ACTIVE_NOT_RECRUITING • Phasen III • Stufe III, IV • HER2 negativ • Medical Oncology • Post-Menopausal • Brain Metastases present • Interventionell
Folgendes wird aus ClinicalTrials.gov importiert:
The study will evaluate the safety and efficacy of datopotamab deruxtecan (also known as Dato-DXd, DS-1062a), when compared with Investigator's choice of standard of care single-agent chemotherapy (eribulin, capecitabine, vinorelbine, or gemcitabine) in participants with inoperable or metastatic HR-positive, HER2- negative breast cancer who have been treated with one or two prior lines of systemic chemotherapy.
The primary objective of this study will assess the safety and efficacy of datopotamab deruxtecan (Dato-DXd) in participants with inoperable or metastatic HR-positive, HER2-negative breast cancer who have been treated with one or two prior lines of systemic chemotherapy. The study will be stratified based on number of previous lines of chemotherapy (1 vs. 2), prior use of CDK4/6 inhibitors (Yes vs. no) and geographic region of participant (US/Canada/Europe vs. rest of world). This study aims to see if datopotamab deruxtecan allows patients to live longer without their breast cancer getting worse, or simply to live longer, compared to patients receiving standard of care chemotherapy. This study is also looking to see how the treatment and the breast cancer affects patients' quality of life.
Breast Cancer
INTERVENTIONAL
732 Teilnehmer
18. Oktober 2021
18 - 999
both
Dato-DXd
Capecitabine
Gemcitabine
Eribulin
Vinorelbine
ACTIVE_NOT_RECRUITING
732
11/23/2024
AstraZeneca
Los Angeles, California, United States
Boston, Massachusetts, United States
Chuo-ku, Japan
New York, New York, United States
Portland, Oregon, United States
Seoul, Korea, Republic of
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