Evidence map›Paper›PMID 36411033›Full record

ReviewSexually transmitted infections2023

Dose selection for a phase III study evaluating gepotidacin (GSK2140944) in the treatment of uncomplicated urogenital gonorrhoea.

Nicole E Scangarella-Oman, Mohammad Hossain, Caroline R Perry, Courtney Tiffany, Marcy Powell, Brandon Swift, Etienne F Dumont

Open access · hybridAbstract readReview
In one paragraph

Review in Sexually transmitted infections, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
3.0field-weighted citation impact, top 8% 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

19 citing papers in PubMed, 23 citations in OpenAlex.

  1. Trial
  2. Article
  3. Article
  4. Article
  5. Article
  6. Fluoroquinolone resistance-conferringbioRxiv : the preprint server for biology · 2026
    Article
  7. Article
  8. Article
  9. Management and prevention of Neisseria meningitidis and Neisseria gonorrhoeae infections in the context of evolving antimicrobial resistance trends.European journal of clinical microbiology & infectious diseases : official publication of the European Society of Clinical Microbiology · 2025
    Review
  10. Article
  11. Article
  12. Review
  13. Interactions between Gepotidacin andACS infectious diseases · 2024
    Article
  14. Journal of clinical medicine · 2023
    Review
  15. Review
  16. Article
  17. Actions of a Novel Bacterial Topoisomerase Inhibitor againstInternational journal of molecular sciences · 2023
    Article
  18. Article
  19. 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 3 institutions in 1 country.

Nicole E Scangarella-OmanGSK Collegeville, Collegeville, Pennsylvania, USA nicole.e.scangarella-oman@gsk.com.ORCID 0000-0003-4211-8261
Mohammad HossainGSK Collegeville, Collegeville, Pennsylvania, USA.
Caroline R PerryGSK Collegeville, Collegeville, Pennsylvania, USA.
Courtney TiffanyGSK Collegeville, Collegeville, Pennsylvania, USA.
Marcy PowellGSK, Research Triangle Park, North Carolina, USA.
Brandon SwiftGSK, Research Triangle Park, North Carolina, USA.
Etienne F DumontGSK Collegeville, Collegeville, Pennsylvania, USA.
Kalamazoo College · USResearch Triangle Park Foundation · USGlaxoSmithKline (United States) · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundGepotidacin is a novel, first-in-class triazaacenaphthylene antibiotic that inhibits bacterial DNA replication by a distinct mechanism of action and is active against most strains of

methodsFor dose selection, prior in vitro minimum inhibitory concentrations (MICs) and PK/PD data were available. PK modelling was conducted to determine a dose that would limit plasma concentrations to less than 14 µg/mL (as concentrations above this are associated with QT prolongation and effects associated with acetylcholinesterase inhibition) while maintaining ≥90% probability of target attainment (PTA) for efficacy and resistance suppression against

resultsTwo 3000 mg gepotidacin doses, administered 10-12 hours apart, resulted in PTA of ≥97.5% and ≥91.7% for gepotidacin MICs ≤1 µg/mL for the ratio of the area under the free drug plasma concentration-time curve over 24 hours to the MIC (

conclusionsTwo gepotidacin 3000 mg oral doses 10-12 hours apart provide ~2-fold higher systemic exposures, increase efficacy for higher gepotidacin MIC

Indexed as

GonorrheaAcenaphthenesAcetylcholinesteraseAnti-Bacterial AgentsClinical Trials, Phase III as TopicHeterocyclic Compounds, 3-RingHumansMicrobial Sensitivity TestsNeisseria gonorrhoeaeAcenaphthenesAcetylcholinesteraseAnti-Bacterial AgentsgepotidacinHeterocyclic Compounds, 3-Ringclinical trialgonorrhoeaneisseria gonorrhoeae

Identifiers

PMID36411033
PMCPMC9887395
OpenAlexW4309496717

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.