drugset / Trial / NCT06388772

Study to Assess PK, Safety and Tolerability Early in Healthy Subjects

NCT06388772

Phase 1 Completed 74 enrolled Changzhou Qianhong Bio-pharma Co., Ltd.
RandomizedParallel-groupQuadruple-blindOther

Summary

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

Timeline

Start
2021-07-05
Primary completion
2022-07-22
Completion
2023-01-06

Drugs

EvaluationDrugModalityDoseRoute
Subject QHRD106 Unknown 250 iu Intramuscular
Subject QHRD106 Unknown 8400 iu Intramuscular

Indications