Pledger G W, Laxer K D, Sahlroot J T, Taylor M R, Cereghino J J, McCormick C, Whitley L, Manning L W
Epilepsy Branch, National Institute of Neurological Disorders and Stroke, National Institutes of Health, Bethesda, Maryland 20892.
Epilepsia. 1992 Jan-Feb;33(1):112-8. doi: 10.1111/j.1528-1157.1992.tb02292.x.
ADD 94057, a metabolite of fluzinamide, manufactured by the A. H. Robins Company, blocks chemically- and electrically-induced seizures in animals. The primary objective of this open add-on study was to evaluate patient tolerability of ADD 94057 at ascending target plasma concentrations. Nine subjects with medically refractory seizures were receiving phenytoin (PHT, 3), carbamazepine (CBZ, 3), or both (3). A pharmacokinetic profile after a single oral 400-mg dose of ADD 94057 was used to calculate ADD 94057 dosages. After a 4-week baseline period, patients were treated for 4 weeks with weekly ADD 94057 dosage escalations. Two patients completed the study at their assigned highest dosage level; the other patients finished the study at lower dosages. The patients receiving PHT (but not CBZ) tolerated higher plasma concentrations of ADD 94057 than did patients receiving CBZ, alone or in combination with PHT. Adverse experiences included headache, ataxia, blurred vision, diplopia, dizziness, lightheadedness, and mild confusion. Eight of nine patients had reductions in seizure frequency from baseline.
氟酰胺的代谢产物ADD 94057由A. H. 罗宾斯公司生产,可阻断动物体内化学诱导和电诱导的癫痫发作。这项开放性附加研究的主要目的是评估在目标血浆浓度上升时患者对ADD 94057的耐受性。九名药物难治性癫痫患者正在接受苯妥英(PHT,3例)、卡马西平(CBZ,3例)或两者联合治疗(3例)。单次口服400毫克ADD 94057后的药代动力学特征用于计算ADD 94057的剂量。经过4周的基线期后,患者接受为期4周的治疗,每周增加ADD 94057的剂量。两名患者在指定的最高剂量水平完成了研究;其他患者在较低剂量时完成了研究。接受PHT(而非CBZ)治疗的患者比单独接受CBZ或同时接受PHT和CBZ治疗的患者能耐受更高血浆浓度的ADD 94057。不良事件包括头痛、共济失调、视力模糊、复视、头晕、头昏和轻度意识模糊。九名患者中有八名癫痫发作频率较基线有所降低。