BENITIONSClinical Trial Intelligence

A Study of Tucatinib vs. Placebo in Combination With Ado-trastuzumab Emtansine (T-DM1) for Patients With Advanced or Metastatic HER2+ Breast Cancer

3期 进行中(已停止招募) NCT03975647

适应症HER2-positive Breast Cancer
分期3期
申办方Seagen, a wholly owned subsidiary of Pfizer
状态进行中(已停止招募)
受试者人数466 人
干预(药物)tucatinib, T-DM1
开始日期2019年10月2日
完成日期2023年6月29日
结果公布日2024年7月30日

摘要

This study is being done to see if tucatinib with ado-trastuzumab emtansine (T-DM1) works better than T-DM1 alone to help patients who have a specific type of breast cancer called HER2 positive breast carcinoma. The breast cancer in this study is either metastatic (spread into other parts of the body) or cannot be removed completely with surgery. Patients in this study will be randomly assigned to get either tucatinib or placebo (a pill with no medicine). This is a blinded study, so neither patients nor their doctors will know whether a patient gets tucatinib or placebo. All patients in the study will get T-DM1, a drug that is often used to treat this cancer. Each treatment cycle lasts 21 days. Patients will swallow tucatinib pills or placebo pills two times every day. Patients will get T-DM1 injections from the study site staff on the first day of every cycle.

Progression-Free Survival (PFS) as Per Response Evaluation Criteria in Solid Tumors (RECIST) Version (v)1.1 Based on Investigator Assessment

From the date of randomization to the date of PD or death from any cause or censoring date, whichever occurred first (maximum up to 43 months) · Months

Tucatinib+ Ado-trastuzumab Emtansine9.5 Months
Placebo+ Ado-trastuzumab Emtansine7.4 Months
p-value0.0163
Hazard Ratio (HR)0.759 (95% CI 0.607–0.950)

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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。