Study of zolbetuximab, pembrolizumab and chemotherapy in adults with HER2-negative, Claudin 18.

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What is this study about?

This clinical trial studies treatment for gastric cancer and gastroesophageal junction adenocarcinoma that cannot be surgically removed or has spread to other parts of the body. The study tests a combination of medications including zolbetuximab, pembrolizumab, and chemotherapy drugs (capecitabine, oxaliplatin, fluorouracil, and folinic acid). The purpose is to evaluate whether adding zolbetuximab to pembrolizumab and chemotherapy works better than chemotherapy and pembrolizumab alone as a first treatment.

The study involves people whose tumors test negative for a protein called HER2 but positive for two other proteins called CLDN18.2 and PD-L1. During the study, participants will receive either zolbetuximab or a placebo along with pembrolizumab and chemotherapy through intravenous infusions. Some chemotherapy medications will be given as tablets to take by mouth.

Researchers will track how long participants live, whether their cancer grows or spreads, and how their tumors respond to treatment. They will also monitor participants for any side effects from the treatment combination. The study will check blood samples to measure drug levels and test for the body’s immune response to the medications.

1 Initial treatment phase

You will receive a combination of medications through different methods:

Zolbetuximab (Vyloy) given through an intravenous infusion

Pembrolizumab (Keytruda) given through an intravenous infusion

– One of two chemotherapy combinations:

2 Chemotherapy option 1 (CAPOX)

CAPOX combination includes:

Oxaliplatin given through an infusion

Capecitabine taken as oral medication

3 Chemotherapy option 2 (mFOLFOX6)

mFOLFOX6 combination includes:

Oxaliplatin given through an infusion

Fluorouracil given through intravenous injection or infusion

Folinic acid given through an infusion

4 Monitoring phase

Regular assessments will include:

– Evaluation of how the cancer responds to treatment

– Physical examinations

– Blood tests

– Heart monitoring (ECG)

– Checking for side effects of the treatment

5 Treatment duration

The study will continue until:

– The cancer shows signs of progression

– Unacceptable side effects occur

– The planned end date of the study (January 2030)

Your doctor will regularly evaluate if continuing the treatment is beneficial for you

Who Can Join the Study?

  • Must be at least 18 years old to sign the consent form
  • Must have a tumor that tests positive for PD-L1 (a protein that helps control immune system responses)
  • Must have confirmed gastric or gastroesophageal adenocarcinoma (cancer of the stomach or where the stomach meets the esophagus)
  • Must have advanced cancer that cannot be surgically removed or has spread to other parts of the body, confirmed by imaging within 28 days before study start
  • Must have cancer that can be measured by imaging scans. If there is only one measurable tumor and previous radiation therapy, the tumor must either be outside the treated area or show growth after radiation
  • Must have good physical function status (ECOG score of 0 or 1), meaning able to perform daily activities with minimal assistance
  • Must have a life expectancy of at least 12 weeks as determined by the doctor
  • Must be able to receive treatment with mFOLFOX6 or CAPOX (types of chemotherapy) and pembrolizumab (an immunotherapy drug)
  • Must have a tumor that is HER2-negative (does not have high levels of a specific protein called HER2)
  • Must have a tumor that is positive for CLDN18.2 (a specific protein found in some stomach cancers)

Who Cannot Join the Study?

  • Known allergy or sensitivity to any of the study medications or their components
  • Previous treatment with chemotherapy for advanced or metastatic (cancer that has spread to other parts of the body) gastric cancer
  • Active autoimmune disease (condition where your immune system attacks healthy cells) requiring systemic treatment
  • Presence of brain metastases (cancer spread to the brain) that are untreated or unstable
  • History of other cancers within the last 5 years, except for successfully treated non-melanoma skin cancer or cervical cancer in situ
  • Significant heart conditions including heart failure, uncontrolled high blood pressure, or recent heart attack
  • Active hepatitis B or hepatitis C infection
  • Active tuberculosis infection
  • Pregnant or breastfeeding women
  • Unable to swallow oral medications
  • Major surgery within 4 weeks before starting the study treatment
  • Participation in another clinical trial within 4 weeks before starting this study
  • Any condition that, in the opinion of the study doctor, would make participation unsafe
  • Unable to understand or provide informed consent

Where you can join this trial?

