This Phase 1 trial consists of two parts: Part 1 is a Single Ascending Dose (SAD) study, and Part 2 is a Multiple Ascending Dose (MAD) study. Both parts adopt a randomized, double-blind, placebo-controlled design.
Part 1 is a randomized, double-blind, placebo-controlled SAD study to evaluate the safety, tolerability, PK, and PD of single oral doses of SK-09 tablets in healthy adult participants. Part 2 is a randomized, double-blind, placebo-controlled MAD study designed to evaluate the safety, tolerability, PK, and PD of multiple oral doses of SK-09 tablets in healthy adult participants.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
DOUBLE
Enrollment
72
Q-Pharm Pty Ltd.
Herston, Queensland, Australia
Safety Evaluation
Number of participants with AE, with abnormal Vital Signs, abnormal Physical Examination findings, abnormal Laboratory Tests results, abnormal 12-lead ECG readings
Time frame: up to 8 days post-dosing for SAD and up to 20 days post-dosing for MAD
PK Evaluation(Cmax)
Pharmacokinetic characteristics after administration (Cmax)
Time frame: up to 72 hours post-dosing for SAD and up to 16 days post-dosing for MAD
PK Evaluation(Tmax)
Pharmacokinetic characteristics after administration
Time frame: up to 72 hours post-dosing for SAD and up to 16 days post-dosing for MAD
PK Evaluation( AUC0-T)
Pharmacokinetic characteristics after administration (AUC0-T)
Time frame: up to 72 hours post-dosing for SAD and up to 16 days post-dosing for MAD
PK Evaluation ( AUC0-∞)
Pharmacokinetic characteristics after administration ( AUC0-∞)
Time frame: up to 72 hours post-dosing for SAD and up to 16 days post-dosing for MAD
PD evaluation
urinary Rac1 levels
Time frame: up to 12 hour post-dosing on Day 1 for SAD and pending for MAD
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