Efficacy of gabapentin as adjunctive therapy in a large, multicenter study

The objective of this study was to determine the efficacy of gabapentin as adjunctive therapy in doses required to achieve the most effective seizure control. There were 2016 patients with partial seizures requiring adjunctive therapy who received gabapentin at doses up to 3600 mg/day in this open-label, multicenter, 16-week study. Of the 1055 patients evaluable for efficacy, 573 received gabapentin < or =1800 mg/day and 482 received > 1800 mg/day as the highest dose received. For the overall efficacy evaluable population, the percentage of patients achieving at least a 50% reduction in seizure frequency was 76.0%; 46.4% of the patients were seizure free. Patients whose highest gabapentin dose did not require > 1800 mg/day had, at baseline, fewer seizures and were receiving fewer concomitant antiepileptic drugs (AEDs) at baseline than those patients requiring > 1800 mg/day. This suggests that patients requiring higher doses of gabapentin were more refractory to drug treatment at the start of the study. Gabapentin was well tolerated at all doses in this study. The results of the study demonstrate that gabapentin is effective as adjunctive therapy in patients with partial seizures whose seizures are inadequately controlled by traditional AEDs.

[1]  R. Ramsay,et al.  Gabapentin as add-on therapy in refractory partial epilepsy: a double-blind, placebo-controlled, parallel-group study. 1993. , 2001, Neurology.

[2]  G. Holmes,et al.  Safety and Tolerability of Gabapentin as Adjunctive Therapy in a Large, Multicenter Study , 1999, Epilepsia.

[3]  J. Liporace,et al.  New antiepileptic drugs. Overcoming the limitations of traditional therapy. , 1997, Postgraduate medicine.

[4]  C. Bazil,et al.  Recent advances in the pharmacotherapy of epilepsy. , 1997, Clinical therapeutics.

[5]  A. Marson,et al.  New antiepileptic drugs: a systematic review of their efficacy and tolerability , 1996, BMJ.

[6]  M. Brodie,et al.  New antiepileptic drugs , 1996, The New England journal of medicine.

[7]  A. Johnson,et al.  Controlling genital chlamydial infection , 1996, BMJ.

[8]  E. Perucca,et al.  The new generation of antiepileptic drugs: advantages and disadvantages. , 1996, British journal of clinical pharmacology.

[9]  J. French Clinical Efficacy of New Antiepileptic Drugs in Refractory Partial Epilepsy: Experience in the United States With Three Novel Drugs , 1996, Epilepsia.

[10]  B. Wilder How About the New Antiepileptic Drugs? , 1994, Canadian Journal of Neurological Sciences / Journal Canadien des Sciences Neurologiques.

[11]  T. Feuerstein,et al.  Gabapentin (Neurontin) as Add‐on Therapy in Patients with Partial Seizures: A Double‐Blind, Placebo‐Controlled Study , 1994, Epilepsia.

[12]  K. Goa,et al.  Gabapentin. A review of its pharmacological properties and clinical potential in epilepsy. , 1993, Drugs.

[13]  G. Woodruff,et al.  Localization of [3H]gabapentin to a novel site in rat brain: autoradiographic studies. , 1993, European journal of pharmacology.

[14]  G. Woodruff,et al.  Characterisation of [3H]gabapentin binding to a novel site in rat brain: homogenate binding studies. , 1993, European journal of pharmacology.

[15]  R. Mattson Drug treatment of partial epilepsy. , 1992, Advances in neurology.

[16]  Uk National Case-Control Study Group Gabapentin in partial epilepsy , 1990, The Lancet.

[17]  D. Chadwick Gabapentin in partial epilepsy , 1990 .

[18]  E. U. Kölle,et al.  Pharmacokinetics and metabolism of gabapentin in rat, dog and man. , 1986, Arzneimittel-Forschung.

[19]  Proposal for Classification of Epilepsies and Epileptic Syndromes , 1985, Epilepsia.