Study of Bemarituzumab with Chemotherapy and Nivolumab in Untreated Advanced Gastric and Gastroesophageal Junction Cancer Patients with FGFR2b Overexpression

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What is this study about?

This clinical trial studies the treatment of gastric cancer and gastroesophageal junction cancer with a specific characteristic called FGFR2b overexpression. The study tests a combination of medications including bemarituzumab (also known as AMG 552), nivolumab, and chemotherapy drugs including oxaliplatin, folinic acid, fluorouracil, and capecitabine. Some participants will receive these medications while others will receive chemotherapy and nivolumab with placebo instead of bemarituzumab.

The purpose of the study is to determine if adding bemarituzumab to standard chemotherapy and nivolumab treatment improves survival for patients with previously untreated advanced stomach cancer. The medications are given through intravenous infusion, except for capecitabine which is taken by mouth. The study is conducted in two parts: a smaller initial phase to evaluate safety, followed by a larger phase to compare the effectiveness of the treatments.

During the study, participants will receive regular doses of the study medications and undergo various medical assessments. The treatment period may last for several months, depending on how well the participant responds to the therapy. Doctors will monitor participants’ health status, check for side effects, and evaluate how well the cancer responds to treatment throughout the study period.

1 Initial treatment assignment

You will be assigned to one of two treatment groups. Each group receives different combinations of medications.

Your treatment will include either mFOLFOX6 or CAPOX chemotherapy regimen, along with nivolumab.

2 Treatment administration – Group 1

If assigned to the first group, you will receive:

Bemarituzumab through intravenous infusion

Nivolumab through intravenous infusion

– Chemotherapy medications including oxaliplatin, folinic acid, and fluorouracil through intravenous infusion, or capecitabine taken orally

3 Treatment administration – Group 2

If assigned to the second group, you will receive:

Placebo (instead of bemarituzumab) through intravenous infusion

Nivolumab through intravenous infusion

– The same chemotherapy medications as Group 1

4 Regular assessments

Throughout the treatment, you will undergo:

– Regular physical examinations

– Laboratory tests to monitor your health

– Imaging scans to evaluate your response to treatment

– Quality of life questionnaires

– Visual acuity checks

5 Treatment duration

The study will continue until January 2027 or until one of the following occurs:

– Your disease shows progression

– You experience unacceptable side effects

– You decide to stop participating

– Your doctor decides to end your participation

Who Can Join the Study?

  • Must be an adult diagnosed with advanced stomach or gastroesophageal junction cancer that cannot be surgically removed or has spread to other parts of the body
  • Must have a good level of physical function, scoring 0 or 1 on the ECOG scale (a measure of daily living abilities)
  • Must have disease that can be measured or evaluated using specific imaging criteria
  • Must be able to receive treatment with nivolumab (an immunotherapy medication) and chemotherapy medications
  • Must have adequate organ function, including:
    • Sufficient blood cell counts
    • Normal or near-normal liver function
    • Adequate kidney function
    • Normal or stable blood clotting measures
  • For Phase 3 participants:
    • No previous treatment for advanced disease except maximum one dose of chemotherapy with or without nivolumab
    • Previous cancer treatments must have been completed more than 6 months before starting the study
    • Must have confirmed presence of specific protein (FGFR2b) in tumor tissue
  • Must be able to take oral medication (for patients receiving specific chemotherapy combination called CAPOX)

Who Cannot Join the Study?

  • Prior treatment with FGFR inhibitors (medications that target specific proteins involved in cancer growth)
  • Previous treatment with immune checkpoint inhibitors (drugs that help the immune system fight cancer)
  • Active or untreated brain metastases (cancer that has spread to the brain)
  • Uncontrolled high blood pressure
  • Major surgery within 28 days before starting the study treatment
  • Active or chronic infections, including hepatitis B, hepatitis C, or HIV
  • Significant heart problems in the past 6 months
  • Other types of cancer within the last 3 years (except for successfully treated non-melanoma skin cancer or cervical cancer in situ)
  • Autoimmune diseases requiring systemic treatment (conditions where the immune system attacks healthy cells)
  • Pregnant or breastfeeding women
  • Known allergies to study medications or their components
  • Participation in another clinical trial within 28 days before starting this study
  • Serious medical conditions that could interfere with study participation

