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Use of a High-Purity Factor X Concentrate in Turkish Subjects With Hereditary Factor X Deficiency: Post Hoc Cohort Subanalysis of a Phase 3 Study

dc.authorid Celkan, Tulin Tiraje/0000-0001-7287-1276
dc.authorscopusid 7005791514
dc.authorscopusid 35584411200
dc.authorscopusid 6506239055
dc.authorscopusid 57146713800
dc.authorscopusid 35885183600
dc.authorwosid Celkan, Tülin/Aai-1729-2019
dc.authorwosid Kavaklı, Kaan/Afp-0928-2022
dc.contributor.author Oner, Ahmet F.
dc.contributor.author Celkan, Tiraje
dc.contributor.author Timur, Cetin
dc.contributor.author Norton, Miranda
dc.contributor.author Kavakli, Kaan
dc.date.accessioned 2025-05-10T17:10:58Z
dc.date.available 2025-05-10T17:10:58Z
dc.date.issued 2018
dc.department T.C. Van Yüzüncü Yıl Üniversitesi en_US
dc.department-temp [Oner, Ahmet F.] Yuzuncu Yil Univ, Fac Med, Dept Pediat Hematol, Van, Turkey; [Celkan, Tiraje] Istanbul Univ, Cerrahpasa Fac Med, Dept Pediat Hematol & Oncol, Istanbul, Turkey; [Timur, Cetin] Istanbul Medeniyet Univ, Goztepe Training & Res Hosp, Clin Pediat Hematol, Istanbul, Turkey; [Norton, Miranda] Bio Prod Lab Ltd, Elstree, Herts, England; [Kavakli, Kaan] Ege Univ, Fac Med, Dept Pediat Hematol, Izmir, Turkey en_US
dc.description Celkan, Tulin Tiraje/0000-0001-7287-1276 en_US
dc.description.abstract Hereditary factor X (FX) deficiency is a rare bleeding disorder more prevalent in countries with high rates of consanguineous marriage. In a prospective, open-label, multicenter phase 3 study, 25 IU/kg plasma-derived factor X (pdFX) was administered as on-demand treatment or short-term prophylaxis for 6 months to 2 years. In Turkish subjects (n=6), 60.7% of bleeds were minor. A mean of 1.03 infusions were used to treat each bleed, and mean total dose per bleed was 25.38 IU/kg. Turkish subjects rated pdFX efficacy as excellent or good for all 84 assessable bleeds; investigators judged overall pdFX efficacy to be excellent or good for all subjects. Turkish subjects had 51 adverse events; 96% with known severity were mild/moderate, and 1 (infusion-site pain) was possibly pdFX-related. These results demonstrate that 25 IU/kg pdFX is safe and effective in this Turkish cohort en_US
dc.description.sponsorship Bio Products Laboratory (Elstree, UK) en_US
dc.description.sponsorship Bio Products Laboratory (Elstree, UK) provided support for this study and funding for medical writing and editorial support in the development of this manuscript. A.F.O.: Received educational support from Pfizer. M.N.: Employee of Bio Products Laboratory. K.K.: Advisory board member for Bayer, Novo Nordisk, Pfizer, and Shire; received educational and investigational support from Bayer, Bio Products Laboratory, CSL Behring, Novo Nordisk, Octapharma, Pfizer, and Shire. en_US
dc.description.woscitationindex Science Citation Index Expanded
dc.identifier.doi 10.4274/tjh.2017.0446
dc.identifier.endpage 133 en_US
dc.identifier.issn 1300-7777
dc.identifier.issn 1308-5263
dc.identifier.issue 2 en_US
dc.identifier.pmid 29545231
dc.identifier.scopus 2-s2.0-85047784869
dc.identifier.scopusquality Q3
dc.identifier.startpage 129 en_US
dc.identifier.uri https://doi.org/10.4274/tjh.2017.0446
dc.identifier.uri https://hdl.handle.net/20.500.14720/7600
dc.identifier.volume 35 en_US
dc.identifier.wos WOS:000433166100006
dc.identifier.wosquality Q3
dc.language.iso en en_US
dc.publisher Galenos Yayincilik en_US
dc.relation.publicationcategory Makale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı en_US
dc.rights info:eu-repo/semantics/openAccess en_US
dc.subject Clinical Trial en_US
dc.subject Clotting Factor Concentrate en_US
dc.subject Efficacy en_US
dc.subject Factor X Deficiency en_US
dc.subject Orphan Drug en_US
dc.subject Safety en_US
dc.title Use of a High-Purity Factor X Concentrate in Turkish Subjects With Hereditary Factor X Deficiency: Post Hoc Cohort Subanalysis of a Phase 3 Study en_US
dc.type Article en_US

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