A Study of Switching From Entecavir to Tenofovir Disoproxil Fumarate in Subjects With Chronic Hepatitis B

GlaxoSmithKline (GSK)

Status and phase: Completed; Phase 4

Conditions: Hepatitis B, Chronic

Treatments: Drug: Tenofovir Disoproxil Fumarate

Study type: Interventional

Funder types: Industry

Identifiers

NCT03258710

205883

Details and patient eligibility

About

Tenofovir Disoproxil Fumarate is a nucleos(t)ide analogue that inhibits Hepatitis B Virus (HBV) growth, and is marketed in Japan with an indication for inhibition of HBV growth in subjects with chronic hepatitis B associated with HBV growth and abnormal liver function. This study has been planned to evaluate the virological effects and safety of switching from ETV to TDF in chronic hepatitis B (hepatitis B e-antigen [HBeAg])-positive and HBV- deoxyribonucleic acid (DNA) undetectable subjects. This study is designed as a multi-center, one-arm, post-marketing clinical study to investigate the HBsAg reduction in subjects who have not achieved the long-term goal, the loss of hepatitis B surface antigen (HBsAg). The study will be conducted in HBeAg-positive and HBV-DNA undetectable subjects treated with ETV. After switching ETV to TDF, TDF will be administered for 96 weeks. Approximately 80 subjects will be screened to achieve 65 evaluable subjects.

Enrollment: 75 patients

Sex: All

Ages: 20 to 69 years old

Volunteers: No Healthy Volunteers

Inclusion criteria

• Subjects must be 20 to 69 years of age inclusive, at the time of signing the informed consent

• Male and female subjects. A female subject is eligible to participate if she is not pregnant and not breastfeeding, and at least one of the following conditions applies:

  • Not a woman of childbearing potential (WOCBP), OR
  • A WOCBP who agrees to follow the contraceptive guidance during the treatment period and for at least 4 days after the last dose of study treatment

• Capable of giving signed informed consent form (ICF)

• Subjects with chronic hepatitis B (CHB) (excluding hospitalized subjects)

• Subjects treated with ETV for at least 2 years prior to initiation of study treatment.

• The serum HBV-DNA level at screening is below the limit of quantitation (< 2.1 Log10 copies/milliliter [mL] or < 20 international unit [IU]/mL).

• Subjects with serum HBeAg positive at screening

• Meet either of the following serum HBsAg levels at screening:

  • Serum HBsAg 80 < to < 800 IU/mL and fluctuation range is equal or more than -0.1 Log10 IU/mL per year
  • Serum HBsAg >=800 IU/mL

• Meet all of the following criteria at screening:

  • Creatinine clearance (CLcr) >=70 mL/minute. CLcr is calculated using the following Cockcroft-Gault formula.

Male: CLcr = (body weight in kilogram [kg] multiplied by [140 minus age in years]) divided by (72 multiplied by serum creatinine [milligram {mg}/deciliter {dL}]) Female: CLcr = CLcr (male) multiplied by 0.85

• Hemoglobin >= 8 gram/dL
• WBC >=1000 per cubic millimeter (mm^3)

Exclusion criteria

• QTc > 450 millisecond (msec) or > 480 msec for subjects with bundle branch block

• Received any interferon or Hepatitis B vaccine therapy within 24 weeks prior to initiation of the study treatment.

• Received overdose of nonsteroidal anti-inflammatory drugs (NSAIDs) (excluding temporary or topical use) within 7 days prior to initiation of the study treatment.

• Received any of the following drugs within 8 weeks prior to initiation of the study treatment (excluding topical products such as ointment and/or cream etc).

  • Drugs causing renal impairment (examples: aminoglycosides, amphotericin B, vancomycin, foscarnet, cisplatin, pentamidine, tacrolimus, cyclosporine, some contrast mediums [ionic high-osmolar contrast media, ionic low-osmolar contrast media]
  • Competitors of renal excretion (except temporary use, example: probenecid)
  • Immunosuppressants (examples: azathioprine, cycolphosphamide) or chemotherapeutics (example: etoposide)
  • Glucocorticoid preparation

• Received TDF, Adefovir pivoxil (ADV) or Tenofovir Alafenamide Fumarate (TAF) within 2 years prior to initiation of the study treatment

• Participation in another clinical study within 6 months prior to screening, or planned participation in another clinical study simultaneously with this study.

• Co-infection with human immunodeficiency virus (HIV) or hepatitis C virus (HCV)

• Subjects with serious complication other than compensated CHB (cancer, significant renal, cardiovascular, pulmonary, or neurological disease, uncontrollable diabetes, etc.)

• Received or have a plan for solid organ or bone marrow transplantation

• Has proximal tubulopathy.

• Subjects with decompensated CHB who meet the following: direct bilirubin > 1.5 times upper limit of normal (ULN), Prothrombin Time (PT) < 60%, platelets < 75,000/mm3 and serum albumin < 3.0 g/dL

• Autoimmune hepatitis (Antinuclear titer > 1:160), excluding CHB

• Subjects with or suspected of having hepatocellular carcinoma (HCC) (including both primary and metastatic) from diagnostic imaging at screening, or with serum alpha-fetoprotein (AFP) > 50 nanogram (ng)/mL at screening

• History of HCC (except subjects who underwent resection or received curative treatment by radiofrequency, and with AFP <=10 ng/mL at screening)

• Woman who is pregnant, possibly pregnant, lactating or planning a pregnancy during the study period.

• Psychiatry disorder or cognitive disorder that may affect the subject's ability to give informed consent or to follow specified study procedures.

• Subjects with a history of alcohol or drug abuse

• Subjects whom the investigator (or sub-investigator) considers ineligible for the study.

• Subjects with hypersensitivity to study treatments or their components, nucleoside and/or nucleotide analogues. Subjects with drug allergy that, in the investigator's (sub-investigator's) [or medical monitor's] opinion, labeled contraindication for participation in the study, or other allergy.

Trial design

Primary purpose: Treatment

Allocation: N/A

Interventional model: Single Group Assignment

Masking: None (Open label)

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75 participants in 1 patient group

All subjects treated with Tenofovir Disoproxil Fumarate

Experimental group

Description:

Subjects with on-going ETV treatment will be switched to Tenofovir Disoproxil Fumarate treatment. Subjects will start TDF on the day ETV is discontinued, without having overlapping treatment periods. All subjects will receive one tablet of TDF 300 mg once daily orally for 96 weeks.

Treatment:

Drug: Tenofovir Disoproxil Fumarate