drugset / Trial / NCT01578239

A Study Comparing Treatment With 177Lu-DOTA0-Tyr3-Octreotate to Octreotide LAR in Patients With Inoperable, Progressive, Somatostatin Receptor Positive Midgut Carcinoid Tumours

NCT01578239

Phase 3 Completed 231 enrolled Advanced Accelerator Applications
RandomizedParallel-groupOpen-labelTreatment

Summary

This was a multicenter, stratified, open, randomized, comparator-controlled, parallel-group phase III study comparing treatment with Lutathera plus best supportive care (30 mg Octreotide LAR) to treatment with high dose (60 mg) Octreotide LAR in participants with metastasized or locally advanced, inoperable, somatostatin receptor positive, histologically proven midgut carcinoid tumours with progression despite LAR treatment.

Timeline

Start
2012-09-06
Primary completion
2015-07-31
Completion
2021-01-18

Publications

Drugs

EvaluationDrugModalityDoseRoute
Subject 177Lu-DOTATATE Peptide 7400 mbq Intravenous
Subject Octreotide Peptide 30 mg Intramuscular
Subject Octreotide Peptide 60 mg Intramuscular