Viewing Study NCT00468286



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Last Modification Date: 2024-10-26 @ 9:32 AM
Study NCT ID: NCT00468286
Status: COMPLETED
Last Update Posted: 2011-03-23
First Post: 2007-04-13

Brief Title: Investigating Efficacy and Safety of Two Degarelix Three-Month Dosing Regimens in Patients With Prostate Cancer Requiring Androgen Ablation Therapy
Sponsor: Ferring Pharmaceuticals
Organization: Ferring Pharmaceuticals

Study Overview

Official Title: An Open-Label Multi-Centre Randomised Parallel-Group Dose-Finding Study Investigating Efficacy and Safety of Two Degarelix Three-Month Dosing Regimens in Patients With Prostate Cancer Requiring Androgen Ablation Therapy
Status: COMPLETED
Status Verified Date: 2011-03
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: The study will have two treatment groups evaluating two Degarelix doses First dose is the initial dose followed by a maintenance dose given every three months The initial dose given to suppress the testosterone level and the three month maintenance dose to maintain the suppressed testosterone level over one year of treatment
Detailed Description: An Open-Label Multi-Centre Randomized Parallel-Group Dose-Finding Study Investigating Efficacy and Safety of Two Degarelix Three-Month Dosing Regimens in Patients with Prostrate Cancer Requiring Androgen Ablation Therapy

Study Oversight

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