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Clinical Trial Summary

The purpose of this study is to describe the safety and tolerability of denosumab administration as measured by adverse events, immunogenicity, and safety laboratory parameters in subjects who previously received either zoledronic acid (Zometa®) or denosumab.


Clinical Trial Description

n/a


Study Design

Endpoint Classification: Safety Study, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Supportive Care


Related Conditions & MeSH terms


NCT number NCT00950911
Study type Interventional
Source Amgen
Contact
Status Completed
Phase Phase 3
Start date July 2009
Completion date April 2012

See also
  Status Clinical Trial Phase
Completed NCT00091832 - Denosumab (AMG 162) in Bisphosphonate Naive Metastatic Breast Cancer Phase 2
Completed NCT01419717 - Open-Label Access Protocol of Denosumab for Subjects With Advanced Cancer Phase 3
Completed NCT00104650 - Study of AMG 162 in Subjects With Advanced Cancer Currently Being Treated With Intravenous (IV) Bisphosphonates Phase 2