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DS-8201a in Pre-treated HER2 Breast Cancer That Cannot be Surgically Removed or Has Spread [DESTINY-Breast02]

Completed · Phase 3 · NCT03523585

Conditions: Breast Cancer

At a glance

Research payments reported, 2025
$213,932
U.S. investigators named
20
Sites paid
18
Planned or actual enrollment
608

About the trial

Sponsor
Daiichi Sankyo (with Daiichi Sankyo Co., Ltd., AstraZeneca)
Tested
Trastuzumab deruxtecan (drug), Capecitabine (drug), Lapatinib (drug), Trastuzumab (drug)
Dates
Started 2018-08-01; completion 2025-12-23
Results posted
Yes

This study will compare DS 8201a to standard treatment. Participants must have HER2 breast cancer that has been treated before. Their cancer: * cannot be removed by an operation * has spread to other parts of the body

From ClinicalTrials.gov, last updated 2026-02-27. Full record, eligibility and contacts (opens in a new tab)

Industry funding

Daiichi Sankyo Inc. reported $213,932 in research payments for this study in 2025 (117 payments).

Products named: Enhertu

Research payments usually go to hospitals, universities and research sites to run a study, not to the investigators personally. A payment is not evidence of wrongdoing.

U.S. investigators named on this study

Clinicians the company named as principal investigators in its Open Payments reports.

Sites paid to run it

Sources: CMS Open Payments research payments (program year 2025) and ClinicalTrials.gov, U.S. National Library of Medicine.