Clinical Trial · NCT04919226

A Prospective, Randomised, Controlled, Open-label, Multicentre Study to Evaluate Efficacy, Safety and Patient-Reported Outcomes of Peptide Receptor Radionuclide Therapy (PRRT) With 177Lu-Edotreotide 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

Overview

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.

Sponsor

ITM Solucin GmbH

Phase

Phase 3

Contacts

Nicolas Schneider, Dr

info-solucin@itm-radiopharma.com

Amanda Rotger, Dr

info-solucin@itm-radiopharma.com

ClinicalTrials.gov

NCT04919226

Drug / Compound

Isotope(s):
Target(s):