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

第3相 実施中(募集終了) NCT03975647

対象疾患HER2-positive Breast Cancer
第3相
スポンサーSeagen, a wholly owned subsidiary of Pfizer
ステータス実施中(募集終了)
参加者数466 名
介入(薬剤)tucatinib, T-DM1
開始日2019年10月2日
完了日2023年6月29日
結果公開日2024年7月30日

概要

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)

BENITIONS で見る ClinicalTrials.gov の原文を見る

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