A Study of ASP2138 Given by Itself or Given With Other Cancer Treatments in Adults With Stomach Cancer, Gastroesophageal Junction Cancer, or Pancreatic Cancer
This is not medical advice. AI-assisted translation — inaccuracies may occur. Always verify the original and consult your oncologist before taking any steps.
About the trial
Claudin 18.2 protein, or CLDN18.2 is a protein found on cells in the digestive system. It is also found on some tumors. Researchers are looking at ways to attack CLDN18.2 to help control tumors. ASP2138 is thought to bind to CLDN18.2 and a protein on a type of immune cell called a T-cell. This "tells" the immune system to attack the tumor. ASP2138 is a potential treatment for people with stomach cancer, gastroesophageal junction cancer (GEJ cancer) or pancreatic cancer. GEJ is where the tube that carries food (esophagus) joins the stomach. Before ASP2138 is available as a treatment, the researchers need to understand how it is processed by and acts upon the body. In this study, ASP2138 will either be given by itself, or given together with standard treatments for gastric, GEJ and pancreatic cancer. Pembrolizumab and mFOLFOX6, and ramucirumab and paclitaxel are standard treatments for gastric and GEJ cancer. mFOLFIRINOX is a standard treatment for pancreatic cancer. This information will help find a suitable dose of ASP2138 given by itself and together with the standard cancer treatments and to check for potential medical problems from the treatments. The main aims of the study are: * To check the safety of ASP2138 and how well people can tolerate medical problems during the study. * To find a suitable dose of ASP2138 to be used later in the study. * These are done for ASP2138 given by itself and when given together with the standard cancer treatments. Adults 18 years or older with stomach cancer, GEJ cancer, or pancreatic cancer can take part. Their cancer is locally advanced unresectable or metastatic. Locally advanced means the cancer has spread to nearby tissue. Unresectable means the cancer cannot be removed by surgery. Metastatic means the cancer has spread to other parts of the body. There should also be the CLDN18.2 marker in a tumor sample. People cannot take part if they need to take medicines to suppress their immune system, have blockages or bleeding in their gut, have specific uncontrollable cancers, have specific infections, have a condition such as hemophagocytic lymphohistiocytosis (HLH) which is when the body over-reacts to a "trigger" such as infection, or have a specific heart condition ("New York Heart Association Class III or IV"). Phase 1: Lower to higher doses of ASP2138 * ASP2138 is either given through a vein (intravenous infusion) or just under the skin (subcutaneous injection). * Different small groups are given lower to higher doses of ASAP2138. * ASP2138 is either given by itself, or given with 1 of 3 standard treatments: * Pembrolizumab and mFOLFOX6 (first treatment for gastric GEJ cancer) * Ramacirumab and paclitaxel (Second treatment for gastric or GEJ cancer) * ASP2138 with mFOLFIRINOX (first treatment for pancreatic cancer) Phase 1b: doses of ASP2138 worked out from Phase 1 * ASP2138 is either given through a vein or just under the skin. This depends on the findings from Phase 1. * People with gastric cancer, GEJ cancer or pancreatic cancer are given doses of ASP2138, worked out from Phase 1. * This includes doses of ASP2138 given by itself and ASP2138 given with the standard cancer treatments. * The standard cancer treatments given depends on the type of cancer they have. End of treatment visit: This is 7 days after final dose of study treatment or if the study doctor decides to stop the person's treatment. People who have locally advanced unresectable pancreatic cancer will not receive ASP2138 by itself.
Original English text from ClinicalTrials.gov
Who can (and can't) join
✓ Qualifies
- •Wiek 18 lat lub więcej
- •Diagnoza raka żołądka, połączenia przełyku ze żołądkiem lub trzustki, która nie może być operowana lub rozprzestrzeniła się na inne części ciała
- •Nowotwór musi mieć dodatni marker CLDN18.2 potwierdzona badaniem próbki
- •Kobieta nie może być w ciąży i musi stosować antykoncepcję przez co najmniej 6 miesięcy po leczeniu
- •Kobieta nie może karmiać piersią i nie może oddawać jajeczek podczas i przez 6 miesięcy po badaniu
- •Mężczyzna musi stosować antykoncepcję i nie może oddawać nasienia podczas i przez 6 miesięcy po badaniu
- •Nowotwór musi być widoczny na badaniach obrazowych wykonanych w ciągu ostatnich 28 dni
- •Nowotwór musi mieć mierzalne zmiany, którym można śledzić postęp leczenia
Simplified criteria — AI translation
Trial details
- Minimum age
- 18 Years
- Last updated (source)
- July 15, 2026
- Sex
- No restrictions
Therapies / drugs in trial
Locations (46)
University of California Irvine Medical Center
Orange, United States
UCLA Dept of Medicine - Hematology/Oncology, Santa Monica
Santa Monica, United States
Northwestern University
Chicago, United States
University of Kansas Cancer Center
Westwood, United States
Rutgers Cancer Institute of New Jersey
New Brunswick, United States
NYU Langone Medical Center - NYU Medical Oncology Associates
New York, United States
Columbia University
New York, United States
Memorial Sloan Kettering Cancer Center
New York, United States
Duke Children's Hospital and Health Center
Durham, United States
Wake Forest University Baptist Health
Winston-Salem, United States
UT Southwestern Medical Center
Dallas, United States
Virginia Mason Medical Center
Seattle, United States
Froedtert Hospital and the Medical College of Wisconsin
Milwaukee, United States
Sun Yat-sen University Cancer Center
Guangzhou, China
Henan Cancer Hospital
Zhengzhou, China
Union Hospital affiliated to Tongji Medical College of Huazhong University of Science and Technology
Wuhan, China
Ruijin Hospital Affiliated to Shanghai Jiao Tong University School of Medicine
Shanghai, China
The First Affiliated Hospital, College of Medicine, Zhejiang University
Hangzhou, China
Site FR33005
Vaillant, France
Site FR33003
Lyon, France
Site FR33004
Marseille, France
Site FR33006
Poitiers, France
Site FR33001
Saint-Herblain, France
Site FR33002
Toulouse, France
Site IT39004
Milan, Italy
Site IT39001
Milan, Italy
Site IT39005
Rozzano, Italy
Site IT39003
Verona, Italy
Aichi Cancer Center
Nagoya, Japan
National Cancer Center Hospital East
Kashiwa, Japan
Kanagawa Cancer Center
Yokohama, Japan
Kindai University Hospital
Sakai, Japan
The University of Osaka Hospital
Suita, Japan
National Cancer Center Hospital
Chuo-ku, Japan
The Cancer Institute Hospital of Japanese Foundation for Cancer Research
Koto-ku, Japan
PanOncology Trials
San Juan, Puerto Rico
Site KR82004
Seongnam-si, South Korea
Site KR82001
Guro-gu, South Korea
Site KR82002
Jongno-gu, South Korea
Site KR82003
Seocho-gu, South Korea
Site KR82005
Seodaemun-gu, South Korea
Site ES34001
Barcelona, Spain
Site ES34002
Barcelona, Spain
Site ES34006
Barcelona, Spain
Site ES34007
El Palmar, Spain
Site ES34004
Zaragoza, Spain
Trial contact
Astellas Pharma Global Development, Inc.
Contact information from ClinicalTrials.gov. Contact in English.
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Data from ClinicalTrials.gov. AI-assisted translation, last sync: 7/16/2026.
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