NCT04014075CompletedPhase 2
DS-8201a in HER2-positive Gastric Cancer That Cannot Be Surgically Removed or Has Spread (DESTINY-Gastric02)
A Phase 2, Open-label, Single-arm Trial of Trastuzumab Deruxtecan (DS 8201a) in HER2-positive, Unresectable or Metastatic Gastric or Gastro-esophageal Junction (GEJ) Adenocarcinoma Subjects Who Have Progressed on or After a Trastuzumab-containing Regimen (DESTINY-Gastric02)
Source: ClinicalTrials.gov · Last updated 3 Apr 2025
Brief summary (registry, in English)
This study will find out if trastuzumab deruxtecan is safe and works for participants with gastric or gastroesophageal junction cancer. They must have human epidermal growth factor receptor 2 (HER2)-positive gastric or gastro-esophageal junction (GEJ) cancer: * that cannot be removed surgically * that has moved to other parts of the body * that got worse during or after treatment that included trastuzumab The study will enroll about 80 participants. Sites will be in North America and the European Union.
- Status (registry)
- Completed
- Phase (registry)
- Phase 2
- Study type
- Interventional
- Enrollment
- 79 (actual)
- First submitted
- 8 Jul 2019
- Start date
- 26 Nov 2019
- Primary completion date
- 8 Nov 2021
- Lead sponsor
- Daiichi Sankyo
- Diseases
- Gastric and esophageal cancer
- NCT number
- NCT04014075
- EudraCT number
- 2019-001512-34
What you commit to
- Study type: Interventional · Phase 2
- Participants enrolled: 79
- From 26 Nov 2019 to the primary completion date, 8 Nov 2021
- 37 sites in 5 countries
- Visits and tests: ask the trial team, the registry does not list them
Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.
Who cannot take part
Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.
Prior treatment
- Has had anticancer therapy after first-line treatment regimen containing trastuzumab
- Clinically severe pulmonary compromise resulting from intercurrent pulmonary illnesses including, but not limited to, any underlying pulmonary disorder (ie, pulmonary emboli within 3 months of the first dose, severe asthma, severe chronic obstructive pulmonary disease (COPD), restrictive lung disease, pleural effusion, etc.), and any autoimmune, connective tissue or inflammatory disorders with pulmonary involvement (ie, rheumatoid arthritis, Sjogren's, sarcoidosis, etc.), or prior pneumonectomy.
- Has pleural effusion, ascites, or pericardial effusion that requires drainage, peritoneal shunt, or Cell-free and Concentrated Ascites Reinfusion Therapy (CART)
- Has spinal cord compression or clinically active central nervous system metastases, defined as untreated and symptomatic or requiring therapy with corticosteroids or anticonvulsants to control associated symptoms (Note: participants with clinically inactive brain metastases may be included in the study as well as participants with treated brain metastases who are no longer symptomatic and no longer require treatment with corticosteroids or anticonvulsants.
Other illness
- Has history of non-infectious interstitial lung disease (ILD)/pneumonitis that required corticosteroid therapy, or current ILD/pneumonitis that cannot be ruled out at screening
Lab values
- Has uncontrolled cardiovascular disease, including any of the following: history of myocardial infarction (MI) within 6 months of first dose or symptomatic congestive heart failure (New York Heart Association Class II to IV), troponin levels consistent with MI as defined according to the manufacturer within 28 days of first dose, or corrected QT interval (QTc) prolongation to \>470 ms (females) or \>450 ms (male) based on screening triplicate 12-lead electrocardiogram (ECG)
Who the study is looking for
- Men or women ≥18 years old (local regulatory guidelines apply)
- Has pathologically documented HER2-positive gastric or GEJ cancer that is unresectable or metastatic, and that progressed during or after treatment regimen containing trastuzumab
- Has at least one measurable lesion per RECIST v1.1, as confirmed by investigator review
- If of reproductive potential, agrees to use a highly effective form of contraception or avoid intercourse during and upon completion of the study and for at least 7 months for females and 4 months for males after the last dose of study drug
Age in the registry: 18 years to - · Sex: All · Does not accept healthy volunteers
Sites (37)
Sites in registry order. Pick your city on the disease page to sort them by distance.
