Treatment Efficacy and Safety of Tenofovir Disoproxil Fumarate (TDF) in naïve Chronic Hepatitis B

Chronic Hepatitis B Clinical Trial

Official title:

Treatment Efficacy and Safety of Tenofovir Disoproxil Fumarate (TDF) in naïve Chronic Hepatitis B : a Real Life Multicenter Cohort Study in Korea

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT02533544
• Other study ID #: IN-US-174-1805
• Status: Completed
• Start date: October 2015
• Est. completion date: October 2018

Study information

• Verified date: January 2019
• Source: The Catholic University of Korea
• Contact: n/a
• Is FDA regulated: No
• Study type: Observational

Clinical Trial Summary

This is an open-label, single arm cohort study to see efficacy and safety of tenofovir disoproxil fumarate (TDF) in naïve chronic hepatitis B, retrospectively and prospectively both.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 572
• Est. completion date: October 2018
• Est. primary completion date: October 2018
• Accepts healthy volunteers: No
• Gender: All
• Age group: 19 Years and older

Eligibility

Inclusion Criteria:

1. Must have the ability to understand and sign a written informed consent form, which must be obtained prior to initiation of study procedures.

2. Adult male and non-pregnant, non-lactating female subjects, 19 years of age and older, based on the date of the screening visit. A negative serum pregnancy test at Screening is required for female subjects of childbearing potential (unless surgically sterile or greater than 2 years post-menopausal).

3. Documented evidence of chronic HBV infection (e.g. HBsAg positive for more than 6 months)

4. Chronic hepatitis B with the following:

• HBeAg-positive and HBeAb negative at Screening

• Screening HBV DNA = 1x 105 copies/mL

• Screening serum ALT level = ×ULN(80 IU/L) and = 10 ×ULN (by center laboratory range) OR

• HBeAg-negative and HBeAb positive at Screening

• Screening HBV DNA = 1x 104 copies/mL

• Screening serum ALT level = ×ULN(80 IU/L) and = 10 ×ULN (by center laboratory range) OR

• Cirrhosis at Screening

• Screening HBV DNA = 1x 104 copies/mL in HBeAg negative or

• Screening HBV DNA = 1x 105 copies/mL in HBeAg positive

• Screening serum ALT level = ×ULN and = 10 ×ULN (by center laboratory range)

5. A patient who treating with TDF as a treatment-naïve for Hepatitis B. Treatment naïve subjects defined as no history of antiviral therapy or < 12 weeks of oral antiviral treatment with any nucleoside or nucleotide analogue, including lamivudine or adefovir, clevudine, telbivudine, entecavir

6. Decompensated liver cirrhosis defined based on a Child-Turcotte-Pugh (CTP) score = 7 (Child B and C) or presence with at least one episode of ascites, jaundice, hepatic encephalopathy or variceal bleeding

7. Any previous treatment with interferon (pegylated or non-pegylated) must have ended at least 6 months prior to the baseline visit

8. Must be willing and able to comply with all study requirements.

Exclusion Criteria:

Subjects who meet any of the following exclusion criteria are not to be enrolled in the study.

1. Pregnant women, women who are breastfeeding or who believe they may wish to become pregnant during the course of the study.

2. Co-infection with HCV, HIV

3. Evidence of hepatocellular carcinoma (e.g. a-fetoprotein> 50 ng/mL or as evidenced by recent ultrasound or other standard of care measure)

4. Malignancy within 5 years prior to screening, with the exception of specific cancers that are cured by surgical resection (basal cell skin cancer, etc). Subjects under evaluation for possible malignancy are not eligible

5. Current alcohol or substance abuse judged by the investigator to potentially interfere with subject compliance

6. Currently receiving therapy with cytotoxic agent, nephrotoxic agents, or agents capable of modifying renal excretion

7. Any other clinical condition or prior therapy that, in the opinion of the Investigator, would make the subject unsuitable for the study or unable to comply with dosing requirements.

