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Clinical Trial Summary

The primary objective of this study will be to evaluate the safety and tolerability of single and multiple oral doses of CCX168, over a range of dose levels, in healthy male and female participants.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT05984251
Study type Interventional
Source Amgen
Contact
Status Completed
Phase Phase 1
Start date December 21, 2009
Completion date April 11, 2011

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