drugset / Trial / NCT06380699
Study to Assess PK, Safety and Tolerability in Healthy Subjects
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
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| 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 |