Phase 2 Ovarian Cancer Trial, Recruiting NCT03184753 Sponsor: Shenzhen Geno-Immune Medical Institute Condition: Ovarian Cancer
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Phase 2 Ovarian Cancer Trial, Recruiting

NCT03184753
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 given written informed consent before any study-related procedures begin.
  • Women aged 20 years or older.
  • People with a general health/activity level rated as 0, 1, or 2 on a standard oncology scale (meaning able to carry out at least some daily activities — confirm with trial site).
  • People with a life expectancy of at least 3 months.
  • People who are able to follow the trial's requirements and schedule.
  • People who have been confirmed through a tissue sample to have high-risk ovarian cancer at an advanced stage (Stage III or IV, using international gynaecology guidelines), and who have achieved a complete remission (no detectable cancer) after treatment for their first recurrence.
  • People who are not pregnant, and who are using appropriate contraception if there is any possibility of becoming pregnant.
  • People whose blood test results show healthy bone marrow function, with sufficient white blood cell and platelet counts.
  • People whose blood test results show that the kidneys and liver are functioning within acceptable levels.

Who may not be able to join:

  • People whose ovarian cancer is of a non-epithelial type (a specific tissue type — confirm with trial site).
  • People with ovarian tumours classified as borderline (low malignant potential).
  • People who have both endometrial cancer and ovarian cancer occurring at the same time.
  • People with signs of free air in the abdomen that cannot be explained by a recent medical procedure.
  • People who have previously received gene-engineered T cell therapy (a type of immune cell treatment — confirm with trial site).
  • People who are currently taking, or have recently taken (within 28 days before the trial start), another experimental drug, or who have previously participated in this same trial.
  • People who have had a minor surgical procedure within 2 days before the trial start date, including procedures such as placement of a central line, tumour biopsy, or needle fluid sampling.
  • People who are pregnant or currently breastfeeding.
  • People whose blood test results show bone marrow function that falls below the required levels for white blood cells, platelets, or haemoglobin.
  • People whose blood test results show liver or kidney function below the required levels, including certain markers of liver health, kidney filtering ability, or protein in the urine above acceptable limits.
  • People who have a serious active infection currently requiring intravenous (IV) antibiotics.
  • People who test positive for HIV, syphilis (Treponema pallidum), 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 8 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 May 2025
Est. completion
30 September 2028

Where this trial is recruiting

🇨🇳 China

Primary endpoints

percentage of adverse effects after OC-IgT cells 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: 8 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