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Pilot Study of Ezetimibe for Chronic Hepatitis C Virus (HCV) Infection (EZE-1)

Primary Purpose

Chronic Hepatitis C

Status
Unknown status
Phase
Phase 1
Locations
Chile
Study Type
Interventional
Intervention
Ezetimibe
Sponsored by
Pontificia Universidad Catolica de Chile
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional basic science trial for Chronic Hepatitis C focused on measuring HCV, Ezetimibe, Cholesterol, Host

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion criteria:

  • Chronic hepatitis C defined as detectable HCV RNA for more than 6 months.
  • Age > 18 years old.
  • Compensated liver disease (bilirubin < 3mg/dL, unless having Gilbert´s syndrome, albumin > 3 g/dL, INR < 2, no hepatic encephalopathy, no ascites or recent -1 month- history of variceal bleeding).
  • HCV RNA level > 10.000 IU/mL.
  • Signed informed consent document.

Exclusion criteria:

  • History of cholecystectomy or known gallstones.
  • Current HCV antiviral treatment.
  • Medications for dyslipidemia in the preceding 2 months.
  • Abdominal surgery that could alter biliary or intestinal anatomy.
  • Evidence of sitosterolemia.
  • Negative pregnancy test in urine (for females).

Sites / Locations

  • Department of Gastroenterology, Pontificia Universidad Católica de ChileRecruiting

Arms of the Study

Arm 1

Arm Type

Experimental

Arm Label

Ezetimibe

Arm Description

Ezetimibe administered by mouth 10 mg BID for 12 weeks

Outcomes

Primary Outcome Measures

HCV plasma viral load

Secondary Outcome Measures

HCV biliary viral load

Full Information

First Posted
April 27, 2014
Last Updated
November 3, 2015
Sponsor
Pontificia Universidad Catolica de Chile
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1. Study Identification

Unique Protocol Identification Number
NCT02126137
Brief Title
Pilot Study of Ezetimibe for Chronic Hepatitis C Virus (HCV) Infection
Acronym
EZE-1
Official Title
A Pilot Study of the Effect of Ezetimibe in Patients With Chronic Hepatitis C Infection
Study Type
Interventional

2. Study Status

Record Verification Date
November 2015
Overall Recruitment Status
Unknown status
Study Start Date
October 2013 (undefined)
Primary Completion Date
January 2016 (Anticipated)
Study Completion Date
March 2016 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Pontificia Universidad Catolica de Chile

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
Infection by hepatitis C virus (HCV) affects more than 170 million people in the World and 80.000 in Chile. It causes more deaths than HIV infection in the US and is a leading cause for liver transplantation in Chile. Even though treatments are evolving with new direct antiviral agents (DAAs) that are increasing response rates, there are several issues with these new approaches, including increased toxicity, need for using interferon and ribavirin, complex algorithms of treatment, high cost, limited effectivity in certain groups (liver transplant patients) and drug interactions. Treatments targeted at host factors required for the viral cycle are becoming increasingly explored as an alternative or complement to DAAs. It has been recently described that Niemann-Pick C1-like 1 (NPC1L1), the intestinal receptor of cholesterol, serves as an entry factor for HCV. NPC1L1 is, therefore, a key transporter in the enterohepatic cycle of cholesterol. NPC1L1 can be blocked with ezetimibe, which is an approved and generally safe drug used for the management of hypercholesterolemia. Our hypothesis posits that blocking HCV entry to the hepatocyte or intestinal HCV reabsorption with ezetimibe may have an antiviral effect. In the study, we will administer ezetimibe 20 mg/d to 20 patients with stable chronic hepatitis C for 12 weeks and assess changes in HCV RNA and core antigen in plasma, bile and feces.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Chronic Hepatitis C
Keywords
HCV, Ezetimibe, Cholesterol, Host

7. Study Design

Primary Purpose
Basic Science
Study Phase
Phase 1
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
20 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Ezetimibe
Arm Type
Experimental
Arm Description
Ezetimibe administered by mouth 10 mg BID for 12 weeks
Intervention Type
Drug
Intervention Name(s)
Ezetimibe
Primary Outcome Measure Information:
Title
HCV plasma viral load
Time Frame
12 weeks
Secondary Outcome Measure Information:
Title
HCV biliary viral load
Time Frame
12 weeks

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion criteria: Chronic hepatitis C defined as detectable HCV RNA for more than 6 months. Age > 18 years old. Compensated liver disease (bilirubin < 3mg/dL, unless having Gilbert´s syndrome, albumin > 3 g/dL, INR < 2, no hepatic encephalopathy, no ascites or recent -1 month- history of variceal bleeding). HCV RNA level > 10.000 IU/mL. Signed informed consent document. Exclusion criteria: History of cholecystectomy or known gallstones. Current HCV antiviral treatment. Medications for dyslipidemia in the preceding 2 months. Abdominal surgery that could alter biliary or intestinal anatomy. Evidence of sitosterolemia. Negative pregnancy test in urine (for females).
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Pilar Labbé, RN
Phone
+56223543820
Email
pililabbe@gmail.com
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Alejandro Soza, MD
Organizational Affiliation
Pontificia Universidad Catolica de Chile
Official's Role
Principal Investigator
Facility Information:
Facility Name
Department of Gastroenterology, Pontificia Universidad Católica de Chile
City
Santiago
State/Province
Metropolitan
ZIP/Postal Code
8330024
Country
Chile
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Pilar Labbé, RN
Phone
+56223543820
Email
pililabbe@gmail.com
First Name & Middle Initial & Last Name & Degree
Alejandro Soza, MD

12. IPD Sharing Statement

Citations:
PubMed Identifier
22231557
Citation
Sainz B Jr, Barretto N, Martin DN, Hiraga N, Imamura M, Hussain S, Marsh KA, Yu X, Chayama K, Alrefai WA, Uprichard SL. Identification of the Niemann-Pick C1-like 1 cholesterol absorption receptor as a new hepatitis C virus entry factor. Nat Med. 2012 Jan 8;18(2):281-5. doi: 10.1038/nm.2581.
Results Reference
background
Links:
URL
http://medicina.uc.cl/CICUC-centro-investigacion-clinica
Description
Centro de Investigación Clínica UC (CICUC)
URL
http://hepatitis.cl
Description
Information related to hepatitis C / Información de hepatitis por virus C (Spanish)

Learn more about this trial

Pilot Study of Ezetimibe for Chronic Hepatitis C Virus (HCV) Infection

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