Related Conditions & MeSH terms

• Chronic Hepatitis B
• Hepatitis
• Hepatitis A
• Hepatitis B
• Hepatitis B, Chronic
• Hepatitis, Chronic

Intervention

Drug:
• tenofovir disoproxil fumarate

Locations

Country	Name	City	State
Korea, Republic of	The Catholic University of Korea, Daejeon St.Mary's Hosptial	Junggu	Daejeon

Sponsors (6)

Lead Sponsor	Collaborator
Myeong Jun Song	Chungnam National University Hospital, Gilead Sciences, Konyang University Hospital, Soonchunhyang University Hospital, Wonkwang University

Country where clinical trial is conducted

Korea, Republic of, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	The proportion of subjects with plasma HBV DNA levels below 116 copies/mL at Week 48	proportion of subjects with plasma HBV DNA levels below 116 copies/mL at Week 48	week 48
Primary	The proportion of subjects with plasma HBV DNA levels below 116 copies/mL at Week 96	proportion of subjects with plasma HBV DNA levels below 116 copies/mL at Week 96	Week 96
Secondary	The proportion of subjects with plasma HBV DNA levels below 116 copies/mL at every visits	The proportion of subjects with plasma HBV DNA levels below 116 copies/mL at every visits	week 12, 24, 36, 48, 60, 72, 84, 96, 108, 120, 132, 144
Secondary	The proportion of the biochemical (alanine aminotransferase normalization) response of TDF for the treatment of chronic hepatitis B at Week 48 and 96	The proportion of the biochemical (alanine aminotransferase normalization) response of TDF for the treatment of chronic hepatitis B at Week 48 and 96	Week 48 and 96
Secondary	The proportion of the serological response (loss of HBeAg and seroconversion to HBeAb) of TDF for the treatment of chronic hepatitis B at Week 48 and 96	The proportion of the serological response (loss of HBeAg and seroconversion to HBeAb) of TDF for the treatment of chronic hepatitis B at Week 48 and 96	Week 48 and 96
Secondary	The proportion of the serological response (loss of HBsAg and seroconversion to HBsAb) of TDF for the treatment of chronic hepatitis B at Week 48 and 96	The proportion of the serological response (loss of HBsAg and seroconversion to HBsAb) of TDF for the treatment of chronic hepatitis B at Week 48 and 96	Week 48 and 96
Secondary	The change from baseline in the decline of HBV DNA at every visits	The change from baseline in the decline of HBV DNA at every visits	week 12, 24, 36, 48, 60, 72, 84, 96, 108, 120, 132, 144
Secondary	The proportion of patients showing virological breakthrough at week 48 and 96	The proportion of patients showing virological breakthrough at week 48 and 96.; Virological Breakthrough defined as any increase in serum HBV DNA by >1 log10 from nadir or redetection of serum HBV DNA at levels =10-fold the lower limit of detection of the HBV DNA assay after having an undetectable result	Week 48 and 96
Secondary	The incidence of resistance of TDF among patients showing virological breakthrough at week 48 and 96	The incidence of resistance of TDF among patients showing virological breakthrough at week 48 and 96.; Virological Breakthrough defined as any increase in serum HBV DNA by >1 log10 from nadir or redetection of serum HBV DNA at levels =10-fold the lower limit of detection of the HBV DNA assay after having an undetectable result	Week 48 and 96
Secondary	The proportion of improvement of liver function including Child Score, Model for End-stage Liver Disease (MELD) score at Week 48 and 96	The proportion of improvement of liver function including Child Score, MELD score at Week 48 and 96	Week 48 and 96
Secondary	The proportion of improvement of Fibrosis marker including Aspartate aminotransferase to Platelet Ratio Index(APRI) at Week 48 and 96	The proportion of improvement of Fibrosis marker including Aspartate aminotransferase to Platelet Ratio Index(APRI) at Week 48 and 96	Week 48 and 96