This study characterizes the pharmacokinetic effects of ASP015K on Tacrolimus in healthy volunteers.
The subjects will be confined to the unit for 13 days and have a brief follow-up visit to obtain hematology blood samples. Numerous blood and urine samples will be taken to determine the pharmacokinetics of the drugs.
Study Type
INTERVENTIONAL
Allocation
NON_RANDOMIZED
Masking
NONE
Enrollment
24
oral
oral
Clinical Pharmacology of Miami
Miami, Florida, United States
Pharmacokinetic assessment of AUC through the analysis of blood and urine samples
Time frame: Up to Day 13
Pharmacokinetic assessment of maximum concentration (Cmax) through the analysis of blood and urine samples
Time frame: Up to Day 13
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