Zonisamide: A Review of Its Use in the Management of Adults with Partial Seizures

被引:15
作者
Hoy, Sheridan M. [1 ]
机构
[1] Adis Int Ltd, Auckland 0754, New Zealand
关键词
CONTROLLED-RELEASE CARBAMAZEPINE; ANTIEPILEPTIC DRUG EFFICACY; NEWLY-DIAGNOSED EPILEPSY; PARTIAL-ONSET SEIZURES; LONG-TERM SAFETY; DOUBLE-BLIND; PHARMACOKINETIC INTERACTIONS; ADJUNCTIVE ZONISAMIDE; CLINICAL-PHARMACOLOGY; INITIAL MONOTHERAPY;
D O I
10.1007/s40265-013-0093-4
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Oral zonisamide (Zonegran (R)) is a benzisoxazole derivative chemically unrelated to other antiepileptic agents. It is indicated in the EU as monotherapy in the treatment of partial seizures, with or without secondary generalization, in adults with newly diagnosed epilepsy and as adjunctive therapy to other antiepileptic drugs (AEDs) in the treatment of adults with partial seizures, with or without secondary generalization. In a double-blind, multinational study in adults newly diagnosed with partial seizures, shorter-term monotherapy with once-daily zonisamide was noninferior to that with twice-daily carbamazepine controlled release in terms of seizure freedom according to the International League Against Epilepsy guidelines, with seizure freedom benefits maintained during longer-term therapy. In four randomized, double-blind, placebo-controlled studies in adults with refractory partial seizures, shorter-term adjunctive therapy with once-or twice-daily zonisamide reduced the frequency of seizures to a significantly greater extent than placebo, with antiepileptic efficacy sustained following longer-term treatment in this patient population. Zonisamide was generally well tolerated in adults with partial seizures participating in these studies, with the majority of adverse events being mild or moderate in severity. Thus, oral zonisamide as monotherapy or adjunctive therapy to other AEDs provides a useful option in the treatment of patients with partial seizures.
引用
收藏
页码:1321 / 1338
页数:18
相关论文
共 55 条
  • [1] Another option for first-line treatment of partial epilepsy?
    Abou-Khalil, Bassel W.
    [J]. LANCET NEUROLOGY, 2012, 11 (07) : 568 - 569
  • [2] [Anonymous], 2012, EP DIAGN MAN EP AD C
  • [3] Antel J, 2012, Handb Exp Pharmacol, P433, DOI 10.1007/978-3-642-24716-3_20
  • [4] Baulac M, 2013, EPILEPSIA, V54, P173
  • [5] Efficacy and tolerability of zonisamide versus controlled-release carbamazepine for newly diagnosed partial epilepsy: a phase 3, randomised, double-blind, non-inferiority trial
    Baulac, Michel
    Brodie, Martin J.
    Patten, Anna
    Segieth, Joanna
    Giorgi, Luigi
    [J]. LANCET NEUROLOGY, 2012, 11 (07) : 579 - 588
  • [6] Clinical guidelines on the identification, evaluation, and treatment of overweight and obesity in adults: The evidence report
    Ben-Menachem, Elinor
    [J]. EPILEPSIA, 2007, 48 : 42 - 45
  • [7] Revised terminology and concepts for organization of seizures and epilepsies: Report of the ILAE Commission on Classification and Terminology, 2005-2009
    Berg, Anne T.
    Berkovic, Samuel F.
    Brodie, Martin J.
    Buchhalter, Jeffrey
    Cross, J. Helen
    Boas, Walter van Emde
    Engel, Jerome
    French, Jacqueline
    Glauser, Tracy A.
    Mathern, Gary W.
    Moshe, Solomon L.
    Nordli, Douglas
    Plouin, Perrine
    Scheffer, Ingrid E.
    [J]. EPILEPSIA, 2010, 51 (04) : 676 - 685
  • [8] Clinical pharmacology and mechanism of action of zonisamide
    Biton, Victor
    [J]. CLINICAL NEUROPHARMACOLOGY, 2007, 30 (04) : 230 - 240
  • [9] Comparison of levetiracetam and controlled-release carbamazepine in newly diagnosed epilepsy
    Brodie, M. J.
    Perucca, E.
    Ryvlin, P.
    Ben-Menachem, E.
    Meencke, H. -J.
    [J]. NEUROLOGY, 2007, 68 (06) : 402 - 408
  • [10] Zonisamide: its pharmacology, efficacy and safety in clinical trials
    Brodie, M. J.
    Ben-Menachem, E.
    Chouette, I.
    Giorgi, L.
    [J]. ACTA NEUROLOGICA SCANDINAVICA, 2012, 126 : 19 - 28