Sign in

NCT04379596Active, not recruitingPhase 2

Ph1b/2 Study of the Safety and Efficacy of T-DXd Combinations in Advanced HER2-expressing Gastric Cancer (DESTINY-Gastric03)

A Phase 1b/2 Multicenter, Open-label, Dose-escalation and Dose-expansion Study to Evaluate the Safety, Tolerability, Pharmacokinetics, Immunogenicity, and Antitumor Activity of Trastuzumab Deruxtecan (T-DXd) Monotherapy and Combinations in Adult Participants With HER2-expressing Gastric Cancer (DESTINY-Gastric-03)

Source: ClinicalTrials.gov · Last updated 28 Aug 2026

Brief summary (registry, in English)

DESTINY-Gastric03 will investigate the safety, tolerability, pharmacokinetics, immunogenicity, and preliminary antitumor activity of trastuzumab deruxtecan (T-DXd) alone or in combination with chemotherapy and/or immunotherapy in HER2-expressing advanced/metastatic gastric/gastroesophageal junction (GEJ) and esophageal adenocarcinoma patients. Study hypotheses: Combination of T-DXd with cytotoxic chemotherapy and/or immunotherapy administered to subjects at the recommended phase 2 dose will show manageable safety and tolerability and preliminary anti-tumor efficacy so as to permit further clinical testing. T-DXd in combination with cytotoxic chemotherapy or immune checkpoint inhibitor administered to HER2-expressing gastric, GEJ and esophageal cancer patients who have not received prior treatment for advanced/metastatic disease will show preliminary evidence of anti-tumour activity and the potential to become a therapeutic option for this patient population.

Status (registry)
Active, not recruiting
Phase (registry)
Phase 2
Study type
Interventional
Enrollment
452 (actual)
First submitted
5 May 2020
Start date
3 Jun 2020
Primary completion date
4 May 2027
Lead sponsor
AstraZeneca
NCT number
NCT04379596
EU CT number
2023-504888-16-00
EudraCT number
2019-004483-22

What you commit to

  • Study type: Interventional · Phase 2
  • Participants enrolled: 452
  • From 3 Jun 2020 to the primary completion date, 4 May 2027
  • 63 sites in 14 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

  • Pleural effusion, ascites or pericardial effusion that requires drainage, peritoneal shunt, or Cell-free and Concentrated Ascites Reinfusion Therapy (CART).

Other illness

  • Part 1 to 4: History of active primary immunodeficiency, known HIV, active chronic, or past hepatitis B infection, or hepatitis C infection. Part 5: evidence of active, uncontroled HIV, HBV or HCV infection.
  • Uncontrolled intercurrent illness.
  • History of non-infectious pneumonitis/ILD, current ILD, or where suspected ILD that cannot be ruled out by imaging at screening.
  • Lung-specific intercurrent clinically significant severe illnesses.
  • Uncontrolled infection requiring intravenous (IV) antibiotics, antivirals, or antifungals.

Other

  • Has spinal cord compression or clinically active central nervous system metastases.

Who the study is looking for

  • Male and female participants must be at least 18 years of age. Other age restrictions may apply as per local regulations
  • Disease Characteristics:
    • Locally advanced, unresectable, or metastatic disease based on most recent imaging
    • For Part 1, 2, 3a, 4a pathologically documented adenocarcinoma of the stomach/GEJ/esophagus, HER2-positive (IHC 3+ or IHC 2+/ISH+) based on local tissue testing results
    • For Part 3b,4b and Part 5, pathologically documented adenocarcinoma of the stomach/GEJ/esophagus, HER2-low (IHC 2+/ISH-negative or IHC 1+) based on local tissue testing results
  • For Part 1, progression on or after at least one prior trastuzumabcontaining regimen For Part 2, Part 3, Part 4 and Part 5, previously untreated for unresectable or metastatic adenocarcinoma of the stomach/GEJ/ esophagus with with HER2-positive (Part 2 and Part 3 \[Arm 3A\] and Part 4 \[Arm 4A\]) or HER2-low (Part 3 \[Arm 3B\], Part 4 \[Arm 4B\] and Part 5)) status
  • Has measurable target disease assessed by the Investigator based on RECIST version 1.1
  • Has protocol defined adequate bone marrow and organ function including cardiac, renal and hepatic function
  • If of reproductive potential, agrees to use a highly effective form of contraception or avoid intercourse during and upon completion of the study.

