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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
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

Full criteria on ClinicalTrials.gov

Sites (37)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
UCL St-Luc
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BrusselsBelgiumUnknown status
Hôpital de Jolimont
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Haine-Saint-PaulBelgiumUnknown status
UZ Leuven
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LeuvenBelgiumUnknown status
Institut Catalan de Oncologia Hospital Duran i Reynals
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BarcelonaSpainUnknown status
Vall d'Hebron University Hospital and Vall d'Hebron Institute of Oncology (VHIO)
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BarcelonaSpainUnknown status
Hospital Clinic de Barcelona
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BarcelonaSpainUnknown status
Hospital La Paz
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MadridSpainUnknown status
Hospital Universitario HM Sanchinarro
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MadridSpainUnknown status
Biomedical Research Institute Hospital de Valencia
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ValenciaSpainUnknown status
Cambridge University Hospitals NHS Foundation Trust
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CambridgeUnited KingdomUnknown status
The Royal Marsden Hospital
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LondonUnited KingdomUnknown status
Christie Hospital
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ManchesterUnited KingdomUnknown status
The Royal Marsden Hospital
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SuttonUnited KingdomUnknown status
Fondazione IRCCS - Istituto Nazionale dei Tumori
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MilanItalyUnknown status
ASST Grande Ospedale Metropolitano Niguarda
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MilanItalyUnknown status
Azienda Ospedaliero - Universitaria di Modena Policlinico
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ModenaItalyUnknown status
Oncology Institute Veneto IOVIRCCS
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PaduaItalyUnknown status
Lehigh Valley Health Network
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AllentownUnited StatesUnknown status
Massachusetts General Hospital (MGH)
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BostonUnited StatesUnknown status
Dana-Farber Cancer Institute
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BostonUnited StatesUnknown status
Beth Israel Deaconess Medical Center (BIDMC)
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BostonUnited StatesUnknown status
University of Chicago Medical Center UCMC Duchossois Center for Advanced Medicine DCAM
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ChicagoUnited StatesUnknown status
City of Hope Medical Center
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DuarteUnited StatesUnknown status
Hartford Hospital
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HartfordUnited StatesUnknown status
The University of Texas MD Anderson Cancer Center
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HoustonUnited StatesUnknown status
Kansas University Cancer Center
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Kansas CityUnited StatesUnknown status
Northwell Health Cancer Institute
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Lake SuccessUnited StatesUnknown status
USC Norris Comprehensive Cancer Center Hospital
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Los AngelesUnited StatesUnknown status
Midstate Medical Center
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MeridenUnited StatesUnknown status
Miami Cancer Institute - Baptist Health South Florida
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MiamiUnited StatesUnknown status
Pacific Cancer Care
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MontereyUnited StatesUnknown status
The Hospital of Central Connecticut
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New BritainUnited StatesUnknown status
Smilow Cancer Hospital at Yale - New Haven
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New HavenUnited StatesUnknown status
Memorial Sloan-Kettering Cancer Center
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New YorkUnited StatesUnknown status
UCLA Health
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Santa MonicaUnited StatesUnknown status
University of Washington - Seattle Cancer Care Alliance
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SeattleUnited StatesUnknown status
Alvin J. Siteman Cancer Center Washington University
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St LouisUnited StatesUnknown status

Related publications

This page is information, not medical advice. Discuss any trial with your doctor.