Evidence map›Paper›PMID 33930706›Full record

Trial reportInternational immunopharmacology2021

Favipiravir in the treatment of patients with SARS-CoV-2 RNA recurrent positive after discharge: A multicenter, open-label, randomized trial.

Hong Zhao, Chi Zhang, Qi Zhu, Xianxiang Chen, Guilin Chen, Wenjin Sun, Zuohan Xiao, Weijun Du, Jing Yao, Guojun Li and 15 more

Open access · greenAbstract readMulticenter StudyRandomized Controlled Trial
In one paragraph

Trial report in International immunopharmacology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers, 5 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed, 5 pooled it
2.3field-weighted citation impact, top 9% 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

23 citing papers in PubMed, 5 syntheses or guidelines pooled it, 42 citations in OpenAlex.

  1. Pooled it
  2. The efficacy and adverse effects of favipiravir on patients with COVID-19: A systematic review and meta-analysis of published clinical trials and observational studies.International journal of infectious diseases : IJID : official publication of the International Society for Infectious Diseases · 2022
    Pooled it
  3. Pooled it
  4. Effectiveness of favipiravir in COVID-19: a live systematic review.European journal of clinical microbiology & infectious diseases : official publication of the European Society of Clinical Microbiology · 2021
    Pooled it
  5. Pooled it
  6. Trial
  7. Article
  8. Review
  9. Antivirals in COVID-19: A Focus on Pediatric Cardiac Patients.The Canadian journal of infectious diseases & medical microbiology = Journal canadien des maladies infectieuses et de la microbiologie medicale · 2025
    Review
  10. Review
  11. Article
  12. Molecules (Basel, Switzerland) · 2023
    Article
  13. Review
  14. Severe COVID-19: Drugs and Clinical Trials.Journal of clinical medicine · 2023
    Review
  15. Article
  16. Article
  17. Baseline uric acid levels and steady-state favipiravir concentrations are associated with occurrence of hyperuricemia among COVID-19 patients.International journal of infectious diseases : IJID : official publication of the International Society for Infectious Diseases · 2022
    Article
  18. Article
  19. Article
  20. Emerging small molecule antivirals may fit neatly into COVID-19 treatment.Drugs & therapy perspectives : for rational drug selection and use · 2022
    Review
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

25 authors at 8 institutions in 1 country.