Verified and Recommended Sites

No sites found in this category

Verified Sites

Other Sites

Site Name City Country Status
Krankenhaus Nordwest GmbH Frankfurt Germany
Klinikum Nuernberg Nürnberg Germany
Centre Antoine Lacassagne Nice France
Unidade Local De Saude De Almada-Seixal E.P.E. Almada Portugal
Centre Hospitalier Universitaire Rouen Rouen France
Institut Jules Bordet Anderlecht Belgium
Hospital Universitari General De Catalunya Sant Cugat Del Valles Spain
Centrul De Oncologie-Euroclinic S.R.L. Iasi Romania
Azienda Socio Sanitaria Territoriale Di Cremona Cremona Italy
Istituto Europeo Di Oncologia S.r.l. Milan Italy
IRCCS Istituto Nazionale Tumori Fondazione Pascale Naples Italy
Centro Ricerche Cliniche Di Verona S.r.l. Verona Italy
Centre Hospitalier Universitaire De Poitiers Poitiers France
Universitair Ziekenhuis Gent Gent Belgium
Leopoldina-Krankenhaus der Stadt Schweinfurt GmbH Schweinfurt Germany
Azienda Sanitaria Universitaria Friuli Centrale Udine Italy
Hospital Universitario 12 De Octubre Madrid Spain
Hospital General Universitario Morales Meseguer Murcia Spain
Hospital Del Mar Barcelona Spain
Masarykuv Onkologicky Ustav Brno-Stred Czechia
Institutul Regional De Gastroenterologie Hepatologie Prof. Dr. Octavian Fodor Cluj Cluj Napoca Romania
Centrum Onkologii Ziemi Lubelskiej Im. Sw. Jana Z Dukli Lublin Poland
Lietuvos sveikatos mokslu universiteto ligonine Kauno klinikos Kaunas Lithuania
Instituto Portugues De Oncologia Do Porto Francisco Gentil E.P.E. Porto Portugal
Instituto Portugues De Oncologia De Coimbra Francisco Gentil E.P.E. Coimbra Portugal
Hospital Clinico Universitario Lozano Blesa Zaragoza Spain
Radiotherapy Center Cluj S.R.L. Floresti Romania
CCAB Centro Clinico Academico Braga Associacao Braga Portugal
Szpital Specjalistyczny W Brzozowie Podkarpacki Osrodek Onkologiczny Im.Ks.B.Markiewicza Brzozow Poland
Szpital Kliniczny Ministerstwa Spraw Wewnetrznych I Administracji Z Warminsko-Mazurskim Centrum Onkologii W Olsztynie Olsztyn Poland
MD Anderson Cancer Center Madrid Spain
Unidade Local De Saude Do Alto Ave E.P.E. Guimaraes Portugal
Fondazione Poliambulanza Brescia Italy
Caritas Traegergesellschaft Saarbruecken mbH (CTS) Saarbrücken Germany
Staedtisches Krankenhaus Kiel GmbH Kiel Germany
HELIOS Klinikum Berlin-Buch GmbH Berlin Germany
Hospital Universitario Ramon Y Cajal Madrid Spain
Hospital General Universitario De Elche Elche Spain
Hopital Prive Jean Mermoz Lyon France
Centrul De Oncologie SF Nectarie S.R.L. Craiova Romania
Institutul Clinic Fundeni Bucharest Romania
Hospital Clinico Universitario De Valencia Valencia Spain
Hospital Unviersitario Miguel Servet Zaragoza Spain
Hospital Universitario Virgen Macarena Sevilla Spain
Universitaetsklinikum Erlangen AöR Erlangen Germany
Ospedale San Raffaele S.r.l. Milan Italy
Universita’ Campus Bio-medico Di Roma Rome Italy
Istituto Di Candiolo Fondazione Del Piemonte Per Loncologia IRCCS Candiolo Italy
Hospital Clinic De Barcelona Barcelona Spain
Hospital Da Luz S.A. Lisbon Portugal
Stichting Radboud University Medical Center Nijmegen The Netherlands
