Study of GSK3965193 in Healthy Participants and Alone and in Combination With Bepirovirsen in Participants Living With Chronic Hepatitis B Infection

• Status: Not yet recruiting
• Trial end date: 2025-12-29
• Target enrollment: 0
• Participant gender: All

Summary

This Phase 1/2a multiple part study is a first-time-in-human (FTIH) study designed to evaluate the safety, tolerability, and pharmacokinetics (PK) of single (Part 1) and repeat doses (Part 2) of GSK3965193 in healthy participants. Part 3 will evaluate the ability of GSK3965193 to lower hepatitis B virus surface antigen (HBsAg) in participants living with chronic hepatitis B infection (PLWCHB). Part 4 will evaluate the safety and tolerability of combination therapy with GSK3965193 and bepirovirsen and the potential to effect sustained virologic response in PLWCHB.

• Phase: Phase 2
• Accepts Healthy Volunteers?: Accepts Healthy Volunteers

Details

• Lead Sponsor: GlaxoSmithKline

Criteria

Inclusion Criteria:

• Parts 1 and 2: Participants between 18 and 55 years of age inclusive, at the time of signing the informed consent.

• Parts 3 and 4: Participants between 18 and 65 years of age inclusive, at the time of signing the informed consent.

• Body weight >=50 kilograms (kg) and body mass index within the range 18-32 kilograms per square meter (kg/m^2) (inclusive).

• Male or female participant: a. Parts 1 and 2: woman of non-childbearing potential only. b. Parts 3 and 4: woman of non-childbearing potential or woman of child-bearing potential who is not pregnant or breastfeeding and is using a contraceptive method that is highly effective.

• Capable of giving signed informed consent.

• Additional Inclusion Criteria for PLWCHB (Parts 3 and 4).

• Participants who have documented chronic hepatitis B virus (HBV) infection >=6 months prior to screening.

• Participants currently receiving stable NA therapy (e.g., tenofovir disoproxil, tenofovir alafenamide, entecavir).

• Plasma or serum HBsAg concentration >100 IU/mL.

• Plasma or serum HBV deoxyribonucleic acid (DNA) concentration <90 IU/mL.

• Hepatitis B virus e-antigen (HBeAg) positive or negative.

• Alanine aminotransferase (ALT) <=2 times the upper limit of normal (ULN)

Exclusion Criteria:

• Exclusion Criteria for Healthy Participants:

• Positive Hepatitis A virus antibody (HAV Ab immunoglobulin M [IgM]), or positive for HBV, hepatitis C virus (HCV) or human immunodeficiency virus (HIV) at screening.

• ALT >1 times ULN.

• Bilirubin >1.5 times ULN (isolated bilirubin >1.5 times ULN is acceptable if bilirubin is fractionated and direct bilirubin <35 percent [%]).

• Corrected QT interval (QTc) >450 milliseconds (msec).

• Signs and symptoms suggestive of Coronavirus Disease 2019 (COVID-19).

• Participants with known COVID-19 positive contacts in the past 14 days.

• For participants in Part 2A: i. Personal history or family history of peripheral neuropathy. ii. A score >=4 on the Toronto clinical scoring system for polyneuropathy.

• Current or previous use of tobacco- or nicotine-containing products (for example (e.g.) cigarettes, nicotine patches or electronic devices) within 6 months before screening and/or have a smoking pack history of >5 pack years.

• Exclusion Criteria for PLWCHB:

• Clinically significant abnormalities in medical history, aside from chronic HBV infection.

• Co-infection with or past history of HCV, HIV or Hepatitis D virus (HDV).

• History of or suspected liver cirrhosis and/or evidence of cirrhosis.

• Diagnosed or suspected hepatocellular carcinoma.

• History of malignancy within the past 5 years with the exception of specific cancers that are cured by surgical resection (e.g., skin cancer).

• 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] or history/presence of other diseases that may be associated with vasculitis condition (e.g., systemic lupus erythematosus, rheumatoid arthritis, relapsing polychondritis, mononeuritis multiplex).

• History of extrahepatic disorders possibly related to HBV immune conditions (e.g., nephrotic syndrome, any type of glomerulonephritis, polyarteritis nodosa, cryoglobulinaemia, uncontrolled hypertension).

• History of alcohol or drug abuse/dependence: a. Current alcohol use as judged by investigator to potentially interfere with participant compliance. b. History of or current drug abuse/dependence as judged by the investigator to potentially interfere with participant compliance.

• History or other evidence of bleeding from esophageal varices.

• Documented history or other evidence of metabolic liver disease within 1 year of randomization.

• Personal history or family history of peripheral neuropathy.

• A score >4 on the Toronto clinical scoring system for polyneuropathy.

• History of having received or currently receiving any systemic anti-neoplastic (including radiation) or immune-modulatory treatment (including systemic oral corticosteroids, interferon or pegylated interferon) within the 8 weeks prior to the first dose of study drug or the expectation that such treatment will be needed at any time during the study.

• Abnormal and clinically significant 12-lead ECG finding.

• Currently taking, or taken 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.

• Participants requiring anti-coagulation therapies.

• Prior treatment with any oligonucleotide or small interfering RNA (siRNA) within 12 months prior to the first dosing day.

• Positive test for COVID-19 infection.

• Participants with known COVID-19 positive contacts in the past 14 days.