Evidence map›Paper›PMID 41017776›Full record

Trial reportJournal of viral hepatitis2025

High Efficiency and Safety of Hepatitis C Treatment Among People Who Inject Drugs in Vietnam.

Didier Laureillard, Nguyen Thanh Binh, Vu Hai Vinh, Tran Thi Hong, Catherine Quillet, Nham Thi Tuyet Thanh, Roselyne Vallo, Bach Thi Nhu Quynh, Jean Pierre Moles, Khuat Thi Hai Oanh and 12 more

Registry-linked trialAbstract readClinical Trial, Phase IV
In one paragraph

Trial report in Journal of viral hepatitis, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT03537196 (Towards HCV Elimination), which is not on this map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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.

NCT03537196 phase4completednot on this map

Towards HCV Elimination: Evaluation of an Integrated Model of HCV Care Targeting People Who Inject Drugs in Hai Phong, Vietnam

TypeinterventionalSponsorANRS, Emerging Infectious DiseasesRan2018 to 2022Enrolled979ConditionsHepatitis C, Drug Use, Viral Hepatitis CArmsSofosbuvir 400 mg and Daclatasvir 60 mg, Sofosbuvir 400 mg and Daclatasvir 90 mg, Ribavirin, Sofosbuvir and Daclatasvir for 24 weeks
3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

  1. Trial
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

22 authors.

Didier LaureillardInfectious and Tropical Diseases Department, University Hospital, Nîmes, France.
Nguyen Thanh BinhInfectious and Tropical Diseases Department, Viet Tiep Hospital, Hai Phong, Vietnam.
Vu Hai VinhInfectious and Tropical Diseases Department, Viet Tiep Hospital, Hai Phong, Vietnam.
Tran Thi HongFaculty of Public Health, Hai Phong University of Medicine and Pharmacy, Hai Phong, Vietnam.
Catherine QuilletPathogenesis and Control of Chronic and Emerging Infections, Université de Montpellier, Inserm, Université des Antilles,, Montpellier, France.
Nham Thi Tuyet ThanhCenter for Supporting Community Development Initiatives, Hanoi, Vietnam.
Roselyne ValloPathogenesis and Control of Chronic and Emerging Infections, Université de Montpellier, Inserm, Université des Antilles,, Montpellier, France.
Bach Thi Nhu QuynhDepartment of Molecular Biology, Hai Phong University of Medicine and Pharmacy, Hai Phong, Vietnam.
Jean Pierre MolesPathogenesis and Control of Chronic and Emerging Infections, Université de Montpellier, Inserm, Université des Antilles,, Montpellier, France.ORCID https://orcid.org/0000-0002-6863-6350
Khuat Thi Hai OanhCenter for Supporting Community Development Initiatives, Hanoi, Vietnam.
Duong Thi HuongFaculty of Public Health, Hai Phong University of Medicine and Pharmacy, Hai Phong, Vietnam.
Delphine RapoudPathogenesis and Control of Chronic and Emerging Infections, Université de Montpellier, Inserm, Université des Antilles,, Montpellier, France.
Jonathan FeelemyerSchool of Global Public Health, New York University, New York, New York, USA.
Laurent MichelCESP Inserm UMRS 1018, Paris Saclay University, Pierre Nicole Center, French Red Cross, Paris, France.
Peter VickermanPopulation Health Sciences, Bristol Medical School, University of Bristol, Bristol, UK.ORCID https://orcid.org/0000-0002-8291-5890
Hannah FraserPopulation Health Sciences, Bristol Medical School, University of Bristol, Bristol, UK.ORCID https://orcid.org/0000-0002-4340-9995
Laurence WeissUniversité Paris Cité, Paris, France.
Maud LemoineDepartment of Metabolism, Digestion and Reproduction, Division of Digestive Diseases, Liver Unit, Imperial College London, London, UK.
Karine LacombeSorbonne Université, Inserm IPLESP, UMR-S1136, Infectious Diseases Department, Saint-Antoine Hospital, AP-HP, Paris, France.
Don Des JarlaisSchool of Global Public Health, New York University, New York, New York, USA.
Pham Minh KhueFaculty of Public Health, Hai Phong University of Medicine and Pharmacy, Hai Phong, Vietnam.ORCID https://orcid.org/0000-0003-2974-3484
Nicolas NagotPathogenesis and Control of Chronic and Emerging Infections, Université de Montpellier, Inserm, Université des Antilles,, Montpellier, France.

Funding

DRIVE (DRug use and blood-borne Infections in ViEtnam): Combined prevention and care to end the HIV epidemic among people who inject drugs in Haiphong, Viet NamR01DA041978 · NIDA · NEW YORK UNIVERSITY · PI DES JARLAIS, DON C · 2016 to 2020
$4.9M
Agence Nationale de Recherches sur le Sida et les Hépatites Virales ANRS 12380NIDA NIH HHS R01 DA041978US NIDA R01DA041978
6 · The paper itself

Abstract

People who inject drugs (PWID) are highly affected by hepatitis C (HCV) worldwide, particularly in low- and middle-income countries (LMICs), where access to addiction services is often limited. Reducing the burden of HCV, as promoted by WHO, requires effective interventions in this high-risk population. Here, we report the safety and efficacy of a pangenotypic generic HCV treatment among PWID in Vietnam, using a sofosbuvir/daclatasvir regimen. PWID were screened for HCV at two community-based organisations (CBO) premises in Haiphong during both a respondent-driven sampling survey and cohort follow-up visits. PWID with detectable HCV RNA were referred to three public hospitals for a 12-week regimen of generic sofosbuvir/daclatasvir, with ribavirin if cirrhosis, and with CBO support for referral and adherence. Treatment safety was assessed over the course of treatment and success was measured by sustained virologic response 12 weeks after the end of treatment (SVR12). Of the 1201 PWID screened with detectable HCV RNA, 1021 were enrolled: 96% male, median age 42 years, 45% HIV-infected, 16% with advanced liver fibrosis, 55% currently injecting, and 71.5% on methadone maintenance therapy (MMT). In total, 979 participants started HCV treatment, and 901 of the 924 participants tested at SVR12 (98%) were cured. Genotype 3, current drug use, lack of MMT, and HIV infection were independently associated with treatment failure. High HCV cure rates can be achieved among PWID in LMICs such as Vietnam using a simple model of care, including a pangenotypic generic direct-acting antiviral combination and CBO support. Trial Registration: ClinicalTrials.gov identifier: NCT03537196.

Indexed as

Antiviral AgentsHepatitis CHepatitis C, ChronicSubstance Abuse, IntravenousAdultCarbamatesDrug Therapy, CombinationFemaleHepacivirusHumansImidazolesMaleMiddle AgedPyrrolidinesRibavirinRNA, ViralAntiviral AgentsCarbamatesdaclatasvirImidazolesPyrrolidinesRibavirinRNA, ViralSofosbuvirValinedaclatasvirgeneric direct‐acting antiviralshepatitis Clow‐ and middle‐income countries (LMICs)people who inject drugssofosbuvir

Identifiers

PMID41017776
PMCPMC12477749

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Registered trials

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.