Goldstein J, Dahlöf C G, Diener H C, Olesen J, Schellens R, Senard J M, Simard D, Steiner T J
Cephalalgia. 1996 Nov;16(7):497-502. doi: 10.1046/j.1468-2982.1996.1607497.x.
Alniditan is a new 5HT1D receptor agonist, belonging to a different chemical class from sumatriptan and other indole derivatives used or being developed for the treatment of acute migraine. In a multinational double-blind randomized parallel-groups dose-finding trial, alniditan was given subcutaneously in hospital to patients with migraine headache of moderate or severe intensity at doses of 0.8 mg (n = 44), 1.0 mg (n = 42), 1.2 mg (n = 46) and 1.4 mg (n = 39). Efficacy, tolerability and safety of each dose were compared with those of placebo (n = 41). At 2 h after injection, headache was absent or mild in 83% and 82% of patients receiving alniditan 1.2 and 1.4 mg respectively compared with 39% for placebo (p < or = 0.002). Complete relief from headache was achieved in 72% (1.4 mg). Time to onset of relief decreased with increasing alniditan dose, and there was a dose-dependent reduction in headache recurrence rate: 25% of patients receiving 1.4 mg had responded by 15 min and headache recurred within 24 h in only 16% of the patients who initially responded to alniditan 1.4 mg, significantly less than for placebo (p = 0.018). Alniditan was superior to placebo in reducing the associated symptoms of nausea, phonophobia and photophobia, and in increasing patients' functional ability. The use of rescue medication was reduced when compared with placebo, and up to 87% of patients said that they would use the drug again if available. No clinically relevant cardiovascular effects were seen, nor consistent changes in clinical laboratory findings. Adverse effects, mainly head pressure, paraesthesia, and hot flushes, were reported by 34% of placebo-treated patients and up to 70% of patients receiving alniditan, but all doses were very well tolerated and no clear relationship with dose was established. Comparison with published findings suggests that alniditan 1.4 mg sc may have advantages over sumatriptan 6 mg sc in providing complete relief from acute migraine headache, and may be associated with fewer headache recurrences within 24 h. Both of these suggestions warrant further and larger trials of alniditan in acute migraine.
阿尼西坦是一种新型5HT1D受体激动剂,与舒马曲坦以及其他已用于或正在研发用于治疗急性偏头痛的吲哚衍生物属于不同的化学类别。在一项跨国双盲随机平行组剂量探索试验中,在医院对中重度偏头痛患者皮下注射阿尼西坦,剂量分别为0.8毫克(n = 44)、1.0毫克(n = 42)、1.2毫克(n = 46)和1.4毫克(n = 39)。将各剂量的疗效、耐受性和安全性与安慰剂(n = 41)进行比较。注射后2小时,接受1.2毫克和1.4毫克阿尼西坦的患者中分别有83%和82%的患者头痛消失或减轻,而安慰剂组为39%(p≤0.002)。1.4毫克剂量组有72%的患者头痛完全缓解。缓解开始时间随阿尼西坦剂量增加而缩短,头痛复发率呈剂量依赖性降低:接受1.4毫克剂量的患者中有