drugset / Trial / NCT06380699

Study to Assess PK, Safety and Tolerability in Healthy Subjects

NCT06380699

Phase 1 Completed 56 enrolled Changzhou Qianhong Bio-pharma Co., Ltd.
RandomizedParallel-groupQuadruple-blindOther

Summary

The purpose of this study is to assess the safety, tolerability, pharmacokinetics (PK) and pharmacodynamics (PD) of QHRD106 in Chinese healthy subjects with single and multiple doses.

Timeline

Start
2023-03-16
Primary completion
2023-11-16
Completion
2023-12-25

Drugs

EvaluationDrugModalityDoseRoute
Comparator Human Urinary Kallidinogenase Protein / enzyme biologic 0.15 unknown Intravenous
Subject QHRD106 Unknown 5600 iu Intramuscular
Subject QHRD106 Unknown 8400 iu Intramuscular
Subject QHRD106 Unknown 12600 iu Intramuscular
Subject QHRD106 Unknown 18900 iu Intramuscular

Indications