Evidence map›Paper›PMID 31712214›Full record

Trial reportAntimicrobial agents and chemotherapy2020

A Randomized, Placebo-Controlled, Respiratory Syncytial Virus Human Challenge Study of the Antiviral Efficacy, Safety, and Pharmacokinetics of RV521, an Inhibitor of the RSV-F Protein.

John DeVincenzo, Dereck Tait, John Efthimiou, Julie Mori, Young-In Kim, Elaine Thomas, Lynn Wilson, Rachel Harland, Neil Mathews, Stuart Cockerill and 2 more

Open access · hybridAbstract readRandomized Controlled Trial
In one paragraph

Trial report in Antimicrobial agents and chemotherapy, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 48 papers.

0numbers the graph read from it
0cells of the map it votes in
48citing papers in PubMed
4.8field-weighted citation impact, top 4% 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

48 citing papers in PubMed, 85 citations in OpenAlex.

  1. Trial
  2. Trial
  3. Trial
  4. Trial
  5. Article
  6. Review
  7. Review
  8. Article
  9. Review
  10. Review
  11. Review
  12. Review
  13. Article
  14. Article
  15. Article
  16. Review
  17. Review
  18. Review
  19. Article
  20. 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

12 authors at 3 institutions in 2 countries.

John DeVincenzoUniversity of Tennessee Center for Health Sciences, Memphis, Tennessee, USA jdevince@uthsc.edu.
Dereck TaitReViral Ltd., Stevenage, Hertfordshire, United Kingdom.
John EfthimiouIndependent Respiratory Specialist, Oxford, United Kingdom.
Julie MorihVIVO Services Limited, London, United Kingdom.
Young-In KimUniversity of Tennessee Center for Health Sciences, Memphis, Tennessee, USA.
Elaine ThomasReViral Ltd., Stevenage, Hertfordshire, United Kingdom.
Lynn WilsonReViral Ltd., Stevenage, Hertfordshire, United Kingdom.
Rachel HarlandReViral Ltd., Stevenage, Hertfordshire, United Kingdom.
Neil MathewsReViral Ltd., Stevenage, Hertfordshire, United Kingdom.
Stuart CockerillReViral Ltd., Stevenage, Hertfordshire, United Kingdom.
Kenneth PowellReViral Ltd., Stevenage, Hertfordshire, United Kingdom.
Edward LittlerReViral Ltd., Stevenage, Hertfordshire, United Kingdom.
hVIVO (United Kingdom) · GBLe Bonheur Children's Hospital · USUniversity of Tennessee Health Science Center · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Effective treatments for respiratory syncytial virus (RSV) infection are lacking. Here, we report a human proof-of-concept study for RV521, a small-molecule antiviral inhibitor of the RSV-F protein. In this randomized, double-blind, placebo-controlled trial, healthy adults were challenged with RSV-A Memphis-37b. After infection was confirmed (or 5 days after challenge virus inoculation), subjects received RV521 (350 mg or 200 mg) or placebo orally every 12 h for 5 days. The primary endpoint was area under the curve (AUC) for viral load, as assessed by reverse transcriptase quantitative PCR (RT-qPCR) of nasal wash samples. The primary efficacy analysis set included subjects successfully infected with RSV who received ≥1 dose of study drug. A total of 66 subjects were enrolled (

Indexed as

AdolescentAdultAntiviral AgentsArea Under CurveDouble-Blind MethodFemaleHumansMaleMiddle AgedPlacebosRespiratory Syncytial Virus, HumanRespiratory Syncytial Virus InfectionsSeverity of Illness IndexTreatment OutcomeViral Fusion ProteinsViral LoadAntiviral AgentsF protein, human respiratory syncytial virusPlacebosViral Fusion Proteinsantiviralrespiratory syncytial virusRV521

Identifiers

PMID31712214
PMCPMC6985722
OpenAlexW2985960182

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.