BENITIONSClinical Trial Intelligence

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

第3相 完了 NCT05899816

対象疾患Atopic Dermatitis, Moderate-to-severe Atopic Dermatitis
第3相
スポンサーAmgen
ステータス完了
参加者数221 名
介入(薬剤)Rocatinlimab
開始日2023年6月7日
完了日2024年8月26日
結果公開日2026年7月23日

概要

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)

BENITIONS で見る ClinicalTrials.gov の原文を見る

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このページは ClinicalTrials.gov の公開データをまとめたものです。医学的助言ではなく、投資助言でもありません。必ず専門医にご相談ください。