BENITIONSClinical Trial Intelligence

A Study Assessing Rocatinlimab on Vaccine Antibody Response in Moderate-to-severe Atopic Dermatitis (AD) (ROCKET - VOYAGER)

3期 已完成 NCT05899816

适应症Atopic Dermatitis, Moderate-to-severe Atopic Dermatitis
分期3期
申办方Amgen
状态已完成
受试者人数221 人
干预(药物)Rocatinlimab
开始日期2023年6月7日
完成日期2024年8月26日
结果公布日2026年7月23日

摘要

The primary objectives of this study are to: * estimate vaccine response in rocatinlimab group vs placebo group, assessed using antibody anti-tetanus response at Week 24 * estimate vaccine response in rocatinlimab group vs placebo group, assessed using antibody anti-meningococcal response at Week 24

Percentage of Participants With a Positive Anti-tetanus Response at Week 24

Week 20 to Week 24 · percentage of participants

Placebo92.3 percentage of participants
Rocatinlimab87.6 percentage of participants
Risk Difference (RD)-4.7 (95% CI -13.5–5.9)

Percentage of Participants With a Positive Anti-meningococcal Response at Week 24

Week 20 to Week 24 · percentage of participants

Placebo53.2 percentage of participants
Rocatinlimab52.5 percentage of participants
Risk Difference (RD)-0.7 (95% CI -18.3–17.1)

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。