🇮🇪Ireland
16°C Partly Cloudy · Dublin
Live Updates
--:--:-- IST
Writer Login
Latest
Clinical Trials in the UK / NCT03529110
Active, not recruiting Phase 3

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]

NCT03529110 · tracked via the Priya Life Science UK tracker
Sponsor
Daiichi Sankyo
Phase
Phase 3
Started
2018-08-09
Last updated
2025-10-21

Condition(s) studied

Breast Cancer

Investigational drug(s) / intervention(s)

Trastuzumab deruxtecan (T-DXd)Ado-trastuzumab emtansine (T-DM1)

Trastuzumab deruxtecan (T-DXd): T-DXd is sterile lyophilized powder reconstituted into a sterile aqueous solution (100 mg/5 mL) to be administered intravenously.

Ado-trastuzumab emtansine (T-DM1): The treatment will be in accordance with the approved label.

Study summary

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.

Eligibility

Sex
ALL
Min age
18 Years
Max age
Healthy volunteers
No
Inclusion Criteria: 1. Must be competent and able to comprehend, sign, and date an Institutional Review Board (IRB) or Ethics Committee (EC) approved ICF before performance of any study-specific procedures or tests. 2. Adults ≥18 y old. (Please follow local regulatory requirements if the legal age of consent for study participation is \>18 y old.) 3. Pathologically documented breast cancer that: 1. is unresectable or metastatic. 2. has confirmed HER2-positive expression as determined according to American Society of Clinical Oncology - College of American Pathologists guidelines evaluated at a central laboratory.23 3. was previously treated with trastuzumab and taxane in the advanced/ metastatic setting or progressed within 6 mo after neoadjuvant or adjuvant treatment involving a regimen including trastuzumab and taxane. 4. Documented radiologic progression (during or after most recent treatment or within 6 mo after completing adjuvant therapy). 5. Subjects must be HER2-positive as confirmed by central laboratory assessment of most recent tumor tissue sample available. If archived tissue is not available, a fresh biopsy is required. 6. Presence of at least 1 measurable lesion per modified Response Evaluation Criteria in Solid Tumors (mRECIST) version 1.1 Exclusion Criteria: 1. Prior treatment with an anti-HER2 ADC (such as T-DM1) in the metastatic setting. Prior treatment in the adjuvant/neoadjuvant setting would be allowed if progression of disease did not occur within 12 mo of end of adjuvant therapy. 2. Uncontrolled or significant cardiovascular disease, including any of the following: 1. History of myocardial infarction within 6 mo before randomization; 2. History of symptomatic congestive heart failure (New York Heart Association Class II to IV); 3. Troponin levels consistent with myocardial infarction as defined according to the manufacturer within 28 d prior to randomization; 4. Corrected QT interval (QTc) prolongation to \> 470 ms (females) or \>450 ms (male) based on average of Screening triplicate 12-lead ECG; 5. LVEF \< 50% within 28 d prior to randomization 3. Has a history of (noninfectious) ILD/pneumonitis that required steroids, has current ILD/pneumonitis, or where suspected ILD/pneumonitis cannot be ruled out by imaging at Screening. 4. Spinal cord compression or clinically active central nervous system (CNS) metastases, defined as untreated or symptomatic, or requiring therapy with corticosteroids or anticonvulsants to control associated symptoms. * Subjects with clinically inactive brain metastases may be included in the study. * Subjects with treated brain metastases that are no longer symptomatic and who require no treatment with corticosteroids or anticonvulsants may be included in the study if they have recovered from the acute toxic effect of radiotherapy. A minimum of 2 wk must have elapsed between the end of whole brain radiotherapy and study enrollment. 5. Has a history of severe hypersensitivity reactions to either the drug substances or inactive ingredients in the drug product. 6. History of severe hypersensitivity reactions to other mAbs.

Primary outcome measure(s)

Trial sites (164)

FacilityCityRegionStatus
UCLA Hematology Oncology Los Angeles California
Sharp Memorial Hospital San Diego California
University of California San Francisco San Francisco California
Innovative Clinical Research Institute Whittier California
Washington Cancer Institute Washington D.C. District of Columbia
Florida Cancer Specialists-Broadway Fort Myers Florida
Florida Cancer Specialists NORTH St. Petersburg Florida
Piedmont Cancer Institute, PC Atlanta Georgia
Loyola University Health System Maywood Illinois
Norton Cancer Institute Louisville Kentucky
Dana-Farber Cancer Institute Boston Massachusetts
University of Nebraska Medical Center Omaha Nebraska
North Shore Hematology Oncology Associates, PC East Setauket New York
University of Rochester Rochester New York
Wake Forest University Baptist Medical Center Winston-Salem North Carolina
University of Cincinnati Medical Center Cincinnati Ohio
Seidman Cancer Center Cleveland Ohio
The Ohio State University Columbus Ohio
Dayton Physicians, LLC Kettering Ohio
Magee-Womens Hospital of UPMC Pittsburgh Pennsylvania
Tennessee Oncology- St Thomas Location Nashville Tennessee
Vanderbilt Breast Center at One Hundred Oaks Nashville Tennessee
UT Southwestern Medical Center Dallas Texas
Houston Methodist Hospital / Houston Methodist Cancer Center Houston Texas
MD Anderson Cancer Center Houston Texas
Millennium Oncology Houston Texas
The University of Texas Health Science Center at Tyler Tyler Texas
MultiCare Health System Institute for Research and Innovation Auburn Washington
The Tweed Hospital Tweed Heads New South Wales
Princess Alexandra Hospital Woolloongabba Queensland
Box Hill Hospital Box Hill Victoria
Peninsula and South Eastern Haematology & Oncology Group Frankston Victoria
Peter MacCallum Cancer Melbourne Victoria
St John of God Subiaco Hospital Subiaco Western Australia
Institut Jules-Bordet Brussels Belgium
Universitair Ziekenhuis Brussel Brussels Belgium
Universitair Ziekenhuis Antwerpen Edegem Belgium
AZ Sint-Lucas - Campus Sint-Lucas Ghent Belgium
Universitaire Ziekenhuizen Leuven Leuven Belgium
CHU UCL Namur site de Sainte Elisabeth Namur Belgium

+ 124 more sites — see the full list on the official registry below.

More Daiichi Sankyo trials in the UK

Other trials for the same condition

Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT03529110 on ClinicalTrials.gov ↗ ← All trials in the UK