Spesolimab: A Review of the First IL-36 Blocker Approved for Generalized Pustular Psoriasis.

IF 2.3 4区 医学 Q3 PHARMACOLOGY & PHARMACY
Annals of Pharmacotherapy Pub Date : 2025-02-01 Epub Date: 2024-05-16 DOI:10.1177/10600280241252688
Gaurav N Pathak, Emily Wang, Jimmy Dhillon, Prachi N Parikh, Reem Esseghir, Babar K Rao, Steven R Feldman
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引用次数: 0

Abstract

Objective: This article reviews clinical trial data that assesses the safety, efficacy, and clinical application of spesolimab, an interleukin-36 (IL-36) blocker, for the treatment of generalized pustular psoriasis (GPP).

Data sources: A review of the literature was conducted using the search terms: "spesolimab," "BI 655130," and "spevigo" in MEDLINE (PubMed) and Clinicaltrials.gov from January 1, 1950 to October 31, 2023.

Study selection and data extraction: Relevant articles in English relating to the pharmacodynamics, pharmacokinetics, efficacy, and safety of spesolimab were included.

Data synthesis: In one phase 2 clinical trial evaluating single dose IV spesolimab for GPP flares at day 8, 54% of patients receiving spesolimab had a GPP physician global assessment (GPPGA) pustulation subscore of 0, and 43% had a GPPGA total score of 0 compared with 6% and 11% for the placebo group, respectively. Another phase 2 clinical trial assessing subcutaneous spesolimab found 23% of patients in low-dose, 29% in medium-dose, and 10% of high-dose spesolimab had flares by week 48 compared with 52% of the placebo group. Hazard ratios for time to GPP flare compared with placebo were 0.16 (P = 0.0005), 0.35 (P = 0.0057), and 0.47 (P = 0.027) for the spesolimab groups, respectively. Infection rates were similar across treatment and placebo groups, and severe adverse events such as drug reactions with eosinophilia and systemic symptom (DRESS), cholelithiasis, and breast cancer occurred with spesolimab.

Relevance to patient care and clinical practice in comparison to existing drugs: Spesolimab is a first-in-class IL-36 monoclonal antibody receptor antagonist approved for the treatment of acute GPP flares. It is a safe and effective therapeutic agent in preventing future GPP flares, with no current comparator trials with other GPP agents.

Conclusion: Spesolimab is a safe and effective treatment for acute GPP flares in adults. Future clinical trials can establish safety and efficacy compared with other agents.

Spesolimab:对首个获批用于泛发性脓疱型银屑病的 IL-36 阻断剂的回顾。
目的:本文回顾了评估白细胞介素-36(IL-36)阻断剂斯派索利单抗治疗泛发性脓疱型银屑病(GPP)的安全性、有效性和临床应用的临床试验数据:数据来源:使用以下检索词对文献进行了综述:数据来源:使用以下检索词对文献进行了综述:"spesolimab"、"BI 655130 "和 "spevigo",检索时间为1950年1月1日至2023年10月31日的MEDLINE(PubMed)和Clinicaltrials.gov:纳入与斯派索利单抗的药效学、药代动力学、疗效和安全性相关的英文文章:一项2期临床试验评估了单剂量静脉注射斯派索利单抗治疗GPP第8天复发的情况,其中54%接受斯派索利单抗治疗的患者的GPP医生总体评估(GPPGA)脓疱子评分为0,43%的患者GPPGA总评分为0,而安慰剂组分别为6%和11%。另一项评估皮下注射斯派索利单抗的 2 期临床试验发现,到第 48 周时,23% 的低剂量患者、29% 的中剂量患者和 10% 的高剂量患者出现复发,而安慰剂组的复发率为 52%。与安慰剂相比,斯派索利单抗组GPP复发时间的危险比分别为0.16(P = 0.0005)、0.35(P = 0.0057)和0.47(P = 0.027)。治疗组和安慰剂组的感染率相似,斯派索利单抗可引起嗜酸性粒细胞增多和全身症状(DRESS)、胆石症和乳腺癌等严重不良事件:斯派索利单抗是第一类IL-36单克隆抗体受体拮抗剂,已被批准用于治疗GPP急性发作。在预防未来 GPP 复发方面,它是一种安全有效的治疗药物,目前尚未与其他 GPP 药物进行比较试验:斯派索利单抗是治疗成人 GPP 急性发作的一种安全有效的药物。结论:斯佩索利单抗是治疗成人 GPP 急性复发的一种安全有效的药物,未来的临床试验可以确定其与其他药物相比的安全性和有效性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
5.70
自引率
0.00%
发文量
166
审稿时长
3-8 weeks
期刊介绍: Annals of Pharmacotherapy (AOP) is a peer-reviewed journal that advances pharmacotherapy throughout the world by publishing high-quality research and review articles to achieve the most desired health outcomes.The articles provide cutting-edge information about the most efficient, safe and cost-effective pharmacotherapy for the treatment and prevention of various illnesses. This journal is a member of the Committee on Publication Ethics (COPE). Average time from submission to first decision: 14 days
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