Phase 2 Peripheral Arterial Disease Trial, Recruiting NCT06607692 Sponsor: Fundación de investigación HM Condition: Peripheral Arterial Disease
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Phase 2 Peripheral Arterial Disease Trial, Recruiting

NCT06607692
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:

  • 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.

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 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.

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

Status
Recruiting
Phase
Phase 2
Sponsor
Fundación de investigación HM
Registry
ClinicalTrials.gov
Start date
20 September 2024
Est. completion
1 July 2029

Where this trial is recruiting

🇪🇸 Spain

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?

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