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DS-8201a Versus T-DM1 for Human Epidermal Growth Factor Receptor 2 (HER2)-Positive, Unresectable and/or Metastatic Breast Cancer Previously Treated With Trastuzumab and Taxane [DESTINY-Breast03]

Completed · Phase 3 · NCT03529110

Conditions: Breast Cancer

At a glance

Research payments reported, 2025
$279,354
U.S. investigators named
17
Sites paid
15
Planned or actual enrollment
524

About the trial

Sponsor
Daiichi Sankyo (with Daiichi Sankyo Co., Ltd., AstraZeneca)
Tested
Trastuzumab deruxtecan (T-DXd) (drug), Ado-trastuzumab emtansine (T-DM1) (drug)
Dates
Started 2018-08-09; completion 2026-08-31
Results posted
Yes

This study is designed to compare the anti-tumor activity as well as the safety and efficacy of DS-8201a versus T-DM1 in HER2-positive, unresectable and/or metastatic breast cancer subjects previously treated with trastuzumab and taxane.

From ClinicalTrials.gov, last updated 2026-10-07. Full record, eligibility and contacts (opens in a new tab)

Industry funding

Daiichi Sankyo Inc. reported $279,354 in research payments for this study in 2025 (203 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.