| Site | City | Country | Site status |
|---|---|---|---|
| UCL St-Luc Coordinator of this site? Confirm its status | Brussels | Belgium | Unknown status |
| Hôpital de Jolimont Coordinator of this site? Confirm its status | Haine-Saint-Paul | Belgium | Unknown status |
| UZ Leuven Coordinator of this site? Confirm its status | Leuven | Belgium | Unknown status |
| Institut Catalan de Oncologia Hospital Duran i Reynals Coordinator of this site? Confirm its status | Barcelona | Spain | Unknown status |
| Vall d'Hebron University Hospital and Vall d'Hebron Institute of Oncology (VHIO) Coordinator of this site? Confirm its status | Barcelona | Spain | Unknown status |
| Hospital Clinic de Barcelona Coordinator of this site? Confirm its status | Barcelona | Spain | Unknown status |
| Hospital La Paz Coordinator of this site? Confirm its status | Madrid | Spain | Unknown status |
| Hospital Universitario HM Sanchinarro Coordinator of this site? Confirm its status | Madrid | Spain | Unknown status |
| Biomedical Research Institute Hospital de Valencia Coordinator of this site? Confirm its status | Valencia | Spain | Unknown status |
| Cambridge University Hospitals NHS Foundation Trust Coordinator of this site? Confirm its status | Cambridge | United Kingdom | Unknown status |
| The Royal Marsden Hospital Coordinator of this site? Confirm its status | London | United Kingdom | Unknown status |
| Christie Hospital Coordinator of this site? Confirm its status | Manchester | United Kingdom | Unknown status |
| The Royal Marsden Hospital Coordinator of this site? Confirm its status | Sutton | United Kingdom | Unknown status |
| Fondazione IRCCS - Istituto Nazionale dei Tumori Coordinator of this site? Confirm its status | Milan | Italy | Unknown status |
| ASST Grande Ospedale Metropolitano Niguarda Coordinator of this site? Confirm its status | Milan | Italy | Unknown status |
| Azienda Ospedaliero - Universitaria di Modena Policlinico Coordinator of this site? Confirm its status | Modena | Italy | Unknown status |
| Oncology Institute Veneto IOVIRCCS Coordinator of this site? Confirm its status | Padua | Italy | Unknown status |
| Lehigh Valley Health Network Coordinator of this site? Confirm its status | Allentown | United States | Unknown status |
| Massachusetts General Hospital (MGH) Coordinator of this site? Confirm its status | Boston | United States | Unknown status |
| Dana-Farber Cancer Institute Coordinator of this site? Confirm its status | Boston | United States | Unknown status |
| Beth Israel Deaconess Medical Center (BIDMC) Coordinator of this site? Confirm its status | Boston | United States | Unknown status |
| University of Chicago Medical Center UCMC Duchossois Center for Advanced Medicine DCAM Coordinator of this site? Confirm its status | Chicago | United States | Unknown status |
| City of Hope Medical Center Coordinator of this site? Confirm its status | Duarte | United States | Unknown status |
| Hartford Hospital Coordinator of this site? Confirm its status | Hartford | United States | Unknown status |
| The University of Texas MD Anderson Cancer Center Coordinator of this site? Confirm its status | Houston | United States | Unknown status |
| Kansas University Cancer Center Coordinator of this site? Confirm its status | Kansas City | United States | Unknown status |
| Northwell Health Cancer Institute Coordinator of this site? Confirm its status | Lake Success | United States | Unknown status |
| USC Norris Comprehensive Cancer Center Hospital Coordinator of this site? Confirm its status | Los Angeles | United States | Unknown status |
| Midstate Medical Center Coordinator of this site? Confirm its status | Meriden | United States | Unknown status |
| Miami Cancer Institute - Baptist Health South Florida Coordinator of this site? Confirm its status | Miami | United States | Unknown status |
| Pacific Cancer Care Coordinator of this site? Confirm its status | Monterey | United States | Unknown status |
| The Hospital of Central Connecticut Coordinator of this site? Confirm its status | New Britain | United States | Unknown status |
| Smilow Cancer Hospital at Yale - New Haven Coordinator of this site? Confirm its status | New Haven | United States | Unknown status |
| Memorial Sloan-Kettering Cancer Center Coordinator of this site? Confirm its status | New York | United States | Unknown status |
| UCLA Health Coordinator of this site? Confirm its status | Santa Monica | United States | Unknown status |
| University of Washington - Seattle Cancer Care Alliance Coordinator of this site? Confirm its status | Seattle | United States | Unknown status |
| Alvin J. Siteman Cancer Center Washington University Coordinator of this site? Confirm its status | St Louis | United States | Unknown status |
Related publications
- Human Epidermal Growth Factor Receptor 2 Quantification Using Computational Pathology to Identify Novel Biomarkers for Trastuzumab Deruxtecan-Treated Human Epidermal Growth Factor Receptor 2-Positive Gastric Cancer.JCO Precis Oncol · 2026 · PMID 42208007
- Trastuzumab deruxtecan in HER2-positive stomach or gastroesophageal junction cancer: a plain language summary of the DESTINY-Gastric02 study.Future Oncol · 2025 · PMID 41294268
This page is information, not medical advice. Discuss any trial with your doctor.