Clinical trial

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

NCT00088608 · Novartis Pharmaceuticals, Industry · Completed

Key facts

NCT number NCT00088608
Title A Study to Assess SOM230 in Patients With Pituitary Cushing's Disease
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
Lead sponsor Novartis Pharmaceuticals, Industry
Status Completed
Phase Phase 2
Study type Interventional
Conditions Cushing's Syndrome
Intervention type Drug
Interventions SOM230 s.c.
Enrollment 26
Start date Apr 1, 2004
Primary completion Jun 1, 2006
First posted Aug 2, 2004
Last update posted Nov 7, 2016
Countries United States

At a glance

  • 1–9 Study sites
  • No Results posted
  • None Linked FDA submissions

Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.

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Source: U.S. National Library of Medicine (NLM), ClinicalTrials.gov · Source date:

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