drugset / Trial / NCT06388772
Study to Assess PK, Safety and Tolerability Early in Healthy Subjects
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
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Subject | QHRD106 | Unknown | 250 iu | Intramuscular |
| Subject | QHRD106 | Unknown | 8400 iu | Intramuscular |