This is a single-center, randomized, double-blind, placebo-controlled, ascending multiple-dose study of VIA-3196 to evaluate the Safety, Pharmacokinetics and Pharmacodynamics of VIA-3196 in Healthy Subjects. Study dosing is organized into cohorts corresponding to escalating doses of VIA-3196 or matching placebo. Subjects will be dosed daily for 14 days.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
QUADRUPLE
Enrollment
48
PRACS Institute (formerly Cetero Research)
Fargo, North Dakota, United States
Number of Adverse Events as a measure of safety and tolerability of VIA-3196
Evaluation will start from predose (Day -1) until the follow-up visit (Day 21)
Time frame: up to 22 days
Plasma concentration of VIA-3196
Assessed without food
Time frame: 0 to 24 hours on Day 1 and Day 14
Lipid level changes following administration of VIA-3196
Time frame: Day 1 to 14
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