Treatment Outcomes in Chronic Hepatitis B Patients on Sequential Therapy With Tenofovir Alafenamide (TAF)

Completed · Phase 4

Conditions studied: Hepatitis B, Chronic

In brief

Primary Objective: To describe rate of persistence and/or improvement of viral suppression with TAF as with previous anti-HBV (hepatitis B virus) treatment

Key facts

Study ID

NCT03471624

Run by

Stanford University

People needed

270

Starts

2018-05-01

Expected to finish

2022-04-19

Last updated by the study team

2023-11-18

Who can join

Age: 18 and older. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• Male or female, age ≥18 years
• Chronic hepatitis B diagnosis confirmed by positive HBsAg or HBV DNA or HBeAg or documented history of chronic hepatitis B in physician note
• Currently maintained on antiviral therapy for at least 48 weeks with any Hepatitis B virus(HBV) DNA value at Screening/Baseline and planned to be switched to TAF by their physician
• Routinely monitored for serum HBV DNA Polymerase chain reaction(PCR), liver chemistry including Aspartate aminotransferase (AST )/alanine transaminase(ALT)/total bilirubin, renal chemistry including Blood urea nitrogen(BUN)/Creatinine/Carbon dioxide (CO2) by their physicians every 3-6 months and a bone density scan at least every 2 years as per routine clinical care (one at baseline and one 2 years after switch).
• Estimated creatinine clearance > 15 ml/min (using the Cockcroft-Gault method) at Screening/Baseline Visit. (Note: multiply estimated rate by 0.85 for women).
• Willing and able to provide informed consent
• Able to comply with dosing instructions for study drug administration and able to complete the study schedule of assessments

You may not qualify if…

• Pregnant women, women who are breastfeeding or who believe they may wish to become pregnant during the course of the study
• Previous recipient of a liver transplant
• Co-infection with human immunodeficiency virus (HIV) or hepatitis C (HCV) or hepatitis D (HDV)
• Severe or uncontrolled comorbidities
• Current or known hepatic decompensation (≤2 years) (e.g ascites, encephalopathy, or variceal hemorrhage) with a Child-Pugh score of B or C
• Malignancy including liver cancer within 5 years except cancers curable by surgical resection (e.g. basal cell skin cancer and squamous cell cancer)
• On any of the disallowed concomitant medications listed in the prior and concomitant medications list (pg. 11). Subjects on prohibited medications who are otherwise eligible will need a wash out period of at least 30 days prior to the Screening/Baseline visit.
• Males and females of reproductive potential who are unwilling to use "effective" protocol-specified method(s) of contraception during the study.
• Current substance or alcohol abuse judged by the investigator to potentially interfere with subject compliance.
• Any other clinical conditions that, in the opinion of the Investigator, would make the subject unsuitable or unable to comply with any of the study procedures

Where it is running

• Stanford University Medical Center — Palo Alto, California, United States
• San Jose Gastroenterology — San Jose, California, United States
• Kyushu University Hospital — Fukuoka, Japan
• Nagoya City University — Nagoya, Japan
• Osaka City University — Osaka, Japan
• Saga University Hospital — Saga, Japan
• Hanyang University Seoul Hospital — Seoul, South Korea
• Nowon Eulji Medical Center, Eulji University College of Medicine, — Seoul, South Korea
• Sanggye Paik Hospital, Inje University College of Medicine — Seoul, South Korea
• Kaohsiung Medical University Hospital — Kaohsiung City, Taiwan
• E-Da Hospital — Kaohsiung City, Taiwan
• China Medical University Hospital — Taichung, Taiwan

Full record on ClinicalTrials.gov

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