Combination Entecavir and Peginterferon Therapy in HBeAg-Positive Immune-Tolerant Adults With Chronic Hepatitis B

Hepatitis B Clinical Trial

— HBRN  

Official title:

Combination Entecavir and Peginterferon Therapy in HBeAg-Positive Immune-Tolerant Adults With Chronic Hepatitis B

Clinical Trial Details — Status: Terminated

Administrative data

• NCT number: NCT01369199
• Other study ID #: DK082864 HBRN IT Adult Trial
• Secondary ID: U01DK082916U01DK
• Status: Terminated
• Phase: Phase 3
• Start date: May 2012
• Est. completion date: February 14, 2017

Study information

• Verified date: May 2022
• Source: National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

The investigators evaluated the safety and efficacy of a short lead-in course (8 weeks) of entecavir followed by combination of entecavir plus peginterferon alfa-2a for 40 weeks.

Description:

To determine the efficacy of treatment with 8 weeks of entecavir followed by 40 weeks of both entecavir and peginterferon in the treatment of chronic hepatitis B in hepatitis B "e" antigen (HBeAg) positive adults who are in the immune tolerant phase.

To evaluate safety and sustained responses after treatment with entecavir and peginterferon alfa-2a in the treatment of chronic hepatitis B in HBeAg positive adults who are in the immune tolerant phase.

A single arm treatment study of 8 weeks of entecavir followed by 40 weeks of both entecavir and peginterferon alfa-2a in adults with HBeAg-positive chronic hepatitis B with normal or near normal alanine aminotransferase (ALT) levels and high serum levels of hepatitis B virus (HBV) DNA ("immune tolerant" HBeAg-positive chronic hepatitis B). All participants followed for 48 weeks after treatment discontinuation (week 96 for those who completed treatment).

Other known NCT identifiers

• NCT01534611

Recruitment information / eligibility

• Status: Terminated
• Enrollment: 28
• Est. completion date: February 14, 2017
• Est. primary completion date: February 14, 2017
• Accepts healthy volunteers: No
• Gender: All
• Age group: 18 Years and older

Eligibility

Inclusion Criteria:

• Enrolled in & completed the baseline evaluation for NCT01263587 or completed the necessary components of NCT01263587 by the end of baseline visit.

• >18 years of age at the baseline visit (day 0). Patients >50 years of age at baseline will need to have a liver biopsy as standard of care with hepatic activity index (HAI) =3 & Ishak fibrosis score =1 within 96 weeks prior to baseline visit.

• Documented chronic HBV infection as evidenced by detection of HBsAg in serum for =24 weeks prior to baseline visit OR at least one positive HBsAg & negative anti-hepatitis B core (HBc) immunoglobulin (IgM) within 24 weeks prior to baseline visit OR at least one positive HBsAg & two positive HBV DNA over a period of =24 weeks prior to baseline visit.

• Presence of HBeAg in serum at last screening visit within 6 weeks of baseline visit.

• Serum HBV DNA level >10^7 IU/mL on at least two occasions at least 12 weeks apart during the 52 weeks before baseline visit. One of the two HBV DNA levels must be within 6 weeks of baseline visit.

• ALT levels persistently =45 U/L in males, =30 U/L in females (approx. 1.5 times the upper limit of normal (ULN) range) as documented by at least three values: one taken 28-52 weeks before baseline visit, one taken 6 to 24 weeks before the baseline visit, & the final value within 6 weeks prior to baseline visit.

• No evidence of hepatocellular carcinoma (HCC) based upon alpha-fetoprotein (AFP) =20 ng/mL at screening visit (up to 6 weeks prior to baseline visit). a. Participants who meet American Association for the Study of Liver Diseases (AASLD) criteria for HCC surveillance must have negative liver imaging as shown by ultrasound, computerized tomography (CT) or magnetic resonance imaging (MRI) within 28 weeks prior to baseline visit. b. Participants with AFP >20 ng/mL must be evaluated clinically with additional imaging & shown not to have HCC on CT or MRI before they can be enrolled.

