drugset / Trial / NCT01886287

P:II Above-Label Octreotide-LAR With Insufficiently Controlled Carcinoid Syndrome

NCT01886287

NaSingle-groupOpen-labelTreatment

Summary

The primary purpose of the study is to investigate the effects of high-dose octreotide on flushing, diarrhea, and quality of life in patients whose disease-related symptoms are inadequately controlled by the maximum approved dose of octreotide LAR.

Timeline

Start
2013-12
Primary completion
2014-08
Completion
2014-10

Drugs

EvaluationDrugModalityDoseRoute
Subject Octreotide Peptide 60 mg Intramuscular