Evidence map›Paper›PMID 29017263›Full record

ReviewClinical infectious diseases : an official publication of the Infectious Diseases Society of America2017

Progress in the Fight Against Multidrug-Resistant Bacteria 2005-2016: Modern Noninferiority Trial Designs Enable Antibiotic Development in Advance of Epidemic Bacterial Resistance.

John H Rex, George H Talbot, Mark J Goldberger, Barry I Eisenstein, Roger M Echols, John F Tomayko, Michael N Dudley, Aaron Dane

Open access · hybridAbstract readReview
In one paragraph

Review in Clinical infectious diseases : an official publication of the Infectious Diseases Society of America, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 28 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
28citing papers in PubMed, 1 pooled it
8.0field-weighted citation impact, top 2% 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

28 citing papers in PubMed, 1 synthesis or guideline pooled it, 63 citations in OpenAlex.

  1. Pooled it
  2. Review
  3. Article
  4. Review
  5. Review
  6. Global Pull Incentives for Better Antibacterials: The UK Leads the Way.Applied health economics and health policy · 2023
    Article
  7. Review
  8. Review
  9. Review
  10. Article
  11. Understanding Early and Late Endpoints in Registrational Trials of Community-acquired Bacterial Pneumonia.Clinical infectious diseases : an official publication of the Infectious Diseases Society of America · 2021
    Article
  12. Article
  13. Article
  14. Article
  15. Article
  16. Article
  17. Review
  18. Article
  19. A shot in the arm for new antibiotics.Nature biotechnology · 2019
    Article
  20. 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

8 authors at 5 institutions in 1 country.

John H RexF2G, Ltd, Eccles, United Kingdom.
George H TalbotTalbot Advisors LLC, Anna Maria, Florida.
Mark J GoldbergerMark Goldberger MD MPH LLC, Potomac, Maryland.
Barry I EisensteinCARB-X, Boston, Massachusetts.
Roger M EcholsInfectious Disease Drug Development Consulting, LLC, Easton, Connecticut.
John F TomaykoSpero Therapeutics, Cambridge, Massachusetts.
Michael N DudleyThe Medicines Company, San Diego, California.
Aaron DaneDaneStat Consulting, Macclesfield, United Kingdom.
Doctors Company (United States) · USHealthcentric Advisors · USInfectious Disease Consultants · USSpero Therapeutics (United States) · USWolstan & Goldberg Eye Associates · US

Funding

Wellcome Trust
6 · The paper itself

Abstract

From a public health perspective, new antibacterial agents should be evaluated and approved for use before widespread resistance to existing agents emerges. However, for multidrug-resistant pathogens, demonstration of superior efficacy of a new agent over a current standard-of-care agent is routinely feasible only when epidemic spread of these dangerous organisms has already occurred. One solution to enable proactive drug development is to evaluate new antibiotics with improved in vitro activity against MDR pathogens using recently updated guidelines for active control, noninferiority trials of selected severe infections caused by more susceptible pathogens. Such trials are feasible because they enroll patients with infections due to pathogens with a "usual drug resistance" phenotype that will be responsive to widely registered standard-of-care comparator antibiotics. Such anticipatory drug development has constructively reshaped the antibiotic pipeline and offers the best chance of making safe and efficacious antibiotics available to the public ahead of epidemic resistance.

Indexed as

Clinical Trials as TopicDrug DiscoveryDrug Resistance, Multiple, BacterialAnti-Bacterial AgentsBacteriaBacterial InfectionsHumansAnti-Bacterial Agentsantibacterial drug developmentantimicrobial drug resistancebacterial resistancenoninferiority trial design

Identifiers

PMID29017263
PMCPMC5850636
OpenAlexW2616409827

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.