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Hepatitis B

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NIH Hepatitis B Research Network

In September 2008, the NIH launched a Hepatitis B Research Network (http://www.hepbnet.org) comprised of 29 clinical centers (adult and pediatric), a data coordinating center, and an immunology laboratory. The University of Michigan is one of the clinical centers and Dr. Anna Lok chairs the network's steering committee.

This network will conduct observational studies as well as clinical studies of new treatment strategies.


Hepatitis B Research Network – Observational Study

 

Enrollment status: Actively enrolling

 

Objective

To study the pattern of hepatitis B in North America and the rates of transition through different phases of chronic HBV infection.

Inclusion/exclusion criteria

Principal investigator: Anna Lok, MD aslok@med.umich.edu

Contact person: Sravanthi Kaza: (734) 615-3853 or sravanth@med.umich.edu


Hepatitis B Research Network – Immune-Tolerant Trial

Combination entecavir and peginterferon alfa-2a therapy in hepatitis B e antigen (HBeAg)–positive immune-tolerant adults with chronic hepatitis B

 

Enrollment status: Actively enrolling

 

Objective

To determine the efficacy of treatment with 8 weeks of entecavir followed by 40 weeks of both entecavir and peginterferon alfa-2a in HBeAg-positive adults who are in the immune-tolerant phase.

Inclusion/exclusion criteria

Adults with chronic hepatitis B infection, HBeAg-positive, normal to slightly abnormal liver enzyme levels, no previous antiviral treatment.

Study design

Open label trial of 8 weeks entecavir followed by 40 weeks of both entecavir and peginterferon alfa-2a).

Principal investigator: Anna Lok, MD aslok@med.umich.edu

Contact person: Sravanthi Kaza: (734) 615-3853 or sravanth@med.umich.edu


Hepatitis B Research Network – Immune-Active Trial

Combination therapy of peginterferon alfa-2a and tenofovir versus tenofovir monotherapy in HBeAg-positive and HBeAg-negative chronic hepatitis B

Enrollment status: Actively enrolling

Objective

To compare the long-term efficacy of initial treatment with combination therapy consisting of peginterferon alfa-2a plus tenofovir DF versus tenofovir DF monotherapy.

Inclusion/exclusion criteria

Study design

This is a randomized (1:1) trial comparing

  1. Tenofovir DF 300 mg daily for 192 weeks (4 years) and

  2. Peginterferon alfa-2a 180 g weekly for 24 weeks plus tenofovir DF 300 mg daily for 192 weeks (4 years).

Note: The cost of medications, clinical evaluations, and tests associated with the study will be covered.

Principal investigator: Anna Lok, MD aslok@med.umich.edu

Contact person: Sravanthi Kaza: (734) 615-3853 or sravanth@med.umich.edu