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Zonisamide: its pharmacology, efficacy and safety in clinical trials

Brodie, M. J. (author)
Ben-Menachem, Elinor, 1945 (author)
Gothenburg University,Göteborgs universitet,Institutionen för neurovetenskap och fysiologi, sektionen för klinisk neurovetenskap och rehabilitering,Institute of Neuroscience and Physiology, Department of Clinical Neuroscience and Rehabilitation
Chouette, I. (author)
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Giorgi, L. (author)
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 (creator_code:org_t)
2012-10-29
2012
English.
In: Acta Neurologica Scandinavica. - : Hindawi Limited. - 0001-6314. ; 126:SI, s. 19-28
  • Journal article (peer-reviewed)
Abstract Subject headings
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  • Zonisamide is a benzisoxazole derivative, chemically unrelated to other antiepileptic drugs, that appears to have multiple mechanisms of action, including inhibition of Na+ channels and reduction of T-type Ca2+ currents. It is currently licensed in Europe and the USA for adjunctive treatment of partial seizures in adults, and in Europe as monotherapy for treatment of partial seizures in adults with newly diagnosed epilepsy. Zonisamide displays predictable, dose-dependent pharmacokinetics and has a half-life of similar to 60 h, allowing once- or twice-daily administration. It has a low potential for interactions with other medications, including oral contraceptives. The clinical efficacy of adjunctive zonisamide therapy has been established in four pivotal, phase III, randomized, double-blind, placebo-controlled trials, which together included approximately 850 patients, aged 12-77 years, with refractory partial epilepsy. In all four trials, zonisamide 300-600 mg/day resulted in significant reductions in median total seizure rates vs placebo, and zonisamide was generally well tolerated; the most frequently reported adverse events being somnolence, dizziness and anorexia/weight loss. Subanalysis of the primary European trial indicated that zonisamide was effective when administered as first-line adjunctive treatment, and a long-term extension to the same trial demonstrated that the efficacy and safety/tolerability of adjunctive zonisamide was sustained for up to 36 months. Once-daily monotherapy with zonisamide (200-500 mg/day) has been shown to be non-inferior to, and as well tolerated as, twice-daily monotherapy with controlled-release carbamazepine (400-1200 mg/day) in adults with newly diagnosed partial epilepsy. Zonisamide has also been shown to have favourable long-term retention rates, an important indication of its overall effectiveness.

Subject headings

MEDICIN OCH HÄLSOVETENSKAP  -- Medicinska och farmaceutiska grundvetenskaper -- Neurovetenskaper (hsv//swe)
MEDICAL AND HEALTH SCIENCES  -- Basic Medicine -- Neurosciences (hsv//eng)

Keyword

antiepileptic drug
clinical trial
efficacy
epilepsy
pharmacokinetics
pharmacology
tolerability
refractory partial seizures
3-substituted 1
2-benzisoxazole
derivatives
steady-state pharmacokinetics
partial epilepsy
double-blind
antiepileptic drugs
anticonvulsant drug
adjunctive
therapy
calcium-channel
in-vitro
kano k
1995
epilepsia
v36
p644

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ref (subject category)
art (subject category)

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Brodie, M. J.
Ben-Menachem, El ...
Chouette, I.
Giorgi, L.
About the subject
MEDICAL AND HEALTH SCIENCES
MEDICAL AND HEAL ...
and Basic Medicine
and Neurosciences
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Acta Neurologica ...
By the university
University of Gothenburg

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