| Eligibility |
Inclusion Criteria:
- Provision of signed and dated informed consent form.
- Positive serum hepatitis delta virus (HDV) antibody results or polymerase chain
reaction (PCR) results for serum/ plasma HDV RNA for at least 6 months before
screening.
- Positive PCR results for serum/ plasma HDV RNA at screening.
- Alanine transaminase level >1 x upper limit of normal (ULN), but less than 10 x ULN.
- Serum albumin >28 g/L.
- Thyroid stimulating hormone (TSH) within normal ranges (including on medication for
control of thyroid function)
- Negative urine pregnancy test for females of childbearing potential.
- Inclusion criteria for female individuals:
- Postmenopausal for at least 2 years, or
- Surgically sterile (total hysterectomy or bilateral oophorectomy, bilateral tubal
ligation, staples, or another type of sterilization), or
- Abstinence from heterosexual intercourse throughout the treatment period, or
- Willingness to use highly effective contraception (double barrier method or
barrier contraception in combination with hormonal or intrauterine contraceptive)
throughout the treatment period and for 6 months after the last dose of the study
medication.
- Male individuals must agree to use a highly effective contraception (double barrier
method or barrier contraception in combination with hormonal or intrauterine
contraceptive used by female partners) and not to donate sperm throughout the
treatment period and for 6 months after the last dose of the study medication.
Exclusion Criteria:
- Child-Pugh hepatic insufficiency score of B-C or over 6 points. Note: Child-Pugh
hepatic insufficiency score of 6 points is allowed. Only individuals with compensated
cirrhosis are allowed. Uncomplicated oesophageal varices allowed; individuals with
current bleeding or ligation, or history of bleeding or ligation within the last 2
years are excluded.
- Hepatitis C virus (HCV) or human immunodeficiency virus (HIV) coinfection. Individuals
with HCV antibodies can be enrolled, if screening HCV RNA test is negative.
- Creatinine clearance < 60 mL/min as estimated using Cockcroft-Gault formula.
- Total bilirubin = 34.2 µmol/L. (Individuals with higher total bilirubin values may be
included after the consultation with the Study Medical Monitor, if such elevation can
be clearly attributed to Gilbert's syndrome associated with low-grade
hyperbilirubinemia.)
- Evidence of an active or suspected malignancy, or an untreated pre-malignancy
disorder, or a history of malignancy within the last 5 years (with the exception of
successfully treated carcinoma of the cervix in situ and successfully treated basal
cell carcinoma and squamous cell carcinoma not less than 1 year prior to screening
[and no more than 3 excised skin cancer within the last 5 years prior to screening])
or history of hepatic carcinoma.
- Systemic connective tissue disorders.
- New York Heart Association (NYHA) class III-IV congestive heart failure.
- Individuals with uncontrolled arterial hypertension: systolic blood pressure > 150 mm
Hg and/ or diastolic blood pressure > 100 mm Hg at Screening.
- Previous or unstable concurrent diseases or conditions that prevent individual's
enrolment into the study.
- Individuals with mental disorders or social circumstances that preclude them from
following protocol requirements.
- Current or previous decompensated liver disease, including coagulopathy, hepatic
encephalopathy and esophageal varices hemorrhage.
- One or more additional known primary or secondary causes of liver disease, other than
hepatitis B (e.g., alcoholism, autoimmune hepatitis, malignancy with hepatic
involvement, hemochromatosis, alpha-1 antitrypsin deficiency, Wilson's Disease, other
congenital or metabolic conditions affecting the liver, congestive heart failure or
other severe cardiopulmonary disease, etc.). Gilbert's syndrome, a benign disorder
associated with low-grade hyperbilirubinemia, will not exclude individauls from
participation in this trial. Autoimmune hepatitis stigmata attributed to HDV infection
in the opinion of the investigator are allowed.
- White blood cells (WBC) count < 3000 cells/mm^3 (<1500 if African individuals).
- Absolute neutrophil count < 1500 cells/mm^3 (<1000 if African individuals).
- Platelet count < 90,000 cells/mm^3.
- Haemoglobin < 12 g/dL.
- Use of prohibited psychotropic agents at Screening.
- Use of interferons within 6 months before Screening.
- History of solid organ transplantation.
- Current alcohol abuse or alcohol abuse within 6 months prior to enrolment in this
study; current drug addict or history of drug use within 2 years prior to Screening.
- History of disease requiring regular use of systemic glucocorticosteroids (inhalative
glucocorticosteroids are allowed) or other immunosuppressants.
- Pregnant or breast-feeding females.
- Participation in another clinical study with investigational drugs within 30 days
prior to randomization.
- Receipt of bulevirtide previously, e.g. in clinical trials.
- Inability to follow protocol requirements and undergo all protocol procedures. Note:
Individuals with medical contraindication for liver biopsy are allowed to participate
in this study. Such individuals will exempt from liver biopsy requirements in this
study. Individuals receiving prohibited treatment at screening cannot be included into
the study unless this treatment is withdrawn prior to randomization.
- Contraindications, intolerance or hypersensitivity to interferons alfa, genetically
engineered E.coli medications, polyethylene glycol or other components of
peginterferon alfa-2?.
- Presence or history of severe retinopathy, significant diabetic or hypertensive
retinopathy.
- Uncontrolled diabetes mellitus.
- Uncontrolled cardiovascular disorders within 6 months before screening.
- History of autoimmune disorder (e.g. myositis, hepatitis, thrombotic thrombocytopenic
purpura, idiopathic thrombocytopenic purpura, severe psoriasis, rheumatoid arthritis,
interstitial nephritis, thyroiditis, and systemic lupus erythematosus)
- Presence or history of significant psychiatric disorder (e.g. severe depression,
suicide attempt, severe neurosis or cognitive disorder).
- Presence or history of chronic lung disease with respiratory malfunction.
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