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NCT05970289CompletedPhase 2

Investigate the Efficacy and Safety of BRII-835 (VIR-2218) and PEG-IFNα Combination Therapy in Chronic HBV Patients

A Phase 2 Multicenter, Randomized, Open-label Study to Investigate the Efficacy and Safety of BRII-835 (VIR-2218) and Pegylated Interferon Alpha (PEG-IFNα) Combination Therapy for the Treatment of Chronic Hepatitis B Virus (HBV) Infection

Source: ClinicalTrials.gov · Last updated 20 Oct 2026

Brief summary (registry, in English)

This study will evaluate the efficacy and safety of PEG-IFNα alone or in combination with different dose levels of BRII-835 (VIR-2218) in participants with chronic hepatitis B virus (HBV) infection.

Status (registry)
Completed
Phase (registry)
Phase 2
Study type
Interventional
Enrollment
86 (actual)
First submitted
21 Jul 2023
Start date
22 Aug 2023
Primary completion date
16 Jul 2025
Lead sponsor
Brii Biosciences Limited
Diseases
Hepatitis B
NCT number
NCT05970289

What you commit to

  • Study type: Interventional · Phase 2
  • Participants enrolled: 86
  • From 22 Aug 2023 to the primary completion date, 16 Jul 2025
  • 28 sites in 5 countries
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • History or evidence of drug or alcohol abuse.

Other illness

  • Any clinically significant chronic or acute medical condition that makes the participant unsuitable for participation.
  • History of intolerance to SC injection.
  • History of chronic liver disease from any cause other than chronic HBV infection.
  • History of hepatic decompensation.

Other

  • Significant liver fibrosis or cirrhosis.
  • Contraindications to the use of Peg-IFNα.

Who the study is looking for

  • Male or female aged 18-60.
  • Body mass index ≥ 18 kg/m2 and ≤ 32 kg/m2.
  • Chronic HBV infection for ≥ 6 months.
  • On NRTI therapy for at least 6 months.

Age in the registry: 18 years to 60 years · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (28)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Investigative Site 61002
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BirtinyaAustraliaUnknown status
Investigative Site 61001
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KingswoodAustraliaUnknown status
Investigative Site 61003
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MelbourneAustraliaUnknown status
Investigative Site 86001
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BeijingChinaUnknown status
Investigative Site 86007
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BeijingChinaUnknown status
Investigative Site 86008
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ChangchunChinaUnknown status
Investigative Site 86004
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ChongqingChinaUnknown status
Investigative Site 86006
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GuangzhouChinaUnknown status
Investigative Site 86011
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HangzhouChinaUnknown status
Investigative Site 85202
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Hong KongChinaUnknown status
Investigative Site 85201
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Hong KongChinaUnknown status
Investigative Site 88601
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KaohsiungChinaUnknown status
Investigative Site 86013
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ShanghaiChinaUnknown status
Investigative Site 88603
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TaipeiChinaUnknown status
Investigative Site 88602
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TaipeiChinaUnknown status
Investigative Site 82001
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BusanSouth KoreaUnknown status
Investigative Site 82002
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ChuncheonSouth KoreaUnknown status
Investigative Site 82004
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DaeguSouth KoreaUnknown status
Investigative Site 82003
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SeoulSouth KoreaUnknown status
Investigative Site 82005
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SeoulSouth KoreaUnknown status
Investigative Site 82006
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SoeulSouth KoreaUnknown status
Investigative Site 65002
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SingaporeSingaporeUnknown status
Investigative Site 65001
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SingaporeSingaporeUnknown status
Investigative Site 66003
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BangkokThailandUnknown status
nvestigative Site 66007
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Chiang MaiThailandUnknown status
Investigative Site 66005
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Khon KaenThailandUnknown status
Investigative Site 66006
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NonthaburiThailandUnknown status
Investigative Site 66008
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SongkhlaThailandUnknown status

This page is information, not medical advice. Discuss any trial with your doctor.