B-Fine: A Mechanistic Study of GSK3228836 With Fine Needle Aspiration (FNA) in Participants With Chronic Hepatitis B
Study Details
Study Description
Brief Summary
Hepatitis B virus (HBV) infection, especially chronic, is a significant worldwide medical problem. This is an exploratory study of the therapeutic mechanism of GSK3228836 in participants with chronic hepatitis B (CHB) on stable nucleos(t)ide therapy (which is the first line therapy for CHB). This study is a Phase IIa, multi-center open label exploratory study of the therapeutic mechanism of GSK3228836 in participants with hepatitis B virus e-antigen (HBeAg)-negative CHB on stable nucleos(t)ide therapy using repeat fine needle aspirations of the liver for intrahepatic immunophenotyping. It will investigate the virologic and immunologic correlates of hepatitis B virus surface antigen (HBsAg) loss observed in participants when treated for 12 weeks with 300 milligrams (mg) GSK3228836. Repeat fine needle aspirates of the liver will be performed to enable analysis of liver-resident immune cells to investigate any immunomodulatory properties of GSK3228836 and to study the biology of underlying treatment-associated liver flares. The study will consist of a screening, treatment, and post-treatment follow-up phase. Approximately 20 participants will be enrolled in the study.
| Condition or Disease | Intervention/Treatment | Phase |
|---|---|---|
|
Phase 2 |
Study Design
Arms and Interventions
| Arm | Intervention/Treatment |
|---|---|
| Experimental: Participants receiving 300 mg GSK3228836 Eligible participants on stable nucleos(t)ide therapy will receive GSK3228836 300 mg subcutaneously (SC) weekly once for 12 weeks along with a loading dose of GSK3228836 300 mg in Week 1 (Day 4) and Week 2 (Day 11). |
Drug: GSK3228836
GSK3228836 will be available as a clear colorless to slightly yellow solution for injection in 150 mg/milliliters (mL) vial to be administered SC once weekly.
Drug: Nucleos(t)ide therapy
Participants receiving nucleos(t)ide therapy upon entry in the study will continue to receive nucleos(t)ide therapy for the duration of the study.
|
Outcome Measures
Primary Outcome Measures
- Percentage of participants achieving serum HBsAg level less than (<) lower limit of quantitation (LLOQ) [From treatment start (Day 1) up to Week 12]
Participants achieving serum HBsAg level <LLOQ will be assessed.
Secondary Outcome Measures
- Percentage of participants with Sustained HBsAg Response (HBsAg <LLOQ) [From Week 12 to Week 36]
Sustained HBsAg response is defined as HBsAg <LLOQ for 24 weeks from end of GSK3228836 treatment.
- Percentage of participants achieving Sustained Virologic Response (HBsAg <LLOQ and HBV DNA<LLOQ) [From Week 12 to Week 36]
Sustained virologic response is defined as HBsAg <LLOQ and HBV DNA <LLOQ for 24 weeks from end of GSK3228836 treatment.
- Percentage of participants achieving HBsAg <LLOQ at indicated time points [Week -1, Week 1, Week 2, Week 3, Week 4, Week 5, Week 6, Week 7, Week 8, Week 9, Week 10, Week 11, Week 12, Week 13, Week 14, Week 16, Week 20, Week 24, Week 28, Week 32 and Week 36]
Participants achieving HBsAg <LLOQ at indicated time points will be assessed.
- Percentage of participants achieving HBV DNA <LLOQ at indicated time points [Week -1, Week 1, Week 2, Week 3, Week 4, Week 5, Week 6, Week 7, Week 8, Week 9, Week 10, Week 11, Week 12, Week 13, Week 14, Week 16, Week 20, Week 24, Week 28, Week 32 and Week 36]
Participants achieving HBV DNA <LLOQ at indicated time points will be assessed.
- Percent of participants achieving HBsAg <LLOQ and HBV DNA <LLOQ at indicated time points [Week -1, Week 1, Week 2, Week 3, Week 4, Week 5, Week 6, Week 7, Week 8, Week 9, Week 10, Week 11, Week 12, Week 13, Week 14, Week 16, Week 20, Week 24, Week 28, Week 32 and Week 36]
Participants achieving HBsAg <LLOQ and HBV DNA <LLOQ at indicated time points will be assessed.
- Categorical change from Baseline in HBsAg at indicated time points [Baseline (Week -1) and Week 1, Week 2, Week 3, Week 4, Week 5, Week 6, Week 7, Week 8, Week 9, Week 10, Week 11, Week 12, Week 13, Week 14, Week 16, Week 20, Week 24, Week 28, Week 32 and Week 36]
Blood samples will be collected from participants at indicated time points to assess HBsAg levels (for example [e.g.]<0.5, greater than or equal to [>=]0.5, >=1, >=1.5, >=3 log10 International units [IU]/mL).
- Percentage of participants with alanine aminotransferase (ALT) greater than (>)3 times upper limit of normal (ULN) at indicated time points [Week -1, Week 1, Week 2, Week 3, Week 4, Week 5, Week 6, Week 7, Week 8, Week 9, Week 10, Week 11, Week 12, Week 13, Week 14, Week 16, Week 20, Week 24, Week 28, Week 32 and Week 36]
Blood samples will be collected from participants at indicated time points to assess ALT levels.