Exclusion Criteria:

• History of hepatic decompensation

• Evidence of decompensated liver disease prior to or during screening, including direct bilirubin >0.5 mg/dL, international normalization ratio (INR) >1.5, or serum albumin <3.5 g/dL.

• Platelet count <120,000/mm3, hemoglobin <13 g/dL (males) or <12 g/dL (females), absolute neutrophil count < 1500 /mm3 (<1000/mm3 for African-Americans) at last screening visit.

• Previous treatment with medications that have established activity against HBV including interferon & nucleos(t)ide analogs =24 weeks. Patients with <24 weeks of prior HBV treatment & a wash-out period >24 weeks are not excluded.

• Known allergy or intolerance to study medications.

• Females who are pregnant or breastfeeding. Females of childbearing potential unable or unwilling to use a reliable method of contraception during the treatment period.

• Renal insufficiency with calculated creatinine clearance <50 mL/min at screening.

• History of alcohol or drug abuse within 48 weeks of baseline visit.

• Previous liver or other organ transplantation (including engrafted bone marrow).

• Any other concomitant liver disease, including hepatitis C or D. Non-alcoholic fatty liver disease (NAFLD) with steatosis &/or mild to moderate steatohepatitis is acceptable but NAFLD with severe steatohepatitis is exclusionary.

• Presence of anti-hepatitis D virus (HDV) or anti-hepatitis C virus (HCV) (unless HCV RNA negative) in serum on any occasion in the 144 weeks prior to baseline visit. Presence of anti-HIV (test completed within 6 weeks prior to baseline visit).

• Pre-existing psychiatric condition(s), including, but not limited to: current moderate or severe depression, history of depression requiring hospitalization within the past 10 years, history of suicidal or homicidal attempt within the past 10 years, history of severe psychiatric disorders as determined by a study physician.

• History of immune-mediated or cerebrovascular disease, chronic pulmonary or cardiac disease associated with functional limitation, retinopathy, uncontrolled thyroid disease, poorly controlled diabetes or uncontrolled seizure disorder, as determined by a study physician.

• Any medical condition that would, in the opinion of a study physician, be predicted to be exacerbated by therapy or that would limit study participation.

• Any medical condition requiring, or likely to require, chronic systemic administration of corticosteroids or other immunosuppressive medications during the course of this study.

• Evidence of active or suspected malignancy, or a history of malignancy within the 144 weeks prior to baseline visit (except adequately treated carcinoma in situ or basal cell carcinoma of the skin).

• Expected need for ongoing use of any antivirals with activity against HBV during the course of the study.

• Concomitant use of complementary or alternative medications purported to have antiviral activity.

• Participation in any other clinical trial involving investigational drugs within 30 days of the baseline visit or intention to participate in another clinical trial involving investigational drugs during participation in this study.

Related Conditions & MeSH terms

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

Intervention

Drug:
• Entecavir and peginterferon
Entecavir 0.5 mg daily orally for 48 weeks plus peginterferon 180 µg sq weekly during weeks 9-48 of treatment.

Locations

Country	Name	City	State
Canada	University of Toronto	Toronto	Ontario
United States	University of Michigan Health System	Ann Arbor	Michigan
United States	NIH Clinical Center	Bethesda	Maryland
United States	Beth Israel Deaconess Medical Center	Boston	Massachusetts
United States	Massachusetts General Hospital	Boston	Massachusetts
United States	University of North Carolina	Chapel Hill	North Carolina
United States	Baylor University Medical Center	Dallas	Texas
United States	University of Texas Southwestern	Dallas	Texas
United States	Duke University Medical Center	Durham	North Carolina
United States	Queen's Medical Center	Honolulu	Hawaii
United States	Cedars Sinai Medical Center	Los Angeles	California
United States	University of California Los Angeles	Los Angeles	California
United States	University of Minnesota	Minneapolis	Minnesota
United States	Virginia Commonwealth University	Richmond	Virginia
United States	Mayo Clinic	Rochester	Minnesota
United States	Saint Louis University	Saint Louis	Missouri
United States	Washington University	Saint Louis	Missouri
United States	California Pacific Medical Center	San Francisco	California
United States	University of California San Francisco	San Francisco	California
United States	University of Washington Medical Center	Seattle	Washington
United States	Virginia Mason Medical Center	Seattle	Washington

