Evidence map›Paper›PMID 35289054›Full record

ArticleJournal of thrombosis and haemostasis : JTH2022

Pharmacological profile of asundexian, a novel, orally bioavailable inhibitor of factor XIa.

Stefan Heitmeier, Mayken Visser, Adrian Tersteegen, Julia Dietze-Torres, Julia Glunz, Christoph Gerdes, Volker Laux, Jan Stampfuss, Susanne Roehrig

Erratum issuedAbstract read
In one paragraph

Article in Journal of thrombosis and haemostasis : JTH, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 54 papers, 3 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
54citing papers in PubMed, 3 pooled it
–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

54 citing papers in PubMed, 3 syntheses or guidelines pooled it.

  1. Pooled it
  2. Pooled it
  3. Evaluating the Safety and Efficacy of Asundexian in Cardiovascular Disease: A Systematic Review and Meta-Analysis of Randomized Controlled Trials.Clinical and applied thrombosis/hemostasis : official journal of the International Academy of Clinical and Applied Thrombosis/Hemostasis
    Pooled it
  4. Trial
  5. Trial
  6. Article
  7. Article
  8. The OCEANIC trial journey: from failure to breakthrough?European heart journal. Cardiovascular pharmacotherapy · 2026
    Article
  9. Review
  10. Review
  11. Article
  12. Inhibition of fibrinolysisResearch and practice in thrombosis and haemostasis · 2026
    Article
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  15. Article
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

9 authors.

Stefan HeitmeierBayer AG, Research and Development Pharmaceuticals, Wuppertal, Germany.ORCID 0000-0003-2108-8286
Mayken VisserBayer AG, Research and Development Pharmaceuticals, Wuppertal, Germany.
Adrian TersteegenBayer AG, Research and Development Pharmaceuticals, Wuppertal, Germany.
Julia Dietze-TorresBayer AG, Research and Development Pharmaceuticals, Wuppertal, Germany.
Julia GlunzBayer AG, Research and Development Pharmaceuticals, Wuppertal, Germany.
Christoph GerdesBayer AG, Research and Development Pharmaceuticals, Wuppertal, Germany.
Volker LauxBayer AG, Research and Development Pharmaceuticals, Wuppertal, Germany.
Jan StampfussBayer AG, Research and Development Pharmaceuticals, Wuppertal, Germany.
Susanne RoehrigBayer AG, Research and Development Pharmaceuticals, Wuppertal, Germany.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundActivated coagulation factor XI (FXIa) contributes to the development and propagation of thrombosis but plays only a minor role in hemostasis; therefore, it is an attractive antithrombotic target.

objectivesTo evaluate the pharmacology of asundexian (BAY 2433334), a small molecule inhibitor targeting FXIa, in vitro and in various rabbit models.

methodsThe effects of asundexian on FXIa activity, selectivity versus other proteases, plasma thrombin generation, and clotting assays were evaluated. Antithrombotic effects were determined in FeCl

resultsAsundexian inhibited human FXIa with high potency and selectivity. It reduced FXIa activity, thrombin generation triggered by contact activation or low concentrations of tissue factor, and prolonged activated partial thromboplastin time in human, rabbit, and various other species, but not in rodents. In the FeCl

conclusionsAsundexian is a potent oral FXIa inhibitor with antithrombotic efficacy in arterial and venous thrombosis models in prevention and intervention settings, without increasing bleeding.

Indexed as

Factor XIaThrombosisAnimalsAnticoagulantsAspirinFibrinolytic AgentsHemorrhageHumansPlatelet Aggregation InhibitorsRabbitsThrombinTicagrelorAnticoagulantsAspirinFactor XIaFibrinolytic AgentsPlatelet Aggregation InhibitorsThrombinTicagreloranticoagulantasundexianBAY 2433334factor XIa inhibitorthrombosis

Identifiers

PMID35289054
PMCPMC9313898

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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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.