Trial of Simplified Treatment Monitoring for 8 Weeks Glecaprevir/Pibrentasvir in Chronic Hepatitis C Patients

The capacity to scale-up interferon-free DAA therapy would be enhanced by simplified
treatment monitoring strategies. The "next generation" DAA regimen of glecaprevir
(300mg)/pibrentasvir (120mg), a protease inhibitor and NS5A inhibitor, provides key features
for HCV treatment simplification, including on-treatment monitoring: 1) pangenotypic activity
with extremely high efficacy (SVR>95%); 2) no relationship between time to undetectable HCV
RNA and SVR; 3) minimal drug-related toxicity; 4) ease of dosing (three pills once daily);
and short duration (8 weeks in non-cirrhosis and 12 weeks in cirrhosis for treatment naïve
patients). In phase II and III clinical trials in participants without cirrhosis, 8 weeks of
glecaprevir (300mg)/pibrentasvir (120mg) has provided intention-to-treat SVR rates of 99.1%,
98%, 97%, and 93.1% in genotype 1, 2, 3, and 4-6 populations, respectively.

Current standard on-treatment monitoring in clinical trials involves clinic-based visits
every 4 weeks. In the DAA era where treatments are highly tolerable, effective and short
duration, this intensive monitoring strategy may no longer be required. A simplified
on-treatment monitoring strategy is hypothesised to be non-inferior to the standard clinical
trial on treatment monitoring strategy. If successful, a simplified on-treatment monitoring
strategy is likely to be highly attractive to patients, clinicians and health care payers. It
has the potential to improve the rapid scale up of treatment providing population level
benefits in the reduction of global hepatitis C disease burden.

This study will be conducted as a Phase IIIb, randomised, controlled, multicentre,
international trial.

There will be a maximum screening period of 6 weeks prior to Baseline. Eligible patients will
be randomised into one of two on-treatment monitoring strategies; standard clinical trial
monitoring (4-weekly on-treatment visits) vs simplified monitoring (no on-treatment visits).
Randomisation will be 1:2 (standard vs simplified) and all participants will receive
treatment with glecaprevir (300mg)/pibrentasvir (120mg) for 8 weeks.

All participants will attend the clinic for screening and baseline visit. Randomisation will
occur at the baseline visit.

The two on-treatment monitoring strategies will differ as follows:

- Standard monitoring arm participants will have on-treatment clinic visits at weeks 4 and
8 (EoT).

- Simplified monitoring arm participants will have no on-treatment clinic visits.

Study nurse phone contact will also be made to participants in BOTH arms 1-2 days prior Week
4 and EoT (Week 8) visits to provide standardized reporting of adverse events, concomitant
medication and adherence. One post treatment clinic visit will be conducted at SVR12 (week
20) for all participants.

Inclusion Criteria:

1. Have voluntarily signed the informed consent form.

2. 18 years of age or older.

3. Chronic HCV infection as defined by anti-HCV antibody or HCV RNA detection for greater
than 6 months.

4. HCV RNA plasma ≥ 10,000 IU/ml at screening.

5. HCV genotype 1-6.

6. HCV treatment naïve (no prior treatment with an approved or investigation anti-HCV
medication).

7. Stage F0-3, based on: hepatic elastography <12.5 kPa on Fibroscan® or APRI <1.0.

8. If co-infection with HIV is documented, the subject must meet the following criteria:

- ART naïve with CD4 T cell count >500 cells/mm3; OR

- On a stable ART regimen (containing only permissible ART - see protocol section
3.2) for >8 weeks prior to screening visit, with CD4 T cell count >200 cells/mm3
and a plasma HIV RNA level below the limit of detection.

9. Negative pregnancy test at screening and baseline (females of childbearing potential
only).

10. All fertile females must be using effective contraception during treatment and during
the 30 days after treatment end.

Exclusion Criteria:

1. History of any of the following:

1. Clinically significant illness (other than HCV) or any other major medical
disorder that may interfere with the participant treatment, assessment or
compliance with the protocol; participants currently under evaluation for a
potentially clinically significant illness (other than HCV) are also excluded.

2. Clinical hepatic decompensation (i.e. ascites, encephalopathy or variceal
haemorrhage).

3. Solid organ transplant.

4. History of severe, life-threatening or other significant sensitivity to any
excipients of the study drugs.

2. Any of the following lab parameters at screening:

1. ALT > 10 x ULN

2. AST > 10 x ULN

3. Direct bilirubin > ULN

4. Platelets < 90,000/μL (cells/mm3) if Fibroscan® <12.5 kPa OR < 150,000/μL
(cells/mm3) if Fibroscan® is unavailable and patient is included with APRI <1

5. Creatinine clearance (CLcr) < 50 mL/min

6. Haemoglobin < 12g/dL for males; <11g/dL for females

7. Albumin < LLN

8. INR > 1.5 ULN unless subject has known haemophilia or is stable on an
anticoagulant regimen affecting INR

3. Pregnant or breastfeeding female.

4. HBV infection (HBsAg positive).

5. Use of prohibited concomitant medications as described in protocol section 5.2.

6. Chronic use of systemically administered immunosuppressive agents (e.g. prednisone
equivalent > 10 mg/day for >2 weeks).

7. Therapy with any anti-neoplastic or immunomodulatory treatment (including
supraphysiologic doses of steroids and radiation) ≤6 months prior to the first dose of
study drug.

8. Any investigational drug ≤6 weeks prior to the first dose of study drug.

9. Ongoing severe psychiatric disease as judged by the treating physician.

10. Positive result of a urine drug screen at the Screening Visit for opiates,
barbiturates, amphetamines, cocaine, benzodiazepines, phencyclidine, propoxyphene, or
alcohol, with the exception of a positive result (including methadone) associated with
documented short-term use or chronic stable use of a prescribed medication in that
class.

11. Injecting drug use within the previous six months.

12. Inability or unwillingness to provide informed consent or abide by the requirements of
the study.