Phase 1 Prostate Cancer Trial, Recruiting NCT07600554 Sponsor: Philogen S.p.A. Condition: Prostate Cancer
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Phase 1 Prostate Cancer Trial, Recruiting

NCT07600554
Recruiting Phase 1

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 and fall into one of these groups: cancer that is suspected to have spread and are being considered for initial treatment; rising PSA levels suggesting the cancer may have returned (confirmed PSA level above 0.2 ng/mL); or metastatic disease where treatment with a specific type of targeted radiation therapy (lutetium-177 PSMA) is being considered — including those with negative or unclear PSMA scan results, as long as prostate cancer has been confirmed by a tissue biopsy
  • People who are biologically capable of fathering children must agree to use effective contraception for three months from the time the study drug is given
  • People aged 18 or older
  • People who are generally well enough to carry out all normal daily activities, or whose illness causes only minor limitations (this is measured by a standard medical scale — confirm with trial site)
  • People who have no current infections or other active illnesses at the time of joining
  • People whose side effects from any previous treatment (such as surgery, radiation, or chemotherapy) have largely resolved — with the exception of hair loss and tiredness, which are allowed
  • People with a life expectancy of more than 12 weeks
  • People who are able to undergo the imaging procedures required by the study
  • People who have read and signed a dated consent form confirming they have been fully informed about the study
  • People who are willing and able to attend all required visits and follow all study procedures

Who may not be able to join:

  • People with chronically reduced kidney function, based on specific blood or urine test results (confirm with trial site)
  • People with an active hepatitis infection
  • People with significant heart problems, such as severe heart failure, a heart attack within the past year, uncontrolled high blood pressure, or irregular heart rhythms
  • People with any other ongoing condition that the study investigators believe could make participation unsafe or affect how well the study can be carried out
  • People who have had a major surgical procedure (such as abdominal, heart, or chest surgery) within 4 weeks before receiving the study drug — note that minor procedures such as biopsies are not considered a reason for exclusion
  • People with a serious wound, ulcer, or bone fracture that has not healed
  • People with a known allergy to the study medication or any of its ingredients
  • People who have received any cancer treatment (such as chemotherapy, immunotherapy, radiation, or surgery) within 3 weeks before the study scan
  • People who have received, or are due to receive, another experimental medication from one month before the study injection through to the end of study participation

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 6 July 2026
Phase 1: approximately ~10% 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: +41 43 544 88 02

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 1
Sponsor
Philogen S.p.A.
Registry
ClinicalTrials.gov
Start date
27 May 2026
Est. completion
1 December 2027

Where this trial is recruiting

🇮🇹 Italy

Primary endpoints

Adverse events (AEs) and Serious Adverse Events (SAEs); Effective dose equivalent (mSv) and absorbed doses (mGy)

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: 6 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