This Phase 1 trial consists of three parts: Part 1 is a Single Ascending Dose (SAD) study, Part 2 is a Multiple Ascending Dose (MAD) study. Both parts adopt a randomized, double-blind, placebo-controlled design. Part 3 is a randomized, open-label, single-dose, two-period crossover self-controlled design FE study.
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. Part 3 is a randomized, open-label, single-dose, two-period crossover self-controlled design FE study to evaluate the food effect on safety, tolerability, and PK of single oral doses of SK-09 tablets in healthy adult participants.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
DOUBLE
Enrollment
84
SAD:Dose groups of 20 mg, 50 mg, 100 mg, 200 mg, 400 mg, and 500 mg were given. MAD:Dose groups (low100 mg BID, 200 mg BID, and 500mg QD or 300mg BID/medium/high, based on Part 1 SAD results) will be given. FE:Dose group (150mg) was given.
SAD:Dose groups of 20 mg, 50 mg, 100 mg, 200 mg, 400 mg, and 500 mg were given. MAD:Dose groups (low100 mg BID, 200 mg BID, and 500mg QD or 300mg BID/medium/high, based on Part 1 SAD results) were given.
Q-Pharm Pty Ltd.
Herston, Queensland, Australia
RECRUITINGSafety 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 ,up to 14 days post-dosing for MAD, up to 14 days first post-dosing for FE.
PK Evaluation(Cmax)
Pharmacokinetic characteristics after administration (Cmax)
Time frame: up to 72 hours post-dosing for SAD and FE,up to 10 days post-dosing for MAD
PK Evaluation(Tmax)
Pharmacokinetic characteristics after administration
Time frame: up to 72 hours post-dosing for SAD and FE,up to 10 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 FE,up to 10 days post-dosing for MAD
PK Evaluation ( AUC0-∞)
Pharmacokinetic characteristics after administration ( AUC0-∞)
Time frame: up to 72 hours post-dosing for SAD and FE,up to 10 days post-dosing for MAD
PD evaluation
urinary Rac1 levels
Time frame: up to 12 hour post-dosing on Day 1 for SAD and up to 12 hour post-dosing on Day 1 & D7 for MAD
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