drugset / Trial / NCT02780882

SOM230 Ectopic ACTH-producing Tumors

NCT02780882

NaSingle-groupOpen-labelTreatment

Summary

The purpose of this prospective open-label phase II study, is to evaluate the efficacy of pasireotide twice daily subcutaneous injections for normalizing 24 hour urine free cortisol in patients with ectopic ACTH-producing tumors as measured by the proportion of patients achieving normal UFC at the end of the study period.

Timeline

Start
2015-12
Primary completion
2018-12
Completion
2019-06

Drugs

EvaluationDrugModalityDoseRoute
Subject Pasireotide Other / unclassified 900 ug Subcutaneous