BENITIONSClinical Trial Intelligence

Long-Term Study (AtDvance) to Evaluate GSK1070806 in Atopic Dermatitis.

2期 提前终止 NCT06447506

适应症Dermatitis, Atopic
分期2期
申办方GlaxoSmithKline
状态提前终止
受试者人数79 人
干预(药物)GSK1070806
开始日期2024年6月5日
完成日期2025年7月29日
结果公布日2026年6月16日

摘要

The study is designed to evaluate the long-term safety and efficacy of GSK1070806 in participants with moderate-to severe atopic dermatitis, who have completed phase 2b parent GSK atopic dermatitis (AtD) study (NCT05999799).

Number of Participants With Treatment Emergent Adverse Events (TEAEs)

Up to Week 59 · Participants

Placebo/Placebo1 Participants
Placebo/GSK1070806 Dose Level 411 Participants
GSK1070806 Dose Level 1/GSK1070806 Dose Level 10 Participants
GSK1070806 Dose Level 1/GSK1070806 Dose Level 46 Participants
GSK1070806 Dose Level 2/GSK1070806 Dose Level 23 Participants
GSK1070806 Dose Level 2/GSK1070806 Dose Level 44 Participants

Number of Participants With TEAEs Leading to Permanent Discontinuation

Up to Week 59 · Participants

Placebo/Placebo1 Participants
Placebo/GSK1070806 Dose Level 40 Participants
GSK1070806 Dose Level 1/GSK1070806 Dose Level 10 Participants
GSK1070806 Dose Level 1/GSK1070806 Dose Level 40 Participants
GSK1070806 Dose Level 2/GSK1070806 Dose Level 20 Participants
GSK1070806 Dose Level 2/GSK1070806 Dose Level 40 Participants

Number of Participants With Serious Adverse Events (SAEs)

Up to Week 59 · Participants

Placebo/Placebo1 Participants
Placebo/GSK1070806 Dose Level 40 Participants
GSK1070806 Dose Level 1/GSK1070806 Dose Level 10 Participants
GSK1070806 Dose Level 1/GSK1070806 Dose Level 41 Participants
GSK1070806 Dose Level 2/GSK1070806 Dose Level 20 Participants
GSK1070806 Dose Level 2/GSK1070806 Dose Level 40 Participants

在 BENITIONS 中查看 查看 ClinicalTrials.gov 原文

同一适应症的其他试验

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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。