Tansey M J, Pilgrim A J, Martin P M
Clinical and Regulatory Directorate, Glaxo Group Research Ltd., Greenford, Middlesex, UK.
Eur Neurol. 1993;33(4):310-5. doi: 10.1159/000116960.
Sumatriptan, a specific 5-hydroxytryptamine agonist, is a novel acute treatment for migraine. The efficacy and safety profiles of sumatriptan have previously been demonstrated in several controlled short-term studies. However, because migraine is a recurrent disorder which may persist throughout adult life, sustained efficacy and tolerability are essential if sumatriptan is to be of value in clinical practice. These aspects were therefore evaluated in a programme of three 12-month studies. Sustained efficacy with long-term use of single 100-mg oral doses has been demonstrated in an open study in which 288 patients treated 8,094 migraine attacks. The long-term safety profile of oral and subcutaneous sumatriptan has been evaluated in a total of 849 patients who treated 24,907 migraine attacks in studies lasting up to 1 year. Sumatriptan was well tolerated. Adverse events did not differ qualitatively or quantitatively from those in short-term studies, irrespective of the frequency of attacks or the number of doses used. Migraine attacks were effectively treated with doses less than the recommended maximum and there was no evidence of any adverse effect on attack frequency. In long-term studies the high efficacy of sumatriptan is maintained, and the adverse event profile is unchanged and unaffected by attack frequency.
舒马曲坦是一种特异性5-羟色胺激动剂,是偏头痛的一种新型急性治疗药物。舒马曲坦的疗效和安全性已在多项对照短期研究中得到证实。然而,由于偏头痛是一种复发性疾病,可能会持续整个成年期,因此如果舒马曲坦要在临床实践中有价值,持续的疗效和耐受性至关重要。因此,在一项由三项为期12个月的研究组成的计划中对这些方面进行了评估。在一项开放研究中,对288例患者治疗的8094次偏头痛发作进行了研究,结果表明长期使用单次100毫克口服剂量具有持续疗效。在总共849例患者中评估了口服和皮下注射舒马曲坦的长期安全性,这些患者在长达1年的研究中治疗了24907次偏头痛发作。舒马曲坦耐受性良好。无论发作频率或使用的剂量数量如何,不良事件在性质或数量上与短期研究中的不良事件没有差异。使用低于推荐最大剂量的药物有效地治疗了偏头痛发作,并且没有证据表明对发作频率有任何不良影响。在长期研究中,舒马曲坦的高效性得以维持,不良事件谱不变,且不受发作频率的影响。