In Patients With Chronic Liver Diseases(Alcoholic Liver Disease and Non-Alcoholic Fatty Liver Disease), LAENNEC(Human Placenta Hydrolysate) is to Evaluate the Efficacy and Safety of Intravenous Drop

Trial statusRecruiting
Trial phasePhase 3
Trial typeInterventional
Biological sexAll
Age19-70
SponsorGreen Cross Wellbeing

About this trial

Control group : LAENNEC subcutaneous injection (4 ml)

Experimental group : LAENNEC intravenous injection (10 ml)

Eligibility criteria

Qualifiers

At the time of screening, 19 or 70 years

Those who have been diagnosed with alcoholic or non-alcoholic fatty liver disease

Those who have increased ALT level (Increased ALT level : 60 IU/L ≤ ALT ≤ 200 IU/L)

A person who can complete the signature agreement and comply with clinical trial requirements.

Disqualifiers

If you have the following disease

Liver cancer or other malignant tumor within 5 years at screening point

Esophageal varix bleeding, hepatic coma, ascites etc. related disease or Child-Pugh Score Class B,C patient within 1 year at screening point

Organs or bone marrow transplant experience

Trial design

Treatments tested in this trial

  • LAENNEC (Human Placenta Hydrolysate) IV
  • LAENNEC (Human Placenta Hydrolysate) SC

Treatment groups

226 Participants
are divided into 2 treatment groups

Sponsors and collaborators