The purpose of the study is to evaluate the effect of food, gender, and age on the single-dose pharmacokinetics (PK) of SUVN-D4010.
The main objective of the study is to evaluate the safety and tolerability of orally administered SUVN-D4010 under single-dose conditions in healthy adult male and female subjects and healthy elderly male subjects.
Study Type
INTERVENTIONAL
Allocation
NON_RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Enrollment
28
Tablets
PRA Health Sciences
Lenexa, Kansas, United States
Area under concentration (AUC)
Time frame: 72 hours
Maximum observed concentration (Cmax)
Time frame: Day 1
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