Clin2
NCT04917484Possibly a fitRecruiting

Higher-precision PRRT dosing versus standard dosing for NEN

Neuroendocrine Neoplasm

Part of Cancer clinical trials.

This Phase 2 study compares a more personalized (precision) radiation dose plan to the standard dose plan using Lu-177-DOTATOC for people with neuroendocrine neoplasms (NEN) that have worsened or caused major symptoms despite usual treatments. The goal is to see if better planning can improve treatment delivery while staying safe.

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

Phase
Phase 2
Enrollment
100 people
Ages
18 years and older
Study type
Interventional

Who can take part

  • Be 18 years or older and able to give informed consent
  • Have NEN confirmed on tissue biopsy (histology)
  • Have disease that is progressing despite standard treatments (or you cannot tolerate them, or symptoms are not controlled)
  • Have an average day-to-day functioning score of 0 to 2 (performance status)
  • Have enough kidney and bone marrow function based on blood tests and kidney clearance results
  • Have a scan showing the cancer takes up Ga-DOTATOC more than the liver (or get a new scan if yours is older than 3 months)

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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