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Clinical Trial Summary

The purpose of the study is to evaluate the efficacy, safety & patient-reported outcomes of peptide receptor radionuclide therapy (PRRT) with 177Lu-Edotreotide as 1st or 2nd line of treatment compared to best standard of care in patients with well-differentiated aggressive grade 2 and grade 3, somatostatin receptor-positive (SSTR+), neuroendocrine tumours of gastroenteric or pancreatic origin.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT04919226
Study type Interventional
Source ITM Solucin GmbH
Contact Nicolas Schneider, Dr
Email info-solucin@itm-radiopharma.com
Status Recruiting
Phase Phase 3
Start date December 21, 2021
Completion date September 2027

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