Sponsors (3)

Lead Sponsor	Collaborator
National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)	National Center for Research Resources (NCRR), University of Pittsburgh

Countries where clinical trial is conducted

United States,  Canada, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Proportion of Participants With HBeAg Loss (Lack of Detectable HBeAg) AND HBV DNA =1,000 IU/mL	Lack of data was considered to be treatment failure.	End of follow-up (up to 96 weeks)
Primary	Incidence of Adverse Events (AEs) Per Person-Year of Observation	The number of AEs includes both AEs and Serious Adverse Events (SAEs). The incidence is calculated as the number of AEs divided by the number of person-years of observation, which is the sum, across all participants, of the number of years between the start of treatment and the end of treatment, or the end of follow-up, respectively.	From first treatment to the end of treatment (up to 48 weeks) and the end of follow-up (up to 96 weeks)
Primary	Incidence of Serious Adverse Events (SAEs) Per Person-Year	The incidence is calculated as the number of SAEs divided by the number of person-years of observation, which is the sum, across all participants, of the number of years between the start of treatment and the end of treatment, or the end of follow-up, respectively.	From first treatment to the end of treatment (up to 48 weeks) and the end of follow-up (up to 96 weeks)
Secondary	Proportion of Participants With HBeAg Loss		End of treatment (up to 48 weeks)
Secondary	Proportion of Participants With HBeAg Loss		End of follow-up (up to 96 weeks)
Secondary	Proportion of Participants With HBeAg Seroconversion		End of treatment (up to 48 weeks)
Secondary	Proportion of Participants With HBeAg Seroconversion		End of follow-up (up to 96 weeks)
Secondary	Proportion of Participants With HBsAg Loss		End of treatment (up to 48 weeks)
Secondary	Proportion of Participants With HBsAg Loss		End of follow-up (up to 96 weeks)
Secondary	Proportion of Participants With HBsAg Seroconversion		End of treatment (up to 48 weeks)
Secondary	Proportion of Participants With HBsAg Seroconversion		End of follow-up (up to 96 weeks)
Secondary	Proportion of Participants With Alanine Aminotransferase (ALT) <45 U/L for Men, <30 U/L for Women		End of treatment (up to 48 weeks)
Secondary	Proportion of Participants With ALT <45 U/L for Men, <30 U/L for Women		End of follow-up (up to 96 weeks)
Secondary	Proportion of Participants With ALT Normalization (Men <30 U/L, Women <20 U/L)		End of treatment (up to 48 weeks)
Secondary	Proportion of Participants With ALT Normalization (Men <30 U/L, Women <20 U/L)		End of follow-up (up to 96 weeks)
Secondary	Proportion of Participants With HBV DNA =1000 IU/mL		End of treatment (up to 48 weeks)
Secondary	Proportion of Participants With HBV DNA =1000 IU/mL		End of follow-up (up to 96 weeks)
Secondary	Proportion of Participants With HBV DNA <20 IU/mL		End of treatment (up to 48 weeks)
Secondary	Proportion of Participants With HBV DNA <20 IU/mL		End of follow-up (up to 96 weeks)
Secondary	Absence of Detectable Antiviral Drug-resistance HBV Mutations	HBV drug resistance variant testing was performed at the CDC laboratory. The sequences of the HBV polymerase spanning nucleotide positions 311-1021 were determined by Sanger sequencing. Drug resistance mutations that were tested in this study included L80VI, L82M, T128N, W153Q, F166L, I169T, V173L, L180M, A181TV, T184ACFGILMS, V191T, A194T, A200V, S202ETV, M204IV, V207I, N236T, M250ILV, and G145R.	End of treatment (up to 48 weeks)

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