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Clinical Trial Summary

The primary objective of this study was to assess the safety, tolerability, and immunogenicity potential of romosozumab following multiple subcutaneous (SC) administrations in healthy men and postmenopausal women with low bone mass.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT01825785
Study type Interventional
Source Amgen
Contact
Status Completed
Phase Phase 1
Start date November 14, 2007
Completion date December 2, 2008

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