drugset / Trial / NCT05050942

A Trial to Assess Efficacy and Safety of Octreotide Subcutaneous Depot in Patients With GEP-NET

NCT05050942

Phase 3 Active not recruiting 332 enrolled Camurus AB
RandomizedParallel-groupOpen-labelTreatment

Summary

The purpose of this study is to compare the effectiveness and safety of CAM2029 to octreotide LAR or lanreotide ATG in patients with advanced, well-differentiated GEP-NET. Patients who experience progressive disease in the randomized part of the study may proceed to an open-label extension part with intensified treatment with CAM2029.

Timeline

Start
2021-10-22
Primary completion
2026-07
Completion
2028-07

Drugs

EvaluationDrugModalityDoseRoute
Comparator Lanreotide Other / unclassified 120 mg Subcutaneous
Subject Octreotide Peptide 20 mg Subcutaneous
Subject Octreotide Peptide 30 mg Subcutaneous