Evidence map›Paper›PMID 26941282›Full record

Trial reportThe Journal of infectious diseases2016

Analysis of Mutations in the Gene Encoding Cytomegalovirus DNA Polymerase in a Phase 2 Clinical Trial of Brincidofovir Prophylaxis.

E Randall Lanier, Scott Foster, Tom Brundage, Sunwen Chou, Mark N Prichard, Steven Kleiboeker, Chad Wilson, Donella Colville, Herve Mommeja-Marin

Registry-linked trialOpen access · hybridAbstract readClinical Trial, Phase IIComparative StudyMulticenter Study
In one paragraph

Trial report in The Journal of infectious diseases, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT00942305 (A Multicenter, Randomized, Double-blind, Placebo-controlled, Dose-escalation Study of the Safety, Tolerability and Ability of CMX001 to Prevent or Control CMV Infection in R+ Hematopoietic Stem Cell Transplant Recipients), which is not on this map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
2.1field-weighted citation impact, top 13% 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.

NCT00942305 phase2completednot on this map

A Multicenter, Randomized, Double-blind, Placebo-controlled, Dose-escalation Study of the Safety, Tolerability and Ability of CMX001 to Prevent or Control CMV Infection in R+ Hematopoietic Stem Cell Transplant Recipients

TypeinterventionalSponsorJazz PharmaceuticalsRan2009 to 2012Enrolled239ConditionsCytomegalovirus InfectionArmsBrincidofovir, Placebo
3 · Its place in the literature

Who cites it

9 citing papers in PubMed, 16 citations in OpenAlex.

  1. Article
  2. Review
  3. Anti-CMV therapy, what next? A systematic review.Frontiers in microbiology · 2023
    Review
  4. Review
  5. Antiviral Drugs Against Herpesviruses.Advances in experimental medicine and biology · 2021
    Article
  6. Review
  7. Article
  8. Article
  9. Article
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

9 authors at 3 institutions in 1 country.

E Randall LanierChimerix, Durham, North Carolina.
Scott FosterChimerix, Durham, North Carolina.
Tom BrundageChimerix, Durham, North Carolina.
Sunwen ChouDivision of Infectious Diseases, Oregon Health and Science University Department of Veterans Affairs Medical Center, Portland, Oregon.
Mark N PrichardDepartment of Pediatrics, University of Alabama at Birmingham.
Steven KleiboekerViracor-IBT Laboratories, Lee's Summit, Missouri.
Chad WilsonChimerix, Durham, North Carolina.
Donella ColvilleChimerix, Durham, North Carolina.
Herve Mommeja-MarinChimerix, Durham, North Carolina.
Chimerix (United States) · USOregon Health & Science University · USUniversity of Alabama at Birmingham · US

Funding

Alternative antiviral drug targets for human cytomegalovirus infectionI01BX000925 · VA · PORTLAND VA MEDICAL CENTER · PI CHOU, SUNWEN · 2011 to 2014
–
BLRD VA I01 BX000925
6 · The paper itself

Abstract

Brincidofovir is an oral antiviral in development for prevention of cytomegalovirus disease. Cytomegalovirus genotyping results from a phase 2 trial comparing brincidofovir to placebo for prophylaxis against cytomegalovirus infection in hematopoietic cell transplant recipients provided initial data on the clinical resistance profile for brincidofovir. In this study, no known resistance-associated mutations were detected in brincidofovir-treated subjects; identified genotypic substitutions did not confer resistance to cytomegalovirus antivirals in vitro, suggesting that these changes represent polymorphisms unrelated to brincidofovir resistance. Lack of evidence for genotypic resistance during prophylaxis suggests that first-line use of brincidofovir for prevention of cytomegalovirus infection may preserve downstream options for patients.

Indexed as

Transplant RecipientsAntiviral AgentsCytomegalovirusCytomegalovirus InfectionsCytosineDNA-Directed DNA PolymeraseDrug Resistance, ViralFemaleGenotypeHematopoietic Stem Cell TransplantationHumansImmunocompromised HostMaleMutationUnited StatesAntiviral AgentsCytosineDNA-Directed DNA PolymerasebrincidofovirCMVCMV (DNA) polymeraseCMV phosphotransferasecytomegalovirusstem cell transplantationUL54UL97

Identifiers

PMID26941282
PMCPMC4907407
OpenAlexW2319786453

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.