BENITIONSClinical Trial Intelligence

Open-label Study of Belimumab Plus Standard Therapy in Chinese Pediatric Participants With Active Systemic Lupus Erythematosus (SLE)

4期 已完成 NCT04908865

适应症Systemic Lupus Erythematosus
分期4期
申办方GlaxoSmithKline
状态已完成
受试者人数67 人
干预(药物)Belimumab, Standard therapy
开始日期2021年10月21日
完成日期2024年5月23日
结果公布日2025年7月23日

摘要

This study will be conducted to evaluate the safety, efficacy and pharmacokinetics of belimumab administered in combination with background standard therapy in pediatric participants with active SLE.

Number of Participants With Adverse Events of Special Interest (AESIs) Through Week 52

Up to Week 52 · Participants

Belimumab0 Participants
Belimumab0 Participants
Belimumab2 Participants
Belimumab0 Participants

Number of Participants With Greater Than Equal to (>=) 4 Points Reduction From Baseline to Week 52 in Safety of Estrogen in Lupus National Assessment - Systemic Lupus Erythematosus Disease Activity Index (SELENA-SLEDAI) Score

Baseline (Day 0) and Week 52 · Participants

Belimumab44 Participants

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。