OncoMatch/Clinical Trials/NCT05365581
A Study of ASP2138 Given by Itself or Given With Other Cancer Treatments in Adults With Stomach Cancer, Gastroesophageal Junction Cancer, or Pancreatic Cancer
Is NCT05365581 recruiting? Yes, currently enrolling (May 2026). This Phase 1 trial studies multiple treatments for gastric adenocarcinoma.
Treatment: Ramucirumab · Paclitaxel · Irinotecan · Capecitabine · ASP2138 · Pembrolizumab · Oxaliplatin · Leucovorin · Fluorouracil — 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.
Check if I qualifyExtracted eligibility criteria
Cancer type
Gastric Cancer
Esophageal Carcinoma
Pancreatic Cancer
Biomarker criteria
Required: CLDN18 overexpression
Participant's tumor sample is positive for claudin (CLDN)18.2 expression by central immunohistochemistry (IHC) testing.
Required: HER2 (ERBB2) negative
Participant has a human epidermal growth factor receptor 2 (HER2)-negative tumor per local testing.
Required: PD-L1 (CD274) CPS ≥ 1 (CPS ≥ 1)
Unique to EU: Participant must have a PD-L1 CPS ≥ 1.
Disease stage
Required: Stage III, IV
Metastatic disease required
radiographically-confirmed, locally advanced, unresectable or metastatic disease within 28 days prior to the first dose of study intervention
Performance status
ECOG 0–1(Restricted strenuous activity)
Prior therapy
Cannot have received: CLDN18.2-targeted therapy (zolbetuximab, chimeric antigen receptor CLDN18.2-specific T cells)
Exception: Allowed in dose expansion cohorts only if >28 days or 5 half-lives prior to first dose and no Grade ≥ 3 GI toxicity
Participant who has received CLDN18.2-targeted therapy (e.g., zolbetuximab or chimeric antigen receptor CLDN18.2-specific T cells) prior to first dose of study intervention administration is not eligible for dose escalation cohorts. However, a participant who has received CLDN18.2-targeted therapy greater than 28 days or 5 half-lives (whichever is longer) prior to first dose study intervention administration is eligible for dose expansion cohorts only, with the exception of participants who have experienced Grade ≥ 3 gastrointestinal toxicity after receiving an CLDN18.2-targeted therapy.
Lab requirements
Blood counts
Must meet all criteria based on laboratory tests within 7 days prior to the first dose of study intervention. If a participant has received a recent blood transfusion, the laboratory tests must be obtained ≥ 1 week after any blood transfusion.
Kidney function
Must meet all criteria based on laboratory tests within 7 days prior to the first dose of study intervention. If a participant has received a recent blood transfusion, the laboratory tests must be obtained ≥ 1 week after any blood transfusion.
Liver function
Must meet all criteria based on laboratory tests within 7 days prior to the first dose of study intervention. If a participant has received a recent blood transfusion, the laboratory tests must be obtained ≥ 1 week after any blood transfusion.
Cardiac function
QTcF ≤ 470 msec; no unstable angina, MI, ventricular arrhythmia, or hospitalization for heart failure within 6 months prior to first dose.
Participant has QT interval by Fredericia (QTcF) ≤ 470 msec. Must meet all of criteria based on laboratory tests within 7 days prior to the first dose of study Intervention. If a participant has received a recent blood transfusion, the laboratory tests must be obtained ≥ 1 week after any blood transfusion. Participant has had within 6 months prior to first dose of study intervention any of the following: unstable angina, myocardial infarction, ventricular arrhythmia requiring intervention or hospitalization for heart failure.
Structured fields extracted by AI. May contain errors — verify against the official protocol.
US trial sites
- University of California Irvine Medical Center · Orange, California
- UCLA Dept of Medicine - Hematology/Oncology, Santa Monica · Santa Monica, California
- Northwestern University · Chicago, Illinois
- University of Kansas Cancer Center · Westwood, Kansas
- Rutgers Cancer Institute of New Jersey · New Brunswick, New Jersey
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