DESTINY-Breast07 will investigate the safety, tolerability, and anti-tumour activity of
trastuzumab deruxtecan (T-DXd) in combination with other anti-cancer agents in patients
with HER2-positive Metastatic Breast Cancer
Additional locations may be listed on ClinicalTrials.gov for NCT04538742.
See trial information on ClinicalTrials.gov for a list of participating sites.
This study is modular in design allowing assessment of safety, tolerability and
anti-tumour activity of T-DXd in combination with other anti-cancer agents.
Combination-treatment modules will have 2 parts: a dose-finding phase (Part 1), and a
dose expansion phase (Part 2); the recommended Phase 2 dose (RP2D) determined in Part 1
will be used for the dose-expansion in Part 2.
The target population of interest in this study is patients with HER2-positive (as per
ASCO/CAP 2018 guidelines) advanced/MBC inclusive of patients with active and stable brain
metastases. Part 1 of each module will enroll patients with locally assessed
HER2-positive advanced/MBC in second-line or later patients. Part 2 of each module will
enroll patients with locally assessed HER2-positive breast cancer who have not received
prior treatment for advanced/metastatic disease.
Lead OrganizationAstraZeneca Pharmaceuticals LP