Single center, randomized, double-blinded, placebo-controlled, single ascending-dose study for the evaluation of the safety, tolerability, and PK following single oral doses of INV-101.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
QUADRUPLE
Enrollment
40
Altasciences
Montreal, Quebec, Canada
Pharmacokinetic parameters - Maximum Concentration (Cmax)
Cmax following single dose
Time frame: 72 hours
Pharmacokinetic parameters - AUC
AUC following single dose
Time frame: 72 hours
Pharmacokinetic parameters - Half-live
Half-live following single dose
Time frame: 72 hours
Adverse events
Safety of INV-101 following single dose
Time frame: 72 hours
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