drugset / Trial / NCT03049189

Efficacy and Safety of 177Lu-edotreotide PRRT in GEP-NET Patients

NCT03049189

Phase 3 Active not recruiting 324 enrolled ITM Solucin GmbH ABX CRO · collabPSI CRO · collab
RandomizedParallel-groupOpen-labelTreatment

Summary

The purpose of the study is 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).

Timeline

Start
2017-02-02
Primary completion
2024-11-27
Completion
2029-11

Drugs

EvaluationDrugModalityDoseRoute
Subject 177Lu-edotreotide Peptide 7500 mbq Intravenous
Comparator Everolimus Small molecule 10 mg Oral