• A5368:Anti-PD-1 Antibody in HBV Infected on Suppressive Antiviral Therapy

    January 24, 2020 Alexis Sexton

    “Safety and Immunotherapeutic Activity of Cemiplimab in Participants with HBV on Suppressive Antiviral Therapy: A Phase I/II Ascending Multiple Dose Study”

    Brief Description: Scientists are looking at ways to cure Hepatitis B (HBV). This study will assess the safety and tolerability of cemiplimab administered in participants with HBV on suppressive antiviral therapy.

    Purpose of this Study: This study is trying to find out if cemiplimab is safe and well tolerated. Participants will receive multiple dose levels (0.3, 1.0, and 3.0 mg/kg) of cemiplimab administered as two infusions at weeks 6 and 12.

    Requirements to Enter Study (things that must be true for you):

    • Have chronic HBV infection (defined as HBsAg positive) and under treatment for ≥12 months with tenofovir- or entecavir-containing therapy: tenofovir disoproxil fumarate (TDF), tenofovir alanfenamide (TAF), TDF/emtricitabine (FTC), TAF/FTC, or entecavir.
    • Be willing to continue HBV antiviral therapy throughout the study.
    • Have certain tests done.
    • Agree to use contraception/birth control methods.
    • Be 18 years old or older but less than 70 years.
    • Weight ≥40 kg.
    • Had evidence of limited or no evidence of fibrosis (F0-F2) by liver biopsy or noninvasive alternative method.
    • Be willing to sign the consent after discussion with the research staff.

    Exclusion Criteria (things that cannot be true about you):

    • Positive for the presence of Hepatitis C Virus.
    • Received investigational drug or device within 60 days prior to study entry.
    • Breastfeeding or pregnancy.
    • Known allergy/sensitivity or any hypersensitivity to components of study drug(s).
    • Active drug or alcohol use or dependence and other conditions that would interfere with adherence to study.
    • Acute or serious illness requiring systemic treatment and/or hospitalization within 35 days prior to study entry.
    • History of immunoglobulin IgG therapy or interferon (IFN) therapy within 12 months prior to study entry.
    • A male participant with a pregnant female partner.
    • Any vaccination within 30 days prior to entry.

    Treatment:

    • Multiple dose levels (0.3, 1.0 and 3.0 mg/kg) of cemiplimab administered as two infusions at weeks 6 and 12.

    Procedures:

    • Blood tests at clinic visits to check mainly hepatic and renal function.
    • Liver biopsy at study entry and at week 18 on study.
    • Leukapheresis for a group of participants.

    Duration of Study: Participants will be on study for up to 90 weeks (78 weeks following the last study drug infusion) with frequent safety evaluations.