Age in the registry: 18 years to 130 years · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (63)

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

SiteCityCountrySite status
Research Site
Coordinator of this site? Confirm its status
LondrinaBrazilUnknown status
Research Site
Coordinator of this site? Confirm its status
Ribeirão PretoBrazilUnknown status
Research Site
Coordinator of this site? Confirm its status
Santa MariaBrazilUnknown status
Research Site
Coordinator of this site? Confirm its status
São José do Rio PretoBrazilUnknown status
Research Site
Coordinator of this site? Confirm its status
São PauloBrazilUnknown status
Research Site
Coordinator of this site? Confirm its status
MontrealCanadaUnknown status
Research Site
Coordinator of this site? Confirm its status
QuébecCanadaUnknown status
Research Site
Coordinator of this site? Confirm its status
TorontoCanadaUnknown status
Research Site
Coordinator of this site? Confirm its status
ChengduChinaUnknown status
Research Site
Coordinator of this site? Confirm its status
GuangzhouChinaUnknown status
Research Site
Coordinator of this site? Confirm its status
HefeiChinaUnknown status
Research Site
Coordinator of this site? Confirm its status
ShanghaiChinaUnknown status
Research Site
Coordinator of this site? Confirm its status
ShenyangChinaUnknown status
Research Site
Coordinator of this site? Confirm its status
WuhanChinaUnknown status
Research Site
Coordinator of this site? Confirm its status
ZhengzhouChinaUnknown status
Krankenhaus Nordwest GmbH
Coordinator of this site? Confirm its status
Frankfurt am MainGermanyActive, not recruiting
Universitaetsklinikum Frankfurt AöR
Coordinator of this site? Confirm its status
Frankfurt Am MainGermanyActive, not recruiting
Haematologisch Onkologische Praxis Eppendorf
Coordinator of this site? Confirm its status
HamburgGermanyActive, not recruiting
Universitaet Leipzig
Coordinator of this site? Confirm its status
LeipzigGermanyActive, not recruiting
Universitaetsklinikum Mannheim GmbH
Coordinator of this site? Confirm its status
MannheimGermanyActive, not recruiting
Klinikum rechts der Isar der TU Muenchen AöR
Coordinator of this site? Confirm its status
MunichGermanyActive, not recruiting
Hospital Universitari Vall d'Hebron
Coordinator of this site? Confirm its status
BarcelonaSpainActive, not recruiting
Hospital General Universitario Gregorio Marañón
Coordinator of this site? Confirm its status
MadridSpainActive, not recruiting
Hospital Universitario Ramón y Cajal
Coordinator of this site? Confirm its status
MadridSpainActive, not recruiting
Hospital Universitario Marqués de Valdecilla
Coordinator of this site? Confirm its status
SantanderSpainActive, not recruiting
University Hospital Virgen Del Rocio S.L.
Coordinator of this site? Confirm its status
SevillaSpainActive, not recruiting
Research Site
Coordinator of this site? Confirm its status
CambridgeUnited KingdomUnknown status
Research Site
Coordinator of this site? Confirm its status
DundeeUnited KingdomUnknown status
Research Site
Coordinator of this site? Confirm its status
LondonUnited KingdomUnknown status
Research Site
Coordinator of this site? Confirm its status
ManchesterUnited KingdomUnknown status
Research Site
Coordinator of this site? Confirm its status
SuttonUnited KingdomUnknown status
ASST Grande Ospedale Metropolitano Niguarda
Coordinator of this site? Confirm its status
MilanItalyActive, not recruiting
Fondazione IRCCS - Istituto Nazionale dei Tumori
