BENITIONSClinical Trial Intelligence

A Study of U3-1402 (Patritumab Deruxtecan) in Subjects With Metastatic Breast Cancer

2期 已完成 NCT04699630

适应症Metastatic Breast Cancer, Locally Advanced Breast Cancer
分期2期
申办方SCRI Development Innovations, LLC
状态已完成
受试者人数121 人
干预(药物)U3-1402
开始日期2021年5月3日
完成日期2025年4月9日
结果公布日2026年5月7日

摘要

This study is to evaluate safety and efficacy of an antibody drug conjugate U3-1402 (patritumab deruxtecan) in patients with locally advanced or metastatic breast cancer (MBC).

Overall Response Rate (ORR) in Participants With HER2-negative MBC (Part A and Part B)

Assessed every 6 weeks for the first 6 months then every 9 weeks thereafter until disease progression or death or study discontinuation, up to 45 months. · percentage of participants

Part A35 percentage of participants
Part B5 percentage of participants

Progression-Free Survival at 6 Months (PFS-6) in Participants With HER2-negative MBC (Part A and Part B)

Assessed every 6 weeks for the first 6 months then every 9 weeks thereafter until disease progression or death or study discontinuation, up to 45 months. · percentage of participants

Part A43.3 percentage of participants
Part B10.0 percentage of participants

在 BENITIONS 中查看 查看 ClinicalTrials.gov 原文

全部试验

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。