Phase 2 Stomach Cancer Trial, Recruiting NCT03614650 Sponsor: Shenzhen Geno-Immune Medical Institute Condition: Stomach Cancer
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Phase 2 Stomach Cancer Trial, Recruiting

NCT03614650
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 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.

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 15 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

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

Status
Recruiting
Phase
Phase 2
Sponsor
Shenzhen Geno-Immune Medical Institute
Registry
ClinicalTrials.gov
Start date
1 July 2025
Est. completion
30 June 2028

Where this trial is recruiting

🇨🇳 China

Primary endpoints

percentage of adverse effects after EIE cell injection

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: 15 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