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Trial · NCT06092333

VIR-2218 and Peginterferon Alfa-2a for Chronic Hepatitis B

NCT06092333, Phase 2, Active not recruiting, National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)

3 sourcestrials-2026-11-12-0.5.0

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ConductScience Library. VIR-2218 and Peginterferon Alfa-2a for Chronic Hepatitis B. Trials, record NCT06092333. Release trials-2026-11-12-0.5.0, 12 Nov 2026. https://conductscience.org/library/trials/NCT06092333

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Trial

As registered on ClinicalTrials.gov, in the graph's capture of the registry.

Title
VIR-2218 and Peginterferon Alfa-2a for Chronic Hepatitis B
NCT number
NCT06092333
Status
Active not recruiting
Phases
Phase 2
Enrollment
12 participants, actual
Lead sponsor
National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)
Conditions
Chronic Hepatitis B
Interventions
VIR-2218 and peginterferon alfa-2a
First posted
2023-10-23
Last updated
2026-10-05

Source ClinicalTrials.gov

Registered outcomes5

Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.

ListOutcomeTime frameDescription
PrimaryDecline in log quantitative HBsAg level6 months after discontinuation of all treatmentTo evaluate the effect of administration of VIR-2218 in combination with peginterferon alfa-2a on qHBsAg levels
SecondaryChanges in innate and adaptive host immune responses to HBV during and after treatment.Within the first 6 hours after peginterferon injection; Baseline to week 12, from Baseline to week 36 and from Baseline to week 84To evaluate the effects of VIR-2218 in combination with peginterferon alfa-2a on peripheral and intrahepatic immune responses in non-cirrhotic adults with chronic HBV infection
SecondaryHBV DNA <10 IU/ml at end of treatment and 6 months off treatment. The response will be reported as HBV DNA <LLOQ target detected (TD) or target not detected (TND)6 months off-treatmentPartial cure. An alternative goal of treatment of chronic hepatitis B
SecondaryFunctional cure which is defined as undetectable HBsAg (<0.085 IU/ml) AND sustained suppression of HBV DNA [< LLOQ], <10 IU/ml)] for more than 6 months after discontinuation of all treatment> 6 months after discontinuation of all treatmentThe goal of treatment of chronic hepatitis B
SecondarySafetyEnd of treatment 6 months off-treatmentTo evaluate the safety and tolerability of VIR-2218 in combination with peginterferon alfa-2a in non-cirrhotic adults with chronic HBV infection

Outcomes0

Each outcome the trial posted results for, in ClinicalTrials.gov's words.

None in this release.

Results by group0

Each measurement the trial posted, group by group, in the words and numbers it posted.

None in this release.

Participant flow0

How many started, completed or left each group, period by period.

None in this release.

Adverse events0

Each adverse event the trial posted, group by group: the participants affected out of those at risk.

None in this release.

Adverse event totals0

The totals the trial posted for each group.

None in this release.

Papers0

The papers the trial lists on ClinicalTrials.gov.

None in this release.

Grants0

The grants NIH RePORTER links to the trial, newest funded first: NIH's, and some of AHRQ's, CDC's, FDA's and VA's. Each shows its title, principal investigators, organization and funder in its newest year.

None in this release.

Trial comparisons0

Comparisons of the trial's two groups, calculated by ConductScience from the counts it posted.

None in this release.

Tests0

The ConductCognition tests this trial's registered outcomes name, as ScienceGraph matched them in trial-tests-2026-11-12-0.2.1.

None in this release.

Data dates

The day each source was copied for this release.

ClinicalTrials.gov
2026-11-12
ClinicalTrials.gov
Results, from AACT
2026-03-23
AACT
NIH grant links
2026-11-13
NIH RePORTER

Sources 3

  • ClinicalTrials.gov's posted results, through CTTI's AACTFreely available. Acknowledgement requested
  • ClinicalTrials.govNo license stated
  • NIH RePORTER's clinical studies and project filesPublic domain
Each source's terms
  • ClinicalTrials.gov's posted results, through CTTI's AACTClinicalTrials.gov data via Aggregate Analysis of ClinicalTrials.gov (AACT), CTTI. CTTI makes its materials freely available and requests acknowledgement. https://aact.ctti-clinicaltrials.org/documentation/299
  • ClinicalTrials.govnone stated
  • NIH RePORTER's clinical studies and project filesPublic domain (NIH RePORTER)

ClinicalTrials.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions.

For software

Read this trial from software.

The record and each of its lists are JSON, twenty rows a page. No key.

GET https://conductscience.org/api/trials/v1/NCT06092333

GET https://conductscience.org/api/trials/v1/NCT06092333/registered