Champalimaud Clinical Centre Lisbon Portugal
Hospital Universitario Fundacion Jimenez Diaz Madrid Spain
Hospital Universitario Quironsalud Madrid Pozuelo De Alarcon Spain
University Clinical Hospital Virgen De La Arrixaca Murcia Spain
Universita’ Politecnica Delle Marche Ancona Italy
Universidade De Santiago De Compostela Santiago De Compostela Spain
Hospital General Universitario De Valencia Valencia Spain
Hospital Universitari Arnau De Vilanova De La Gerencia Territorial De Lleida Lleida Spain
Hospital Universitario Virgen De Valme Sevilla Spain
Oncomed S.R.L. Timisoara Romania
Institute Of Oncology Prof. Dr. Ion Chiricuta Cluj-Napoca Cluj Napoca Romania
Medical Center – University Of Freiburg Freiburg Im Breisgau Germany
CHC MontLegia Liege Belgium
Muenchen Klinik gGmbH Munich Germany
Fundacio Assistencial De Mutua De Terrassa Fpc Terrassa Spain
Hopital Prive Des Cotes D’armor Plerin France
Samodzielny Publiczny Zespol Opieki Zdrowotnej W Swidnicy Swidnica Poland
Vseobecna Fakultni Nemocnice V Praze Prague Czechia
Lux Med Onkologia Sp. z o.o. Warsaw Poland
University Hospital Olomouc Olomouc Czechia
Centro Hospitalar Universitario De Santo Antonio E.P.E. Porto Portugal
Centre Hospitalier Lyon Sud Pierre Benite France
Hopital Beaujon Clichy France
Fondazione I.R.C.C.S. Istituto Neurologico Besta Milan Italy
Fakultni Thomayerova nemocnice Prague Czechia
Centre Hospitalier Universitaire De Caen Normandie Caen France
Centre Regional Lutte Contre Le Cancer STRASBOURG, Alsace France
Azienda Ospedaliero Universitaria Pisana Pisa Italy
Cnpwcemom Uiptthhwqjiejq Sqmorqjuu Woluwe-Saint-Lambert Belgium
Irazufmn Rmpmzgnr Do Cwcekb Dm Mdiqxpraazu Montpellier France
Vciqvrofq ihmjucgg Vhtrcqdi umnnuoofhcrh lokavpdtz Syfrsyvk kxtonxk fwncmazm Nuttmklxcgmi vjysd cuwoqkb Vilnius Lithuania
Uxpxamjyjhwjhrrbwmotm Eafmu Atn Essen Germany
Ifnqvynm Cbxskb Dtoysciopkmuaykos L'hospitalet De Llobregat Spain
Ifobus Bonheiden Belgium
Iotqmgwf Bqexeyhd Bordeaux France
Pdvtzasi Wghsxyzme Wolfsburg Germany
Fdiihulu nmdhegqhm Mrtop a Hocuafs Prague Czechia
Igulduhy Rxbgmorvr Pzk Ln Sivtlg Dbw Twybwu Dpgk Avpdjke Ibha Sabzfv Meldola Italy
Ehdervm Umolgykeqnbl Mamvblv Cgowoxe Rfkuflqec (huvnodh Mpv Rotterdam The Netherlands
Aykymbk Ohaejidtojx Uhvepesdcbtel Seugnn Siena Italy
Cdvvck Hckhxcxtzjv Di Cngkwgyjmqh Carcassonne France
Nempuhku Iglivdwl Ollxzqyjl Img Mmzbh Sziovmdelglsizgdhnhmqqwvjvcl Igfjqcvx Bpnnafsl Cracow Poland
Apxpwrr Ufa Idxij Dw Rneqdi Esadwu Reggio Emilia Italy
Autdilb Uqezc Slfwroxac Lrpgfv Da Bixzjqe Bologna Italy
Hhrwlpvy De Lk Szbrd Cuwc I Sadk Pts Barcelona Spain
Urtnovvnpo Om Avdkhzl Edegem Belgium
Avvucth Oilymugkbpg Pjbf Gtfxjjfu Xyref Bergamo Italy
Fazdxuqtn Pmao Lp Itdnrwqozmlcb Butiisjdn Dle Hzrqfacp Uazsulsunxdem Lw Pmk Madrid Spain
Hgqsjsrp Utjwieotugngo Hzcwyucb Tllqt y Plcisj Irzpqnpd Ciybzu dxfmpjautjlnoknhi (tmra Badalona Spain
Hmysddbd Vmvh dkghoulz Barcelona Spain
Cyltzl Ohzjn Lbncxbe Lille France
Hbwipmmu Uguinxliabkxv de A Cvxjdl A Coruna Galicia Spain
Wnvedsntjr Sivibpi Ilt Sqkuvms Psz W Ppeckdfce Przemysl Poland

