A Trial of IDN-6556 in Post Orthotopic Liver Transplant for Chronic HCV (POLT-HCV-SVR)

Conatus Pharmaceuticals

Status and phase: Completed; Phase 2

Conditions: Hepatic Cirrhosis; Liver Cirrhosis; Hepatic Fibrosis; Liver Fibrosis

Treatments: Drug: Placebo; Drug: IDN-6556

Study type: Interventional

Funder types: Industry

Identifiers

NCT02138253

IDN-6556-07

Details and patient eligibility

About

This is a double-blind, multicenter study involving patients with chronic HCV infection who had a liver transplantation; developed HCV-related liver fibrosis and/or incomplete cirrhosis; achieved a sustained virologic response (SVR) following anti-HCV therapy; but still have fibrosis and/or incomplete cirrhosis on liver biopsy to see if treatment with IDN-6556 is better than placebo in reversing or stopping the progression of the damage to the new liver caused by HCV.

Full description

There are data to suggest that with eradication of the HCV virus, improvements in liver fibrosis can be seen in the post-transplant population. However, amelioration of inflammatory activity, and deceleration of fibrosis progression is a gradual process over the course of many years. This placebo-controlled study is designed to evaluate the effects of IDN-6556, compared to placebo, on markers of apoptosis and inflammation, and liver histology.

Enrollment: 64 patients

Sex: All

Ages: 18+ years old

Volunteers: No Healthy Volunteers

Inclusion criteria

• Male or female subjects of minimum adult legal age (according to local laws for signing the informed consent document), able to provide written informed consent, and able to understand and willing to comply with the requirements of the study
• History of orthotopic liver transplantation for HCV-induced liver disease
• Diagnosis of HCV infection (HCV-RNA detectable in serum) and liver fibrosis and/or incomplete cirrhosis status post liver transplantation, and achieved a sustained virologic response (SVR) with anti-viral HCV treatment within 18 months of Day 1
• Liver fibrosis on liver histology as read by central histopathologist of Ishak F2 to F6 within three months of Day 1 (Up to 15 subjects with an Ishak score of F6 can be enrolled)
• Willingness to utilize two reliable forms of contraception (for both males and females of childbearing potential) from Screening to one month after the last dose of study drug

Exclusion criteria

• Known infection with hepatitis B virus (HBV) and/or human immunodeficiency virus (HIV)
• History of renal transplant and/or severe renal impairment defined as eGFR (estimated glomerular filtration rate) of less than 30 mL/min/1.73 m2
• Evidence of tumor burden >Milan criteria, or evidence of micro- or macrovascular invasion in explanted liver
• Hepatocellular carcinoma (HCC) at entry into the study
• Concurrent sirolimus (rapamycin) use
• History or presence of clinically concerning cardiac arrhythmias, or prolongation of Screening (pre-treatment) QT or QTc interval of > 480 milliseconds (msec)
• Subjects with diagnosed or suspected systemic lupus erythematosus (SLE) and/or rheumatoid arthritis (RA)
• If female: known pregnancy, positive urine or serum pregnancy test, or lactating/breastfeeding

Trial design

Primary purpose: Treatment

Allocation: Randomized

Interventional model: Parallel Assignment

Masking: Quadruple Blind

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64 participants in 2 patient groups, including a placebo group

IDN-6556

Experimental group

Description:

IDN-6556 25 mg BID

Treatment:

Drug: IDN-6556

Placebo

Placebo Comparator group

Description:

Placebo BID

Treatment:

Drug: Placebo