Skip to content

A Biomarker Exploratory Study of Zolbetuximab-Based Treatment for Gastric Cancer

Phosphoproteomic Analysis to Elucidate Resistance Mechanisms and Identify Novel Therapeutic Targets in Zolbetuximab-Based Treatment for Gastric Cancer - Phosphoproteomic Analysis to Elucidate Resistance Mechanisms and Identify Novel Therapeutic Targets in Zolbetuximab-Based Treatment for Gastric Cancer

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
JPRN
Registry ID
JPRN-UMIN000061994
Enrollment
15
Registered
2026-06-22
Start date
2025-05-09
Completion date
Unknown
Last updated
2026-09-14

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Patients with unresectable advanced or recurrent gastric cancer scheduled to receive zolbetuximab-containing chemotherapy

Interventions

None listed

Sponsors

National Cancer Center
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1) Patients who have been histologically diagnosed with gastric cancer. 2) Patients whose gastric cancer tumor tissue is confirmed to be CLDN18.2-positive by additional testing, including those who have already been confirmed to be CLDN18.2-positive at another institution prior to referral. 3) Patients who are scheduled to receive, or may potentially receive, anticancer drug therapy using zolbetuximab at the participating institution. 4) Patients aged 18 years or older at the time of informed consent. 5) Patients from whom at least one tumor tissue sample and at least one non-tumor sample can be obtained from the following specimens: Tumor samples: Tumor tissue samples newly collected after consent for this study. Non-tumor samples: Non-tumor tissue samples newly collected for this study and/or peripheral blood samples. If newly collected samples are difficult to obtain or if archived samples are considered useful for analysis, the use of archived samples will be permitted. 6) Patients who have provided written informed consent before study registration after receiving a sufficient explanation of the study. 7) Patients may be enrolled even if they are participating in other clinical trials, including investigational new drug trials.

Exclusion criteria

Exclusion criteria: 1) Patients who are considered unsuitable for enrollment in this study by the attending physician.

Design outcomes

Primary

MeasureTime frame
Comprehensive phosphoproteomic profiling

Secondary

MeasureTime frame
Comprehensive gene expression analysis Protein profiling of circulating extracellular vesicles in blood

Countries

Japan

Contacts

Public ContactShotaro Yamaguchi

National Cancer Center Japan Department of Gastrointestinal Medical Oncology

shyamag4@ncc.go.jp03-3542-2511

Outcome results

None listed

Source: JPRN (via WHO ICTRP) · Data processed: Sep 19, 2026