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 질환 | HER2-positive Breast Cancer |
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| 임상 단계 | 3상 |
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| 스폰서 | Seagen, a wholly owned subsidiary of Pfizer |
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| 상태 | 진행 중(모집 완료) |
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| 참여자 수 | 466 명 |
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| 중재(약물) | tucatinib, T-DM1 |
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| 시작일 | 2019년 10월 2일 |
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| 완료일 | 2023년 6월 29일 |
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| 결과 공개일 | 2024년 7월 30일 |
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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 Emtansine | 9.5 Months |
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| Placebo+ Ado-trastuzumab Emtansine | 7.4 Months |
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| p-value | 0.0163 |
| Hazard Ratio (HR) | 0.759 (95% CI 0.607–0.950) |
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