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An Open Label, Single Arm, Extension Study to Evaluate the Long Term Safety of Denosumab for Prolonging Bone Metastasis-Free Survival in Men With Hormone-Refractory Prostate Cancer
This is a multi-national, multi-center, open-label, single-arm extension study for the prolongation of bone metastasis-free survival in men with hormone-refractory (androgen independent) prostate cancer. Patients currently participating in the phase 3 study 20050147 (NCT00286091) will be offered this study if a positive benefit:risk compared with placebo is determined in the 20050147 study. The primary endpoint of the 20050147 study is bone metastases-free survival determined by the time to first occurrence of bone metastases (either symptomatic or asymptomatic) or death from any cause. Participants will receive open-label denosumab administered once every 4 weeks (Q4W) subcutaneously (SC) until they developed a bone metastasis or for up to 3 years, whichever comes first.
Age
18 - No limit years
Sex
MALE
Healthy Volunteers
No
Research Site
Hradec Králové, Czechia
Research Site
Pelhřimov, Czechia
Research Site
Prague, Czechia
Research Site
Prague, Czechia
Research Site
Tábor, Czechia
Research Site
Newcastle, United Kingdom
Research Site
Northwood, United Kingdom
Research Site
Sheffield, United Kingdom
Research Site
Sutton, United Kingdom
Start Date
January 1, 2011
Primary Completion Date
February 1, 2014
Completion Date
February 1, 2014
Last Updated
March 5, 2015
18
ACTUAL participants
Denosumab
BIOLOGICAL
Lead Sponsor
Amgen
NCT02266745
NCT04053062
Data Source & Attribution
This clinical trial information is sourced from ClinicalTrials.gov, a service of the U.S. National Institutes of Health.
Modifications: This data has been reformatted for display purposes. Eligibility criteria have been parsed into inclusion/exclusion sections. Location data has been geocoded to enable distance-based search. For the authoritative and most current information, please visit ClinicalTrials.gov.
Neither the United States Government nor Clareo Health make any warranties regarding the data. Check ClinicalTrials.gov frequently for updates.
View ClinicalTrials.gov Terms and ConditionsNCT01681433