This is a sequential, randomized, double-blind, placebo-controlled Phase 1 single (SAD) and multiple (MAD) ascending dose study to evaluate the safety, tolerability, and pharmacokinetics (PK) of orally or intravenously administered LTG-001 in healthy male and female participants
Protocol Amendment History
3 changes
criticalTrial status changed: Recruiting → Active, Not Recruiting2026-06-17