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 who have signed a written consent form before any study procedures begin.
- People whose cancer tissue samples test positive for at least one of a specific set of proteins found on tumour cells (such as GD2, mesothelin, CEA, P16, MMP, Melan A, MAGE A1, MAGE A3, or MAGE A4).
- People with a general health status rated as 0, 1, or 2 on a standard medical scale (meaning able to carry out daily activities, with or without some limitations).
- People with a life expectancy of at least 3 months.
- People who are able to follow the requirements of the study as assessed by the trial team.
- People with a confirmed diagnosis of high-risk gynaecological cancer at an advanced stage (Stage III or IV, based on the FIGO classification system).
- People who are not pregnant, and who are using appropriate contraception if there is a possibility of becoming pregnant.
- People whose blood test results show adequate bone marrow function, including sufficient levels of white blood cells and platelets.
- People whose blood test results show that their kidneys and liver are functioning within acceptable ranges as defined by the trial.
Who may not be able to join:
- People whose cancer tissue samples test negative for all of the specific tumour-associated proteins being studied.
- People who have taken part in any other cell therapy trial within the past year.
- People who have received another experimental drug within the 28 days before the study start date.
- People who have had a minor surgical procedure (such as biopsy, needle aspiration, or placement of a central line) within 2 days before the study start date.
- People who are pregnant or currently breastfeeding.
- People who are unable to meet the requirements of the trial.
- People whose blood test results show that bone marrow function is below the levels required by the trial (low white blood cell count, low platelets, or low haemoglobin).
- People whose liver or kidney function test results fall outside the acceptable ranges defined by the trial.
- People who have a serious active infection that requires intravenous (IV) antibiotics at the time of screening.
- People who test positive for HIV, syphilis (Treponema pallidum), or tuberculosis (TB).
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.
Contact this trial
Principal Investigator: Lung-Ji Chang, PhD, Shenzhen Geno-Immune Medical Institute
Phone: +86 0755-86573763
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
Where this trial is recruiting
Primary endpoints
percentage of adverse effects after EIE cell injection
Can't join this trial?
Data last synced from ClinicalTrials.gov: 15 July 2026. Trial status can change. Always verify current status directly with the trial site before making any decision.