Clinical Trials Directory

Trials / Withdrawn

WithdrawnNCT02780882

SOM230 Ectopic ACTH-producing Tumors

A Proof of Concept and Open-label Study to Test the Efficacy and Safety of Pasireotide in Patients With Ectopic ACTH-producing Tumors

Status
Withdrawn
Phase
Phase 2
Study type
Interventional
Enrollment
0 (actual)
Sponsor
Cedars-Sinai Medical Center · Academic / Other
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

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.

Conditions

Interventions

TypeNameDescription
DRUGPasireotide

Timeline

Start date
2015-12-01
Primary completion
2018-12-01
Completion
2019-06-01
First posted
2016-05-24
Last updated
2018-01-26

Locations

1 site across 1 country: United States

Source: ClinicalTrials.gov record NCT02780882. Inclusion in this directory is not an endorsement.

SOM230 Ectopic ACTH-producing Tumors (NCT02780882) · Clinical Trials Directory