Phase 1 Prostate Cancer Trial, Recruiting
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.
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
Where this trial is recruiting
Primary endpoints
Adverse events (AEs) and Serious Adverse Events (SAEs); Effective dose equivalent (mSv) and absorbed doses (mGy)
Can't join this trial?
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.