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NCT05870423Possibly a fitRecruiting

Testing PARP inhibitors with peptide radiation for NET

Neuroendocrine TumorsPeptide Receptor Radionuclide Therapy

Treatments studied

Part of Cancer clinical trials.

This early-phase study tests whether adding a medicine called a PARP inhibitor to peptide receptor radionuclide therapy (PRRT) can better control advanced or metastatic neuroendocrine tumors (NET). It may help by targeting tumor DNA repair while PRRT delivers targeted radiation.

Summary written for real people, not researchers, by Clin2.

Phase
Phase 1
Enrollment
24 people
Ages
18 years and older
Study type
Interventional

Who can take part

  • You are 18 or older and have a NET that has spread or is locally advanced
  • Your tumor is “well-differentiated” (grade 1–3) based on biopsy results
  • Your disease has progressed after PRRT using 177Lu-DOTATATE, and you may still be able to have two more PRRT cycles
  • Your scans show the right docking sites (“somatostatin receptors”) on the tumors using a 68Ga-DOTATATE (or related) PET scan
  • You have measurable tumors on CT or MRI, and you are able to do study activities (Karnofsky score over 60)
  • Your blood and organ tests are safe enough for treatment (lower limits for blood counts, kidney, and liver function apply)

View the official record on ClinicalTrials.gov

Quick eligibility check

Answer a few plain-language questions, based on this study's own requirements, to get a preliminary sense of fit.

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