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Objective: The PERPRISE study (Study 509; NCT04202159) was a prospective, observational, non-interventional study in a real-world setting in Germany. This study was conducted to evaluate the effectiveness of perampanel as the only adjunctive treatment for 12 months in patients aged ≥18 years with focal to bilateral tonic-clonic seizures (FBTCS) or generalized tonic-clonic seizures (GTCS) in clinical practice.
Methods: Adult patients with FBTCS or GTCS received perampanel as an adjunctive therapy to anti-seizure medication (ASM) monotherapy (add-on therapy) or as a substitute for one ASM in dual therapy (substitution therapy) per the approved indication. The primary endpoint was the 12-month retention rate of perampanel; the secondary endpoints were the 6-month retention rate, seizure freedom for FBTCS or GTCS at 12 months, and safety and tolerability. Exploratory endpoints included efficacy assessments by seizure type at 6 and 12 months and patient-reported outcomes.
Results: Of the 185 patients enrolled in the study, 183 patients were included in the full analysis set (add-on, 86 patients; substitution, 96 patients; missing, 1 patient). The 12-month retention rate was 66.7% (add-on, 67.4%; substitution, 66.7%); the 6-month retention rate was 80.3% (add-on, 82.6%; substitution, 78.1%). At 12 months, the seizure-freedom rate for FBTCS or GTCS was 42.3% (add-on, 51.7%; substitution, 35.1%). Treatment-emergent adverse events (TEAEs) occurred in 44.0% of patients; 6.0% of patients reported serious TEAEs, and 16.5% of patients withdrew from the study due to TEAEs. Treatment with perampanel did not adversely affect cognitive function in patients with FBTCS or GTCS, and improvements in quality of life were reported by patients at both 6 and 12 months following perampanel initiation.
Significance: Findings from the PERPRISE study suggest that perampanel as an only adjunctive therapy is associated with favorable retention rates and good tolerability in patients with FBTCS or GTCS in a real-world clinical setting in Germany.
Plain Language Summary: Patients with epilepsy often take multiple treatments to control their seizures. It is important to look at how well they work in everyday life. This study looked at adult patients in Germany taking perampanel added to one other epilepsy treatment. After 1 year, 58 of 137 patients suffering from the most severe type of seizure were free of them. Side effects occurred in 80 patients (most commonly dizziness, fatigue, and nausea) and caused 30 of them to withdraw from treatment. Perampanel was effective and did not seem to negatively affect patients' thinking ability or quality of life.
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http://dx.doi.org/10.1002/epi4.70117 | DOI Listing |
Epilepsia Open
August 2025
Department of Neurology, University of Saarland, Homburg, Germany.
Objective: The PERPRISE study (Study 509; NCT04202159) was a prospective, observational, non-interventional study in a real-world setting in Germany. This study was conducted to evaluate the effectiveness of perampanel as the only adjunctive treatment for 12 months in patients aged ≥18 years with focal to bilateral tonic-clonic seizures (FBTCS) or generalized tonic-clonic seizures (GTCS) in clinical practice.
Methods: Adult patients with FBTCS or GTCS received perampanel as an adjunctive therapy to anti-seizure medication (ASM) monotherapy (add-on therapy) or as a substitute for one ASM in dual therapy (substitution therapy) per the approved indication.
Epilepsia
April 2025
Formerly: Eisai Inc., Nutley, New Jersey, USA.
Objective: Study 311 (NCT02849626) Extension A assessed long-term outcomes of adjunctive perampanel treatment in children (ages 4 to <12 years) with uncontrolled focal-onset seizures (FOS), with/without focal to bilateral tonic-clonic seizures (FBTCS), or generalized tonic-clonic seizures (GTCS).
Methods: Patients completing the 23-week Core Study could enter Extension A (29-week Maintenance and 4-week Follow-up Periods) to receive perampanel at the dose achieved during the Core Study. Dose adjustments were permitted per the investigator's discretion during Extension A.
Epilepsia
August 2024
Reference Center for Rare Epilepsies, Necker Enfants Malades Hospital, APHP, U1163 Institut Imagine, Université Paris Cité, Paris, France.
Epilepsia Open
June 2024
Mainz Comprehensive Epilepsy and Sleep Medicine Center, Department of Neurology, University Medical Center of the Johannes Gutenberg University, Mainz, Germany.
Objective: To report the interim results of the PERPRISE study (Study 509; NCT04202159), which is evaluating perampanel as the only adjunctive anti-seizure medication (ASM) in adults with focal to bilateral tonic-clonic seizures (FBTCS) or primary generalized tonic-clonic seizures (GTCS).
Methods: PERPRISE is an ongoing 12-month multicenter, prospective, observational, non-interventional study of perampanel in a real-world setting in Germany. Patients are aged ≥18 years with FBTCS or GTCS due to focal or idiopathic generalized epilepsy.
Seizure
August 2023
Eisai Inc., Nutley, NJ, United States of America. Electronic address:
Purpose: To evaluate the safety and tolerability of adjunctive perampanel in a Japanese subpopulation of Study 311 (NCT02849626), which was a global, multicenter, open-label, single-arm study of children (aged 4 to <12 years) with inadequately controlled focal-onset seizures (FOS), with or without focal to bilateral tonic-clonic seizures (FBTCS) or generalized tonic-clonic seizures (GTCS).
Methods: Study 311 comprised a Core Study, Extension A, and Extension B; this report focuses on the Japanese patient subgroup in the Core Study only. In the Core Study, Japanese patients (FOS only) received adjunctive perampanel ≤12 mg/day in a 23-week Treatment Phase.