ClinicalTrials.gg
CompletedNCT03343925SHARP-CUpdated Apr 14, 2022

Direct-acting Antiviral Therapy and Reinfection Among PWID With Chronic HCV in Community-based Settings

An observational study in Hepatitis C, Chronic, sponsored by Kirby Institute. Completed at 4 sites in Australia. Open to participants aged 18 Years and older, including healthy volunteers. Per ClinicalTrials.gov, last updated 2022-04-14.

Sponsored by Kirby Institute · Observational

Study type
Observational
Model
Cohort
Time perspective
Prospective
Enrollment
140
Ages
18 Years and older
Sex
All
01

Where this study stands

Counted across the records on this site · 2026-11-12

Among 11 studies in Hepatitis C, Chronic by Kirby Institute — none open to participants now, none under way, none of them phase 3. Hepatitis C, Chronic · Kirby Institute.

Started
2018
the only one that year
Observational
3 of 11
none open now
Registered
8th of 11
by date

Among the 11 studies in Hepatitis C, Chronic by Kirby Institute, this one is the only one that started in 2018, is one of 3 observational ones, and was the 8th registered.

By phase

11 studies; the count open now beside each. This study's row is marked.

Phase 45 · 0 open
Observationalthis study3 · 0 open
No phase2 · 0 open
Phase 31 · 0 open

By the year they started

First in 2011; this study’s year is marked. 1 started in 2018.

Size and results

Median enrollment 90 across the 8 interventional studies, 140 across the 3 observational. Of the 9 that completed or were terminated, 3 (33%) have results posted.

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Download CSVWith an account: the 11 studies in Hepatitis C, Chronic by Kirby Institute as a file.
02

Study summary

SHARP-C is an observational cohort study investigating the effect of direct-acting antiviral (DAA) therapy and reinfection in people with chronic hepatitis C virus (HCV) and recent injecting drug use. A prospective, observational cohort design will be used to enrol patients attending tertiary drug and alcohol and primary health care services.

Participants will be prescribed a direct-acting HCV medication as per the standard of care. The on treatment phase will vary dependent on the type of a direct-acting antiviral prescribed as per the standard of care. Once patients have completed their treatment course they will be followed up every 3 months for up to 3 years following the end of treatment phase.

The study will aim to evaluate the incidence of HCV reinfection following successful DAA treatment over the three years of follow up. The study will also evaluate the proportion of patients with undetectable HCV RNA at 12 weeks post end of treatment (SVR12) with direct-acting anti-viral HCV therapy.

Read the detailed description

In Australia, hepatitis C virus (HCV)-related morbidity and mortality have doubled in the past decade, with health care costs of $220 million per annum1. This is due to a large, ageing population with chronic infection (230,000), and low uptake of existing interferon-based therapy (1-2% per year) due to side-effects, and sub-optimal therapy efficacy. The majority of new (90%) and existing (80%) cases of HCV infection occur among people who inject drugs (PWID).

In the community, 15-20% of current PWID report recent (last month) receptive needle/syringe sharing2. Qualitative research shows that decisions about sharing equipment are multi-factorial and can include issues ranging from service access (such as distance to service and opening hours), concerns about anonymity, perceptions that HCV is ubiquitous and unavoidable3 to socially-located concerns that promote use of sterile equipment such as a desire to avoid "track marks"4. There is no research that examines sharing of injecting equipment in those with successful therapy in either community or prison settings.

Increasing access to HCV therapy is a key objective of national and NSW Hepatitis C Strategies5,6. The advent of well-tolerated, simple, oral hepatitis C virus (HCV) regimens - direct acting antivirals (DAAs) - has the potential to transform this landscape. These are much shorter, tolerable treatment regimens with cure >95%, providing an opportunity to reverse the rising burden of advanced liver disease. From 1st March 2016, these highly efficacious HCV therapies have been listed on the Pharmaceutical Benefit Scheme, and people with recent injecting drug use are eligible to receive them. This is an important feature of the listing. In many countries, people who have not ceased injecting drug use are ineligible to receive DAA therapy7, despite the fact that they comprise a significant proportion of HCV cases. Australia is therefore poised to lead the world in the scale-up of new therapies to an extent that many countries with such exclusions will not be able to achieve.

This feature of DAA access also affords unique opportunities with respect to the implementation of treatment scale-up in community drug treatment clinics. Australia has good treatment coverage for people who are opioid dependent, with over 50% of opioid dependent people estimated to engage in opioid substitution therapy (OST) 8. Community-based drug treatment clinics represent another logical venue for expansion of HCV care beyond existing tertiary HCV treatment centres 9,10.

