BENITIONSClinical Trial Intelligence

A Single Arm Phase 2 Study to Evaluate Efficacy and Safety of Trastuzumab Deruxtecan for Patients With HER2 Mutant NSCLC

2期 进行中(已停止招募) NCT05246514

适应症HER2-mutant Non-Small Cell Lung Cancer
分期2期
申办方AstraZeneca
状态进行中(已停止招募)
受试者人数72 人
干预(药物)Trastuzumab deruxtecan
开始日期2022年7月13日
完成日期2024年11月4日
结果公布日2024年12月4日

摘要

The purpose of this study is to evaluate the efficacy and safety of T-DXd in participants with HER2 mutant metastatic non-squamous NSCLC.

ICR-assessed ORR (Objective Response Rate)

Tumour assessments (per RECIST 1.1) every 6 weeks for the first 48 weeks relative to the date of enrolment and then every 9 weeks thereafter. Assessed up to 28 months. (from date of enrolment to final analysis data cut-off) · Percentage of participants

T-DXd Arm56.9 Percentage of participants

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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。