Evidence map›Paper›PMID 34694880›Full record

Trial reportAntimicrobial agents and chemotherapy2022

Safety, Tolerability, Pharmacokinetics, and Pharmacodynamics of Coadministered Ruxolitinib and Artemether-Lumefantrine in Healthy Adults.

M Farouk Chughlay, Karen I Barnes, Myriam El Gaaloul, Nada Abla, Jörg J Möhrle, Paul Griffin, Paul van Giersbergen, Stephanie E Reuter, Hayley B Schultz, Anita Kress and 9 more

Open access · hybridAbstract readClinical Trial, Phase IRandomized Controlled Trial
In one paragraph

Trial report in Antimicrobial agents and chemotherapy, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
1.6field-weighted citation impact, top 16% 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

9 citing papers in PubMed, 15 citations in OpenAlex.

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  8. Journal of clinical medicine · 2023
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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 6 institutions in 3 countries.

M Farouk ChughlayMedicines for Malaria Venturegrid.452605.0, Geneva, Switzerland.
Karen I BarnesDivision of Clinical Pharmacology, Department of Medicine, University of Cape Towngrid.7836.a, Cape Town, South Africa.ORCID 0000-0002-5547-820X
Myriam El GaaloulMedicines for Malaria Venturegrid.452605.0, Geneva, Switzerland.
Nada AblaMedicines for Malaria Venturegrid.452605.0, Geneva, Switzerland.
Jörg J MöhrleMedicines for Malaria Venturegrid.452605.0, Geneva, Switzerland.ORCID 0000-0002-0769-9649
Paul GriffinQIMR Berghofer Medical Research Institutegrid.1049.c, Brisbane, Queensland, Australia.
Paul van GiersbergenVan Giersbergen Consulting, Wuenheim, France.
Stephanie E ReuterUniSA Clinical and Health Sciences, University of South Australiagrid.1026.5, Adelaide, South Australia, Australia.
Hayley B SchultzUniSA Clinical and Health Sciences, University of South Australiagrid.1026.5, Adelaide, South Australia, Australia.
Anita KressSwiss BioQuant, Reinach, Switzerland.
Peter TapleyTetraQ, Brisbane, Queensland, Australia.
Rebecca A WebsterQIMR Berghofer Medical Research Institutegrid.1049.c, Brisbane, Queensland, Australia.
Timothy WellsMedicines for Malaria Venturegrid.452605.0, Geneva, Switzerland.
James S McCarthyQIMR Berghofer Medical Research Institutegrid.1049.c, Brisbane, Queensland, Australia.
Bridget E BarberQIMR Berghofer Medical Research Institutegrid.1049.c, Brisbane, Queensland, Australia.
Louise MarquartQIMR Berghofer Medical Research Institutegrid.1049.c, Brisbane, Queensland, Australia.
Michelle J BoyleQIMR Berghofer Medical Research Institutegrid.1049.c, Brisbane, Queensland, Australia.
Christian R EngwerdaQIMR Berghofer Medical Research Institutegrid.1049.c, Brisbane, Queensland, Australia.
Stephan ChalonMedicines for Malaria Venturegrid.452605.0, Geneva, Switzerland.ORCID 0000-0002-9306-1851
Medicines for Malaria Venture · CHQIMR Berghofer Medical Research Institute · AUUniversity of South Australia · AUMater Health Services · AUThe University of Queensland · AUUniversity of Cape Town · ZA

Funding

Gates Foundation INV-007155
6 · The paper itself

Abstract

Despite repeated malaria infection, individuals living in areas where malaria is endemic remain vulnerable to reinfection. The Janus kinase (JAK1/2) inhibitor ruxolitinib could potentially disrupt the parasite-induced dysfunctional immune response when administered with antimalarial therapy. This randomized, single-blind, placebo-controlled, single-center phase 1 trial investigated the safety, tolerability, and pharmacokinetic and pharmacodynamic profile of ruxolitinib and the approved antimalarial artemether-lumefantrine in combination. Ruxolitinib pharmacodynamics were assessed by inhibition of phosphorylation of signal transducer and activator of transcription 3 (pSTAT3). Eight healthy male and female participants ages 18 to 55 years were randomized to either ruxolitinib (20 mg) (

Indexed as

AntimalarialsMalaria, FalciparumAdolescentAdultArtemetherArtemether, Lumefantrine Drug CombinationDrug CombinationsEthanolaminesFemaleFluorenesHumansLumefantrineMaleMiddle AgedNitrilesPyrazolesAntimalarialsArtemetherArtemether, Lumefantrine Drug CombinationDrug CombinationsEthanolaminesFluorenesLumefantrineNitrilesPyrazolesPyrimidinesruxolitinibartemether-lumefantrineclinical trialhealthy volunteersmalariapharmacokineticsphase 1 studyruxolitinibsignal transducer and activator of transcription 3

Identifiers

PMID34694880
PMCPMC8765294
OpenAlexW3210099779

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.