drugset / Trial / NCT06867393

Safety, Tolerability, and Pharmacokinetics of HL-003 in Healthy Subjects

NCT06867393 ↗

Phase 1 Recruiting 52 enrolled Shanghai Kechow Pharma, Inc.
RandomizedParallel-groupTriple-blindOther

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.

Timeline

Start
2025-02-28
Primary completion
2025-08
Completion
2025-09

Drugs

EvaluationDrugModalityDoseRoute
Comparator HL-003 Unknown 25 mg Oral
Comparator HL-003 Unknown 100 mg Oral
Comparator HL-003 Unknown 250 mg Oral
Comparator HL-003 Unknown 500 mg Oral
Comparator HL-003 Unknown 1000 mg Oral
Comparator HL-003 Unknown 1500 mg Oral

Indications

No indication recorded.