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
Istituto Oncologico Veneto Padua Italy
Centre Antoine Lacassagne Nice France
Centre Hospitalier Universitaire Rouen Rouen France
Institut Jules Bordet Anderlecht Belgium
Orszagos Onkologiai Intezet Budapest Hungary
Klinikum der Technischen Universitaet Muenchen (TUM Klinikum) Munich Germany
Azienda Socio Sanitaria Territoriale Di Cremona Cremona Italy
IRCCS Istituto Nazionale Tumori Fondazione Pascale Naples Italy
CHU Gabriel-Montpied Clermont Ferrand France
Centre hospitalier universitaire de Liege Liege Belgium
Universitair Ziekenhuis Gent Gent Belgium
Universitaetsklinikum Schleswig-Holstein AöR Kiel Germany
Hospital General Universitario Gregorio Maranon Madrid Spain
Hospital Universitario 12 De Octubre Madrid Spain
Hospital Del Mar Barcelona Spain
Institutul Regional De Gastroenterologie Hepatologie Prof. Dr. Octavian Fodor Cluj Cluj Napoca Romania
Instituto Portugues De Oncologia Do Porto Francisco Gentil E.P.E. Porto Portugal
AZ Turnhout Turnhout Belgium
Mtz Clinical Research Powered By Pratia Warsaw Poland
Grand Hopital De Charleroi Charleroi Belgium
Jasz-Nagykun-Szolnok Varmegyei Hetenyi Geza Korhaz-Rendelointezet Szolnok Hungary
Komarom-Esztergom Varmegyei Szent Borbala Korhaz Tatabanya Hungary
CCAB Centro Clinico Academico Braga Associacao Braga Portugal
National Institute Of Gastroenterology Saverio De Bellis Research Hospital Castellana Grotte Italy
Hopital De Libramont Libramont-Chevigny Belgium
RKH Klinken Ludwigsburg-Bietigheim gGmbH Ludwigsburg Germany
Szpital Kliniczny Ministerstwa Spraw Wewnetrznych I Administracji Z Warminsko-Mazurskim Centrum Onkologii W Olsztynie Olsztyn Poland
Mazowiecki Szpital Wojewodzki Im. Sw. Jana Pawła II W Siedlcach Sp. z o.o. Siedlce Poland
Spitalul Municipal Ploiesti Ploiesti Romania
Unidade Local De Saude De Matosinhos E.P.E. Senhora Da Hora Portugal
Unidade Local De Saude Do Alto Ave E.P.E. Guimaraes Portugal
Multiprofile Hospital For Active Treatment-Uni Hospital Ltd. Panagyurishte Bulgaria
MBAL Serdika Ltd. Sofia Bulgaria
Beskidzkie Centrum Onkologii Szpital Miejski Im. Jana Pawla II W Bielsku-Bialej SPZOZ Bielsko-Biala Poland
University Multiprofile Hospital For Active Treatment Saint Georgi EAD Plovdiv Bulgaria
Hospital Universitario Ramon Y Cajal Madrid Spain
Hospital Universitario Central De Asturias Oviedo Spain
Institut De Cancerologie Strasbourg Europe STRASBOURG, Alsace France
Hospital General Universitario De Elche Elche Spain
Centrul De Oncologie SF Nectarie S.R.L. Craiova Romania
Tolna Vármegyei Balassa János Kórház Szekszard Hungary
University Of Debrecen Debrecen Hungary
Institutul Clinic Fundeni Bucharest Romania
Hospital Clinico Universitario De Valencia Valencia Spain
Institutul Regional De Oncologie Iasi Iasi Romania
Virgen del Rocío University Hospital Sevilla Spain
Universitaetsklinikum Tuebingen AöR Tuebingen Germany
Ospedale San Raffaele S.r.l. Milan Italy
Hospital Clinic De Barcelona Barcelona Spain
Charite Universitaetsmedizin Berlin KöR Berlin Germany
Hospital Da Luz S.A. Lisbon Portugal
Fakultni Nemocnice Hradec Kralove Novy Hradec Kralove Czechia
Vorarlberger Krankenhaus-Betriebsgesellschaft mbH Feldkirch Austria
IRCCS Ospedale Policlinico San Martino Genoa Italy
Universita’ Di Pisa Pisa Italy
Universita’ Politecnica Delle Marche Ancona Italy
Hospital General Universitario De Valencia Valencia Spain
Szabolcs-Szatmar-Bereg Varmegyei Oktatokorhaz Nyiregyhaza Hungary
Del-Pesti Centrumkorhaz Orszagos Hematologiai Es Infektologiai Intezet Budapest Hungary
Oncomed S.R.L. Timisoara Romania
Pratia S.A. Skorzewo Poland
Multidisciplinary Hospital For Active Treatment Haskovo AD Haskovo Bulgaria
Institute Of Oncology Prof. Dr. Ion Chiricuta Cluj-Napoca Cluj Napoca Romania
Samodzielny Publiczny Szpital Kliniczny Nr 1 W Lublinie Lublin Poland
Vseobecna Fakultni Nemocnice V Praze Prague Czechia
Centre Hospitalier Universitaire Amiens Picardie Amiens France
Centre Hospitalier Universitaire De Rennes Rennes France
Lux Med Onkologia Sp. z o.o. Warsaw Poland
University Hospital Olomouc Olomouc Czechia
Institut fuer Klinische Transfusionsmedizin und Immungenetik Ulm gGmbH Ulm Germany
Hopital Beaujon Clichy France
Vrije Universiteit Brussel Jette Belgium
Fondazione I.R.C.C.S. Istituto Neurologico Besta Milan Italy
Fakultni Thomayerova nemocnice Prague Czechia
Fakultni Nemocnice Kralovske Vinohrady Prague Czechia
Institut de Cancérologie de l’Ouest Saint-Herblain France
Hospital CUF Porto S.A. Porto Portugal
Uniklinikum Salzburg Salzburg Austria
Fakultni Nemocnice Ostrava Ostrava Czechia
Csidahelv Uasuclwollqiup Sygjndybv Woluwe-Saint-Lambert Belgium
Skvvbklrlq Emmtbgn Budapest Hungary
Nuc Lvr Gpprhkbpbj Tmpkguoxpmlkg Gvqw Wiener Neustadt Austria
Cfrzag Lebe Bqgwfh Lyon France
Hxwhliqw Umdxrwttcbqxx Munibuj Du Vylxlbdawd Santander Spain
Igffcdui Crmutk Drvlpklxijzttxvlu L'hospitalet De Llobregat Spain
Ijjfcxgn Mukbntdbnp Mcnqhlequm Paris France
Ibsheaol Bnszbnwj Bordeaux France
Pgkkhjjlxeb Lgqmsxpx &jfnzoegtwutdszdfhra Rulee Khohkdrmfol Konin Poland
Plmtifll Wroejygcy Wolfsburg Germany
Cbcilx Hqvhaxmrfky En Uifufanoepemv Dk Lteqzuy Limoges France
Aazwmzusff Pwqljleu Htoqbasb Db Pqkxd Paris France
Bxxctijy Ulglaghirn Hztveqjt Ckgoli Besançon France
Nhfdqpda Ibmpftgu Onmkeezwu Ikk Mdjwe Sthqdtkphaddsgxpunmezktsahlk Ipyjaqxk Btgktgqz Cracow Poland
Kqoondly dit Ucrebqbgdhao Mpawfizj Agw Munich Germany
Mekeghmm Mzsrkvr Asvgbco Pleven Bulgaria
Cmfarpv Odeixxdz Cfgdbq Bjbmgz Edpg Burgas Bulgaria
Umiddzcxon Of Amtbwdv Edegem Belgium
Afvdsll Ouirtvamoru Pfuu Gnvjhmhd Xbdqw Bergamo Italy
Ikenvynm df Cxnllcieilsr Hsuiiomhyqg Ubpmxpnqhwtlf dq Seixj Empetbf (geeoxby Saint Priest En Jarez France
Hrgqqodn Vdlb dbodnavs Barcelona Spain
Hhpmnisx Ukppyrvxoujgm dh A Cmhtvo A Coruna Galicia Spain

