Evidence map›Paper›PMID 37633256›Full record

ArticleClinical infectious diseases : an official publication of the Infectious Diseases Society of America2024

Chronic Hepatitis B Finite Treatment: Similar and Different Concerns With New Drug Classes.

Marion G Peters, Man-Fung Yuen, Norah Terrault, John Fry, Pietro Lampertico, Ed Gane, Carey Hwang, Luisa M Stamm, Mitchell Leus, Mala K Maini and 9 more

Open access · hybridAbstract read
In one paragraph

Article in Clinical infectious diseases : an official publication of the Infectious Diseases Society of America, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed, 1 pooled it
1.7field-weighted citation impact, top 15% of its field
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

7 citing papers in PubMed, 1 synthesis or guideline pooled it, 8 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Article
  4. Review
  5. Article
  6. Article
  7. [Current status and challenges of clinical research and development of new drugs for liver diseases].Zhonghua gan zang bing za zhi = Zhonghua ganzangbing zazhi = Chinese journal of hepatology · 2024
    Article
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

19 authors at 16 institutions in 8 countries.

Marion G PetersDepartment of Medicine, Northwestern University, Chicago, Illinois, USA.ORCID 0000-0002-1484-4752
Man-Fung YuenDepartment of Medicine, School of Clinical Medicine & State Key Laboratory of Liver Research, The University of Hong Kong, Hong Kong, China.
Norah TerraultKeck School of Medicine, University of Southern California, Los Angeles, California, USA.
John FryAligos Therapeutics, Clinical Development Consultant, San Francisco, California, USA.
Pietro LamperticoDivision of Gastroenterology and Hepatology, Foundation IRCCS Ca' Granda Ospedale Maggiore Policlinico, Milan, Italy.
Ed GaneDepartment of Medicine, University of Auckland, Auckland, New Zealand.
Carey HwangVir Biotechnology, San Francisco, California, USA.
Luisa M StammAssembly Biosciences, South San Francisco, California, USA.
Mitchell LeusForum for Collaborative Research, University of California, Berkeley School of Public Health, Washington, DC, USA.
Mala K MainiInstitute of Immunity and Transplantation, University College London, London, United Kingdom.
Patricia MendezGilead Sciences, Warren, New Jersey, USA.
Isabelle Lonjon-DomanecJanssen Pharmaceutica, Issy les Moulineaux, France.
Thomas BergDepartment of Medicine, Leipzig University Medical Center, Leipzig, Germany.
Su WangCooperman Barnabas Medical Center, RWJBarnabas-Rutgers Medical Group, Livingston, New Jersey, USA.
Poonam MishraDivision of Antivirals, Center for Drug Evaluation and Research, US Food and Drug Administration, Silver Spring, Maryland, USA.
Eric DonaldsonDivision of Antivirals, Center for Drug Evaluation and Research, US Food and Drug Administration, Silver Spring, Maryland, USA.
Stephanie BuchholzDepartment 32 Infectiology, Dermatology and Allergology, Federal Institute for Drugs and Medical Devices, Germany.
Veronica MillerForum for Collaborative Research, University of California, Berkeley School of Public Health, Washington, DC, USA.
Oliver LenzJanssen Pharmaceutica, Beerse, Belgium.
United States Food and Drug Administration · USUniversity of California, Berkeley · USAssembly Biosciences (United States) · USFederal Institute for Drugs and Medical Devices · DEGilead Sciences (United States) · USJanssen (Belgium) · BEJanssen (France) · FRLeipzig University · DENorthwestern University · USRutgers, The State University of New Jersey · USUniversity College London · GBUniversity of Auckland · NZUniversity of Hong Kong · HKUniversity of Milan · ITUniversity of Southern California · USVIR Biotechnology (United States) · US

Funding

AbbottGilead SciencesGlaxoSmithKlineRoche
6 · The paper itself

Abstract

Chronic hepatitis B, a major cause of liver disease and cancer, affects >250 million people worldwide. Currently there is no cure, only suppressive therapies. Efforts to develop finite curative hepatitis B virus (HBV) therapies are underway, consisting of combinations of multiple novel agents with or without nucleos(t)ide reverse-transcriptase inhibitors. The HBV Forum convened a webinar in July 2021, along with subsequent working group discussions to address how and when to stop finite therapy for demonstration of sustained off-treatment efficacy and safety responses. Participants included leading experts in academia, clinical practice, pharmaceutical companies, patient representatives, and regulatory agencies. This Viewpoints article outlines areas of consensus within our multistakeholder group for stopping finite therapies in chronic hepatitis B investigational studies, including trial design, patient selection, outcomes, biomarkers, predefined stopping criteria, predefined retreatment criteria, duration of investigational therapies, and follow-up after stopping therapy. Future research of unmet needs are discussed.

Indexed as

Hepatitis BHepatitis B, ChronicAntiviral AgentsBiomarkersDNA, ViralHepatitis B Surface AntigensHepatitis B virusHumansTreatment OutcomeAntiviral AgentsBiomarkersDNA, ViralHepatitis B Surface Antigenschronic hepatitis Bfunctional cureHBV biomarkersnew combination therapystopping finite therapy

Identifiers

PMID37633256
PMCPMC11006103
OpenAlexW4386187511

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.