Phase 2 Prostate Cancer Trial, Recruiting NCT07068555 Sponsor: Shenzhen Geno-Immune Medical Institute Condition: Prostate Cancer
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Phase 2 Prostate Cancer Trial, Recruiting

NCT07068555
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 prostate cancer (specifically a type called adenocarcinoma), confirmed by a laboratory tissue test
  • People who are generally healthy and active, or have only mild limitations in daily activity (this is measured by a standard medical scale called ECOG 0–1)
  • People with a life expectancy of at least 12 weeks
  • People whose blood test results show white blood cell counts, platelet counts, and haemoglobin levels within the required ranges (confirm with trial site for exact values)
  • People whose kidney and liver function blood tests fall within the required ranges (confirm with trial site for exact values)
  • People who are able to produce sperm must be willing to use effective contraception during the trial
  • People who are willing to provide blood samples for research purposes
  • People who are able to complete questionnaires, either on their own or with help
  • People who are able to undergo a procedure called leukapheresis, where blood is drawn to collect certain blood cells
  • People who do not have a known immune system deficiency
  • People who have not had another type of cancer in the past 5 years, except for certain skin cancers (basal cell or squamous cell) that were treated with local surgical removal only
  • People who do not have another serious illness at the time of joining
  • People who have no known history of a positive tuberculosis (PPD) skin test
  • People whose HIV and Hepatitis C virus (HCV) tests have come back negative

Who may not be able to join:

  • People who were still taking a steroid medication called dexamethasone at a dose greater than 4 mg per day at the time of a specific blood cell collection procedure
  • People who have a history of autoimmune diseases, or any condition that requires long-term use of hormonal or immune-suppressing medications
  • People who have a history of allergic reactions to immune cells or to the supporting substances used in cell-based treatments
  • People who have an active infection with a fever at the time of joining
  • People who have had a prolonged low white blood cell count (lasting more than 10 days) that has been difficult to correct with treatment
  • People with a bacterial, fungal, or viral infection that is not under control
  • People who are living with HIV, active Hepatitis B (HBV), or active Hepatitis C (HCV)
  • People who have severe failure of a major organ, such as the heart, liver, kidneys, or lungs
  • People who have previously received a cell therapy treatment and have been assessed by the trial team as not suitable for this type of treatment
  • People who, in the opinion of the researchers, have any other factor that could increase risk or affect the reliability of the trial results (confirm with trial site)

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 23 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: +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
15 June 2025
Est. completion
15 June 2028

Where this trial is recruiting

🇨🇳 China

Primary endpoints

Events of adverse effects after the DC vaccine 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: 23 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