Metformin Therapy in HCV Infection
A Study of the Antiviral Activity of Metformin as an Anti-Hepatitis C Virus Agent in Patients With Chronic Hepatitis C Virus Infection
2 other identifiers
interventional
16
1 country
1
Brief Summary
Hepatitis C virus infection (HCV) is a major cause of cirrhosis and death from liver disease worldwide. Current therapy for HCV with interferon based therapies results in cure rates of around 5055% which leaves a significant number of patients without effective therapy. HCV induces (can bring on) insulin resistance and insulin resistance is a factor known to reduce the response to antiHCV therapy. This finding stimulated initial studies looking at agents that may reduce insulin resistance as additional therapy in HCV infection. A study using metformin in addition to interferon and ribavirin showed a nonsignificant increase in cure rates (53% vs. 42%), but this was limited to patients with type 1 infection AND demonstrable insulin resistance. The assumption was made that the potential effect of metformin was likely to be on insulin resistance and thus by modulating this enhances response. The investigators (Prof M Harris, University of Leeds) have data (currently unpublished)suggesting that metformin may have an antiviral effect independent of its effect on insulin resistance, thus raising the possibility that metformin may have a direct antiviral effect in vivo. Given that the development of specific antiHCV agents which target viral proteins such as its polymerase and protease are in trial development but have so far proved either highly toxic or are likely to have a huge cost there is considerable rationale for looking at alternative potential antiHCV agents and in this context metformin is cheap, readily available and has an excellent safety profile. This pilot study therefore addresses the question "Does metformin therapy result in a significant drop in HCV viral load in chronically infected patients?"
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at below P25 for phase_4
Started Mar 2011
Shorter than P25 for phase_4
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
March 1, 2011
CompletedPrimary Completion
Last participant's last visit for primary outcome
September 1, 2011
CompletedStudy Completion
Last participant's last visit for all outcomes
December 1, 2011
CompletedFirst Submitted
Initial submission to the registry
October 27, 2016
CompletedFirst Posted
Study publicly available on registry
November 23, 2016
CompletedNovember 23, 2016
November 1, 2016
6 months
October 27, 2016
November 22, 2016
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
Drop of viral load by at least 1 log in patients receiving Metformin
14 days
Study Arms (1)
Metformin therapy, single arm
EXPERIMENTALOpen label trial, participants will be expected to take Metformin twice a day for 2 weeks
Interventions
Oral Metformin 1g bd. (total = 2g per day) for 14 days
Eligibility Criteria
You may qualify if:
- Adult Males and Females (18-70 yrs old) able to give consent
- Chronic hepatitis C virus infection
- Women of child bearing potential (who have a negative pregnancy test) must agree to use methods of medically acceptable forms of contraception during the study; (e.g.intra-uterine device (IUD) or a double-barrier method of oral contraception with condom)
You may not qualify if:
- Type 2 diabetes.
- Patients with impaired renal function.
- Decompensated liver cirrhosis (stable patients with cirrhosis would be eligible).
- Patients who in the opinion of the Investigator are considered unsuitable.
- Pregnant females.
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Secondary care Hepatitis clinic at Nottingham University Hospital
Nottingham, Nottingham, NG7 2UH, United Kingdom
MeSH Terms
Interventions
Intervention Hierarchy (Ancestors)
Study Officials
- PRINCIPAL INVESTIGATOR
Stephen Dr Ryder
Nottingham University Hospitals NHS Trust
Study Design
- Study Type
- interventional
- Phase
- phase 4
- Allocation
- NA
- Masking
- NONE
- Intervention Model
- SINGLE GROUP
- Sponsor Type
- OTHER
- Responsible Party
- SPONSOR
Study Record Dates
First Submitted
October 27, 2016
First Posted
November 23, 2016
Study Start
March 1, 2011
Primary Completion
September 1, 2011
Study Completion
December 1, 2011
Last Updated
November 23, 2016
Record last verified: 2016-11