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

3상 진행 중(모집 완료) NCT03975647

대상 질환HER2-positive Breast Cancer
임상 단계3상
스폰서Seagen, a wholly owned subsidiary of Pfizer
상태진행 중(모집 완료)
참여자 수466 명
중재(약물)tucatinib, T-DM1
시작일2019년 10월 2일
완료일2023년 6월 29일
결과 공개일2024년 7월 30일

요약

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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