Phase 2 Prostate Cancer Trial, Recruiting NCT07332000 Sponsor: Candel Therapeutics, Inc. Condition: Prostate Cancer
Back to Prostate Cancer

Phase 2 Prostate Cancer Trial, Recruiting

NCT07332000
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 their written agreement to take part in this specific study before enrolling
  • People who have been diagnosed with prostate cancer (a specific type called adenocarcinoma), confirmed through a tissue sample test
  • People whose prostate cancer is classified as "intermediate-risk" according to a standard set of guidelines used by cancer specialists (called NCCN criteria)
  • People whose doctors have determined they are medically suitable to receive a standard course of external beam radiation therapy to the prostate, and — for one group in the trial — who are also able to tolerate several injections into the prostate guided by ultrasound
  • People aged 18 or older
  • People who are reasonably active and able to care for themselves, based on a standard medical scoring system (rated 0, 1, or 2 on the ECOG scale — confirm with trial site if unsure what this means)
  • For one group in the trial only, people whose blood test results meet certain minimum levels for liver enzymes, kidney function, and blood cell counts (the trial site will check these specific values)

Who may not be able to join:

  • People with active liver disease, such as cirrhosis or active hepatitis
  • People currently taking high-dose steroid medications (more than 10 mg of prednisone per day) or other medicines that suppress the immune system
  • People known to be living with HIV
  • People whose cancer has spread to nearby lymph nodes or to other parts of the body
  • People who are planning to receive radiation treatment covering the whole pelvic area, rather than the prostate only
  • People who currently have another type of cancer, with the exception of certain common skin cancers (squamous cell or basal cell)
  • People with other serious health conditions or significant organ problems that, in the trial doctor's judgment, would interfere with treatment or follow-up — for example, severe prostate inflammation or inflammatory bowel disease, which can make radiation to the prostate unsuitable
  • People who have previously received treatment for prostate cancer, except for a specific surgical procedure called a TURP (a procedure to clear a blocked urethra); people with a prior TURP may still be considered if the trial doctor determines they are able to receive the prostate injections
  • People who have had, or are planning to have, surgical removal of the testicles as a form of hormone treatment
  • For one group in the trial only, people with a known allergy or sensitivity to the medications acyclovir or valacyclovir

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 27 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.

GP referral letter

Print a one-page summary to share with your doctor.

Trial details

Status
Recruiting
Phase
Phase 2
Sponsor
Candel Therapeutics, Inc.
Registry
ClinicalTrials.gov
Start date
30 October 2025
Est. completion
1 August 2026

Where this trial is recruiting

🇺🇸 United States

Primary endpoints

Biodistribution of aglatimagene besadenovec

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: 27 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