Efficacy and Safety of Oltipraz in the Patients With Liver Fibrosis and Cirrhosis

NCT ID: NCT00956098

Last Updated: 2009-08-11

Basic Information

• Recruitment Status: COMPLETED
• Clinical Phase: PHASE2
• Total Enrollment: 81 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2006-02-28
• Study Completion Date: 2007-02-28

Brief Summary

This study investigated the effectiveness and safety of oltipraz therapy in treating patients with cirrhosis induced by chronic hepatitis type B or C.

Detailed Description

Oltipraz [5-(2-pyrazinyl)-4-methyl-1,2-dithiol-3-thione] has been extensively studied as a cancer chemopreventive agent. Comprehensive mechanistic and phase IIa studies supported the notion that oltipraz exerts chemopreventive effects, as supported by Phase IIa human clinical studies of oltipraz on cancer chemoprevention, conducted in Qidong, China. Hepatic stellate cells cause synthesis of large quantities of extracellular matrix. Transforming growth factor beta1 (TGF-beta1), as a key fibrogenic mediator for fibrogenesis after injuries through deposition of extracellular matrix and inhibition of collagenase activity in the liver, is associated with the regulation of cell growth and differentiation and causes synthesis of extracellular matrix proteins and cellular receptors for matrix proteins. Previously, we reported the effectiveness of oltipraz in regeneration of cirrhotic liver, which includes reduction of the intensities of liver fibrotic and cirrhotic nodules, elimination of accumulated extracellular matrix, and regeneration of cirrhotic liver in animal models. Oltipraz completely resolves fibrosis in the cirrhotic liver, thereby improving viability. TGF-beta1 signaling plays an important role in liver fibrogenesis and cirrhosis as evidenced by receptor knockout experiments. No therapeutic agent that is active in interrupting TGF-beta1 signaling is available, proposing that C/EBP serve as a molecular target for the treatment of liver cirrhosis.

Conditions

Liver Fibrosis; Liver Cirrhosis

Study Design

• Allocation Method: RANDOMIZED
• Intervention Model: PARALLEL
• Primary Study Purpose: TREATMENT
• Blinding Strategy: DOUBLE

Study Groups

placebo

Group Type: PLACEBO_COMPARATOR

placebo

Intervention Type: DRUG

oltipraz

Group Type: EXPERIMENTAL

oltipraz

Intervention Type: DRUG

60mg bid 90mg qd

Interventions

oltipraz

60mg bid 90mg qd

Intervention Type: DRUG

placebo

Intervention Type: DRUG

Eligibility Criteria

Inclusion Criteria

• patients with fibrosis and cirrhosis induced by chronic hepatitis type B or C
• patients with HbsAg, Anti-HCV or HCV RNA positive

Exclusion Criteria

• treatment with antiviral agents, immunosuppressants, glucocorticoids, within the 6 months or with biphenyl dimethyl dicarboxylate one month
• treatment with any investigational drug (except CJ11555PK or CJ-OPZ-201PK) within one month
• Child-Pugh class C, Use of a mean daily dose of 80 g alcohol with the one month, of enzyme inducers or inhibitors, or of drug abuse that might affect this study
• a known hypersensitivity to oltipraz or its structurally related compounds
• ascites, hemorrhage from varicoses, uncompensated LC with the history of hepatic encephalopathy within the 6 months
• hepatocellular carcinoma (a rising serum level of α-fetoprotein or a suspicious foci on hepatic ultrasonography at screening or), liver transplantation
• pregnancy or lactation, unwillingness of contraception during the study period
• other serious concurrent illness (e.g., severe hemorrhagic GI, renal, pulmonary, neurological, cardiovascular (CHF of class III or above; a history of MI within the past 6 months) diseases, or cancer, autoimmunity or psychological diseases)
• any patients who is inappropriate or has unwillingness of clinical study as judged by participating clinicians
• bilirubin content greater than 2.0 mg/dL, prothrombin time longer than 4 sec, and serum albumin below 2.5 g/dL

• Minimum Eligible Age: 25 Years
• Maximum Eligible Age: 65 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

HK inno.N Corporation

INDUSTRY

Sponsor Role: lead

Locations

The Catholic University of Korea Holy Family Hospital

Sosa-Dong, Wonmi-Gu, Gyeonggi-do, South Korea

The Catholic University of Korea Seoul St. Mary's Hospital

Banpo-Dong, Seocho-Gu, Seoul, South Korea

Countries

South Korea

Other Identifiers

CJ-OPZ-201 study

Identifier Type: -

Identifier Source: org_study_id