Evidence map›Paper›PMID 41404410›Full record

ArticleMolecular therapy. Methods & clinical development2025

HBVZ10, an AAV8 vector-based new HBV therapy candidate for cccDNA elimination.

Bai-Hua Zhang, Yuanping Zhou, Stephen Horrigan, Laura Luckenbaugh, Jianming Hu, Fabien Zoulim, Yong-Yuan Zhang

Abstract read
In one paragraph

Article in Molecular therapy. Methods & clinical development, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

7 authors.

Bai-Hua ZhangVirology, HBVtech, Rockville, MD, USA.
Yuanping ZhouDepartment of Infectious Diseases, The Third Affiliated Hospital, Southern Medical University, Guangzhou, China.
Stephen HorriganPreclinical Department, Noble Life Sciences, Sykesville, MD, USA.
Laura LuckenbaughDepartment of Microbiology and Immunology, Penn State College of Medicine, Hershey, PA, USA.
Jianming HuDepartment of Microbiology and Immunology, Penn State College of Medicine, Hershey, PA, USA.
Fabien ZoulimPaThLiv INSERM U1350, Université Claude Bernard Lyon 1, Hospices Civils de Lyon, Lyon Hepatology Institute, Lyon, France.
Yong-Yuan ZhangVirology, HBVtech, Rockville, MD, USA.

Funding

Mechanisms of Hepadnavirus Assembly and ReplicationR37AI043453 · NIAID · PENNSYLVANIA STATE UNIV HERSHEY MED CTR · PI Jianming Hu · 2018 to 2026
$3.8M
NIAID NIH HHS R37 AI043453
6 · The paper itself

Abstract

Eliminating hepatitis B virus (HBV) covalently closed circular DNA (cccDNA) remains a major challenge, requiring innovative treatment strategies and drug candidates. Clinical studies reveal that wild-type HBV in the blood is often replaced by gradually rising mutant populations. This replacement reflects loss of the early cccDNA pool, then replenished predominantly through

Indexed as

AAV gene therapycccDNA eliminationchronic HBV infectionde novo infectionHBVZ10

Identifiers

PMID41404410
PMCPMC12704295

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.