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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 hepati...
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Lead Sponsor
AbbVie
NCT07269301 · Hepatic Impairment, Healthy
NCT07457229 · Hepatic Impairment
NCT07324616 · Hepatic Impairment (HI)
NCT07023354 · Healthy, Hepatic Impairment
NCT04271488 · Hepatic Impairment
Clinical Pharmacology of Miami /ID# 246573
Miami, Florida
Orlando Clinical Research Ctr /ID# 246052
Orlando, Florida
TX Liver Inst, Americ Res Corp /ID# 246572
San Antonio, Texas
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This clinical trial information is sourced from ClinicalTrials.gov, a service of the U.S. National Institutes of Health.
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