- Actual values of HBsAg at indicated time points [Week -1, Week 1, Week 2, Week 3, Week 4, Week 5, Week 6, Week 7, Week 8, Week 9, Week 10, Week 11, Week 12, Week 13, Week 14, Week 16, Week 20, Week 24, Week 28, Week 32 and Week 36]
Blood samples will be collected from participants at indicated time points to assess HBsAg levels.
- Change from Baseline in HBsAg at indicated time points [Baseline (Week -1) and Week 1, Week 2, Week 3, Week 4, Week 5, Week 6, Week 7, Week 8, Week 9, Week 10, Week 11, Week 12, Week 13, Week 14, Week 16, Week 20, Week 24, Week 28, Week 32 and Week 36]
Blood samples will be collected from participants at indicated time points to assess HBsAg levels.
- Actual values of HBV DNA at indicated time points [Week -1, Week 1, Week 2, Week 3, Week 4, Week 5, Week 6, Week 7, Week 8, Week 9, Week 10, Week 11, Week 12, Week 13, Week 14, Week 16, Week 20, Week 24, Week 28, Week 32 and Week 36]
Blood samples will be collected from participants at indicated time points to assess HBV DNA levels.
- Change from Baseline in HBV DNA at indicated time points [Baseline (Week -1) and Week 1, Week 2, Week 3, Week 4, Week 5, Week 6, Week 7, Week 8, Week 9, Week 10, Week 11, Week 12, Week 13, Week 14, Week 16, Week 20, Week 24, Week 28, Week 32 and Week 36]
Blood samples will be collected from participants at indicated time points to assess HBV DNA levels.
- Actual values of HB surface antibody (anti-HBsAg) levels at indicated time points [Week -1, Week 5, Week 9, Week 13, Week 14, Week 16, Week 20, Week 24, Week 28, Week 32 and Week 36]
Blood samples will be collected from participants at indicated time points to assess anti-HBsAg levels.
- Actual values of HBe antibody (anti-HBeAg) levels at indicated time points [Week -1, Week 5, Week 9, Week 13, Week 14, Week 16, Week 20, Week 24, Week 28, Week 32 and Week 36]
Blood samples will be collected from participants at indicated timepoints to assess anti-HBeAg levels.
- Area under the concentration-time curve (AUC) of ALT at indicated time points [From Day 1 to Week 36]
Blood samples will be collected from participants to assess ALT levels.
Eligibility Criteria
Criteria
Inclusion Criteria:
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Participants should be at least 18 years of age at the time of signing the informed consent.
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Participants who have documented chronic HBV infection >=6 months prior to screening and currently receiving stable nucleos(t)ide analogue therapy, defined as no changes to their nucleos(t)ide regimen from at least 6 months prior to screening and with no planned changes to the stable regimen over the duration of the study.
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Plasma or serum HBsAg concentration >100 IU/mL
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Plasma or serum HBV DNA concentration must be adequately suppressed, defined as plasma or serum HBV DNA <90 IU/mL.
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HBeAg-negative
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ALT less than or equal to (<=)2 times ULN
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No gender restriction.
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A male participant is eligible to participate if they agree to the following during the intervention period and for at least 90 days after the last dose of study treatment i. Refrain from donating sperm ii. and be abstinent from heterosexual intercourse as their preferred and usual lifestyle (abstinent on a long term and persistent basis) and agree to remain abstinent or Must agree to use contraception/barrier as detailed below
- Agree to use a male condom (and should also be advised of the benefit for a female partner to use a highly effective method of contraception as a condom may break or leak) when having sexual intercourse with a woman of childbearing potential (WOCBP) who is not currently pregnant.
- A female participant is eligible to participate:
- If she is not pregnant or breastfeeding. ii. and at least one of the following conditions applies:
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Is not a WOCBP
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or is a WOCBP and using a contraceptive method that is highly effective (with a failure rate of <1 percent [%] per year), preferably with low user dependency during the intervention period and for at least 90 days after the last dose of study treatment iii. A WOCBP must have both
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A confirmed menstrual period prior to the first dose of study intervention (additional evaluation [e.g. amenorrhea in athletes, birth control] should also be considered)
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and a negative highly sensitive pregnancy test (urine or serum) within 24 hours before the first dose of study treatment
- Capable of giving signed informed consent which includes compliance with the requirements and restrictions listed in the informed consent form (ICF) and in this protocol.
Exclusion Criteria:
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Clinically significant abnormalities, aside from chronic HBV infection in medical history (e.g., moderate-severe liver disease other than chronic HBV, acute coronary syndrome within 6 months of screening, major surgery within 3 months of screening, significant/unstable cardiac disease, uncontrolled diabetes, bleeding diathesis or coagulopathy) or physical examination.
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Co-infection with:
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Current or past history of Hepatitis C virus (HCV)
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Human immunodeficiency virus (HIV)
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Hepatitis D virus (HDV).
