Evidence map›Paper›PMID 33235105›Full record

Trial reportMedicine2020

First clinical study using HCV protease inhibitor danoprevir to treat COVID-19 patients.

Hongyi Chen, Zhicheng Zhang, Li Wang, Zhihua Huang, Fanghua Gong, Xiaodong Li, Yahong Chen, Jinzi J Wu

Open access · goldAbstract readClinical Trial
In one paragraph

Trial report in Medicine, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 74 papers, 4 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
74citing papers in PubMed, 4 pooled it
2.1field-weighted citation impact, top 7% 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

74 citing papers in PubMed, 4 syntheses or guidelines pooled it, 93 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. Pooled it
  4. Pooled it
  5. Article
  6. Article
  7. Article
  8. Article
  9. Review
  10. Review
  11. Article
  12. Review
  13. Review
  14. Article
  15. Article
  16. Small molecules in the treatment of COVID-19.Signal transduction and targeted therapy · 2022
    Review
  17. Review
  18. Review
  19. Article
  20. Identification of potential SARS-CoV-2 MJournal of biomolecular structure & dynamics · 2022
    Article

14 more citing papers are in PubMed but not listed here.

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 at 4 institutions in 3 countries.

Hongyi ChenThe First Department of Infectious Disease.
Zhicheng ZhangThe Intensive Care Unit.
Li WangThe First Department of Infectious Disease.
Zhihua HuangThe Radiology Department.
Fanghua GongThe Second Department of Infectious Disease, The Ninth Hospital of Nanchang, Nanchang 330002, Jiangxi Province.
Xiaodong LiAscletis Bioscience Co., Ltd., Hangzhou 310051.
Yahong ChenAscletis Bioscience Co., Ltd., Hangzhou 310051.
Jinzi J WuAscletis Bioscience Co., Ltd., Hangzhou 310051.
Bioscience (China) · CNIntensive Care Society · GBNinth Hospital of Nanchang · CNUniversity Radiology · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

introductionAs coronavirus disease 2019 (COVID-19) outbreak globally, repurposing approved drugs is emerging as important therapeutic options. Danoprevir boosted by ritonavir (Ganovo) is a potent hepatitis C virus (HCV) protease (NS3/4A) inhibitor, which was approved and marketed in China since 2018 to treat chronic hepatitis C patients.

methodsThis is an open-label, single arm study evaluating the effects of danoprevir boosted by ritonavir on treatment naïve and experienced COVID-19 patients for the first time. Patients received danoprevir boosted by ritonavir (100 mg/100 mg, twice per day). The primary endpoint was the rate of composite adverse outcomes and efficacy was also evaluated.

resultsThe data showed that danoprevir boosted by ritonavir is safe and well tolerated in all patients. No patient had composite adverse outcomes during this study. After initiation of danoprevir/ritonavir treatment, the first negative reverse real-time PCR (RT-PCR) test occurred at a median of 2 days, ranging from 1 to 8 days, and the obvious absorption in CT scans occurred at a median 3 days, ranging from 2 to 4 days. After 4 to 12-day treatment of danoprevir boosted by ritonavir, all enrolled 11 patients were discharged from the hospital.

conclusionOur findings suggest that repurposing danoprevir for COVID-19 is a promising therapeutic option.

Indexed as

COVID-19 Drug TreatmentAdolescentAdultAgedAntiviral AgentsCOVID-19CyclopropanesDrug Therapy, CombinationFemaleHumansIsoindolesLactams, MacrocyclicMaleMiddle AgedPandemicsProlineAntiviral AgentsCyclopropanesdanoprevirIsoindolesLactams, MacrocyclicProlineRitonavirSulfonamides

Identifiers

PMID33235105
PMCPMC7710192
OpenAlexW3110533165

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.