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Clinical Trials in the UK / NCT05152147
Active, not recruiting Phase 3

A Study of Zanidatamab in Combination With Chemotherapy Plus or Minus Tislelizumab in Patients With HER2-positive Advanced or Metastatic Gastric and Esophageal Cancers

NCT05152147 · tracked via the Priya Life Science UK tracker
Sponsor
Jazz Pharmaceuticals
Phase
Phase 3
Started
2021-12-02
Last updated
2026-09-01

Condition(s) studied

Gastric NeoplasmsGastroesophageal AdenocarcinomaEsophageal Adenocarcinoma

Investigational drug(s) / intervention(s)

ZanidatamabTislelizumabTrastuzumabCapecitabineOxaliplatinCisplatin5-Fluorouracil

Zanidatamab: Administered IV

Tislelizumab: Administered IV

Trastuzumab: Administered intravenously (IV)

Capecitabine: Administered orally (PO bid)

Oxaliplatin: Administered IV

Cisplatin: Administered IV

5-Fluorouracil: Administered IV

Study summary

This study is being done to find out if zanidatamab, when given with chemotherapy plus or minus tislelizumab, is safe and works better than trastuzumab given with chemotherapy.

The patients in this study will have advanced human epidermal growth factor 2 (HER2)-positive stomach and esophageal cancers that are no longer treatable with surgery (unresectable) or chemoradiation, and/or have grown or spread to other parts of the body (metastatic).

Eligibility

Sex
ALL
Min age
18 Years
Max age
Healthy volunteers
No
Inclusion Criteria: * Histologically confirmed unresectable locally advanced, recurrent or metastatic HER2-positive gastroesophageal adenocarcinoma (adenocarcinomas of the stomach or esophagus, including the gastroesophageal junction), defined as 3+ HER2 expression by IHC or 2+ HER2 expression by IHC with ISH positivity per central assessment. Subjects with esophageal adenocarcinoma must not be eligible for combined chemoradiotherapy at the time of enrollment * Assessable (measurable or non-measurable) disease as defined by RECIST 1.1 * Eastern Cooperative Oncology Group (ECOG) performance status score of 0 or 1, assessed within 3 days prior to randomization * Adequate organ function * Left ventricular ejection fraction (LVEF) ≥ 50% as determined by either echocardiogram or multiple gated acquisition scan (MUGA) Exclusion Criteria: * Prior treatment with a HER2-targeted agent, with the exception of subjects who received HER2-targeted treatment for breast cancer \> 5 years prior to initial diagnosis of GEA * Prior treatment with an anti-PD-1, anti-PD-L1, anti-PD-L2 or any other antibody or drug specifically targeting T-cell co-stimulation or checkpoint pathways * Prior treatment with systemic antineoplastic therapy or intraperitoneal chemotherapy for unresectable locally advanced, recurrent or metastatic GEA * Untreated central nervous system (CNS) metastases, symptomatic CNS metastases, or radiation treatment for CNS metastases within 4 weeks prior to randomization. Stable, treated brain metastases are allowed (defined as subjects who are completely off steroids and anticonvulsants and are neurologically stable with no evidence of radiographic progression for at least 4 weeks prior to randomization) * Known history of or ongoing leptomeningeal disease (LMD) * Known additional malignancy that is not considered cured or that has required treatment within the past 3 years * Known active hepatitis * Any history of human immunodeficiency virus (HIV) infection * Known SARS-CoV-2 infection; subjects with prior infection that has resolved per local institutions' requirements and screening guidance are eligible * QTc Fridericia (QTcF) \> 470 ms * Clinically significant cardiac disease, such as ventricular arrhythmia requiring therapy, uncontrolled hypertension or any history of symptomatic congestive heart failure (CHF)

Primary outcome measure(s)

Trial sites (227)

FacilityCityRegionStatus
Hospital de Gastroenterología Dr Bonorino Udaondo Buenos Aires Argentina
Instituto de Investigaciones Metabólicas - IDIM Buenos Aires Argentina
Hospital Italiano de Buenos Aires Buenos Aires Argentina
Fundación Centro de Medicina Nuclear y Molecular ER Córdoba Argentina
Centro Médico Privado CEMAIC Córdoba Argentina
Centro de Investigación Pergamino S.A. Pergamino Argentina
Centro de Investigación Clínica - Clínica Viedma Viedma Argentina
Flinders Medical Centre Bedford Park Australia
Austin Health Heidelberg Australia
Liverpool Hospital Liverpool Australia
Fiona Stanley Hospital Murdoch Australia
Imelda VZW Bonheiden Belgium
Cliniques Universitaires Saint-Luc Brussels Belgium
UZ Gent Ghent Belgium
UZ Leuven Leuven Belgium
CHU de Liège Liège Belgium
Centro Integrado de Pesquisa - CIP Barretos Brazil
Fundação Pio XII Hospital de Câncer de Barretos Barretos Brazil
Cenantron - Centro Avancado de Tratamento Oncologico Ltda Belo Horizonte Brazil
Centro de Pesquisas Clínicas/Fundação Doutor Amaral Carvalho Brasília Brazil
Instituto Do Câncer Do Ceará ICC Fortaleza Brazil
Hospital de Clinicas de Porto Alegre (HCPA) - PPDS Porto Alegre Brazil
Irmandade Da Santa Casa de Misericordia de Porto Alegre Porto Alegre Brazil
Hospital Nossa Senhora Da Conceição Porto Alegre Brazil
Núcleo de Pesquisa Clínica da Rede São Camilo Santo André Brazil
Instituto do Cancer do Estado de São Paulo ICESP São Paulo Brazil
Instituto de Oncologia de Sorocaba Sorocaba Brazil
Princess Margaret Cancer Centre Toronto Canada
Centro Internacional de Estudios Clinicos CIEC Santiago Region Metropolitan
Fundación Arturo López Pérez (FALP) - PPDS Providencia Santiago Metropolitan
Centro de Estudios Clínicos SAGA SpA Providencia Chile
Sociedad Oncovida S.A Santiago Chile
Icegclinic Santiago Chile
BIOCINETIC SpA Santiago Chile
Sociedad de Investigaciones Medicas Limitada Temuco Chile
Beijing Chao-Yang Hospital, Capital Medical University Beijing China
Cancer Hospital Chinese Academy of Medical Sciences Beijing China
Beijing Cancer Hospital Beijing China
Peking University Third Hospital Beijing China
Beijing Luhe Hospital, Capital Medical University Beijing China

+ 187 more sites — see the full list on the official registry below.

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 NCT05152147 on ClinicalTrials.gov ↗ ← All trials in the UK