Ezetimibe as a Safe and Efficacious Treatment for Chronic Hepatitis C

VA Office of Research and Development

Status and phase: Terminated; Phase 2

Conditions: Chronic Hepatitis C

Treatments: Drug: 40mg ezetimibe; Drug: Placebo; Drug: 20mg ezetimibe

Study type: Interventional

Funder types: Other U.S. Federal agency

Identifiers

NCT02971033

INFA-015-16S

Details and patient eligibility

About

To address the need for more affordable hepatitis C virus (HCV) antivirals with high barriers to viral resistance and strategies to shorten the current treatment duration, the goal is to develop affordable therapeutic regimens to prevent HCV entry/spread and test the efficacy of those inhibitors for treating HCV infection. The investigators recently discovered that a major cholesterol uptake receptor is required for HCV entry into hepatocytes and that there is already an FDA-approved drug that inhibits cholesterol uptake by this receptor. Importantly the same drug also potently blocks HCV entry in human liver cells both in cell culture and in a small animal model. Further, looking back at people who were previously treated for HCV infection, the investigators found treatment response to be better (i.e. larger viral log reduction) in patients who happened to be taking ezetimibe (EZE). Hence, the objective of this study is to assess whether the FDA-approved drug (ezetimibe) is useful for the treatment of chronic HCV. The investigators predict that when administered as monotherapy ezetimibe will reduce HCV viremia perhaps allowing for viral clearance and that when included in combination treatment regimens that EZE will increase HCV decline resulting in faster viral clearance (i.e. shorter/cheaper direct-acting antiviral [DAA] therapy). To test these hypotheses, the investigators will execute the following aims: (1) Assess the efficacy of EZE monotherapy in chronically HCV infected and predict time to cure; (2) Assess the efficacy of EZE as an adjunct therapy in chronically HCV infected patients undergoing currently approved HCV DAA treatment.

Full description

To address the need for more affordable HCV antivirals with high barriers to viral resistance and/or strategies to shorten the current treatment duration, the goal is to develop affordable therapeutic regimens to prevent HCV entry/spread and test the efficacy of those inhibitors for treating HCV infection. The investigators recently discovered that the Niemann-Pick C1 Like-1 (NPC1L1) cellular cholesterol uptake receptor is required for HCV entry into hepatocytes and that ezetimibe, an FDA-approved drug that inhibits NPC1L1-mediated cholesterol uptake potently blocks HCV entry in human hepatoma cells and human hepatocytes transplanted into urokinase-type plasminogen activator-severe combined immunodeficiency (uPA-SCID) mice. Further, retrospective analysis of the National VA database using multivariable logistic regression models to control for age, sex, race, alcohol use, drug use, and other co-morbidities, the investigators found HCV prevalence to be lower (p <.001) and interferon/ribavirin (IFN/RBV) treatment response to be better (i.e. larger viral log reduction) in patients taking ezetimibe. Hence, the specific objective of this application is to assess the efficacy of EZE for the treatment of chronic HCV. Based on preliminary in vitro, in vivo, clinical retrospective data and HCV/DAA modeling, the investigators hypothesize that when administered as monotherapy EZE will reduce HCV viremia perhaps allowing for viral clearance and that when included in combination treatment regimens that EZE will augment 2nd phase HCV decline resulting in faster viral clearance (i.e. shorter/cheaper DAA therapy). To test these hypotheses, the investigators will execute the following aims: (1) Assess the efficacy of EZE monotherapy in chronically HCV infected and predict time to cure; (2) Assess the efficacy of EZE as an adjunct therapy in chronically HCV infected patients undergoing currently approved HCV DAA treatment.

Enrollment: 2 patients

Sex: All

Ages: 18 to 70 years old

Volunteers: No Healthy Volunteers

Inclusion criteria

• Males/females 18 - 70 yrs of age

• Serum HCV RNA >2,000 IU/ml

• Hepatitis C genotype 1

• Other causes of chronic liver disease excluded by appropriate clinical, laboratory, or histologic evaluation

• The following hematological criteria must be met:

  • Hemoglobin > 12 g/dl
  • Absolute neutrophil count (ANC) > 1.0x109 /L
  • Platelets 150 x 108 /L (i.e normal)

• Serum creatinine <1.5 times the upper limit of normal (ULN) at screening.

• Fasting blood sugar normal for non-diabetics or hemoglobin A1C < 8.5% with diabetes

• Women of childbearing potential must have a negative pregnancy test prior to receiving treatment. Sexually active women must take adequate precautions to prevent pregnancy during the study. Pregnancy tests will be done at the final clinic visits and every 4 weeks

• Patient provides written informed consent

Exclusion criteria

• Evidence of liver disease other than HCV:

  • Antinuclear antibodies (ANA) >1:160
  • Active alcoholic liver disease.
  • Hepatitis B surface antigen positive
  • Hemochromatosis
  • Wilson disease
  • Alpha-1-antitrypsin deficiency
  • Recent hepatotoxic drug exposure
  • Cirrhosis with complications of portal hypertension including esophageal varices (> grade 1 by endoscopy), ascites, or hepatic encephalopathy, or bilirubin >2.0 mg/dl

• Patients with advanced fibrosis (defined herein as decompensated cirrhosis, FIB4 > 2.5, platelet count <150 x 103/uL, clinical or radiographic evidence of cirrhosis)

• Extrahepatic manifestations of liver disease or HIV co-infection

• Use of fibric acid, Fenofibrate or cholestyramine

• Active substance abuse including, but not limited to alcohol or i.v./inhaled drugs

• Use of chemotherapy or systemic steroid therapy within 30 days prior to enrollment

• Pregnancy, females who are breast feeding, or females of child bearing potential who are not using adequate birth control measures

• History of a medical condition that could interfere with participation or completion of the protocol

• Organ transplant recipient

• History of hypersensitivity to ezetimibe

Trial design

Primary purpose: Treatment

Allocation: Randomized

Interventional model: Parallel Assignment

Masking: Double Blind

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2 participants in 3 patient groups, including a placebo group

placebo

Placebo Comparator group

Description:

placebo

Treatment:

Drug: Placebo

20mg/day ezetimibe

Experimental group

Description:

20mg/day ezetimibe

Treatment:

Drug: 20mg ezetimibe

40mg/day ezetimibe

Experimental group

Description:

40mg/day ezetimibe

Treatment:

Drug: 40mg ezetimibe