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Open-Label Study of AB-729, Nucleos(t)Ide Analogue and Pegylated Interferon Alfa-2a in Subjects With Chronic Hepatitis B Infection

← catalyst calendar

NCT04980482 · results posted

Sponsored by Arbutus Biopharma Corporation (industry) · ABUS — their whole pipeline →.

Phase
Phase 2
Status
Completed
Study type
Interventional
Design
Randomized · None · Treatment
Enrollment
43actual
Sites
17
Countries
Australia, Hong Kong, Moldova +4

Every value on this page is a field the sponsor filed with ClinicalTrials.gov, reproduced. Dates are their own estimates, revised as a study runs, unless the registry marks them actual. sources →

Source: ClinicalTrials.gov, retrieved 2026-08-19

Dates

each axis at the precision it was filed, with the registry's own basis
DateFiledBasisWhat it is
Start2021-10-29actualWhen the study began enrolling
Primary completion2025-03-13actualThe date the last participant is measured for the primary outcome — the readout window
Study completion2025-05-21actualThe whole study's end, after follow-up
First posted2021-07-28actualWhen this record first appeared on the registry
Results posted2026-04-29actualWhen the sponsor posted results to the registry
Record updated2026-04-29actualThe sponsor's own last edit to this record — every projection above is as current as this date

What it studies

Condition

  • Chronic Hepatitis b

Interventions

  • Drug: AB-729
  • Drug: Peg-IFNα-2a — also filed as pegylated interferon alpha 2a

Primary outcome

what the primary-completion date above is the date OF
The Frequency and Severity of Treatment Emergent Adverse Events (TEAEs), Discontinuations Due to AEs and Lab Abnormalities After Dosing With AB-729 Plus Peg-IFNα-2a
measured Up to 124 weeks

Posted documents

hosted by the registry — we link, never re-serve
Study Protocolposted 2022-06-17 · 18.6 MB · Prot_000.pdf
Statistical Analysis Planposted 2025-07-23 · 851 KB · SAP_001.pdf

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