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Clinical Trial Summary

The primary objective of this study is to evaluate the pharmacokinetics (PK) of miricorilant in the presence and absence of the strong cytochrome P450 [(CYP) 2C19] inhibitor, fluvoxamine, in healthy participants. Participants will receive a single dose of miricorilant under fed conditions with a standard breakfast after an overnight fast alone and in combination with once-daily doses of fluvoxamine. Blood samples will be collected at regular intervals for PK and safety analysis between admission and discharge from the clinical unit.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT05712265
Study type Interventional
Source Corcept Therapeutics
Contact
Status Completed
Phase Phase 1
Start date January 24, 2023
Completion date February 23, 2023

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