Coordinator of this site? Confirm its status
MilanItalyActive, not recruiting
IRCCS Istituto Nazionale Tumori Fondazione Pascale
Coordinator of this site? Confirm its status
NaplesItalyActive, not recruiting
Istituto Oncologico Veneto
Coordinator of this site? Confirm its status
PadovaItalyActive, not recruiting
Fondazione Policlinico Universitario Agostino Gemelli IRCCS
Coordinator of this site? Confirm its status
RomeItalyActive, not recruiting
Centro Ricerche Cliniche di Verona s.r.l.
Coordinator of this site? Confirm its status
VeronaItalyActive, not recruiting
Research Site
Coordinator of this site? Confirm its status
ChūōkuJapanUnknown status
Research Site
Coordinator of this site? Confirm its status
KashiwaJapanUnknown status
Research Site
Coordinator of this site? Confirm its status
Seongnam-siSouth KoreaUnknown status
Research Site
Coordinator of this site? Confirm its status
SeoulSouth KoreaUnknown status
Stichting Amsterdam UMC
Coordinator of this site? Confirm its status
AmsterdamNetherlandsActive, not recruiting
Het Nederlands Kanker Instituut-Antoni van Leeuwenhoek Ziekenhuis Stichting
Coordinator of this site? Confirm its status
AmsterdamNetherlandsActive, not recruiting
Universitair Medisch Centrum Utrecht
Coordinator of this site? Confirm its status
UtrechtNetherlandsActive, not recruiting
Samodzielny Publiczny Zaklad Opieki Zdrowotnej Szpital Uniwersytecki W Krakowie
Coordinator of this site? Confirm its status
CracowPolandActive, not recruiting
Uniwersyteckie Centrum Kliniczne
Coordinator of this site? Confirm its status
GdanskPolandActive, not recruiting
Przychodnia Lekarska "KOMED"
Coordinator of this site? Confirm its status
KoninPolandActive, not recruiting
Szpital Wojewodzki im. Mikolaja Kopernika w Koszalinie
Coordinator of this site? Confirm its status
KoszalinPolandActive, not recruiting
Opolskie Centrum Onkologii Im. Prof. Tadeusza Koszarowskiego W Opolu Samodzielny Publiczny Zaklad Opieki Zdrowotnej
Coordinator of this site? Confirm its status
OpolePolandActive, not recruiting
Specjalistyczny Szpital Onkologiczny NU-MED Sp. z o.o.
Coordinator of this site? Confirm its status
Tomaszów MazowieckiPolandActive, not recruiting
Narodowy Instytut Onkologii im Marii Sklodowskiej Curie Panstwowy Instytut Badawczy
Coordinator of this site? Confirm its status
WarsawPolandActive, not recruiting
Research Site
Coordinator of this site? Confirm its status
KostromaRussiaUnknown status
Research Site
Coordinator of this site? Confirm its status
MoscowRussiaUnknown status
Research Site
Coordinator of this site? Confirm its status
NovosibirskRussiaUnknown status
Research Site
Coordinator of this site? Confirm its status
Saint PetersburgRussiaUnknown status
Research Site
Coordinator of this site? Confirm its status
Kaohsiung CityTaiwanUnknown status
Research Site
Coordinator of this site? Confirm its status
TainanTaiwanUnknown status
Research Site
Coordinator of this site? Confirm its status
TaipeiTaiwanUnknown status
Research Site
Coordinator of this site? Confirm its status
TaoyuanTaiwanUnknown status
Research Site
Coordinator of this site? Confirm its status
BaltimoreUnited StatesUnknown status
Research Site
Coordinator of this site? Confirm its status
BostonUnited StatesUnknown status
Research Site
Coordinator of this site? Confirm its status
HoustonUnited StatesUnknown status
Research Site
Coordinator of this site? Confirm its status
New YorkUnited StatesUnknown status

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