Phase 2 Prostate Cancer Trial, Recruiting NCT06575257 Sponsor: Xijing Hospital Condition: Prostate Cancer
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Phase 2 Prostate Cancer Trial, Recruiting

NCT06575257
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 aged 18 to 75 years old.
  • People who have been diagnosed with prostate cancer through a tissue or cell sample test, and whose doctors have determined that surgery to remove the prostate (radical prostatectomy) is an appropriate treatment option.
  • People who are largely able to carry out daily activities with no more than mild limitations (based on a standard medical fitness scale called ECOG, with a score of 0 or 1).
  • People who are able to complete specialised prostate imaging scans (mpMRI or 68Ga-PSMA PET/CT) both before and after the pre-surgery treatment phase.
  • People whose cancer meets at least one of the following staging conditions: the imaging scans show the tumour has reached a certain size or has spread to nearby lymph nodes; the tumour has a Gleason score (a measure of cancer aggressiveness) of 8 or higher; or the PSA blood level (a prostate cancer marker) is 20 ng/ml or above.
  • People whose blood tests and organ function results fall within acceptable ranges, as checked within 28 days before joining the trial (confirm specific values with the trial site).
  • People who are willing to voluntarily sign a consent form and follow all study requirements.

Who may not be able to join:

  • People whose cancer has spread to lymph nodes in or beyond the local area, to bones, or to other organs, based on clinical or scan findings.
  • People who have previously received hormone therapy, surgery to remove hormone-producing organs, targeted local treatment, radiotherapy, or chemotherapy for prostate cancer.
  • People with a severe or uncontrolled active infection.
  • People with severe heart failure classified as Class III or IV by standard heart failure guidelines (New York Heart Association scale).
  • People with uncontrolled severe high blood pressure, persistently uncontrolled diabetes, lung disease requiring ongoing oxygen use, chronic liver disease, or HIV infection.
  • People with a mental illness, intellectual disability, or any condition that prevents them from being able to give informed consent.
  • People who have had another type of cancer in the past 5 years, except for certain fully treated skin cancers (basal cell or squamous cell skin cancers that have been cured may still be considered eligible — confirm with the 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 12 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: Weijun Qin, MD, The First Affillated Hospital, the Air Force Medical University

Phone: 029-84771579

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
Xijing Hospital
Registry
ClinicalTrials.gov
Start date
1 May 2024
Est. completion
1 May 2026

Where this trial is recruiting

🇨🇳 China

Primary endpoints

Pathologic Complete Response Rate; Proportion of Subjects With Minimal Residual Disease

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: 12 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