Phase 2 Stomach Cancer Trial, Recruiting NCT06519591 Sponsor: Ruijin Hospital Condition: Stomach Cancer
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Phase 2 Stomach Cancer Trial, Recruiting

NCT06519591
Recruiting Phase 2

Who may be able to join

AI generated eligibility summary. Written by an AI model from the official source data and checked on a sample basis. It can contain mistakes, so confirm anything important against the original source. How we use AI

Who might be able to join this trial:

  • People who have been diagnosed with stomach (gastric) cancer of a specific type called adenocarcinoma, where lab tests show the tumour is HER2-negative, and who have not had surgery to remove the primary tumour or any spread of the cancer
  • People whose stomach cancer has spread to the lining of the abdomen (peritoneal metastases), confirmed or requiring confirmation by a keyhole surgical procedure called laparoscopy, and who do not have a blockage in the stomach outlet or intestines
  • People whose tumour tests positive for a protein called Claudin 18.2 at specific levels (confirm with trial site for exact thresholds)
  • People aged 18 or older at the time of registration
  • People who are generally able to carry out daily activities with little or no difficulty, based on a standard performance scale (ECOG score of 0 or 1)
  • People who are expected to live for more than 3 months
  • People whose bone marrow, liver, and kidneys are functioning well enough, as shown by blood tests

Who may not be able to join:

  • People whose cancer has spread to places other than the abdominal lining, such as the liver, lungs, or nearby lymph nodes
  • People who are pregnant, have given birth within the last 28 days, or are currently breastfeeding
  • People who have previously received certain immune therapies (such as PD-1, PD-L1, or CTLA-4 treatments) or targeted therapy directed at the Claudin 18.2 protein
  • People who have had another cancer diagnosis either at the same time or within the past 5 years
  • People with severe mental illness, uncontrolled epilepsy, or significant disease of the brain or nervous system
  • People with serious active heart problems, such as significant heart failure, troublesome irregular heartbeat requiring medication, or a heart attack within the past 12 months
  • People with a blockage or significant problem in the upper digestive tract that could prevent a study medication called S-1 from being properly absorbed
  • People with known nerve damage in the hands or feet beyond a mild level (confirm with trial site)
  • People who are taking steroids or immune-suppressing medications following an organ transplant
  • People with severe infections that cannot be controlled, or other severe uncontrolled health conditions
  • People with moderate or severe kidney problems, based on specific kidney function test results (confirm with trial site for exact thresholds)
  • People known to be missing an enzyme called DPD, which is needed to process certain chemotherapy drugs safely
  • People who have had a severe allergic reaction to paclitaxel (a chemotherapy drug) or to any ingredient in the study medications
  • People with an active autoimmune disease (where the immune system attacks the body) or a history of a hard-to-treat autoimmune condition
  • People who are HIV-positive, or who have active hepatitis B or hepatitis C infections at specific levels requiring antiviral treatment (confirm with trial site for exact definitions)
  • People who have used steroids or other immune-suppressing medicines in the 14 days before joining the trial, with some exceptions for low-dose or locally applied treatments (confirm with trial site)
  • People with uncontrolled irregular heartbeat, a heart attack in the 12 months before joining, or active tuberculosis

Important: Always verify eligibility with the trial site directly before applying.

Based on publicly available eligibility criteria from ClinicalTrials.gov. Verify directly with the trial site before acting. This is not medical advice.

This is a simplified plain English summary of the eligibility criteria. Full criteria are set by the trial investigators and may include additional requirements not shown here. Never self-exclude from a trial based on this summary. Contact the trial site directly to confirm your eligibility.
Last synced 26 July 2026
Phase 2: approximately ~30% of drugs entering this phase reach regulatory approval, based on published industry-wide historical data. This is not specific to this trial.
Phase success rates shown are historical industry-wide averages based on published data. They are not a prediction for this specific trial or your individual situation.

Contact this trial

Phone: 8621-64370045

Contact details sourced from ClinicalTrials.gov. Verify directly with the trial site before attending.

GP referral letter

Print a one-page summary to share with your doctor.

Trial details

Status
Recruiting
Phase
Phase 2
Sponsor
Registry
ClinicalTrials.gov
Start date
25 February 2025
Est. completion
1 May 2026

Where this trial is recruiting

🇨🇳 China

Primary endpoints

1-year survival rate

Can't join this trial?

Expanded access pathways

If this trial is not available to you, other access pathways may exist. In Australia, the TGA Special Access Scheme allows access to unapproved therapeutic goods for individual patients.

TGA Special Access Scheme information

Find other recruiting trials on ClinicalTrials.gov

Data last synced from ClinicalTrials.gov: 26 July 2026. Trial status can change. Always verify current status directly with the trial site before making any decision.

Trial recruitment status can change without notice between our nightly data updates. Always contact the trial site directly to confirm current recruitment status before making any decisions or travel arrangements.

View original record on ClinicalTrials.gov