Although response to DAA HCV therapy is high, lower responses have been observed among people with previous treatment experience9, cirrhosis9 and those with baseline or emergent resistance associated variants10. Such resistance associated variants can persist for up to two years after treatment11, affect re-treatment options12, and be transmitted to new hosts13. Further, PWID are likely to be exposed to multiple HCV infections as a result of ongoing high-risk behaviours and might commonly harbour mixed HCV infections (infection with two or more distinct viruses) 14. Underlying mixed HCV infection can contribute to nonresponse during therapy14, which has implications for DAA regimens that are preferentially active against specific viral genotypes or subtypes. These data argue for surveillance of HCV resistance and mixed HCV infection among PWID to resolve residual concerns regarding their clinical and public health significance.

Two systematic reviews assessing interferon-based therapy for PWID have demonstrated responses comparable to randomised controlled trials excluding PWID15, 16. These data have supported international recommendations for the management of HCV for PWID 17. However, there are limited data on DAA therapy among recent PWID. As treatment is broadened to include more marginalised individuals, many clinicians are reluctant to treat HCV among PWID with recent injecting drug use with new DAA therapies. Major concerns include poor adherence/response, increased risk behaviour and HCV reinfection.

A major concern is that ongoing injecting risk behaviours following DAA therapy in PWID will lead to HCV reinfection, reversing the benefits of cure. Ongoing risk behaviours following successful HCV therapy may lead to reinfection and compromised treatment outcomes14. In a systematic review and meta-analysis of HCV reinfection among PWID performed by the investigators, the pooled estimate of re-infection was 2.2/100 p-yrs (95% CI, 0.9-6.1) overall and 6.4/100 p-yrs (95% CI, 2.5-16.7) among individuals who reported injecting drug use post-SVR16. The one study of HCV reinfection post-therapy in prison performed to date was small (n=74), retrospective, and did not assess the rate of HCV reinfection18. Studies of reinfection following HCV therapy are limited by small sample sizes, retrospective study designs, incomplete follow-up, and a lack of sensitive methods to detect reinfection. Further, there are no data on HCV reinfection among recent PWID treated with DAAs.

Although DAA therapy could limit HCV-related disease burden, as treatment is broadened to include more marginalised individuals, many clinicians are reluctant to treat HCV among recent PWID, given concerns about poor adherence (and lower response to therapy), increased risk behaviours (due to the ease and high cure rates of DAA HCV therapy) and HCV reinfection (thereby reversing cure). However, no data exist on the extent to which this should be a concern. Given that DAA HCV therapy is highly expensive, we urgently need data on the magnitude of risk for, and predictors of, HCV reinfection. It is also unclear whether PWID treated in these two settings will vary in their response to DAA therapy and risk for reinfection.

The investigators have an excellent track record of conducting high quality cohort studies and clinical trials among PWID in the community19-23 and prison24, with high participant retention in follow-up. The investigators have developed a network of clinical sites providing HCV care in nine community-based drug treatment clinics20, 25. In SHARP-C the investigators will explore the risk of HCV reinfection and treatment efficacy among recent PWID with chronic HCV and recent injecting drug use.

03

Conditions studied

  • Hepatitis C, Chronic

Keywords

  • Reinfection
04

Who can participate

Ages eligible
18 Years and older
Sexes eligible
All
Accepts healthy volunteers
Yes
Sampling method
Non-probability sample

Study population

Participants with chronic HCV infection and recent injecting drug use who are 18 years or over and are eligible for DAA therapy as per the PBS criteria.

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  1. Participants have voluntarily signed the form.
  2. Be ≥18 years of age on day of signing informed consent form.
  3. Have chronic infection.
  4. Recent injecting drug use (previous 6 months).
  5. Eligible for DAA therapy as per the Pharmaceutical Benefits Scheme (PBS) criteria
  6. -1 infected participants enrolled in the study must meet the following criteria:

    1. Have HIV infection documented by any licensed rapid HIV test or HIV enzyme or chemiluminescence immunoassay (E/CIA) test kit at any time prior to study entry (Baseline) and confirmed by a licensed Western blot or a second antibody test by a method other than the initial rapid HIV and/or E/CIA, or by HIV-1 p24 antigen, or plasma HIV-1 RNA viral load.
    2. Be on HIV Antiretroviral Therapy (ART) for at least 4 weeks prior to study entry using an ART regimen that is allowable with the intended DAA regimen as determined by the current PI and the Liverpool drug interaction website (http://www.hiv-druginteractions.org/) OR be naive to treatment with any antiretroviral therapy (ART) with a baseline of >200 and have no plans to initiate ART treatment while participating in this study and through to at least Follow-up Week 4.

