This study is a First in Human, three-parts, double-blind, randomized, placebo-controlled, single and multiple ascending dose study. The purpose of this study is to evaluate the safety, tolerability, pharmacokinetics (PK), and pharmacodynamics (PD) of TT5 at different doses in healthy and surgical participants.
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Incidence of Adverse Events (AEs) and serious adverse events (SAEs)
Timeframe: SAD cohorts: Day-1 through Day 8; MAD cohorts: Day-1 through Day 14
Clinically significant changes in physical examinations
Timeframe: SAD cohorts: Baseline through Day 8; MAD cohorts: Baseline through Day 14
Clinically significant changes in vital signs
Timeframe: SAD cohorts: Day-1 through Day 8; MAD cohorts: Day-1 through Day 14
Clinically significant changes in laboratory analysis
Timeframe: SAD cohorts: Day-1 through Day 8; MAD cohorts: Day-1 through Day 14
Bond and Lader Visual Analog Scale (VAS)
Timeframe: SAD cohorts: Day 1 through Day 8; MAD cohorts: Day 1 through Day 14