Evidence map›Paper›PMID 38365949›Full record

Trial reportNature medicine2024

A first-in-class leucyl-tRNA synthetase inhibitor, ganfeborole, for rifampicin-susceptible tuberculosis: a phase 2a open-label, randomized trial.

Andreas H Diacon, Clifton E Barry, Alex Carlton, Ray Y Chen, Matt Davies, Veronique de Jager, Kim Fletcher, Gavin C K W Koh, Irina Kontsevaya, Jan Heyckendorf and 9 more

Open access · hybridAbstract readRandomized Controlled TrialClinical Trial, Phase II
In one paragraph

Trial report in Nature medicine, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 26 papers.

0numbers the graph read from it
0cells of the map it votes in
26citing papers in PubMed
16.3field-weighted citation impact, top 1% 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

26 citing papers in PubMed, 42 citations in OpenAlex.

  1. Article
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  11. Selectivity of the Time-DependentACS chemical biology · 2025
    Article
  12. Review
  13. New drugs for the management of tuberculosis.Current opinion in infectious diseases · 2025
    Review
  14. Review
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  16. Article
  17. Review
  18. Article
  19. Identification of novelFuture medicinal chemistry · 2025
    Article
  20. Chemical genetic interactions elucidate pathways controlling tuberculosis antibiotic efficacy during infection.Proceedings of the National Academy of Sciences of the United States of America · 2025
    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

19 authors at 8 institutions in 5 countries.

Andreas H DiaconTASK, Cape Town, South Africa.
Clifton E BarryNational Institutes of Health, Bethesda, MD, USA.ORCID 0000-0002-2927-270X
Alex CarltonGSK, London, UK.
Ray Y ChenNational Institutes of Health, Bethesda, MD, USA.
Matt DaviesGSK, London, UK.ORCID 0000-0001-7545-8460
Veronique de JagerTASK, Cape Town, South Africa.
Kim FletcherGSK, London, UK.
Gavin C K W KohGSK, London, UK.ORCID 0000-0002-7336-1566
Irina KontsevayaResearch Center Borstel, Leibniz Lung Center, Borstel, Germany.
Jan HeyckendorfDepartment of Internal Medicine I, University Medical Center Schleswig-Holstein, Kiel, Germany.
Christoph LangeResearch Center Borstel, Leibniz Lung Center, Borstel, Germany.ORCID 0000-0002-9691-4741
Maja ReimannResearch Center Borstel, Leibniz Lung Center, Borstel, Germany.
Sophie L PenmanGSK, London, UK.
Rhona ScottGSK, London, UK.
Gareth Maher-EdwardsGSK, London, UK.
Simon TiberiGSK, London, UK.
Georgios VlasakakisGSK, Philadelphia, PA, USA.
Caryn M UptonTASK, Cape Town, South Africa.ORCID 0000-0002-7503-3320
David Barros AguirreGSK, Tres Cantos, Spain. david.a.barros@gsk.com.ORCID 0000-0002-4099-0438
Task Applied Science · ZAGerman Center for Infection Research · DENational Institutes of Health · USBaylor College of Medicine · USGlaxoSmithKline (Spain) · ESGlaxoSmithKline (United States) · USIntarcia Therapeutics (United States) · USQueen Mary University of London · GB

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

New tuberculosis treatments are needed to address drug resistance, lengthy treatment duration and adverse reactions of available agents. GSK3036656 (ganfeborole) is a first-in-class benzoxaborole inhibiting the Mycobacterium tuberculosis leucyl-tRNA synthetase. Here, in this phase 2a, single-center, open-label, randomized trial, we assessed early bactericidal activity (primary objective) and safety and pharmacokinetics (secondary objectives) of ganfeborole in participants with untreated, rifampicin-susceptible pulmonary tuberculosis. Overall, 75 males were treated with ganfeborole (1/5/15/30 mg) or standard of care (Rifafour e-275 or generic alternative) once daily for 14 days. We observed numerical reductions in daily sputum-derived colony-forming units from baseline in participants receiving 5, 15 and 30 mg once daily but not those receiving 1 mg ganfeborole. Adverse event rates were comparable across groups; all events were grade 1 or 2. In a participant subset, post hoc exploratory computational analysis of

Indexed as

Amino Acyl-tRNA SynthetasesTuberculosisTuberculosis, PulmonaryAntitubercular AgentsHumansMaleRifampinAmino Acyl-tRNA SynthetasesAntitubercular AgentsRifampin

Identifiers

PMID38365949
PMCPMC10957473
OpenAlexW4391882834

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.