Evidence map›Paper›PMID 40338896›Full record

ArticlePLoS neglected tropical diseases2025

Unprecedented in vivo activity of telacebec against Mycobacterium leprae.

Aurélie Chauffour, Emmanuelle Cambau, Kevin Pethe, Nicolas Veziris, Alexandra Aubry

Abstract read
In one paragraph

Article in PLoS neglected tropical diseases, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
–field-weighted citation impact
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

2 citing papers in PubMed.

  1. Review
  2. New drugs for the management of tuberculosis.Current opinion in infectious diseases · 2025
    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

5 authors.

Aurélie ChauffourSorbonne Université, CNRS, INSERM, Centre d'Immunologie et des Maladies Infectieuses, CIMI, Paris, France.
Emmanuelle CambauUniversité Paris Cité, IAME Inserm UMR 1137, Service de Mycobactériologie Spécialisée et de Référence, Laboratoire Associé du CNR des Mycobactéries et de La Résistance des Mycobactéries Aux Antituberculeux (CNR-MyRMA) APHP GHU Paris Nord, Hôpital Bichat, Paris, France.
Kevin PetheLee Kong Chian School of Medicine, Nanyang Technological University, Experimental Medicine Building, Nanyang, Singapore.
Nicolas VezirisSorbonne Université, CNRS, INSERM, Centre d'Immunologie et des Maladies Infectieuses, CIMI, Paris, France.
Alexandra AubrySorbonne Université, CNRS, INSERM, Centre d'Immunologie et des Maladies Infectieuses, CIMI, Paris, France.ORCID 0000-0003-4230-4793

Funding

Association Française Raoul Follereau
6 · The paper itself

Abstract

backgroundNew drugs targeting the electron transport chain (ETC) seem to be a promising advance in leprosy treatment. In this study, we evaluated the bactericidal activity of telacebec (TCB), a phase 2 drug candidate for tuberculosis, alongside known ETC-targeting antibiotics, bedaquiline (BDQ) and clofazimine (CFZ), as monotherapy or in combination. METHODOLOGY/ PRINCIPAL

findingsWe used the reference leprosy proportional bactericidal mouse footpad model. Four hundred and ten mice were inoculated in the footpads with 5x104 to 5x100 bacilli of M. leprae strain THAI53 for the untreated control group and groups treated with drug-monotherapies, and with 5x104 to 5x101 for groups treated with drug-combinations. Mice were randomly allocated into the following groups: 2 control groups (untreated or standard multi drug therapy (MDT), rifampin, dapsone and clofazimine with dosing equipotent to human dosing) and 7 test groups (TCB 10mg/kg, bedaquiline 25mg/kg (BDQ), clofazimine 20mg/kg (CFZ), CFZ + BDQ, TCB + BDQ, TCB + CFZ, TCB + CFZ + BDQ). Mice in the test groups received either one month treatment (MDT) or a single dose of the drugs (TCB, RIF, BDQ, CFZ). Twelve months later, mice were sacrificed to enumerate M. leprae bacilli in the footpad. All the footpads became negative in the MDT, TCB and combination groups except in the TCB + CFZ group where 2 mice remained positive in the 5x104 inoculum.

conclusionWe demonstrated that monotherapy of TCB exhibited bactericidal activity against M. leprae comparable to that of MDT and that all combination therapies were as effective as MDT, except the combination TCB + CFZ, possibly due to an antagonism between these two drugs.

Indexed as

Leprostatic AgentsLeprosyMycobacterium lepraeAnimalsClofazimineDiarylquinolinesDisease Models, AnimalDrug Therapy, CombinationElectron Transport Chain Complex ProteinsFemaleImidazolesMiceMice, NudeMicrobial Sensitivity TestsPiperidinesPyridinesbedaquilineClofazimineDiarylquinolinesElectron Transport Chain Complex ProteinsImidazolesLeprostatic AgentsPiperidinesPyridinestelacebec

Identifiers

PMID40338896
PMCPMC12061105

What OpenQuestion holds

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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.