BENITIONSClinical Trial Intelligence

A Study to Evaluate the Efficacy and Safety of Bimekizumab in the Treatment of Subjects With Active Psoriatic Arthritis

3期 已完成 NCT03896581

适应症Psoriatic Arthritis
分期3期
申办方UCB Biopharma SRL
状态已完成
受试者人数400 人
干预(药物)Bimekizumab
开始日期2019年3月28日
完成日期2021年12月8日
结果公布日2024年10月16日

摘要

This is a study to demonstrate the clinical efficacy, safety and tolerability of bimekizumab administered subcutaneously (sc) compared with placebo in the treatment of tumor necrosis factor alpha-inadequate responders (TNFα-IR) subjects with active Psoriatic Arthritis (PsA).

Percentage of Participants With American College of Rheumatology 50 (ACR50) Response

From Baseline to Week 16 · percentage of participants

Placebo6.8 percentage of participants
Bimekizumab 160mg43.4 percentage of participants
p-value<0.001
Odds Ratio (OR)11.139 (95% CI 5.402–22.969)

在 BENITIONS 中查看 查看 ClinicalTrials.gov 原文

同一适应症的其他试验

全部试验

本页整理自 ClinicalTrials.gov 的公开数据,不构成医疗建议,也不构成投资建议。请务必咨询专业医师。