drugset / Trial / NCT05932888

Safety, Tolerability, and Pharmacokinetic Study of QLM3003 in Healthy Adult Subjects

NCT05932888 ↗

Phase 1 Completed 40 enrolled Qilu Pharmaceutical Co., Ltd.
RandomizedParallel-groupQuadruple-blindTreatment

Summary

The purpose of the study is to evaluate the safety and tolerability of single ascending (SAD) doses of QLM3003 compared to placebo. Also, pharmacokinetics (PK) of qlm3003 will be evaluated.

Timeline

Start
2023-06-25
Primary completion
2023-08-05
Completion
2023-08-30

Drugs

EvaluationDrugModalityDoseRoute
Subject QLM3003 Unknown 1 % —
Subject QLM3003 Unknown 1.5 % —
Subject QLM3003 Unknown 2 % —

Indications