LY3451838是一种pacap中和单克隆抗体,在随机、双盲、安慰剂对照的1期和2期研究中进行临床前和临床评估,该研究涉及健康成人和治疗抵抗性偏头痛的成人。

IF 4.6 2区 医学 Q1 CLINICAL NEUROLOGY
Cephalalgia Pub Date : 2025-08-01 Epub Date: 2025-08-21 DOI:10.1177/03331024251368757
Michael P Johnson, Judith Krikke-Workel, Chetan N Patel, S Michelle Morin, P Kellie Turner, Kristie A Clark, David Donley, Yan Jin, Kirk W Johnson, Maurice Vincent, John R Stille, Lisa M Broad, Ashok Patel
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引用次数: 0

摘要

AimLY3451838是一种针对垂体腺苷酸环化酶激活肽(PACAP)的单克隆抗体,是偏头痛研究的靶点。本研究旨在评估LY3451838作为治疗难治性偏头痛参与者的预防性治疗。在对LY3451838进行临床前评估(包括药代动力学和药效学研究)后,在健康受试者中进行了LY3451838 (n = 33)与安慰剂(n = 13)的1期研究,以评估其安全性。一项2期试验在慢性偏头痛(CM) (n = 16)或发作性偏头痛(EM) (n = 22)的治疗抵抗参与者中进行。在第二阶段,参与者接受单次静脉(IV)剂量1500 mg LY3451838 (n = 19)或安慰剂(n = 19),并完成ePRO每日日记。为了安全起见,研究人员对参与者进行了140天的随访。结果在第2期,在给药后1个月,接受单次静脉注射LY3451838的患者在CM和EM亚组的平均每月偏头痛天数比基线变化更大(CM: -4.7天对-3.0天;EM: -1.7天对-1.2天),但两亚组的治疗对比均无统计学意义。在三个月时间点观察到类似的无显著性结果。报告LY3451838和安慰剂治疗后出现的不良事件的参与者百分比相似,在LY3451838治疗的参与者中出现了一次严重的b细胞淋巴瘤不良事件,导致研究终止。结论LY3451838在治疗难治性CM或EM患者中并没有表现出优于安慰剂的疗效。然而,LY3451838与安慰剂在CM患者中观察到的差异与最近主要由CM患者组成的HOPE试验中报道的统计学显著差异相似。进一步的临床研究需要更大的样本量,以了解阻断PACAP在不同偏头痛人群中的效用。临床试验注册网站:NCT03692949(一期);NCT04498910(第二阶段)。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Preclinical and clinical evaluation of LY3451838, a PACAP-neutralizing monoclonal antibody, in randomized, double-blind, placebo-controlled phase 1 and phase 2 studies involving healthy adults and adults with treatment-resistant migraine.

AimLY3451838 is a monoclonal antibody against pituitary adenylate cyclase-activating peptide (PACAP), a target in migraine research. The present study aimed to evaluate LY3451838 as a preventive treatment for participants with treatment-resistant migraine.MethodsFollowing preclinical assessment of LY3451838, including pharmacokinetic and pharmacodynamic studies, safety was evaluated in a phase 1 study of LY3451838 (n = 33) versus placebo (n = 13) in healthy participants. A phase 2 trial was carried out in treatment-resistant participants with chronic migraine (CM) (n = 16) or episodic migraine (EM) (n = 22). In phase 2, participants received a single intravenous (IV) dose of 1500 mg LY3451838 (n = 19) or placebo (n = 19) and completed ePRO daily diaries. Participants were followed for safety for 140 days.ResultsIn phase 2, at one-month post-dose, patients who had received a single IV dose of LY3451838 exhibited greater changes from baseline than placebo in mean monthly migraine headache days in both the CM and EM subgroups (CM: -4.7 days vs. -3.0 days; EM: -1.7 days vs. -1.2 days), but the treatment contrast was not statistically significant in either subgroup. Similar non-significant results were seen at the three-month time point. The percentage of participants reporting treatment-emergent adverse events was similar for LY3451838 and placebo, with one serious adverse event of B-cell lymphoma in an LY3451838-treated participant that led to study discontinuation.ConclusionsLY3451838 did not demonstrate superior efficacy over placebo in patients with treatment-resistant CM or EM. However, the difference observed between LY3451838 and placebo among CM patients is similar to the statistically significant difference reported in the recent HOPE trial, which primarily consisted of CM patients. Further clinical research with larger sample sizes is needed to inform on the utility of blocking PACAP in various migraine populations.Trial RegistrationClinicalTrials.gov: NCT03692949 (phase 1); NCT04498910 (phase 2).

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来源期刊
Cephalalgia
Cephalalgia 医学-临床神经学
CiteScore
10.10
自引率
6.10%
发文量
108
审稿时长
4-8 weeks
期刊介绍: Cephalalgia contains original peer reviewed papers on all aspects of headache. The journal provides an international forum for original research papers, review articles and short communications. Published monthly on behalf of the International Headache Society, Cephalalgia''s rapid review averages 5 ½ weeks from author submission to first decision.
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