NCT02972723

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 The investigators (Prof M Harris, University of Leeds) have data (currently unpublished)suggesting that metformin may have an antiviral effect independent of its effect on insulin resistance, thus raising the possibility that metformin may have a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

87
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
16

participants targeted

Target at below P25 for phase_4

Timeline
Completed

Started Mar 2011

Shorter than P25 for phase_4

Geographic Reach
1 country

1 active site

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Start

First participant enrolled

March 1, 2011

Completed
6 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

September 1, 2011

Completed
3 months until next milestone

Study Completion

Last participant's last visit for all outcomes

December 1, 2011

Completed
4.9 years until next milestone

First Submitted

Initial submission to the registry

October 27, 2016

Completed
27 days until next milestone

First Posted

Study publicly available on registry

November 23, 2016

Completed
Last Updated

November 23, 2016

Status Verified

November 1, 2016

Enrollment Period

6 months

First QC Date

October 27, 2016

Last Update Submit

November 22, 2016

Conditions

Keywords

Metformin Therapy in HCV

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

EXPERIMENTAL

Open label trial, participants will be expected to take Metformin twice a day for 2 weeks

Drug: Metformin

Interventions

Oral Metformin 1g bd. (total = 2g per day) for 14 days

Also known as: Glucophage
Metformin therapy, single arm

Eligibility Criteria

Age18 Years - 70 Years
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64), Older Adult (65+)

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

Location

MeSH Terms

Interventions

Metformin

Intervention Hierarchy (Ancestors)

BiguanidesGuanidinesAmidinesOrganic Chemicals

Study Officials

  • Stephen Dr Ryder

    Nottingham University Hospitals NHS Trust

    PRINCIPAL INVESTIGATOR

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

Locations