- History of or suspected liver cirrhosis and/or evidence of cirrhosis as determined by
- Both Aspartate aminotransferase (AST)-Platelet Index (APRI) >2 and FibroSure/FibroTest result >0.7
- If only one parameter (APRI or FibroSure/FibroTest) result is positive, a discussion with the Medical Monitor is required before inclusion in study is permitted.
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Regardless of APRI or Fibrosure/FibroTest score participants will be excluded from the study if their past history includes one of the following criteria:
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Liver biopsy showing Metavir 4 or equivalent
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Liver stiffness >12 kilopascals (kPa)
- Diagnosed or suspected hepatocellular carcinoma as evidenced by the following
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Alpha-fetoprotein concentration >=200 nanograms (ng)/mL
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If the screening alpha fetoprotein concentration is >=50 ng/mL and <200 ng/mL, the absence of liver mass must be documented by imaging within 6 months before enrolment.
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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.
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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).
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History of extrahepatic disorders possibly related to HBV immune conditions (e.g., nephrotic syndrome, any type of glomerulonephritis, polyarteritis nodosa, cryoglobulinemia, uncontrolled hypertension).
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Anti-neutrophil cytoplasmic antibody (ANCA) at screening by itself won't be an exclusion criterion - but if results are borderline positive or positive:
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Myeloperoxidase (MPO)-ANCA (perinuclear [p] ANCA) and Proteinase 3 (PR3)-ANCA (Cytoplasmic [c] ANCA) analysis will be conducted
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A discussion with the Medical Monitor will be required to review participant's complete medical history to ensure no past history or current manifestations of a vasculitic/inflammatory/auto-immune condition before inclusion in study is permitted.
- Low compliment (C)3 at screening or Baseline by itself won't be an exclusion criterion-but if it is present
- A discussion with the Medical Monitor is required to review participant's complete medical history to ensure no past history or current manifestations of vasculitic/inflammatory/auto-immune conditions.
- History of alcohol or drug abuse/dependence
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Current alcohol use as judged by investigator to potentially interfere with participant compliance.
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History of or current drug abuse/dependence as judged by the investigator to potentially interfere with participant compliance.
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Refers to illicit drugs and substances with abuse potential. Medications that are used by the participant as directed, whether over-the-counter or through prescription, are acceptable and would not meet the exclusion criteria.
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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.
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Participants for whom immunosuppressive treatment is not advised, including therapeutic doses of steroids, will be excluded.
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Currently taking, or took within 12 months of screening, any interferon-containing therapy.
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Participants requiring anti-coagulation therapies (for example warfarin, Factor Xa inhibitors or anti-platelet agents like clopidogrel).
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The participant has participated in a clinical trial and has received an investigational product within the following time period prior to the first dosing day in the current study: 5 half-lives (if known) or twice the duration (if known) of the biological effect of the study treatment (whichever is longer) or 90 days (if half-life or duration is unknown).
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Prior treatment with any oligonucleotide or small interfering RNA (siRNA) within 12 months prior to the first dosing day.
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Fridericia's QT correction formula (QTcF) >=450 milliseconds (msec) (if single electrocardiogram [ECG] at screening shows QTcF >=450 msec, a mean of triplicate measurements should be used to confirm that participant meets exclusion criterion).
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Laboratory results as follows
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Serum albumin <3.5 grams per deciliter (g/dL)
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Glomerular filtration rate (GFR) <60 mL/minute/1.73 per meter square as calculated by the Chronic kidney disease- Epidemiologic Collaboration (CKD-EPI) formula.
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International normalized Ratio (INR) >1.25
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Platelet count <140 times 10^9/liter (L)
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Total bilirubin >1.25 times ULN
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For participants with benign unconjugated hyperbilirubinemia with total bilirubin >1.25 times ULN, discussion for inclusion to the study is required with the Medical Monitor
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Urine albumin to creatinine ratio (ACR) >=0.03 mg/mg (or >=30 mg/g). In the event of an ACR above this threshold, eligibility may be confirmed by a second measurement 1) In cases where participants have low urine albumin and low urine creatinine levels resulting in a urine ACR calculation >=0.03 mg/mg (or >=30 mg/g), the investigator should confirm that the participant does not have a history of diabetes, hypertension or other risk factors that may affect renal function and discuss with the Medical Monitor, or designee.
- History of/sensitivity to GSK3228836 or components thereof or a history of drug or other allergy that, in the opinion of the investigator or Medical Monitor, contraindicates their participation.
Contacts and Locations
Locations
| Site | City | State | Country | Postal Code | |
|---|---|---|---|---|---|
| 1 | GSK Investigational Site | Boston | Massachusetts | United States | 02114 |
| 2 | GSK Investigational Site | Toronto | Ontario | Canada | M5G 2C4 |
| 3 | GSK Investigational Site | Rotterdam | Netherlands | 3015 GD | |
| 4 | GSK Investigational Site | London | United Kingdom | E1 1BB |
Sponsors and Collaborators
- GlaxoSmithKline
Investigators
- Study Director: GSK Clinical Trials, GlaxoSmithKline
Study Documents (Full-Text)
None provided.More Information
Publications
None provided.- 212602