Prostate Cancer Trial, Recruiting NCT07219303 Sponsor: Fox Chase Cancer Center Condition: Prostate Cancer
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Prostate Cancer Trial, Recruiting

NCT07219303
Recruiting Not Applicable

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 (adenocarcinoma) confirmed by a tissue biopsy, at an intermediate or favorable high-risk stage (classified as stage IIA–IIC under a specific staging system)
  • People aged 18 or older
  • People whose general physical health and ability to carry out daily activities meets a certain minimum level (confirm with trial site)
  • People whose prostate is no larger than 100cc in size, as measured by MRI or ultrasound within the past 24 months (or within 6 months if hormone therapy has been used)
  • People who have had a specific type of prostate MRI scan (multiparametric MRI) showing certain findings, or a particular type of nuclear medicine scan (PSMA PET/CT), within 12 months of joining the study
  • People whose urinary symptom score is 15 or below on a standard questionnaire (use of medications to help urinary flow is allowed)
  • People who are able to fully understand and are willing to sign a consent form for the study

Who may not be able to join:

  • People who are currently experiencing severe bowel or urinary side effects (grade 3 or higher on a standard scale)
  • People who are currently taking part in another clinical trial involving an experimental treatment
  • People who have previously had radiation therapy to the pelvic area
  • People whose cancer has spread to the lymph nodes
  • People whose cancer has been found to have grown outside the prostate on MRI (scanned within the past 24 months, or before hormone therapy began if hormone therapy was used)
  • People who have previously had procedures that destroy prostate tissue, such as cryotherapy, HIFU, or nanoknife treatment
  • People who have previously had a full surgical removal of the prostate (simple prostatectomy) — however, people who have had certain other prostate procedures (TURP or laser enucleation) may still be eligible
  • People currently receiving other cancer-fighting drugs, including methotrexate — however, people who have previously received hormone therapy (ADT) may still be eligible if the total course was less than 6 months, the last dose was more than 6 months ago, and hormone levels have recovered to a certain level (confirm with trial site)
  • People who have another serious uncontrolled health condition, such as an active infection, unstable heart condition, uncontrolled heart rhythm problems, or a mental health or social situation that would make it difficult to follow the study requirements
  • People with any other condition that their treating doctor considers makes it unsafe to receive the radiation treatment used in this trial
  • People with active inflammatory bowel disease or an active connective tissue disorder affecting blood vessels
  • People who are unable to have small marker seeds (fiducials) placed in the prostate
  • People who are unable to have a spacer device placed between the prostate and rectum (people with an iodine allergy who can only receive a non-contrast spacer may still be eligible)
  • People who are unable to have a prostate MRI scan
  • People with artificial hip replacements on both sides — people with a replacement on one side only may be eligible if the radiation treatment plan meets all required safety limits (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 26 July 2026
This study is not part of the standard drug-approval phase pathway (for example an observational, device, behavioural, or registry study), so a phase success rate does not apply.

Contact this trial

Principal Investigator: Mark A Hallman, MD, PhD, FCCC

Phone: 215-728-2581

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
Not Applicable
Sponsor
Fox Chase Cancer Center
Registry
ClinicalTrials.gov
Start date
25 September 2025
Est. completion
1 August 2033

Where this trial is recruiting

🇺🇸 United States

Primary endpoints

Severe (CTCAE grade ≥ 3) treatment-related (possibly, probably or definitely) toxicity occurring within 90 days of treatment.

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: 26 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