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A Study to Assess SOM230 in Patients With Pituitary Cushing's Disease

Cushing's Syndrome Clinical Trial

Official title:
A Multicenter, Open Label Study to Assess the Safety and Efficacy of 600 µg SOM230, Administered Subcutaneously, b.i.d. in Patients With Cushing's Disease

Clinical Trial Summary

The study treatment period is 15 days in length and includes patients with pituitary Cushing's disease who are candidates for surgical intervention as well as and patients who have recurrent Cushing's post operatively.

Clinical Trial Description

n/a

Study Design

Endpoint Classification: Safety/Efficacy Study, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Treatment

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT00088608
Study type Interventional
Source Novartis
Contact
Status Completed
Phase Phase 2
Start date April 2004
View Details
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