Evidence map›Paper›PMID 32094138›Full record

ArticleAntimicrobial agents and chemotherapy2020

Antiviral Properties and Mechanism of Action Studies of the Hepatitis B Virus Capsid Assembly Modulator JNJ-56136379.

Jan Martin Berke, Pascale Dehertogh, Karen Vergauwen, Wendy Mostmans, Koen Vandyck, Pierre Raboisson, Frederik Pauwels

Abstract read
In one paragraph

Article in Antimicrobial agents and chemotherapy, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 38 papers.

0numbers the graph read from it
0cells of the map it votes in
38citing 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

38 citing papers in PubMed.

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  19. The progress of molecules and strategies for the treatment of HBV infection.Frontiers in cellular and infection microbiology · 2023
    Review
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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.

Jan Martin BerkeJanssen Research and Development, Beerse, Belgium jberke@its.jnj.com.
Pascale DehertoghJanssen Research and Development, Beerse, Belgium.
Karen VergauwenJanssen Research and Development, Beerse, Belgium.
Wendy MostmansJanssen Research and Development, Beerse, Belgium.
Koen VandyckJanssen Research and Development, Beerse, Belgium.
Pierre RaboissonJanssen Research and Development, Beerse, Belgium.
Frederik PauwelsJanssen Research and Development, Beerse, Belgium.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Capsid assembly is a critical step in the hepatitis B virus (HBV) life cycle, mediated by the core protein. Core is a potential target for new antiviral therapies, the capsid assembly modulators (CAMs). JNJ-56136379 (JNJ-6379) is a novel and potent CAM currently in phase II trials. We evaluated the mechanisms of action (MOAs) and antiviral properties of JNJ-6379

Indexed as

Antiviral AgentsCapsidCapsid ProteinsCell LineDNA ReplicationDNA, ViralDose-Response Relationship, DrugDrug SynergismHepatitis BHepatitis B virusHepatocytesHumansMicrobial Sensitivity TestsOrganic ChemicalsPrimary Cell CultureVirus ReplicationAntiviral AgentsCapsid ProteinsDNA, ViralJNJ-56136379Organic Chemicalscapsidcapsid assembly modulatorcccDNAhepatitishepatitis B virusprimary human hepatocytes

Identifiers

PMID32094138
PMCPMC7179615

What OpenQuestion holds

Textmetadata
Read underepoch 390

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.