Viewing Study NCT01374906


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Study NCT ID: NCT01374906
Status: COMPLETED
Last Update Posted: 2018-05-22
First Post: 2011-06-14
Is NOT Gene Therapy: False
Has Adverse Events: True

Brief Title: Efficacy and Safety of Pasireotide Administered Monthly in Patients With Cushing's Disease
Sponsor: Novartis Pharmaceuticals
Organization:

Study Overview

Official Title: A Randomized, Double-blind, Multicenter, Phase III Study to Evaluate the Efficacy and Safety of Pasireotide LAR in Patients With Cushing's Disease
Status: COMPLETED
Status Verified Date: 2018-04
Last Known Status: None
Delayed Posting: No
If Stopped, Why?: Not Stopped
Has Expanded Access: False
If Expanded Access, NCT#: N/A
Has Expanded Access, NCT# Status: N/A
Acronym: None
Brief Summary: This is a randomized, double-blind, multicenter, phase III study to evaluate the safety and efficacy of 2 dosing regiments of Pasireotide long acting release (LAR) in patients with Cushing's disease.
Detailed Description: None

Study Oversight

Has Oversight DMC: None
Is a FDA Regulated Drug?: True
Is a FDA Regulated Device?: False
Is an Unapproved Device?: None
Is a PPSD?: None
Is a US Export?: None
Is an FDA AA801 Violation?:

Secondary ID Infos

Secondary ID Type Domain Link View
2009-011128-70 EUDRACT_NUMBER None View