Evidence map›Paper›PMID 39536817›Full record

ArticleJournal of thrombosis and haemostasis : JTH2025

Examining downstream effects of concizumab in hemophilia A with a mathematical modeling approach.

Kenji Miyazawa, Alan E Mast, Adam R Wufsus, Michael Dockal, Marianne Kjalke, Karin Leiderman

Abstract read
In one paragraph

Article in Journal of thrombosis and haemostasis : JTH, 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

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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. Article
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

6 authors.

Kenji MiyazawaQuantitative Biosciences and Engineering Program, Colorado School of Mines, Golden, Colorado, USA.
Alan E MastThrombosis and Hemostasis Program, Versiti Blood Research Institute, Milwaukee, Wisconsin, USA.
Adam R WufsusRare Disease, Novo Nordisk, Inc., Plainsboro, NJ, USA.
Michael DockalRare Blood Disorders, Novo Nordisk A/S, Novo Nordisk Park, Maaloev, Denmark.
Marianne KjalkeRare Blood Disorders, Novo Nordisk A/S, Novo Nordisk Park, Maaloev, Denmark.
Karin LeidermanDepartment of Mathematics, University of North Carolina at Chapel Hill, Chapel Hill, NC; Computational Medicine Program, University of North Carolina at Chapel Hill, Chapel Hill, North Carolina, USA. Electronic address: karin.leiderman@unc.edu.

Funding

Tissue Factor Pathway Inhibitor Binding Proteins on EndoR01HL068835 · NHLBI · VERSITI WISCONSIN, INC. · PI Alan E Mast · 2002 to 2026
$9.7M
An integrated computational and experimental approach to understanding the hemostatic response during treatment of bleedingR01HL151984 · NHLBI · UNIV OF NORTH CAROLINA CHAPEL HILL · PI FOGELSON, AARON L, LEIDERMAN, KARIN · 2020 to 2023
$2.8M
NHLBI NIH HHS R01 HL068835NHLBI NIH HHS R01 HL151984
6 · The paper itself

Abstract

backgroundTissue factor (TF) pathway inhibitor (TFPI) is an anticoagulant protein that inhibits factor (F)Xa, the TF-FVIIa-FXa complex, and early forms of the prothrombinase complex. Concizumab is a monoclonal antibody that blocks FXa inhibition by TFPI and reduces bleeding in hemophilia.

objectivesTo examine how concizumab impacts various reactions of TFPI to restore thrombin generation in hemophilia A using mathematical models.

methodsA compartment model was used to estimate plasma concentrations of free concizumab and its complexes with TFPIα and TFPIβ. Concizumab was integrated into a flow-mediated mathematical model of coagulation, and a small injury was simulated under hemophilia A conditions. Simulations were then analyzed to determine how concizumab's blockade of TFPI anticoagulant activities, specifically the inhibition of FXa in plasma and on platelets, inhibition of TF:FVIIa at the subendothelium, and prior sequestration of plasma TFPIα to the endothelium via TFPIβ, altered thrombin generation.

resultsConcizumab improved simulated thrombin generation in hemophilia A by simultaneously altering all 3 mechanisms of the TFPI anticoagulant blockade examined. Concizumab sequestered ∼75% of plasma TFPIα through the formation of ternary TFPIα-concizumab-TFPIβ-complexes. For all TF levels, reducing the TFPIα plasma concentration had the largest impact on the lag time, followed by blocking TFPIα inhibition of TF:FVIIa:FXa and subsequently by blocking TFPIα inhibition of FXa in plasma and on the platelet surface.

conclusionThe effectiveness of concizumab is mediated through the blockade of TFPI anticoagulant activities in plasma and on multiple physiological surfaces. An important and previously unrecognized function of concizumab was the sequestration of plasma TFPIα to the endothelium.

Indexed as

Antibodies, Monoclonal, HumanizedBlood CoagulationHemophilia AComputer SimulationFactor XaHumansLipoproteinsModels, BiologicalThrombinAntibodies, Monoclonal, HumanizedconcizumabFactor Xalipoprotein-associated coagulation inhibitorLipoproteinsThrombinconcizumabhemophilia Amathematical modelingTFPI-antibody

Identifiers

PMID39536817
PMCPMC12336664

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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.