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.

NCT05532124 ↗

Phase 2 Completed 49 enrolled Green Cross Wellbeing
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

EvaluationDrugModalityDoseRoute
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

Indications