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HER-TEMPO - Real World Treatment-related Outcomes on T-DXd in Canada
Sponsor: AstraZeneca
Summary
Trastuzumab deruxtecan (T-DXd) has been studied in multiple global prospective DESTINY-Breast trials and has a marketing authorization from Health Canada for patients with HER2-positive metastatic breast cancer (mBC) and HER2-low mBC, respectively. Multiple stakeholders, including clinicians, patients, regulators, and healthcare decision makers, are interested in real-world treatment-related outcomes in order to better represent the effectiveness of therapies in routine care settings.
Official title: Real World Study of TrEatment Discontinuations and Modifications for Patients With HER2+ and HER2-low Metastatic Breast Cancer On Trastuzumab Deruxtecan
Key Details
Gender
All
Age Range
18 Years - 130 Years
Study Type
OBSERVATIONAL
Enrollment
22
Start Date
2024-04-22
Completion Date
2025-07-07
Last Updated
2026-07-08
Healthy Volunteers
No
Conditions
Interventions
Trastuzumab deruxtecan
This is a non-interventional, observational study. Patients who are enrolled by their clinician will receive T-DXd per routine clinical practice through the PSP.
Locations (1)
Research Site
Oakville, Ontario, Canada