Phase 2 Stomach Cancer Trial, Recruiting
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 aged between 18 and 75 years
- People who have had surgery to fully remove their stomach cancer, including removal of surrounding lymph nodes (called D2 or wider dissection), with no cancer left behind after surgery
- People who did not receive any cancer treatment (such as chemotherapy) before their surgery
- People whose cancer has been confirmed by laboratory testing to be a type called gastric adenocarcinoma (a specific type of stomach cancer)
- People whose cancer is classified as stage III gastric or gastroesophageal junction adenocarcinoma (where the stomach meets the oesophagus), according to a standard cancer staging system (AJCC 8th edition)
- People whose cancer shows a moderate-to-high level of a protein called HER2 (confirmed by a specific lab test result of IHC 3+ or 2+)
- People who are largely able to carry out daily activities, with only minor limitations (rated 0 or 1 on a standard activity scale called ECOG PS)
- People whose life expectancy is estimated to be at least 3 months
- People who are able to understand the study, are willing to take part voluntarily, and can sign a consent form
- People who are willing and able to follow the treatment plan required by the study
- People who have complete medical imaging and pathology records available
- People whose liver, kidneys, and blood counts are functioning well enough to safely participate (confirm with trial site)
Who may not be able to join:
- People whose stage III stomach or gastroesophageal junction cancer has not been confirmed by laboratory tissue or cell testing
- People who are unable to receive the specific treatments used in this trial (a drug called disitamab vedotin or a chemotherapy regimen called SOX)
- People who are unable to attend the required follow-up appointments
- People who are unwilling or unable to follow the treatment plan set out in the study
- People who are unable or unwilling to have required scans during the study (such as CT scans)
- People who have an active autoimmune disease (where the immune system attacks the body's own tissues)
- People with a history of substance abuse that cannot be stopped, or who have a severe or poorly controlled mental health condition, or a severe or poorly controlled serious illness affecting the whole body
- People who have another medical condition that the study doctor believes could put them at significant risk or prevent the study from being completed safely
- People who have had another type of cancer in the past 5 years, unless it was a type considered fully cured by treatment — such as thyroid cancer, a very early-stage cervical condition, certain skin cancers, or early breast duct cancer treated with surgery (confirm with trial site)
- Women who are currently breastfeeding
- People who received cancer treatment before surgery (neoadjuvant therapy) or chemotherapy delivered directly into the abdomen during surgery
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.
GP referral letter
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Trial details
Where this trial is recruiting
Primary endpoints
3-year-DFS rate
Can't join this trial?
Data last synced from ClinicalTrials.gov: 21 July 2026. Trial status can change. Always verify current status directly with the trial site before making any decision.