Clin2
NCT03206060Possibly a fitRecruiting

Lu-177 DOTATATE for hard-to-remove pheochromocytoma or paraganglioma

PheochromocytomaParagangliomaNeuroendocrine TumorsNeuroendocrine Neoplasms

Treatments studied

Part of Cancer, Heart & circulation clinical trials.

This trial studies Lu-177 DOTATATE (Lutathera), a targeted radiation medicine, for tumors that cannot be safely removed with surgery. It aims to shrink or control pheochromocytoma/paraganglioma that is showing recent growth and has a specific target signal on a special PET scan.

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

Phase
Phase 2
Enrollment
130 people
Ages
18 years to 100 years
Study type
Interventional

Who can take part

  • Your tumor type is pheochromocytoma (PHEO) or paraganglioma (PGL), and it can be proven by tumor testing on tissue (site review preferred, but not required).
  • Surgery can’t be done (inoperable), or the main tumor can’t be fully removed, even if the cancer is only at the original spot.
  • Your cancer has been growing within the last 12 months on scans (measurable disease).
  • Your tumor must not have certain inherited gene causes—except SDHx—based on genetic testing you had before the study.
  • Your Ga-68 DOTATATE PET scan must be positive (at least one qualifying spot that is big enough and clearly higher than background, within 12 weeks).
  • You must be able to do study visits/scans and sign consent; your general health scores must be good enough (Karnofsky ≥60 or ECOG ≤2).

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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