Literature DB >> 25495693

The clinical pharmacology profile of the new antiepileptic drug perampanel: A novel noncompetitive AMPA receptor antagonist.

Philip N Patsalos1.   

Abstract

The clinical pharmacology profile of a drug critically determines its therapeutics, and this review summarizes the characteristics associated with the antiepileptic drug (AED) perampanel. A PubMed literature search was performed for perampanel. Congress abstract data are included where necessary and Eisai Ltd provided access to unpublished data on file. After oral ingestion, perampanel is rapidly absorbed and peak plasma concentrations occur 0.5-2.5 h later; its bioavailability is ~100%. Although the rate of perampanel absorption is slowed by food co-ingestion, the extent absorbed remains unchanged; therefore, perampanel can be administered without regard to meal times. The pharmacokinetics of perampanel are linear and predictable over the clinically relevant dose range (2-12 mg); perampanel is 95% protein-bound to albumin and α1-acid glycoprotein. Perampanel is extensively metabolized (>90%) in the liver, primarily by cytochrome P450 (CYP) 3A4, to various pharmacologically inactive metabolites. In healthy volunteers, the apparent terminal half-life is ~105 h, whereas the calculated effective half-life is 48 h. These half-life values allow for once-daily dosing, which will aid patient compliance and in the event of a missed dose, will have minimal impact on seizure control. In healthy volunteers prescribed carbamazepine, half-life decreases to 25 h. Clearance values are not significantly different in adolescents (~13.0 ml/min) and the elderly (~10.5 ml/min) compared with adults (10.9 ml/min). Perampanel has minimal propensity to cause pharmacokinetic interactions. However, it is the target of such interactions and CYP3A4-inducing AEDs enhance its clearance; this can be used to advantage because dose titration can be faster and thus optimum therapeutic outcome can be achieved sooner. Perampanel 12 mg, but not 4 or 8 mg, enhances the metabolism of the progesterone component of the oral contraceptive pill, necessitating the need for an additional reliable contraceptive method. Overall, perampanel has a favorable clinical pharmacology profile, which should aid its clinical use. Wiley Periodicals, Inc.
© 2014 International League Against Epilepsy.

Entities:  

Keywords:  Clinical pharmacology; Drug-drug interactions; Pharmacodynamics; Pharmacokinetics; Plasma protein binding

Mesh:

Substances:

Year:  2014        PMID: 25495693     DOI: 10.1111/epi.12865

Source DB:  PubMed          Journal:  Epilepsia        ISSN: 0013-9580            Impact factor:   5.864


  47 in total

1.  The Orally Active Noncompetitive AMPAR Antagonist Perampanel Attenuates Focal Cerebral Ischemia Injury in Rats.

Authors:  Hong-Xia Niu; Jun-Zhe Wang; Dong-Liang Wang; Jun-Jie Miao; Hua Li; Zhi-Gang Liu; Xing Yuan; Wei Liu; Jing-Ru Zhou
Journal:  Cell Mol Neurobiol       Date:  2017-04-11       Impact factor: 5.046

Review 2.  Feasibility of Using Oral Fluid for Therapeutic Drug Monitoring of Antiepileptic Drugs.

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Review 3.  Antiepileptic Drug Removal by Continuous Renal Replacement Therapy: A Review of the Literature.

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Journal:  Clin Drug Investig       Date:  2017-01       Impact factor: 2.859

Review 4.  [Cenobamate-a new perspective for epilepsy treatment].

Authors:  Bernhard J Steinhoff
Journal:  Nervenarzt       Date:  2020-09-29       Impact factor: 1.214

Review 5.  Practice Update: Review of Anticonvulsant Therapy.

Authors:  Derek J Chong; Andrew M Lerman
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Review 6.  The AMPA receptor antagonist perampanel in the adjunctive treatment of partial-onset seizures: clinical trial evidence and experience.

Authors:  Bernhard J Steinhoff
Journal:  Ther Adv Neurol Disord       Date:  2015-05       Impact factor: 6.570

Review 7.  The Pharmacology and Toxicology of Third-Generation Anticonvulsant Drugs.

Authors:  Paul LaPenna; Laura M Tormoehlen
Journal:  J Med Toxicol       Date:  2017-08-16

Review 8.  Perampanel: A Review in Drug-Resistant Epilepsy.

Authors:  James E Frampton
Journal:  Drugs       Date:  2015-09       Impact factor: 9.546

Review 9.  Pharmacotherapy for Focal Seizures in Children and Adolescents.

Authors:  Clare E Stevens; Carl E Stafstrom
Journal:  Drugs       Date:  2018-09       Impact factor: 9.546

10.  Structural Bases of Noncompetitive Inhibition of AMPA-Subtype Ionotropic Glutamate Receptors by Antiepileptic Drugs.

Authors:  Maria V Yelshanskaya; Appu K Singh; Jared M Sampson; Chamali Narangoda; Maria Kurnikova; Alexander I Sobolevsky
Journal:  Neuron       Date:  2016-09-08       Impact factor: 17.173

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