Phase 2 Peripheral Arterial Disease 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:
- You were first diagnosed between the ages of 18 months and 18 years, and you are at least 3 years old at the time of joining the trial.
- You have a solid tumour that has come back or stopped responding to treatment, and a recent scan (done within the last 3 months) showed that your tumour has enough of a specific protein called somatostatin receptors on its surface (a score of 2 or higher on the scan).
- You are generally well enough to carry out some daily activities, as measured by a standard health scale used for children and young people.
- Your doctors expect you to live for at least 3 more months.
- You are able to swallow tablets or capsules.
- Your blood counts, kidney function, liver function, and protein levels are within acceptable ranges based on tests done in the last 28 days (confirm specific values with trial site).
- If you are female and have started your periods, or are 12 years old or older, a pregnancy test must come back negative before joining.
- If you could become pregnant or father a child, you must agree to use reliable contraception during the trial and for several months after the last dose of the study treatments.
- You (and your parent or guardian if you are under 18) are willing and able to give written consent to take part in the trial.
- You have recovered well enough from any major surgery before starting the study treatment.
- There are no significant personal, family, social, or location-related reasons that would make it hard for you to follow the trial schedule and attend appointments.
Who may not be able to join:
- You have previously had a serious liver reaction caused by a medication that required dose changes or stopping treatment, or that the doctor feels could pose a risk.
- You have already received more than one treatment with a type of radioactive drug similar to the one used in this trial (radiolabelled somatostatin analogues).
- You are unable to swallow tablets or capsules.
- You are currently receiving any other cancer treatments or experimental treatments, or it has been less than 28 days since your last cancer treatment (or less than 4 months if that treatment was a type of immunotherapy called a checkpoint inhibitor).
- You have received a specific type of long-acting hormone-blocking drug (long-acting somatostatin analogue) within the last 28 days.
- You have a known allergy to any of the ingredients in the study medications (confirm with trial site).
- You currently have an infection that is not under control.
- You are currently breastfeeding.
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
Principal Investigator: Marta Osuna Marco, PhD, HM Monteprincipe
Phone: +34 917 08 99 35
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
To estimate the safety of the combination of 177LUDOTATATE and olaparib.; To estimate the preliminary activity of the combination of 177LUDOTATATE and olaparib.
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.