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

Acute Ischemic Stroke Clinical Trial

Official title:
Phase I Clinical Study of Tolerability, Safety and Pharmacokinetics of QHRD106 Injection in Chinese Healthy Subjects With Single Doses

Clinical Trial 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.

Clinical Trial Description

Eight dose groups were initially set up. The experimental groups were increased from low to high dose according to the principle of increasing dose, and Placebo was added as the control group. All the selected subjects in the experimental group were given the drug once. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT06388772
Study type Interventional
Source Changzhou Qianhong Bio-pharma Co., Ltd.
Contact
Status Completed
Phase Phase 1
Start date July 5, 2021
Completion date January 6, 2023
View Details
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