Effect of LEGALON SIL on Hepatitis C Virus Recurrence in Stable Liver Transplanted Patients

Hepatitis C Virus Recurrence Clinical Trial

— LEG-SIL-LTX-02  

Official title:

A Randomized, Double-blind, Placebo-controlled Study to Investigate the Efficacy and Safety of LEGALON SIL for the Treatment of HCV Recurrence in Stable Liver Transplanted Patients

Clinical Trial Details — Status: Terminated

Administrative data

• NCT number: NCT01518933
• Other study ID #: LEG-SIL-LTX-02
• Status: Terminated
• Phase: Phase 2
• First received: January 23, 2012
• Last updated: March 4, 2015
• Start date: August 2011
• Est. completion date: April 2012

Study information

• Verified date: March 2015
• Source: Rottapharm
• Contact: n/a
• Is FDA regulated: No
• Health authority: Italy: The Italian Medicines Agency
• Study type: Interventional

Clinical Trial Summary

Hepatitis C virus (HCV)-related liver disease is the most common indication for liver transplantation (LT). However, LT does not cure the infection, and therapeutic strategies resulted in very limited efficacy and tolerability in LT recipients. In view of its postulated safety profile, Silibinin seems an ideal drug to be used in the setting of HCV recurrent patients after liver transplantation.

Description:

Hepatitis C virus (HCV)-related liver disease continues to be the most common indication for liver transplantation (LT) in both the United States and Europe. However, LT does not cure the infection, and re-infection of the liver allograft universally occurs. Recurrent HCV hepatitis often follows an accelerated course after LT, and histological recurrence occurs in approximately 50% of patients within 1 year after LT; 15-30% of them develop cirrhosis within 5 years. In this context, a peculiar feature is represented by the rapid course of liver fibrosis. Therapeutic strategies for managing the primary cause of liver damage, i.e. HCV infection, irrespective of application in pre-, peri-, and/or post-LT periods resulted in very limited efficacy and tolerability in LT recipients.

In view of its postulated safety profile, Silibinin seems an ideal drug to be used in the setting of HCV recurrent patients after liver transplantation.

Silibinin, a flavonolignan representing the main component (60%) of Silymarin and proposed as an anti-hepatotoxic agent for the treatment of various liver diseases has been recently reported to beneficially modulate the pro-fibrogenic potential of HSC, thus representing a very attractive possibility in the transplanted population. Besides the anti-inflammatory properties, Silibinin is able to inhibit Tumor necrosis factor-alpha (TNF-α). This is a proinflammatory cytokine with a major role in both acute and chronic viral, bacterial and fungal infections.

The primary objective is to determine the effect of post-transplant treatment with Legalon SIL on HCV viral load 30 days after the beginning of treatment.

44 stable liver transplanted patients with HCV recurrence will be randomized 3:1 to receive Legalon-SIL or Placebo. Randomized patients will be treated for 14 consecutive days with Legalon-SIL or Placebo. Patients dropping-out before the end of treatment period will be replaced.

Patients will be followed up for 1 year to monitor the effect of treatment on liver fibrosis, liver functional state, lymphocyte activation, and viral load.

Recruitment information / eligibility

• Status: Terminated
• Enrollment: 20
• Est. completion date: April 2012
• Est. primary completion date: April 2012
• Accepts healthy volunteers: No
• Gender: Both
• Age group: 18 Years to 70 Years

Eligibility

Inclusion Criteria:

• Patients must provide signed and dated informed consent before undergoing any trial related procedure.

• Males or females aged = 18 and = 70.

• Patients with HCV recurrent chronic hepatitis after liver transplantation, not responding to treatment with peginterferon/ribavirin (i.e. the so called standard of care, SOC).

• Stable (= 1 year) liver transplanted patients with HCV recurrence (as indicated by positive serum HCV-RNA, increase in transaminases, signs of graft damage according to HCV recurrence and/or presence of liver fibrosis as assessed by Fibroscan).

• Patients without biochemical, clinical and/or histological suspicion of rejection.

• Patients must be able to communicate, participate and comply with the requirements of the entire study.

• Female patients of child-bearing potential must agree on using a contraceptive method (oral contraceptive, intra-uterine device [IUD], transdermal contraceptive patch) and must have a negative pregnancy test at screening.

Exclusion Criteria:

• Patients with active hepatocellular carcinoma or other neoplasia (excluding cutaneous carcinoma in view of the high prevalence in the transplanted population).

• Patients with active biliary tract anomalies.

• Patients with a rejection episode in the 6 months preceding study inclusion.

• Patients on active interferon treatment.

• Female patients who are pregnant or breast-feeding.

• Patients with clinically significant laboratory abnormalities at screening.

• Patients with creatinine clearance < 50 ml.

• Patients with any abnormality on physical examination, vital signs (sitting systolic blood pressure greater than 140 mmHg, sitting diastolic blood pressure greater than 90 mmHg and pulse greater than 80 bpm) and ECG, unless these abnormalities are judged to be not clinically significant by the Investigator (a note about this must be made on the electronic Case Report Form - e-CRF).

• Patients taking any concomitant medication that is not allowed and that cannot be discontinued for the entire study period.

• Patients who are already taking other investigational drugs/treatments or have taken part in a clinical study within the previous 3 months or 5 half lives (whichever is longer).

• Patients with known hypersensitivity to any of the test materials or related compounds.

• Patients with a history of drug, alcohol or other substance abuse or other factors limiting their ability to co-operate during the study.

• Patients not available to attend all the test days and investigations as foreseen by the protocol, or unable to understand the aim, procedure or possible hazards of the study.

Study Design

Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Double Blind (Subject, Caregiver, Investigator, Outcomes Assessor), Primary Purpose: Treatment

Related Conditions & MeSH terms

• Hepatitis
• Hepatitis C
• Hepatitis C Virus Recurrence
• Recurrence

Intervention

Drug:
• Silibinin (Legalon-SIL)
20 mg/kg Silibinin (Legalon SIL), as per randomization schedule, will be administered daily as a 2-h infusion for 14 days.
• Saline
Placebo

Locations

Country	Name	City	State
Italy	Azienda Ospedaliero-Universitaria Policlinico Consorziale	Bari

Sponsors (2)

Lead Sponsor	Collaborator
Rottapharm	Azienda Ospedaliera Universitaria Policlinico

Country where clinical trial is conducted

Italy, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Viral load	To determine the effect of post-transplant treatment with Legalon SIL on HCV viral load 30 days after the beginning of treatment.	30 days after the beginning of treatment	No
Secondary	Viral load and lymphocyte activation	To determine the effect of post-transplant treatment with Legalon SIL on HCV viral load and lymphocyte activation one year after the beginning of treatment.	1 year after the beginning of the treatment	No
Secondary	Fibrosis	To determine the effect of post-transplant treatment with Legalon SIL on fibrosis and functional state.	1 year after the beginning of the treatment	No
Secondary	Safety	To determine the safety and tolerability of post-transplant treatment with Legalon SIL, including evaluation of its effect on the levels of immunomodulators.	1 year	Yes