Evidence map›Paper›PMID 42139005›Full record

Trial reportJournal of clinical pharmacology2026

Randomized, Placebo-Controlled, First-in-Human Study of the Safety, Tolerability, and Pharmacokinetics of Single and Repeat Oral Doses of Novel Antitubercular Drug Candidate, GSK2556286, in Healthy Adults.

Emma Ilsley, Edward Banham-Hall, Tetyana Chaychenko, Katerina Chinenyeze, Gareth Maher-Edwards, Catherine Muya, Katie Rolfe, Raman Sharma, Simon Tiberi, David Barros-Aguirre

Registry-linked trialAbstract readRandomized Controlled TrialClinical Trial, Phase I
In one paragraph

Trial report in Journal of clinical pharmacology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT04472897 (A Randomised, Double Blind), which is not on this map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing 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.

NCT04472897 phase1terminatednot on this map

A Randomised, Double Blind (Sponsor Unblinded), Placebo-controlled, First Time in Human Study to Evaluate the Safety, Tolerability and Pharmacokinetics of Single and Repeat Oral Doses and the Food Effect of GSK2556286 in Healthy Adult Participants

TypeinterventionalSponsorGlaxoSmithKlineRan2020 to 2024Enrolled92ConditionsTuberculosisArmsGSK2556286, Placebo
3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

10 authors.

Edward Banham-HallGSK, Cambridge, UK.
Tetyana ChaychenkoGSK, London, UK.
Katerina ChinenyezeGSK, London, UK.
Gareth Maher-EdwardsGSK, London, UK.
Catherine MuyaGSK, Stevenage, UK.
Katie RolfeGSK, Stevenage, UK.
Raman SharmaGSK, Stevenage, UK.
Simon TiberiGSK, London, UK.
David Barros-AguirreGSK, Tres Cantos, Spain.

Funding

GSK NCT04472897Innovative Medicines Initiative 2 Joint Undertaking (JU) 853989
6 · The paper itself

Abstract

This first-in-human study (ClinicalTrials.gov identifier: NCT04472897) evaluated the safety, tolerability, pharmacokinetics, and food effect of single ascending and repeat oral doses of GSK2556286 (GSK286), a novel antitubercular drug candidate with efficacy in animal models of tuberculosis. In part A, 56 participants received single GSK286 doses (25-1000 mg; 10 cohorts) and 19 participants received a placebo. In part B, GSK286 and placebo doses were administered once daily for up to 14 days. Cohorts received repeat doses of GSK286 (225 or 650 mg; 13 participants) or placebo (four participants) in part B before the study was placed on hold due to reaching the stopping criterion, defined as clinically significant, non-serious adverse events (AEs) that are considered to be at least possibly related to GSK286 in two or more participants on active treatment. Single GSK286 doses were well tolerated; all reported AEs were mild, apart from moderate AEs in two participants administered GSK286 1000 mg, and there were no serious AEs (SAEs). In part B (repeat dosing), three participants reported moderate AEs, one reported a severe AE, and there were no SAEs. However, four of six participants in the 650 mg repeat dose cohort discontinued treatment due to the AEs (at least one) of headache, photophobia, fatigue, nausea, and vomiting. There was high intraindividual variability in the pharmacokinetics of GSK286 in both parts of the study, and the effect of food in modulating this variability was unclear. The combination of unexpected pharmacokinetic variability and exposure-related AEs led to termination of the study.

Indexed as

Antitubercular AgentsAdministration, OralAdolescentAdultDose-Response Relationship, DrugDouble-Blind MethodFemaleFood-Drug InteractionsHumansMaleMiddle AgedYoung AdultAntitubercular Agentsdose escalationfirst‐in‐humanGSK2556286pharmacokineticssafetytuberculosis

Identifiers

PMID42139005
PMCPMC13178715

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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.