Safety, Tolerability, and Pharmacokinetics of HL-003 in Healthy Subjects
Phase I Clinical Study of the Safety, Tolerability, and Pharmacokinetics of Single and Multiple Oral Doses of HL-003 in Healthy Subjects
Shanghai Kechow Pharma, Inc.
52 participants
Feb 28, 2025
INTERVENTIONAL
Conditions
Summary
This clinical study aims to evaluate the safety, tolerability, and pharmacokinetic characteristics of HL-003 tablets in healthy subjects. It is conducted in two sequential clinical phases: single-dose and multiple-dose escalation.
Eligibility
Plain Language Summary
Simplified for easier understanding
This summary was AI-generated to explain the trial in plain language. It is not medical advice. Always discuss eligibility with your doctor before enrolling in a clinical trial.
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Interventions
100mg、250mg、500mg、1000mg、1500mg,SAD
25mg、100mg、250mg、500mg、1000mg、1500mg,SAD
Locations(1)
View Full Details on ClinicalTrials.gov
For the most up-to-date information, visit the official listing.
NCT06867393