Suppr超能文献

比美吉珠单抗自我注射装置:两项多中心、随机、开放标签研究,评估银屑病患者自我给药。

Bimekizumab Self-Injection Devices: Two Multicenter, Randomized, Open-Label Studies on Self-Administration by Patients With Psoriasis.

出版信息

J Drugs Dermatol. 2022 Feb 1;21(2):162-171. doi: 10.36849/jdd.6274.

Abstract

BACKGROUND

Bimekizumab is a monoclonal IgG1 antibody that selectively inhibits interleukin (IL)-17F in addition to IL-17A.

OBJECTIVES

To assess patients' ability to self-inject bimekizumab subcutaneously using a 1 mL safety syringe or auto-injector.

METHODS

DV0002 and DV0006 were sub-studies of BE BRIGHT, a multicenter, phase 3 open-label extension study. Patients with moderate to severe plaque psoriasis received bimekizumab 320 mg (2x160 mg injections) every 4 or 8 weeks and were randomized 1:1 to the safety syringe or the auto-injector. The ability of patients to safely and effectively self-inject bimekizumab was assessed at 8 weeks (primary endpoint) and immediately after self-injection training at Baseline (secondary endpoint). Patient experience was evaluated using the pain visual analog scale (VAS; 0–100 mm; 100 being worst pain), and the Self-Injection Assessment Questionnaire (SIAQ; 0–10; 10 being most positive experience).

RESULTS

All evaluable patients in DV0002 (n=125) and DV0006 (n=86) safely and effectively self-injected bimekizumab at Week 8. All evaluable patients in DV0002 who used the safety syringe (n=64) and 97.1% (n=66/68) who used the auto-injector, as well as all evaluable DV0006 patients (n=88) also self-injected bimekizumab safely and effectively at Baseline. Median VAS scores were low (range: 7.0–20.0), and median pre-injection and post-injection SIAQ scores were high (range: 5.8–10.0 and 7.1–10.0, respectively) across both devices, sub-studies, and timepoints.

CONCLUSIONS

Both devices provide a safe and effective option for patients to self-administer bimekizumab. Furthermore, patients reported a positive self-injection experience.

TRIAL REGISTRATION

NCT03766685 J Drugs Dermatol. 2022;21(2):162-171. doi:10.36849/JDD.6274THIS ARTICLE HAD BEEN MADE AVAILABLE FREE OF CHARGE. PLEASE SCROLL DOWN TO ACCESS THE FULL TEXT OF THIS ARTICLE WITHOUT LOGGING IN. NO PURCHASE NECESSARY. PLEASE CONTACT THE PUBLISHER WITH ANY QUESTIONS.

摘要

背景

比美吉珠单抗是一种单克隆 IgG1 抗体,除了抑制白细胞介素(IL)-17A 外,还能选择性抑制白细胞介素(IL)-17F。

目的

评估患者使用 1 毫升安全注射器或自动注射器皮下注射比美吉珠单抗的能力。

方法

DV0002 和 DV0006 是多中心、3 期开放标签扩展研究 BE BRIGHT 的子研究。中重度斑块状银屑病患者接受比美吉珠单抗 320mg(2x160mg 注射),每 4 或 8 周一次,并按 1:1 随机分配至安全注射器或自动注射器组。在第 8 周(主要终点)和基线时(次要终点)在自我注射培训后立即评估患者安全有效地自我注射比美吉珠单抗的能力。使用疼痛视觉模拟量表(VAS;0–100mm;100 为最痛)和自我注射评估问卷(SIAQ;0–10;10 为最佳体验)评估患者的体验。

结果

DV0002 中所有可评估的患者(n=125)和 DV0006 中所有可评估的患者(n=86)在第 8 周安全有效地自我注射了比美吉珠单抗。在 DV0002 中使用安全注射器的所有可评估患者(n=64)和 97.1%(n=66/68)使用自动注射器的患者,以及所有可评估的 DV0006 患者(n=88)在基线时也安全有效地自我注射了比美吉珠单抗。两种设备、两个子研究和各个时间点的中位 VAS 评分均较低(范围:7.0–20.0),中位预注射和注射后 SIAQ 评分均较高(范围:5.8–10.0 和 7.1–10.0)。

结论

两种设备都为患者自行给药提供了安全有效的选择。此外,患者报告了积极的自我注射体验。

试验注册

NCT03766685 J 皮肤病药物杂志。2022;21(2):162-171. doi:10.36849/JDD.6274 本文已免费提供。请向下滚动访问本文的全文,无需登录。无需购买。如有任何问题,请与出版商联系。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验