Evidence map›Paper›PMID 39818980›Full record

ArticleJournal of the American Heart Association2025

Comparative Effects of Glenzocimab and Eptifibatide on Bleeding Severity in 2 Mouse Models of Intracranial Hemorrhage.

Sébastien Dupont, Héloïse Lebas, Sabrina Mavouna, Eloïse Pascal, Astride Perrot, Adrien Cogo, Marie-Charlotte Bourrienne, Carine Farkh, Mialitiana Solo Nomenjanahary, Véronique Ollivier and 9 more

Abstract readComparative Study
In one paragraph

Article in Journal of the American Heart Association, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. 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

19 authors.

Sébastien DupontUniversité Paris Cité, Inserm, UMRS-1144, Optimisation Thérapeutique en Neuropsychopharmacologie Paris France.
Héloïse LebasUniversité Paris Cité, Inserm, UMRS-1148, Laboratory for Vascular Translational Science Paris France.
Sabrina MavounaUniversité Paris Cité, Inserm, UMRS-1144, Optimisation Thérapeutique en Neuropsychopharmacologie Paris France.ORCID 0009-0003-0619-0917
Eloïse PascalUniversité Paris Cité, Inserm, UMRS-1144, Optimisation Thérapeutique en Neuropsychopharmacologie Paris France.ORCID 0009-0002-6281-7772
Astride PerrotUniversité Paris Cité, Inserm, UMRS-1144, Optimisation Thérapeutique en Neuropsychopharmacologie Paris France.
Adrien CogoUniversité Paris Cité, Inserm, UMRS-1144, Optimisation Thérapeutique en Neuropsychopharmacologie Paris France.
Marie-Charlotte BourrienneUniversité Paris Cité, Inserm, UMRS-1144, Optimisation Thérapeutique en Neuropsychopharmacologie Paris France.ORCID 0000-0003-0125-9236
Carine FarkhUniversité Paris Cité, Inserm, UMRS-1144, Optimisation Thérapeutique en Neuropsychopharmacologie Paris France.ORCID 0000-0001-9840-0077
Mialitiana Solo NomenjanaharyUniversité Paris Cité, Inserm, UMRS-1144, Optimisation Thérapeutique en Neuropsychopharmacologie Paris France.
Véronique OllivierUniversité Paris Cité, Inserm, UMRS-1144, Optimisation Thérapeutique en Neuropsychopharmacologie Paris France.ORCID 0000-0003-1318-1712
Fatima ZemaliUniversité Paris Cité, Inserm, UMRS-1144, Optimisation Thérapeutique en Neuropsychopharmacologie Paris France.
Bernhard NieswandtInstitute of Experimental Biomedicine I, University Hospital, University of Würzburg Würzburg Germany.
Stéphane LoyauUniversité Paris Cité, Inserm, UMRS-1148, Laboratory for Vascular Translational Science Paris France.ORCID 0000-0001-8748-501X
Martine Jandrot-PerrusUniversité Paris Cité, Inserm, UMRS-1148, Laboratory for Vascular Translational Science Paris France.ORCID 0000-0002-8450-9247
Eric CamererUniversité Paris Cité, Inserm, PARCC Paris France.ORCID 0000-0002-6271-7125
Jean-Philippe DesillesUniversité Paris Cité, Inserm, UMRS-1144, Optimisation Thérapeutique en Neuropsychopharmacologie Paris France.ORCID 0000-0001-8395-6312
Mikael MazighiUniversité Paris Cité, Inserm, UMRS-1144, Optimisation Thérapeutique en Neuropsychopharmacologie Paris France.ORCID 0000-0003-0911-8999
Yacine BoulaftaliUniversité Paris Cité, Inserm, UMRS-1148, Laboratory for Vascular Translational Science Paris France.ORCID 0000-0003-4870-2098
Benoît Ho-Tin-NoéUniversité Paris Cité, Inserm, UMRS-1144, Optimisation Thérapeutique en Neuropsychopharmacologie Paris France.ORCID 0000-0002-7428-1760

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundAntiplatelet drugs represent potential candidates for protecting the penumbral microcirculation during cerebral ischemia and improving the benefits of arterial recanalization in ischemic stroke. Yet while the efficacy of such adjuvant strategies has been shown to be highly time dependent, antiplatelet therapy at the acute phase of ischemic stroke cannot be envisioned until the diagnosis of stroke and its ischemic nature have been confirmed because of the presumed risk of worsening bleeding in case of intracranial hemorrhage (ICH). Here, we investigated this risk for 2 antiplatelet drugs currently being tested in clinical trials for ischemic stroke, glenzocimab and eptifibatide, in 2 mouse models of ICH. METHODS AND

resultsThe severity of ICH was assessed in mice humanized for glycoprotein VI treated or not with glenzocimab or eptifibatide at effective dose, in a model of primary ICH caused by unilateral striatal injection of collagenase type VII, and in a model of hyperglycemia-induced hemorrhagic transformation of cerebral ischemia-reperfusion injury. Glenzocimab had no impact on bleeding severity in either model of ICH. Conversely, eptifibatide caused a significant increase in intracranial bleeding in both models, and a drastic increase in death after hyperglycemia-induced hemorrhagic transformation of cerebral ischemia-reperfusion injury.

conclusionsUnlike eptifibatide, glenzocimab is safe in the setting of ICH. These results suggest that glenzocimab could be administered upon suspicion of ischemic stroke, before assessment of its ischemic nature, thus opening the way to hastening of treatment initiation.

Indexed as

Antibodies, Monoclonal, HumanizedEptifibatideIntracranial HemorrhagesPlatelet Aggregation InhibitorsAnimalsDisease Models, AnimalMaleMiceMice, Inbred C57BLSeverity of Illness IndexAntibodies, Monoclonal, HumanizedEptifibatidePlatelet Aggregation Inhibitorsantiplatelet drugsintracranial hemorrhageischemic strokeplateletssafety

Identifiers

PMID39818980
PMCPMC12074769

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Registered trials

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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.