Evidence map›Paper›PMID 40281127›Full record

Trial reportScientific reports2025

Time required to achieve optimum viral load suppression with Ravidasvir/sofosbuvir in chronic hepatitis C patients with or without compensated cirrhosis.

Nor Asiah Muhamad, Izzah Athirah Rosli, Nur Hasnah Maamor, Rozainanee Mohd Zain, Fatin Norhasny Leman, Huan-Keat Chan, Muhammad Radzi Abu Hassan, Shahnaz Murad

Abstract readMulticenter StudyClinical Trial, Phase IIClinical Trial, Phase III
In one paragraph

Trial report in Scientific reports, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Trial
  2. 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

8 authors.

Nor Asiah MuhamadSector for Evidence-Based Healthcare, National Institutes of Health, Ministry of Health, Selangor, Malaysia. norasiahdr@gmail.com.
Izzah Athirah RosliSector for Evidence-Based Healthcare, National Institutes of Health, Ministry of Health, Selangor, Malaysia.
Nur Hasnah MaamorSector for Evidence-Based Healthcare, National Institutes of Health, Ministry of Health, Selangor, Malaysia.
Rozainanee Mohd ZainInstitute for Medical Research, National Institutes of Health, Ministry of Health, Selangor, Malaysia.
Fatin Norhasny LemanSector for Evidence-Based Healthcare, National Institutes of Health, Ministry of Health, Selangor, Malaysia.
Huan-Keat ChanOffice of the Director General of Health, Ministry of Health, Putrajaya, Malaysia.
Muhammad Radzi Abu HassanOffice of the Director General of Health, Ministry of Health, Putrajaya, Malaysia.
Shahnaz MuradFormer Office of the Deputy Director General of Health (Research and Technical Support), Ministry of Health, Putrajaya, Malaysia.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

A study indicated that ravidasvir (RDV) has excellent safety and tolerability when used with sofosbuvir (SOF) to treat chronic HCV infection. The aim of this study was to determine the time taken by RDV/SOF to achieve optimum viral load suppression in chronic hepatitis C patients with or without compensated cirrhosis. Data from the open-label, multicentre, single-arm, phase II/III clinical trial (STORM-C-1) were utilized. Time‒to-event analysis via Kaplan-Meier curves was performed to determine the time required to achieve optimum viral load suppression in both the cirrhotic and noncirrhotic groups. Multivariate logistic regression analyses were performed to identify potential predictors of achieving suppression within four and eight weeks. The time to achieve optimum viral load suppression ranged from six to 85 days and from five to 148 days among noncirrhotic and cirrhotic patients, respectively. Among noncirrhotic patients, 80.6% achieved optimum viral load suppression within 4 weeks, and 92.6% achieved this within 8 weeks. Among cirrhotic patients, 76.1% and 90.4% achieved optimum viral load suppression within 4 and 8 weeks, respectively. Notably, optimum viral load suppression differs from sustained virological response (SVR12), which is defined as undetectable HCV RNA 12 weeks after treatment completion. While the study demonstrates promising early viral suppression, it does not evaluate the efficacy of a shortened regimen. Further research is needed to assess whether shorter treatment durations maintain high SVR12 rates without compromising treatment success.

Indexed as

Antiviral AgentsHepatitis C, ChronicLiver CirrhosisSofosbuvirViral LoadAdultAgedBenzimidazolesDrug Therapy, CombinationFemaleHepacivirusHumansMaleMiddle AgedTime FactorsTreatment OutcomeAntiviral AgentsBenzimidazolesravidasvirSofosbuvirValineHepatitisRavidasvirSofosbuvirSTORM-C-1Time-to-eventVirologic response

Identifiers

PMID40281127
PMCPMC12032149

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Registered trials

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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.