Evidence map›Paper›PMID 21369346›Full record

ReviewViruses2011

Efficacy of CMX001 as a prophylactic and presymptomatic antiviral agent in New Zealand white rabbits infected with rabbitpox virus, a model for orthopoxvirus infections of humans.

Amanda D Rice, Mathew M Adams, Bernhard Lampert, Scott Foster, Alice Robertson, George Painter, Richard W Moyer

Open access · goldAbstract readReview
In one paragraph

Review in Viruses, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed
1.4field-weighted citation impact, top 22% 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

22 citing papers in PubMed, 53 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. Managing Monkeypox Virus Infections: A Contemporary Review.Iranian journal of medical sciences · 2024
    Review
  4. Review
  5. Comprehensive literature review of monkeypox.Emerging microbes & infections · 2022
    Review
  6. Monkeypox: epidemiology, pathogenesis, treatment and prevention.Signal transduction and targeted therapy · 2022
    Review
  7. Therapeutic strategies to address monkeypox.Expert review of anti-infective therapy · 2022
    Article
  8. Article
  9. Article
  10. Article
  11. Skin lesions caused byPostepy dermatologii i alergologii · 2020
    Article
  12. Drug Development against Smallpox: Present and Future.Antimicrobial agents and chemotherapy · 2020
    Review
  13. Review
  14. Article
  15. Article
  16. Article
  17. Article
  18. Review
  19. Article
  20. Poxvirus DNA replication.Cold Spring Harbor perspectives in biology · 2013
    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

7 authors at 2 institutions in 1 country.

Amanda D RiceDepartment of Molecular Genetics and Microbiology, University of Florida, Gainesville, FL 32610, USA. amandar@ufl.edu
Mathew M Adams
Bernhard Lampert
Scott Foster
Alice Robertson
George Painter
Richard W Moyer
Chimerix (United States) · USUniversity of Florida · US

Funding

DEVELOPMENT OF AN ORAL DRUG FOR SMALLPOX TREATMENTU01AI057233 · NIAID · CHIMERIX, INC. · PI PAINTER, GEORGE R · 2003 to 2007
$36.3M
NIAID NIH HHS U01 AI057233
6 · The paper itself

Abstract

CMX001, a lipophilic nucleotide analog formed by covalently linking 3-(hexdecyloxy)propan-1-ol to cidofovir (CDV), is being developed as a treatment for smallpox. CMX001 has dramatically increased potency versus CDV against all dsDNA viruses and, in contrast to CDV, is orally available and has shown no evidence of nephrotoxicity in healthy volunteers or severely ill transplant patients to date. Although smallpox has been eliminated from the environment, treatments are urgently being sought due to the risk of smallpox being used as a bioterrorism agent and for monkeypox virus, a zoonotic disease of Africa, and adverse reactions to smallpox virus vaccinations. In the absence of human cases of smallpox, new treatments must be tested for efficacy in animal models. Here we first review and discuss the rabbitpox virus (RPV) infection of New Zealand White rabbits as a model for smallpox to test the efficacy of CMX001 as a prophylactic and early disease antiviral. Our results should also be applicable to monkeypox virus infections and for treatment of adverse reactions to smallpox vaccination.

Indexed as

AnimalsAntiviral AgentsBioterrorismCytosineDisease Models, AnimalDisease Transmission, InfectiousHumansMpox, MonkeypoxOrganophosphonatesRabbitsSmallpoxSmallpox VaccineVaccinia virusAntiviral AgentsbrincidofovirCytosineOrganophosphonatesSmallpox VaccineantiviralCMX001poxvirusrabbitpoxsmallpox treatment

Identifiers

PMID21369346
PMCPMC3045966
OpenAlexW2055062957

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.