Efficacy and Safety of Oltipraz in the Patients With Non-alcoholic Fatty Liver Disease

About this trial

Last updated 12 years ago

Study ID

PMK-N01GI1

Status

Completed

Type

Interventional

Phase

Phase 2

Placebo

Yes

Accepting

18 to 75 Years

All Sexes

Trial Timing

Ended 13 years ago

What is this trial about?

Dithiolethiones, a novel class of adenosine monophosphate-activated protein kinase (AMPK) activators, prevent insulin resistance through AMPK-dependent p70 ribosomal S6 kinase-1 (S6K1) inhibition. And it is well known that the modulation of S6K1 by oltipraz inhibited the development of insulin resistance and hyperglycemia through the AMPK-S6K1 pathway.Also some research reported that LXRg (a member of the nuclear hormone receptor)-mediated increases in SREBP-1c (the sterol regulatory element-binding protein-1c gene) promote the expression of lipogenic genes and enhance fatty acid synthesis and oltipraz inhibits LXRg and SREBP-c. Therefore, Oltipraz inhibits fatty acid synthesis through AMPK-S6K1 pathway and LXRg-SREBP-1c pathway in liver.

What are the participation requirements?

Inclusion Criteria

* Patients over 18, under 75 years of age * Patients with non-alcoholic fatty liver disease

Exclusion Criteria

* Over 2 ratio of AST to ALT * Type 1 diabetes mellitus (insulin-dependent diabetes mellitus) * Disorder in liver function with an exception of non-alcoholic fatty liver (e.g. Virus infection, biliary atresia, autoimmune hepatitis and etc.) * Patients who have been taken drugs induced fatty liver for over 3 month within 1 year of participation in this study; amiodarone, tamoxifen, methotrexate, tetracyclines, glucocorticoids, anabolic steroids, over usual dose of estrogen for hormone replacement therapy and valproate * Patients who has been taken any medications that could affect the treatment for non-alcoholic steatohepatitis: insulin, insulin sensitizer(metformin, thiazolidinedione), high dose of vitamin E, high dose of UDCA, pentoxifylline, SAM-e, Betaine, types of Statin, types of fibrate and orlistat * Patients who had a Bariatric surgery less than 6 month prior to the participation in the study * Patients who are judged by investigator that participation of the study is difficult due to disease as follow; hepatic cirrhosis, Wilson's disease, malignant tumor, serious metabolic disease, severe renal disease, severe pulmonary disease, severe cardiovascular disease, severe nervous disease/psychiatric disorder, muscle disease and etc * Any history of immune disorder which affect the changes in cytokine: inflammatory bowel disease, autoimmune thrombocytopenic purpura, system lupus erythematosus, autoimmune hemolytic anemia, severe psoriasis, rheumatic arthritis and etc * Patients who have received treatment that may affect liver function within 1 month prior to the participation in the study * Patient who has been administered other investigational product within 1 month prior to the participation in the study * Patient who is not allowed to get MRS test: pacemaker, shunt and etc * Pregnant or nursing women * Patient who considered ineligible for participation in the study as Investigator's judgment