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Clinical Trial Summary

Determine the safety and effectiveness of Lu-177 DOTATOC in adult subjects with somatostatin receptor-expressing Pulmonary, Pheochromocytoma, Paraganglioma, Unknown primary, and Thymus neuroendocrine tumors or any other non-.GEP-NET. The treatment regimen will consist of 4 doses of 200 (±10%) mCi 177Lu-DOTATOC administered at 8+/- 1-week intervals.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT04276597
Study type Interventional
Source Excel Diagnostics and Nuclear Oncology Center
Contact
Status Withdrawn
Phase Phase 2
Start date March 4, 2020
Completion date July 15, 2021

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