drugset / Trial / NCT05532124
Part A: In Patients With Chronic Liver Diseases, LAENNEC (Human Placenta Hydrolysate) is to Assess Safety and Tolerability After the Doses of Doses. Part B: Part A, it is to Determine the Optimal Dose by Evaluating Two Capacity and Placebo Groups.
RandomizedParallel-groupDouble-blindTreatment
Summary
Part A: In Patients With Chronic Liver Diseases, LAENNEC (Human Placenta Hydrolysate) is to Assess Safety and Tolerability After the Doses of Doses. Part B: Part A, it is to Determine the Optimal Dose by Evaluating Two Capacity and Placebo Groups.
Timeline
- Start
- 2021-06-01
- Primary completion
- 2023-05-25
- Completion
- 2023-09-27
Drugs
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Subject | LAENNEC (Human Placenta Hydrolysate) | Unknown | 4 ml | Intravenous |
| Subject | LAENNEC (Human Placenta Hydrolysate) | Unknown | 6 ml | Intravenous |
| Subject | LAENNEC (Human Placenta Hydrolysate) | Unknown | 10 ml | Intravenous |