Evidence map›Paper›PMID 20923374›Full record

ArticleThe Journal of infectious diseases2010

Efficacy of CMX001 against herpes simplex virus infections in mice and correlations with drug distribution studies.

Debra C Quenelle, Bernhardt Lampert, Deborah J Collins, Terri L Rice, George R Painter, Earl R Kern

Open access · greenAbstract read
In one paragraph

Article in The Journal of infectious diseases, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 36 papers.

0numbers the graph read from it
0cells of the map it votes in
36citing papers in PubMed
4.7field-weighted citation impact, top 5% 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

36 citing papers in PubMed, 76 citations in OpenAlex.

  1. A Randomized, Double-Blind, Placebo-Controlled Phase 3 Trial of Oral Brincidofovir for Cytomegalovirus Prophylaxis in Allogeneic Hematopoietic Cell Transplantation.Biology of blood and marrow transplantation : journal of the American Society for Blood and Marrow Transplantation · 2019
    Trial
  2. Article
  3. Article
  4. Article
  5. Review
  6. Review
  7. Article
  8. Monkeypox: epidemiology, pathogenesis, treatment and prevention.Signal transduction and targeted therapy · 2022
    Review
  9. Article
  10. Article
  11. Review
  12. Review
  13. Review
  14. Antiviral Properties ofFrontiers in pharmacology · 2019
    Article
  15. Article
  16. Article
  17. Review
  18. Brincidofovir for polyomavirus-associated nephropathy after allogeneic hematopoietic stem cell transplantation.American journal of kidney diseases : the official journal of the National Kidney Foundation · 2015
    Article
  19. Article
  20. Antiviral Drug- and Multidrug Resistance in Cytomegalovirus Infected SCT Patients.Computational and structural biotechnology journal · 2015
    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

6 authors at 2 institutions in 1 country.

Debra C QuenelleThe University of Alabama at Birmingham School of Medicine, Birmingham, Alabama 35233-1711, USA. dquenelle@peds.uab.edu
Bernhardt Lampert
Deborah J Collins
Terri L Rice
George R Painter
Earl R Kern
University of Alabama at Birmingham · USChimerix (United States) · US

Funding

NIAID NIH HHS N01 AI015439NIAID NIH HHS N01 AI030049NIAID NIH HHS N0I-AI-15439NIAID NIH HHS N0I-AI-30049
6 · The paper itself

Abstract

CMX001, an orally active lipid conjugate of cidofovir, is 50 times more active in vitro against herpes simplex virus (HSV) replication than acyclovir or cidofovir. These studies compared the efficacy of CMX001 to acyclovir in BALB/c mice inoculated intranasally with HSV types 1 or 2. CMX001 was effective in reducing mortality using doses of 5 to 1.25 mg/kg administered orally once daily, even when treatments were delayed 48-72 h post viral inoculation. Organ samples obtained from mice treated with CMX001 had titers 3-5 log(10) plaque-forming units per gram of tissue lower than samples obtained from mice treated with acyclovir, including 5 different regions of the brain. Detectable concentrations of drug-related radioactivity were documented in the central nervous system of mice after oral administration of (14)C-CMX001. These studies indicate that CMX001 penetrates the blood-brain barrier, is a potent inhibitor of HSV replication in disseminated infections and central nervous system infections, and is superior to acyclovir.

Indexed as

Herpesvirus 1, HumanHerpesvirus 2, HumanAdministration, OralAnimalsAntiviral AgentsCytosineDisease Models, AnimalDrug Evaluation, PreclinicalFemaleHerpes SimplexMiceMice, Inbred BALB COrganophosphonatesTissue DistributionAntiviral AgentsbrincidofovirCytosineOrganophosphonates

Identifiers

PMID20923374
PMCPMC2957530
OpenAlexW2164098750

What OpenQuestion holds

Textmetadata
LicenceTDM
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.