The purpose of this study is to describe the safety and tolerability of up to 5 years (ie, 3 years under the 20040138 Amgen study and 2 years on this study) denosumab administration as measured by adverse events, immunogenicity, and safety laboratory parameters in subjects who previously received denosumab for non-metastatic prostate cancer.
Study Type
INTERVENTIONAL
Allocation
NA
Purpose
TREATMENT
Masking
NONE
Enrollment
384
60 mg SC of Denosumab will be administered on study day 1, month 6, month 12, and month 18
Overall Survival Through Month 24
Time frame: 24 months
This platform is for informational purposes only and does not constitute medical advice. Always consult a qualified healthcare professional.
Research Site
Huntsville, Alabama, United States
Research Site
Anaheim, California, United States
Research Site
Laguna Hills, California, United States
Research Site
Long Beach, California, United States
Research Site
San Bernardino, California, United States
Research Site
San Diego, California, United States
Research Site
San Diego, California, United States
Research Site
Santa Monica, California, United States
Research Site
Middlebury, Connecticut, United States
Research Site
New Britain, Connecticut, United States
...and 64 more locations