Intravenous perampanel as an alternative to the oral formulations in Japanese patients with epilepsy

Author:

Hanaya Ryosuke1ORCID,Kubota Yuichi2ORCID,Mizobuchi Masahiro3,Iida Koji4,Ono Tomonori5ORCID,Motooka Hiromichi6,Nakano Naoki7,Fujimoto Ayataka8ORCID,Iwasaki Masaki9ORCID,Fukuda Masafumi10,Kondo Akihiko11,Uruno Katsuhisa12,Yamamuro Shintaro13,Yamaguchi Kohei13,Onishi Kisaki13,Ngo Leock Y14,Inoue Yushi15

Affiliation:

1. Department of Neurosurgery Kagoshima University, Graduate School of Medical and Dental Sciences Kagoshima Japan

2. Epilepsy Center, TMG Asaka Medical Center Asaka Japan

3. Department of Neurology Nakamura Memorial Hospital Sapporo Japan

4. Epilepsy Center, Hiroshima University Hospital Hiroshima Japan

5. Epilepsy Center, National Hospital Organization Nagasaki Medical Center Omura Japan

6. Department of Neuropsychiatry Kurume University Kurume Japan

7. Department of Neurosurgery Kindai University Osakasayama Japan

8. Comprehensive Epilepsy Center, Seirei Hamamatsu General Hospital Hamamatsu Japan

9. Department of Neurosurgery National Center Hospital, National Center of Neurology and Psychiatry Kodaira Japan

10. Department of Neurosurgery National Hospital Organization Nishiniigata Chuo Hospital Niigata Japan

11. Department of Neurosurgery National Hospital Organization, Shizuoka Institute of Epilepsy and Neurological Disorders Shizuoka Japan

12. Department of Neurology National Hospital Organization Yamagata Hospital Yamagata Japan

13. Eisai Co., Ltd. Bunkyo Japan

14. Eisai Inc. Nutley New Jersey USA

15. National Hospital Organization, Shizuoka Institute of Epilepsy and Neurological Disorders Shizuoka Japan

Abstract

AbstractObjectivePerampanel is an oral anti‐seizure medication, which is approved in Japan for focal‐onset seizures, with/without focal to bilateral tonic–clonic seizures, as monotherapy/adjunctive therapy in patients aged 4 years and older. Treatment for generalized tonic–clonic seizures as adjunctive therapy in patients aged 12 years and older is approved as well. We evaluated the feasibility of intravenous (IV) administration of perampanel as an alternative to oral administration.MethodsStudy 240 (NCT03754582) was an uncontrolled, open‐label study of IV perampanel, conducted in 21 Japanese patients with epilepsy who received a stable dose of 8–12 mg/day of oral perampanel. Patients received 30‐minute IV infusions at equivalent daily doses of oral perampanel for 4 days, then were switched back to oral perampanel. Safety, tolerability, plasma concentration, and maintenance of efficacy throughout the transition between IV and oral dosing of perampanel were assessed. As supportive data, a subgroup analysis was also conducted using data from healthy Japanese subjects (n = 18) who were enrolled in Study 050 (NCT03376997) investigating the pharmacokinetics and safety of IV perampanel in healthy subjects who received an IV infusion (30‐, 60‐, or 90‐minute) of perampanel 12 mg and a single oral administration of perampanel 12‐mg tablet.ResultsIn Study 240, the transition between 30‐minute IV and oral perampanel dosing was associated with a ≤1.4‐fold increase in the mean change in maximum observed concentration of perampanel. Seizure outcomes demonstrated no considerable changes in efficacy before, during, or after 30‐minute IV dosing of perampanel. The safety profiles were similar between IV and oral formulations. In Study 050, the pharmacokinetics of 30‐ or 60‐minute IV infusion of perampanel further support the interchangeability between oral and IV formulations in the Japanese subjects.SignificanceThese results support that 30‐minute IV perampanel may be a potential short‐term alternative to oral formulations for patients with epilepsy.

Funder

Eisai Canada

Publisher

Wiley

Subject

Neurology (clinical),Neurology

Reference27 articles.

1. Perampanel: A novel, orally active, noncompetitive AMPA-receptor antagonist that reduces seizure activity in rodent models of epilepsy

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4. Food and Drug Administration.FYCOMPA® Prescribing Information.2019. Available from:https://www.fycompa.com/‐/media/Files/Fycompa/Fycompa_Prescribing_Information.pdf. Accessed Sep 28 2021

5. PMDA.FYCOMPA® Prescribing Information.2020. Available from:https://www.pmda.go.jp/PmdaSearch/iyakuDetail/ResultDataSetPDF/170033_1139014F1022_1_08. Accessed Sep 28 2021

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