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A Pharmacokinetic Study of Omaveloxolone in Subjects With Hepatic Impairment and Normal Hepatic Function

NCT03902002 PHASE1 COMPLETED

This study will examine the pharmacokinetics (PK) of omaveloxolone following a single oral dose of omaveloxolone in subjects with mild, moderate, or severe hepatic impairment compared to healthy subjects with normal hepatic function.

Details

Lead sponsorBiogen
PhasePHASE1
StatusCOMPLETED
Enrolment48
Start dateFri Jul 19 2019 00:00:00 GMT+0000 (Coordinated Universal Time)
CompletionMon Jan 27 2020 00:00:00 GMT+0000 (Coordinated Universal Time)

Conditions

Interventions

Countries

United States