroencephalogram (United States); 50% responder rate (≥50% reduction in ADF of focal seizures) during maintenance (European Union).ResultsIn total, 255 patients were randomized (lacosamide/placebo: 128/127) and received ≥1 trial medication dose. Percentage reduction in ADF of focal seizures for lacosamide (116 patients) versus placebo (120 patients) was 3.2% (95% confidence interval = −13.6 to 17.5, p = 0.69). 50% responder rate was 41.4% for lacosamide (116 patients), 37.5% for placebo (120 patients) (p = 0.58). Treatment‐emergent adverse events were reported by 44.5% of lacosamide‐treated patients (placebo 51.2%).InterpretationAdjunctive lacosamide did not show superior efficacy versus placebo in young children with focal seizures. However, efficacy variables were potentially affected by high variability and low reliability between readers in video‐electroencephalogram interpretation. Lacosamide was generally well tolerated; safety profile was acceptable and consistent with that in adults and children aged ≥4 years.

Funder

UCB Pharma

Publisher

Wiley

Reference15 articles.

1. Incidence and Prevalence of Childhood Epilepsy: A Nationwide Cohort Study

2. Emerging Antiepileptic Drugs for Severe Pediatric Epilepsies

3. The Safety and Tolerability of Newer Antiepileptic Drugs in Children and Adolescents

4. UCB Inc.VIMPAT (Lacosamide) US Prescribing Information.2023[November 7 2023];https://www.ucb‐usa.com/vimpat‐prescribing‐information.pdf

5. UCB Pharma SA.VIMPAT (Lacosamide) EU Summary of Product Characteristics.2022[November 8 2023];https://www.ema.europa.eu/en/documents/product‐information/vimpat‐epar‐product‐information_en.pdf

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