Evidence map›Paper›PMID 40765904›Full record

ArticleBlood vessels, thrombosis & hemostasis2025

Treatment of severe bleeds with eptacog beta in hemophilia A or B with inhibitors: a post hoc analysis of the PERSEPT 1 and 2 trials.

Guy Young, Johnny Mahlangu, Lisa N Boggio, Manuel Carcao, Yesim Dargaud, Miguel Escobar, Adam Giermasz, Cédric Hermans, Philip Kuriakose, Wolfgang Miesbach and 6 more

2 registry-linked trialsAbstract read
In one paragraph

Article in Blood vessels, thrombosis & hemostasis, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to 2 registered trials, which are not on this map. Not yet cited in PubMed.

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

NCT02020369 phase3completednot on this map

A Phase III Study on the Safety, Pharmacokinetics and Efficacy of Coagulation Factor VIIa (Recombinant) in Congenital Hemophilia A or B Patients With Inhibitors to Factor VIII or IX

TypeinterventionalSponsorrEVO BiologicsRan2014 to 2015Enrolled27ConditionsHemophilia A With Inhibitors, Hemophilia B With InhibitorsArmsCoagulation Factor VIIa (Recombinant)
NCT02448680 phase3completednot on this map

A Phase III Study on the Safety, Pharmacokinetics, and Efficacy of Coagulation Factor VIIa (Recombinant) in Congenital Hemophilia A or B Pediatric Patients From Birth to <12 Years Old With Inhibitors to Factor VIII or IX: PerSept 2

TypeinterventionalSponsorLaboratoire français de Fractionnement et de BiotechnologiesRan2015 to 2017Enrolled25ConditionsHemophilia A With Inhibitors, Hemophilia B With InhibitorsArmsCoagulation FVIIa (Recombinant)
3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

16 authors.

Guy YoungCancer and Blood Disease Institute, Children's Hospital Los Angeles, Los Angeles, CA.
Johnny MahlanguDepartment of Molecular Medicine and Haematology, Hemophilia Comprehensive Care Center, University of the Witwatersrand and National Health Laboratory Service, Johannesburg, South Africa.
Lisa N BoggioDepartment of Pediatrics, Rush Hemophilia and Thrombophilia Center, Rush University Medical Center, Chicago, IL.
Manuel CarcaoDepartment of Pediatrics, The Hospital for Sick Children, Toronto, ON, Canada.
Yesim DargaudDivision of Hemostasis and Thrombosis, Lyon University Hospitals, Lyon, France.
Miguel EscobarUniversity of Texas Health Science Center at Houston, Houston, TX.
Adam GiermaszDivision of Hematology/Oncology, University of California Davis, Sacramento, CA.
Cédric HermansDivision of Haematology, Cliniques Saint-Luc, Université Catholique de Louvain, Brussels, Belgium.
Philip KuriakoseDepartment of Internal Medicine, Henry Ford Hospital, Detroit, MI.
Wolfgang MiesbachDepartment of Haemostaseology, Goethe University Hospital, Frankfurt, Germany.
Danielle NanceDivision of Hematology, Banner MD Anderson Cancer Center, Phoenix, AZ.
Amina RafiqueDepartment of Pediatric Hematology and Oncology, Atrium Health Levine Cancer, Charlotte, NC.
Robert F SidonioDepartment of Pediatrics, Emory University and Aflac Cancer and Blood Disorders Center of Children's Healthcare of Atlanta, Atlanta, GA.
Kateryna V VilchevskaDepartment of Pediatrics, National Specialized Children's Hospital Okhmatdyt, Kyiv, Ukraine.
Michael WangDepartment of Pediatrics, Hemophilia and Thrombosis Center, University of Colorado, Aurora, CO.
Steven W PipeDepartments of Pediatrics and Pathology, University of Michigan, Ann Arbor, MI.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Severe bleeding episodes (BEs) in persons with hemophilia A or B and inhibitors (PwHABIs) represent challenging clinical situations and can require treatment regimens lasting days or weeks before hemostatic control is achieved. Eptacog beta is a recombinant activated human factor VII bypassing agent approved for treating and controlling bleeding in PwHABIs aged ≥12 years. The aim of this study is to assess the efficacy and safety of eptacog beta for severe bleed treatment in PwHABIs during 2 phase 3 trials (PERSEPT 1 and PERSEPT 2). Patients could treat severe BEs with initial doses of 75 or 225 μg/kg eptacog beta at home, followed by subsequent 75 μg/kg eptacog beta infusions administered at predefined intervals in a hospital or hemophilia treatment center. Satisfactory treatment responses to eptacog beta were typically defined in this post hoc analysis by physician- and patient-reported hemostasis evaluations of "excellent" or "good." Hemostatic control of an intracranial hemorrhage (ICH) in 1 patient was assessed by computed tomography. Seven PwHABIs (aged 1-50 years) treated 8 BEs considered severe or otherwise life threatening with eptacog beta during PERSEPT 1 and PERSEPT 2. Hemostatic control of 7 of these BEs (including 3 ICH events) was achieved. Eptacog beta treatment durations ranged from 25 minutes to 96 hours. No thrombotic events were reported, and eptacog beta was well tolerated. Most severe BEs resolved with eptacog beta treatment during PERSEPT 1 and PERSEPT 2. The PERSEPT 1 and PERSEPT 2 trials were registered at www.clinicaltrials.gov as #NCT02020369 and #NCT02448680, respectively.

Identifiers

PMID40765904
PMCPMC12320391

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Registered trials

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.