This study will evaluate the efficacy and safety of bepirovirsen compared to placebo in participants with human immunodeficiency virus (HIV)/hepatitis B virus (HBV) co-infection.
Eligibility
Sex
ALL
Min age
18 Years
Max age
—
Healthy volunteers
No
Inclusion Criteria:
1. Documented chronic hepatitis B virus (HBV) infection and documented human immunodeficiency virus (HIV)-1 infection greater than equal to (\>=) 12 months prior to Screening.
2. Must be on uninterrupted antiretroviral therapy (ART) containing at least tenofovir disoproxil (TDF) or tenofovir alafenamide (TAF) plus lamivudine (3TC) or emtricitabine (FTC) for greater than (\>)12 months, with no planned changes to the stable regimen over the duration of the study.
o Switch in ART is permitted \>=6 months prior to Screening for reasons not related to loss of HIV or HBV control (e.g., change in formulary, tolerability, side effects).
3. Documented evidence of at least 2 plasma HIV-1 ribonucleic acid (RNA) measurements less than (\<) 50 copies per milliliter (copies/mL) are required in the 12 months prior to Screening: 1 within 6 to 12 months prior to Screening and 1 within 6 months prior to Screening.
4. Plasma or serum HBV deoxyribonucleic acid (DNA) concentration must be adequately suppressed, defined as plasma or serum HBV DNA \<90 international units per milliliter (IU/mL).
5. Plasma or serum HBsAg concentration \>100 IU/mL and \<=3000 IU/mL.
6. Plasma HIV-1 RNA concentration must be undetectable, defined as plasma HIV 1 RNA \<50 copies/mL.
7. Cluster of differentiation 4 (CD4) count \>=350 cells per cubic millimeter (cells/mm\^3).
8. Alanine aminotransferase (ALT) \<=2 times upper limit of normal (ULN).
Exclusion Criteria:
1. History of or suspected liver cirrhosis and/or evidence of cirrhosis.
2. Diagnosed or suspected hepatocellular carcinoma (HCC).
3. History of extrahepatic disorders possibly related to HBV immune conditions (e.g., nephrotic syndrome, any type of glomerulonephritis, polyarteritis nodosa, cryoglobulinemia, uncontrolled hypertension).
4. Coinfection with:
1. Hepatitis C virus (HCV) with positive HCV antibody and detectable HCV RNA at Screening.
I. HCV treatment should have completed \>12 months prior to Screening.
2. Hepatitis D virus (HDV) defined as positive or equivocal HDV antibody regardless of HDV RNA level.
5. Clinically significant abnormalities, aside from HIV-1 infection and chronic HBV infection in medical history (e.g., moderate severe liver disease other than chronic HBV/HIV, acute coronary syndrome within 6 months of Screening, major surgery within 3 months of Screening, significant/unstable cardiac disease, uncontrolled diabetes, bleeding diathesis coagulopathy) or clinically significant physical examination findings.
6. Untreated syphilis infection (positive rapid plasma reagin \[RPR\] at Screening without clear documentation of treatment) are excluded unless they complete treatment during the Screening period and 7 days prior to randomization.
7. History of malignancy within the past 5 years with the exception of specific cancers that are cured by surgical resection (e.g., skin cancer). Participants under evaluation for possible malignancy are not eligible.
8. History of vasculitis or presence of symptoms and signs of potential vasculitis (e.g., vasculitic rash, skin ulceration, repeated blood detected in urine without identified cause), current or history of an autoimmune condition or history/presence of other diseases that may be associated with vasculitis condition (e.g., systemic lupus erythematosus, rheumatoid arthritis, relapsing polychondritis, mononeuritis multiplex).
9. Participants who in the investigator's judgment, have a significant risk of suicide or self-harm.
10. Alcohol or drug abuse/dependence
11. Currently taking, or took within 3 months of Screening, any immunosuppressing drugs (e.g., prednisone), other than a short course of therapy (\<=2 weeks) or topical/inhaled steroid use.
12. Participants to whom immunosuppressive treatment, including therapeutic doses of steroids, is contraindicated should not be considered for enrolment in the study.
13. Currently taking, or has taken within 12 months of Screening, any interferon containing therapy.
14. Participants requiring anti coagulation therapies (e.g., warfarin, Factor Xa inhibitors) or anti platelet agents (including but not limited to clopidogrel or aspirin) unless treatment can safely be discontinued throughout duration of study intervention, by the discretion of the investigator. Occasional use is permitted.
15. Treatment with an HIV-1 immunotherapeutic vaccine within 90 days of Screening.
16. Prior treatment with any oligonucleotide or small interfering ribonucleic acid (siRNA) within 12 months prior to the first dosing day.
17. Prior treatment with bepirovirsen.
Primary outcome measure(s)
Percentage of participants achieving hepatitis B virus (HBV) virologic response at 36 weeks after scheduled end of study treatment in absence of rescue medication — At study week 60 HBV virologic response defined as HBV surface antigen (HBsAg) not detected and HBV deoxyribonucleic acid (DNA) less than (\<) lower limit of quantification (LLOQ).
Trial sites (51)
Facility
City
Region
Status
GSK Investigational Site
Bakersfield
California
GSK Investigational Site
San Francisco
California
GSK Investigational Site
Orlando
Florida
GSK Investigational Site
West Palm Beach
Florida
GSK Investigational Site
Baltimore
Maryland
GSK Investigational Site
Minneapolis
Minnesota
GSK Investigational Site
Hillsborough
New Jersey
GSK Investigational Site
Almagro
Argentina
GSK Investigational Site
Buenos Aires
Argentina
GSK Investigational Site
Buenos Aires
Argentina
GSK Investigational Site
Buenos Aires
Argentina
GSK Investigational Site
La Plata
Argentina
GSK Investigational Site
Rosario
Argentina
GSK Investigational Site
Aracaju
Brazil
GSK Investigational Site
Campinas
Brazil
GSK Investigational Site
Curitiba
Brazil
GSK Investigational Site
Manaus
Brazil
GSK Investigational Site
Salvador
Brazil
GSK Investigational Site
São Paulo
Brazil
GSK Investigational Site
Ottawa
Ontario
GSK Investigational Site
Toronto
Ontario
GSK Investigational Site
Montreal
Quebec
GSK Investigational Site
Montreal
Quebec
GSK Investigational Site
Québec
Quebec
GSK Investigational Site
Marseille
France
GSK Investigational Site
Melun
France
GSK Investigational Site
Montpellier
France
GSK Investigational Site
Nantes
France
GSK Investigational Site
Paris
France
GSK Investigational Site
Paris
France
GSK Investigational Site
Genova
Italy
GSK Investigational Site
Milan
Italy
GSK Investigational Site
Milan
Italy
GSK Investigational Site
Naples
Italy
GSK Investigational Site
Roma
Italy
GSK Investigational Site
Sassari
Italy
GSK Investigational Site
Durban
KwaZulu-Natal
GSK Investigational Site
Ekurhuleni
South Africa
GSK Investigational Site
Johannesburg
South Africa
GSK Investigational Site
Barcelona
Spain
+ 11 more sites — see the full list on the official registry below.
This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.
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