BENITIONSClinical Trial Intelligence

A Study of Baricitinib in Participants With Rheumatoid Arthritis

4期 已完成 NCT04086745

适应症Rheumatoid Arthritis
分期4期
申办方Eli Lilly and Company
状态已完成
受试者人数1,050 人
干预(药物)Baricitinib, TNF Inhibitor
开始日期2020年2月14日
完成日期2025年5月19日
结果公布日2026年7月10日

摘要

This post-marketing study is designed to compare the safety of baricitinib versus tumor necrosis factor (TNF) inhibitors with respect to venous thromboembolic events (VTEs) when given to participants with rheumatoid arthritis (RA).

Pooled JAJA and JAJD: Time From First Dose of Study Treatment to First Event of Venous Thromboembolism (VTE) [Combined Baricitinib Dose Versus TNF Inhibitor]

From the first dose of study treatment up to 30 days after the last dose or the last study visit, whichever occurs first (approximately up to 6.1 years for JAJA and 5.3 years for JAJD participants) · Days

Baricitinib 2/4 mgNA Days
TNF InhibitorNA Days
Hazard Ratio (HR)1.606 (95% CI 0.969–2.660)

在 BENITIONS 中查看 查看 ClinicalTrials.gov 原文

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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。