Exclusion criteria

Exclusion Criteria:

  1. The participant must be excluded from participating in the trial if the subject is unable or unwilling to provide or abide by the requirements of the study.
Terms in these criteria, in plain language(4)

Underlined terms in the criteria open these too. Explained by clinicaltrials.gg, not part of the registry record. The study team decides who can take part.

Informed consent

Before you join, the study team explains what taking part involves — its purpose, what happens, the risks and possible benefits — and answers your questions, so you can decide freely. Consent is usually recorded on a form (the informed consent form, ICF) signed by you or, where the law allows, by someone legally authorised to decide for you.

You can keep asking questions during the study, you are told of new information that matters, and you can choose to leave at any time.

Hepatitis C tests

Hepatitis C is a virus that infects the liver. An HCV antibody test can stay positive after an infection has cleared (and is occasionally positive without one); an HCV RNA test shows whether the virus is there now.

After treatment, hepatitis C counts as cured when HCV RNA is still undetectable 12 weeks or more after the treatment ended. Studies often accept people cured this way.

HIV

The human immunodeficiency virus, which weakens the immune system.

Many studies now accept people whose HIV is controlled on treatment, judged by the viral load and the CD4 count. Check the limits this study sets.

CD4 count

The number of CD4 cells, a type of white blood cell, in a given amount of blood. It is used to follow how well the immune system is doing in HIV.

05

Study design

Observational model
Cohort
Time perspective
Prospective
Enrollment
140 participants (actual)
Patient registry
No
Biospecimen retention
Samples with dna
06

What researchers measure

Primary outcomes

  1. Reinfection

    Incidence of HCV reinfection following successful DAA therapy.

    Time frame: 3 years

Secondary outcomes

  1. Undetectable HCV RNA at SVR12

    The proportion of participants with a treatment response at SVR12

    Time frame: 2.5 years

  2. Treatment completion

    The proportion of participants who complete treatment

    Time frame: 3 years

  3. Undetectable HCV RNA at the end of treatment

    The proportion of participants with undetectable HCV RNA at the end of treatment

    Time frame: 3 years

07

Study locations

4 sites
  • St Vincent's Hospital
    Darlinghurst, New South Wales 2010, Australia
  • Nepean Hospital
    Kingswood, New South Wales 2751, Australia
  • Drug and Alcohol Services (Hunter)
    Newcastle, New South Wales 2300, Australia
  • Infectious Diseases Clinic, Royal Adelaide Hospital
    Adelaide, South Australia 5000, Australia
08

Timeline

Tracking since Sep 25, 2026
ElapsedEstimatedEstimated, not yet reachedSimilar studies: half by the dot; the band is the middle halfHalf of similar studies reached it by the dot; the band is the middle half, from a quarter to three quarters

Ran from Aug 2018 to primary completion in Jul 2021, 34 months.

Of 38 non-industry observational studies under Hepatitis C, Chronic, half reached primary completion within 43 months of starting (the median), counting those still running; a quarter within 26 and three quarters within 110. This study's 34 months is below that.

Counting every sponsor, half of 72 studies reached it within 32 months; a quarter within 22 and three quarters within 54.

How these figures are worked out, and which studies are left out of them.

Registered
Nov 8, 2017
First posted
Nov 17, 2017
StartActual
Aug 17, 2018
Primary completionActual
Jul 1, 2021
CompletionActual
Apr 11, 2022
Last update
Apr 14, 2022
What these dates mean
Start.
When the first participant enrolled; while estimated, when the study expects to open to recruitment.
Primary completion.
When the last participant was examined or treated to collect data for the study's main question, its primary outcome. A study that stopped early gives the date its data collection stopped.
Completion.
When the last participant's last visit took place, for every outcome, secondary ones and side effects included: the end of the study. Often later than primary completion, sometimes the same day.
Actual and Est.
Actual means the registry says the date has happened. Est. (estimated) is a date the sponsor plans or expects. It can still move, and the sponsor is expected to change it to actual once it has passed.
No changes since tracking began. The registry record was last updated on Apr 14, 2022, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
09

Registry details

Key details

Study ID
NCT03343925
Lead sponsor
Kirby Institute
Responsible party
Sponsor
First posted
Nov 17, 2017
Start date
Aug 17, 2018
Primary completion
Jul 1, 2021
Completion
Apr 11, 2022
Last update
Apr 14, 2022

Study contacts

Jason Grebely
principal investigator · Kirby Institute

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is completed, as verified in Apr 2022. You cannot join it, but the record below documents what was studied.

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Discussion

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