Department of Pharmacology, Burdwan Medical College, Kolkata, West Bengal, India.
Department of Neonatology, AMRI Hospital, Kolkata, West Bengal, India.
Neurol India. 2021 Nov-Dec;69(6):1759-1762. doi: 10.4103/0028-3886.333495.
Migraine is characterized by severe, intermittent headache attacks with associated symptoms including nausea, vomiting, phonophobia, and photophobia. Still Triptans (selective 5-HT agonists) are considered as the first-line therapy in acute attack of migraine. Recently two new drugs Lasmiditan and Ubrogepant were approved by United States Food and Drug Administration in acute attack of migraine with or without aura in adults. Lasmiditan is a highly selective 5-HT receptor agonist which demonstrated superiority to placebo in the acute treatment of migraine in adults with moderate/severe migraine disability in two similarly designed phase-3 trials, SAMURAI and SPARTAN. Ubrogepant is a novel small molecule oral calcitonin gene-related peptide receptor antagonist. The approval was supported by two pivotal phase-3, randomized, double-blind, placebo-controlled trials (ACHIEVE I and ACHIEVE II) that evaluated the efficacy, safety, tolerability. Hopefully, these two drugs may soon be a new addition to the mounting armory of drugs against migraine and may fulfill a substantial unmet need.
偏头痛的特征是严重的、间歇性的头痛发作,并伴有相关症状,包括恶心、呕吐、恐声和畏光。曲坦类药物(选择性 5-HT 激动剂)仍被认为是偏头痛急性发作的一线治疗药物。最近,两种新药物拉米地坦和ubrogepant 被美国食品和药物管理局批准用于成人偏头痛急性发作,无论有无先兆。拉米地坦是一种高度选择性的 5-HT 受体激动剂,在两项设计相似的 III 期临床试验(SAMURAI 和 SPARTAN)中,与安慰剂相比,在有中度/重度偏头痛残疾的成人偏头痛急性治疗中表现出优势。Ubrogepant 是一种新型小分子口服降钙素基因相关肽受体拮抗剂。这一批准得到了两项关键的 III 期、随机、双盲、安慰剂对照试验(ACHIEVE I 和 ACHIEVE II)的支持,这些试验评估了疗效、安全性和耐受性。希望这两种药物很快成为对抗偏头痛的新武器,并满足大量未满足的需求。