drugset / Trial / NCT05050942
A Trial to Assess Efficacy and Safety of Octreotide Subcutaneous Depot in Patients With GEP-NET
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
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Comparator | Lanreotide | Other / unclassified | 120 mg | Subcutaneous |
| Subject | Octreotide | Peptide | 20 mg | Subcutaneous |
| Subject | Octreotide | Peptide | 30 mg | Subcutaneous |