To evaluate the effect of rifampin, a cytochrome P450 3A (CYP3A) inducer, on the pharmacokinetics (PK) of IPI-145; to assess the safety and tolerability of IPI-145 when administered with rifampin in healthy subjects
* In Treatment Period 1, subjects will receive a single 25 mg oral dose of IPI-145 * In Treatment Period 2, on Days 3-9, the same subjects will receive once daily (QD) oral doses of 600 mg rifampin; on Day 9, subjects will receive a single oral dose of 25 mg IPI-145 concomitantly administered with 600 mg of rifampin
Study Type
INTERVENTIONAL
Allocation
NA
Purpose
BASIC_SCIENCE
Masking
NONE
Enrollment
14
PRA International, Inc
Lenexa, Kansas, United States
Pharmacokinetic parameters (AUC) of IPI-145 and its metabolite, IPI-656
Time frame: Over 48 hours
Pharmacokinetic parameters (Cmax) of IPI-145 and its metabolite, IPI-656
Time frame: Over 48 hours
Pharmacokinetic parameters (t1/2) of IPI-145 and its metabolite, IPI-656
Time frame: Over 48 hours
Plasma concentrations of IPI-145 and its metabolite, IPI-656
Time frame: Over 48 hours
Incidence of adverse events following administration of IPI-145, rifampin, and the combination.
Safety Findings
Time frame: 2 weeks
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