Evidence map›Paper›PMID 32290293›Full record

ReviewInternational journal of molecular sciences2020

A Review of SARS-CoV-2 and the Ongoing Clinical Trials.

Yung-Fang Tu, Chian-Shiu Chien, Aliaksandr A Yarmishyn, Yi-Ying Lin, Yung-Hung Luo, Yi-Tsung Lin, Wei-Yi Lai, De-Ming Yang, Shih-Jie Chou, Yi-Ping Yang and 2 more

2 registry-linked trialsOpen access · goldAbstract readReview
In one paragraph

Review in International journal of molecular sciences, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to 2 registered trials, which are not on this map. Cited by 340 papers, 5 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
340citing papers in PubMed, 5 pooled it
17.6field-weighted citation impact, top 1% 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.

NCT04798716 phase1 / phase2unknown statusnot on this mapstarted 2023, after this paper: background citation

Mesenchymal Stem Cell Exosomes for the Treatment of COVID-19 Positive Patients With Acute Respiratory Distress Syndrome and/or Novel Coronavirus Pneumonia

TypeinterventionalSponsorAVEM HealthCareRan2023 to 2024Enrolled55ConditionsCovid19, Novel Coronavirus Pneumonia, Acute Respiratory Distress SyndromeArmsMSC-exosomes delivered intravenously every other day on an escalating dose: (2:4:8), MSC-exosomes delivered intravenously every other day on an escalating dose (8:4:8), MSC-exosomes delivered intravenously every other day (8:8:8)
NCT05739513 nacompletednot on this map

A Specific miRNA Encoded by SARS-CoV-2 as a Diagnostic Tool to Predict Disease Severity in COVID-19 Patients

TypeinterventionalSponsorFondazione Policlinico Universitario Agostino Gemelli IRCCSRan2020 to 2021Enrolled120ConditionsCOVID-19ArmsmiRNA analysis in plasma
3 · Its place in the literature

Who cites it

340 citing papers in PubMed, 5 syntheses or guidelines pooled it, 720 citations in OpenAlex.

  1. Globally approved vaccines for COVID-19: a systematic review.Brazilian journal of microbiology : [publication of the Brazilian Society for Microbiology] · 2025
    Pooled it
  2. Pooled it
  3. Pooled it
  4. Recent advances in the diagnosis of COVID-19: a bird's eye view.Expert review of molecular diagnostics · 2021
    Pooled it
  5. Pooled it
  6. Trial
  7. Review
  8. Review
  9. Article
  10. Article
  11. Article
  12. Review
  13. Article
  14. Review
  15. Article
  16. The One Health Concept.British journal of biomedical science · 2024
    Review
  17. Potential Drugs in COVID-19 Management.Current medicinal chemistry · 2024
    Review
  18. Review
  19. Article
  20. Review

280 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

12 authors at 2 institutions in 1 country.

Yung-Fang TuDepartment of Medical Research, Taipei Veterans General Hospital, Taipei 11217, Taiwan.
Chian-Shiu ChienDepartment of Medical Research, Taipei Veterans General Hospital, Taipei 11217, Taiwan.
Aliaksandr A YarmishynDepartment of Medical Research, Taipei Veterans General Hospital, Taipei 11217, Taiwan.
Yi-Ying LinDepartment of Medical Research, Taipei Veterans General Hospital, Taipei 11217, Taiwan.
Yung-Hung LuoSchool of Medicine, National Yang-Ming University, Taipei 11221, Taiwan.
Yi-Tsung LinSchool of Medicine, National Yang-Ming University, Taipei 11221, Taiwan.
Wei-Yi LaiDepartment of Medical Research, Taipei Veterans General Hospital, Taipei 11217, Taiwan.
De-Ming YangDepartment of Medical Research, Taipei Veterans General Hospital, Taipei 11217, Taiwan.
Shih-Jie ChouDepartment of Medical Research, Taipei Veterans General Hospital, Taipei 11217, Taiwan.
Yi-Ping YangDepartment of Medical Research, Taipei Veterans General Hospital, Taipei 11217, Taiwan.
Mong-Lien WangDepartment of Medical Research, Taipei Veterans General Hospital, Taipei 11217, Taiwan.
Shih-Hwa ChiouDepartment of Medical Research, Taipei Veterans General Hospital, Taipei 11217, Taiwan.
National Yang Ming Chiao Tung University · TWTaipei Veterans General Hospital · TW

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The sudden outbreak of 2019 novel coronavirus (2019-nCoV, later named SARS-CoV-2) in Wuhan, China, which rapidly grew into a global pandemic, marked the third introduction of a virulent coronavirus into the human society, affecting not only the healthcare system, but also the global economy. Although our understanding of coronaviruses has undergone a huge leap after two precedents, the effective approaches to treatment and epidemiological control are still lacking. In this article, we present a succinct overview of the epidemiology, clinical features, and molecular characteristics of SARS-CoV-2. We summarize the current epidemiological and clinical data from the initial Wuhan studies, and emphasize several features of SARS-CoV-2, which differentiate it from SARS-CoV and Middle East respiratory syndrome coronavirus (MERS-CoV), such as high variability of disease presentation. We systematize the current clinical trials that have been rapidly initiated after the outbreak of COVID-19 pandemic. Whereas the trials on SARS-CoV-2 genome-based specific vaccines and therapeutic antibodies are currently being tested, this solution is more long-term, as they require thorough testing of their safety. On the other hand, the repurposing of the existing therapeutic agents previously designed for other virus infections and pathologies happens to be the only practical approach as a rapid response measure to the emergent pandemic, as most of these agents have already been tested for their safety. These agents can be divided into two broad categories, those that can directly target the virus replication cycle, and those based on immunotherapy approaches either aimed to boost innate antiviral immune responses or alleviate damage induced by dysregulated inflammatory responses. The initial clinical studies revealed the promising therapeutic potential of several of such drugs, including

Indexed as

BetacoronavirusCoronavirus InfectionsPandemicsPneumonia, ViralViral VaccinesAntiviral AgentsClinical Trials as TopicCOVID-19COVID-19 Drug TreatmentCOVID-19 SerotherapyCOVID-19 VaccinesGenome, ViralHumansImmunization, PassiveImmunologic FactorsSARS-CoV-2Antiviral AgentsCOVID-19 VaccinesImmunologic FactorsViral VaccinesACE2clinical trialsCOVID-19immunotherapypneumoniareplicaseSARS-CoV-2vaccine

Identifiers

PMID32290293
PMCPMC7177898
OpenAlexW3015807479

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

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.