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Clinical Trial Summary

The objective of this study is to evaluate the pharmacokinetics and safety of cedirogant following oral administration of multiple doses in adult participants with hepatic impairment and normal hepatic function.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT05376839
Study type Interventional
Source AbbVie
Contact
Status Terminated
Phase Phase 1
Start date July 6, 2022
Completion date November 8, 2022

See also
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