Denosumab for Prolonging Bone Metastasis-Free Survival in Men with Hormone-Refractory Prostate Cancer
Study Details
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.
Protocol Summary
Incidence of treatment-emergent adverse events
Timeframe: 4 weeks after the last dose of open label treatment
Changes in laboratory values
Timeframe: 4 weeks after the last dose of open label treatment
Incidence of anti-denosumab neutralising antibody formulation
Timeframe: 4 weeks after the last dose of open label treatment