Drug-drug interaction (DDI) and Cardiodynamic Evaluation Study To assess the effect of multiple oral doses of edasalonexent on the single-dose pharmacokinetics (PK) of midazolam (a cytochrome P450 \[CYP\]3A4 sensitive substrate) and of deflazacort (a CYP3A4 moderate sensitive substrate) in healthy adult subjects.
This is an open-label, fixed-sequence DDI and cardiodynamic study in healthy adult subjects. Twenty-six (26), healthy, adult male and female (non-childbearing potential) subjects will be enrolled. Screening of subjects will occur within 28 days prior to the first dosing. To assess the effect of multiple oral doses of edasalonexent on the single-dose pharmacokinetics (PK) of midazolam (a cytochrome P450 \[CYP\]3A4 sensitive substrate) and of deflazacort (a CYP3A4 moderate sensitive substrate) in healthy adult subjects. Visit assessments include Clinical laboratory tests, Safety ECGs and Cardiodynamic ECGs. Subjects will be housed on Day -3 of Period 1, until after the 24-hour blood draw and/or study procedures are completed on Day 12 of Period 2.
Study Type
INTERVENTIONAL
Allocation
NON_RANDOMIZED
Purpose
HEALTH_SERVICES_RESEARCH
Masking
NONE
Enrollment
26
CAT-1004 capsules
2 mg/ml syrup
36 mg tablets
Celerion Clinical Research Unit
Tempe, Arizona, United States
AUC of edasalonexent with midazolam and deflazacort
Time frame: 12 Days
QTc interval with edasalonexent
Time frame: 12 Days
Number of participants with reported treatment-related adverse events
Time frame: 12 days
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