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

Trial status

Country Status Recruitment Start
Austria Austria
Not recruiting
20.10.2022
Belgium Belgium
Not recruiting
20.10.2022
Bulgaria Bulgaria
Not recruiting
20.10.2022
Czechia Czechia
Not recruiting
20.10.2022
France France
Not recruiting
20.10.2022
Germany Germany
Not recruiting
20.10.2022
Hungary Hungary
Not recruiting
20.10.2022
Italy Italy
Not recruiting
20.10.2022
Poland Poland
Not recruiting
20.10.2022
Portugal Portugal
Not recruiting
20.10.2022
Romania Romania
Not recruiting
20.10.2022
Spain Spain
Not recruiting
20.10.2022

Trial locations

Bemarituzumab
This is a targeted therapy medication that works by targeting a specific protein called FGFR2b found on some cancer cells. It is being studied in the treatment of gastric (stomach) and gastroesophageal junction cancer.

Nivolumab
This is an immunotherapy medication that helps your immune system fight cancer cells. It works by blocking a protein that prevents your immune system from attacking cancer cells, allowing your body’s immune system to better fight the cancer.

FOLFOX
This is a combination chemotherapy treatment that includes several medications used together to treat cancer. It is commonly used to treat various types of gastrointestinal cancers, including stomach cancer. The combination includes fluorouracil, leucovorin, and oxaliplatin.

Investigated diseases:

Gastric and Gastroesophageal Junction Cancer – A disease that begins when cancer cells form in the tissues of the stomach or the area where the stomach connects to the esophagus (gastroesophageal junction). In this specific type, there is an overexpression of a protein called FGFR2b in the cancer cells. The cancer typically develops slowly over many years, starting with changes in the inner lining of these organs. As the disease progresses, it can grow through the stomach’s wall and spread to nearby lymph nodes and other organs. This particular form of cancer is characterized by abnormal cell growth driven by excessive amounts of FGFR2b protein on the surface of cancer cells.

Trial ID:
2023-505458-16-00
Protocol code:
20210098
NCT ID:
NCT05111626
Trial Phase:
Therapeutic confirmatory (Phase III)

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