Want to learn more about this study or check if you can participate? Contact us.

Trial status

Country Status Recruitment Start
Belgium Belgium
Not recruiting
01.07.2025
Czechia Czechia
Not recruiting
01.07.2025
France France
Not recruiting
01.07.2025
Germany Germany
Not recruiting
01.07.2025
Italy Italy
Not recruiting
01.07.2025
Lithuania Lithuania
Not recruiting
01.07.2025
Poland Poland
Not recruiting
01.07.2025
Portugal Portugal
Not recruiting
01.07.2025
Romania Romania
Not recruiting
01.07.2025
Spain Spain
Not recruiting
01.07.2025
The Netherlands The Netherlands
Not recruiting
01.07.2025

Trial locations

Zolbetuximab is an antibody medication that targets a specific protein called Claudin 18.2, which is found on the surface of some stomach and gastroesophageal junction cancer cells. It works by helping the immune system recognize and attack cancer cells.

Pembrolizumab is an immunotherapy medication that helps the body’s immune system detect and fight cancer cells. It works by blocking a protein called PD-L1 that cancer cells use to hide from the immune system.

CAPOX is a combination chemotherapy treatment that includes two medications: capecitabine and oxaliplatin. These medications work together to kill cancer cells or stop them from growing.

mFOLFOX6 is another combination chemotherapy treatment that includes several medications: fluorouracil, leucovorin, and oxaliplatin. These medications work together in different ways to kill cancer cells or prevent them from multiplying.

Gastric Adenocarcinoma – A type of stomach cancer that begins in the glandular cells of the stomach lining. These cells normally produce mucus and other fluids that help with digestion. The disease typically develops slowly over many years, starting with changes in the stomach’s inner lining. As the cancer grows, it can spread deeper into the stomach walls and potentially to other parts of the body.

Gastric Cancer – A disease where abnormal cells form in the tissues of the stomach. It usually starts in the mucus-producing cells that line the stomach. The condition can develop in any part of the stomach and can spread throughout the stomach and to other organs. Early stages may have minimal symptoms, while the disease progresses gradually over time.

Gastroesophageal Junction Adenocarcinoma – A cancer that forms in the area where the esophagus joins the stomach. This type of cancer develops in the glandular tissue near the junction of these two organs. The disease begins in the cells that make and release mucus and other fluids. As it progresses, it can affect both the lower esophagus and upper portion of the stomach.

Trial ID:
2024-519773-19-00
Protocol code:
8951-CL-0305
NCT ID:
NCT06901531
Trial Phase:
Therapeutic confirmatory (Phase III)

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