Hong ZhaoDepartment of Infectious Disease, Center for Liver Disease, Peking University First Hospital, Beijing, China; Department of Infectious Disease, Peking University International Hospital, Beijing, China.
Chi ZhangDepartment of Infectious Disease, Center for Liver Disease, Peking University First Hospital, Beijing, China.
Qi ZhuDepartment of Tuberculosis, Wuhan Pulmonary Hospital, Wuhan, China.
Xianxiang ChenAdministrative Office, Wuhan Pulmonary Hospital, Wuhan, China.
Guilin ChenDepartment of Tuberculosis, Wuhan Pulmonary Hospital, Wuhan, China.
Wenjin SunDepartment of Infectious Disease, Ezhou Central Hospital, Ezhou, China.
Zuohan XiaoDepartment of Infectious Disease, Ezhou Central Hospital, Ezhou, China.
Weijun DuDepartment of Internal Medicine, Fankou Branch of Ezhou Central Hospital, Ezhou, China.
Jing YaoDepartment of Obstetrics and Gynecology, Fankou Branch of Ezhou Central Hospital, Ezhou, China.
Guojun LiDepartment of Hepatology III, The Third People's Hospital of Shenzhen, Shenzhen, China.
Yanhua JiDepartment of Hepatology III, The Third People's Hospital of Shenzhen, Shenzhen, China.
Niuniu LiDepartment of Hepatology III, The Third People's Hospital of Shenzhen, Shenzhen, China.
Yujin JiangDepartment of Hepatology III, The Third People's Hospital of Shenzhen, Shenzhen, China.
Ying WangDepartment of Hepatology III, The Third People's Hospital of Shenzhen, Shenzhen, China.
Qingjin ZengDepartment of Hepatology III, The Third People's Hospital of Shenzhen, Shenzhen, China.
Wei LiDepartment of Respiratory Medicine, The First Affiliated Hospital of Bengbu Medical College, Bengbu, China.
Beilei GongDepartment of Respiratory Medicine, The First Affiliated Hospital of Bengbu Medical College, Bengbu, China.
Xianyou ChangDepartment of Respiratory Medicine, Bengbu Fifth People's Hospital, Bengbu, China.
Feng ZhuDepartment of Respiratory Medicine, Wuxi Fifth People's Hospital, Wuxi, China.
Xiufeng JiangDepartment of Respiratory Medicine, Wuxi Fifth People's Hospital, Wuxi, China.
Jiawen LiDepartment of Infectious Disease, Center for Liver Disease, Peking University First Hospital, Beijing, China.
Zhao WuDepartment of Infectious Disease, Center for Liver Disease, Peking University First Hospital, Beijing, China.
Yingxia LiuAdministrative Office, The Third People's Hospital of Shenzhen, Shenzhen, China. Electronic address: yingxialiu@hotmai.com.
Peng PengAdministrative Office, Wuhan Pulmonary Hospital, Wuhan, China. Electronic address: PengPengwg@126.com.
Guiqiang WangDepartment of Infectious Disease, Center for Liver Disease, Peking University First Hospital, Beijing, China; Department of Infectious Disease, Peking University International Hospital, Beijing, China. Electronic address: john131212@126.com.
Shenzhen Third People’s Hospital · CNEzhou Central Hospital · CNFirst Affiliated Hospital of Bengbu Medical College · CNWuhan Pulmonary Hospital · CNPeking University First Hospital · CNWuxi People's Hospital · CNBengbu Medical College · CNPeking University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundThe clinical characteristics and treatment of patients who tested positive for COVID-19 after recovery remained elusive. Effective antiviral therapy is important for tackling these patients. We assessed the efficacy and safety of favipiravir for treating these patients.

methodsThis is a multicenter, open-label, randomized controlled trial in SARS-CoV-2 RNA re-positive patients. Patients were randomly assigned in a 2:1 ratio to receive either favipiravir, in addition to standard care, or standard care alone. The primary outcome was time to achieve a consecutive twice (at intervals of more than 24 h) negative RT-PCR result for SARS-CoV-2 RNA in nasopharyngeal swab and sputum sample.

resultsBetween March 27 and May 9, 2020, 55 patients underwent randomization; 36 were assigned to the favipiravir group and 19 were assigned to the control group. Favipiravir group had a significantly shorter time from start of study treatment to negative nasopharyngeal swab and sputum than control group (median 17 vs. 26 days); hazard ratio 2.1 (95% CI [1.1-4.0], p = 0.038). The proportion of virus shedding in favipiravir group was higher than control group (80.6% [29/36] vs. 52.6% [10/19], p = 0.030, respectively). C-reactive protein decreased significantly after treatment in the favipiravir group (p = 0.016). The adverse events were generally mild and self-limiting.

conclusionFavipiravir was safe and superior to control in shortening the duration of viral shedding in SARS-CoV-2 RNA recurrent positive after discharge. However, a larger scale and randomized, double-blind, placebo-controlled trial is required to confirm our conclusion.

Indexed as

COVID-19 Drug TreatmentAdministration, OralAdultAgedAmidesAntiviral AgentsCOVID-19FemaleHumansLymphocyte SubsetsMaleMiddle AgedPatient DischargePyrazinesReinfectionRNA, ViralAmidesAntiviral AgentsfavipiravirPyrazinesRNA, ViralCOVID-19FavipiravirRecurrent positiveSARS-CoV-2

Identifiers

PMID33930706
PMCPMC8059985
OpenAlexW3158369907

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.