Evidence map›Paper›PMID 40534246›Full record

ArticleHaemophilia : the official journal of the World Federation of Hemophilia2025

Evaluation of One-Stage Assays for the Monitoring of Recombinant Human Factor IX Padua Activity After Etranacogene Dezaparvovec Gene Therapy.

Jan Astermark, Wolfgang Miesbach, Michiel Coppens, Sander Gielen, Jaap Twisk, Ricardo Dolmetsch, Stephanie Verweij, Paul E Monahan, Bruce M Ewenstein, Silpa Nuthalapati and 3 more

Abstract read
In one paragraph

Article in Haemophilia : the official journal of the World Federation of Hemophilia, 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. Laboratory Challenges in the Era of Novel Haemophilia Therapies.Transfusion medicine and hemotherapy : offizielles Organ der Deutschen Gesellschaft fur Transfusionsmedizin und Immunhamatologie · 2026
    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

13 authors.

Jan AstermarkInstitution of Translational Medicine, Lund University and Department of Hematology, Oncology and Radiation Physics, Skåne University Hospital, Malmö, Sweden.ORCID https://orcid.org/0000-0001-8500-2483
Wolfgang MiesbachMedical Clinic 2, Frankfurt University Hospital, Frankfurt, Germany.ORCID https://orcid.org/0000-0002-4506-0061
Michiel CoppensDepartment of Vascular Medicine, Amsterdam UMC, University of Amsterdam, Amsterdam, The Netherlands.
Sander GielenuniQure biopharma B.V., Amsterdam, The Netherlands.
Jaap TwiskuniQure biopharma B.V., Amsterdam, The Netherlands.
Ricardo DolmetschuniQure biopharma B.V., Amsterdam, The Netherlands.
Stephanie VerweijuniQure biopharma B.V., Amsterdam, The Netherlands.
Paul E MonahanCSL Behring, King of Prussia, Pennsylvania, USA.
Bruce M EwensteinCSL Behring, King of Prussia, Pennsylvania, USA.
Silpa NuthalapatiCSL Behring, King of Prussia, Pennsylvania, USA.
Nick GalanteCSL Behring, King of Prussia, Pennsylvania, USA.
Guy YoungKeck School of Medicine of the University of Southern California, Los Angeles, California, USA.ORCID https://orcid.org/0000-0001-6013-1254
HOPE‐B study investigators

Funding

CSL Behring
6 · The paper itself

Abstract

introductionAccurate and reproducible measures of factor activity are required to guide clinical decision-making following gene therapy for haemophilia B (HB). Highly significant discrepancies have been observed in measurements of various factor IX (FIX) concentrates that carry molecular modifications to extend their half-life, arguing for the need for careful analysis of new HB treatment modalities with respect to FIX assay performance.

aimTo further characterise variability in FIX activity measured using different one-stage assays (OSAs) and chromogenic assays (CAs) in patients with HB receiving gene therapy utilising the FIX Padua variant and to assess whether assay differences were due to the FIX-Padua variant.

methodsFIX activity was assessed centrally (OSA and CA) and locally (OSA only) using plasma samples collected from a phase 2b and phase 3 study of etranacogene dezaparvovec and in an in vitro study of wild-type (wt) recombinant human FIX (rhFIX) and rhFIX-Padua.

resultsLower CA than OSA FIX activity for plasma samples from the phase 3 trial was observed (CA:OSA ratio: 0.408 [±0.049]-0.547 [±0.062]). Local OSA:central OSA FIX activity ratios were 0.789 (±0.314)-1.021 (±0.159). Local OSA:central OSA FIX activity ratios across methods and/or reagents were 0.81 (±0.02)-1.28 (±0.04) for rhFIX-wt-spiked samples and 0.67 (±0.02)-1.13 (±0.09) for rhFIX-Padua-spiked samples.

conclusionFIX activity differences between central and local OSAs were modest; similar differences were observed in vitro with rhFIX-wt versus rhFIX-Padua. Commonly available OSAs can be used to monitor patients post-etranacogene dezaparvovec administration; we recommend using the same assay platform throughout the post-treatment period.

Indexed as

DependovirusFactor IXGene Therapy AgentsGenetic TherapyHemophilia BHumansRecombinant Proteinsetranacogene dezaparvovecFactor IXRecombinant Proteinschromogenic assayfactor IXgene therapyhaemophilia Bone‐stage assay

Identifiers

PMID40534246
PMCPMC12311899

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.