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Phase III Study to Evaluate Efficacy and Safety of Peptide Receptor Radionuclide Therapy (PRRT) With 177Lu-Edotreotide Compared to Targeted Molecular Therapy With Everolimus in Patients With Inoperable, Progressive, Somatostatin Receptor-positive (SSTR+), Neuroendocrine Tumours of Gastroenteric or Pancreatic Origin (GEP-NET) (COMPETE)

Summary

The purpose of this phase III study is to evaluate the safety and efficacy of Peptide Receptor Radionuclide Therapy (PRRT) with 177Lu-Edotreotide compared to targeted molecular therapy with Everolimus in patients with inoperable, progressive, somatostatin receptor-positive (SSTR+), neuroendocrine tumours of gastroenteric or pancreatic origin (GEP-NET).

General Information

NCT#: NCT03049189
Study ID: ITM-LET-01
Trial Phase: Phase III

Trial Sponsor: ITM Isotopen Technologien München AG
Therapies Used in This Trial: Everolimus, Peptide Receptor Radionuclide Therapy (PRRT), 177Lu-Edotreotide

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