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Sumatriptan iontophoretic transdermal system: A review of its use in patients with acute migraine

机译:Sumatriptan离子电渗疗法透皮系统:在急性偏头痛患者中的应用综述

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摘要

The sumatriptan iontophoretic transdermal system (ZECUITY?) [hereafter referred to as sumatriptan TDS] is the first transdermal treatment for migraine to be approved by the US FDA. This article reviews the available pharmacologic properties of sumatriptan TDS and its clinical efficacy and tolerability for the acute treatment of adult patients with migraine with or without aura. Sumatriptan, a selective 5-hydroxy-tryptamine receptor subtype 1 (5-HT 1) agonist, is presumed to exert its therapeutic effect on migraine patients by binding to the 5-HT1B/1D receptors on intracranial blood vessels and sensory nerves of the trigeminal system, resulting in cranial vessel constriction and the inhibition of the release of pro-inflammatory neuropeptides and plasma extravasation. In a well designed, phase III clinical trial, sumatriptan TDS was shown to be more effective than placebo at treating a single migraine attack, with significantly more sumatriptan TDS than placebo recipients being headache pain free and nausea free at 2 hours. These data were supported by a long-term, repeat-use study over 12 months. Additionally, sumatriptan TDS was generally well tolerated in clinical trials; the most common adverse events were application-site reactions. The sumatriptan TDS formulation avoids the gastrointestinal tract, and has a controlled, sustained delivery, allowing for patients with migraine-associated nausea and vomiting to receive treatment without the risk of inconsistent absorption or avoidance of tablet use (associated with oral delivery of the drug in these patients). Moreover, it may offer a useful alternative to the nasal spray or subcutaneous sumatriptan formulations. However, definitive conclusions on the comparative efficacy and tolerability of sumatriptan TDS versus other sumatriptan formulations or other migraine drugs are not as yet possible, and data from comparative trials would be of great interest. Sumatriptan TDS is a useful addition to the treatment options available to migraine patients.
机译:舒马曲坦离子电渗透皮系统(ZECUITY?)[以下简称舒马普坦TDS]是美国FDA批准的首个偏头痛透皮治疗方法。本文综述了舒马普坦TDS的可用药理特性及其对急性偏头痛伴或不伴有先兆的成年患者进行急性治疗的临床疗效和耐受性。 Sumatriptan是一种选择性的5-羟色胺受体1亚型(5-HT 1)激动剂,被认为通过结合颅内血管和三叉神经的感觉神经上的5-HT1B / 1D受体对偏头痛患者发挥治疗作用。系统,导致颅骨血管收缩,抑制促炎性神经肽释放和血浆外渗。在一项精心设计的III期临床试验中,舒马普坦TDS在治疗单发偏头痛方面显示出比安慰剂更有效,舒马普坦TDS比安慰剂接受者在2小时内无头痛,无恶心的情况明显多。这些数据得到了为期12个月的长期重复使用研究的支持。此外,舒马曲坦TDS在临床试验中通常被很好地耐受。最常见的不良事件是应用现场反应。舒马普坦TDS制剂可避免胃肠道,并具有可控的持续分娩功能,使偏头痛相关的恶心和呕吐患者可以接受治疗,而不会出现吸收不一致或避免使用片剂的风险(与口服口服药物有关)这些患者)。而且,它可以提供鼻喷雾剂或皮下舒马普坦制剂的有用替代品。然而,关于舒马普坦TDS与其他舒马普坦制剂或其他偏头痛药物的比较功效和耐受性的确切结论尚不明确,来自比较试验的数据将引起极大关注。 Sumatriptan TDS是可用于偏头痛患者的治疗选择的有用补充。

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