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.authorid0000-0001-7287-1276
dc.contributor.authorOner, Ahmet F.
dc.contributor.authorCelkan, Tiraje
dc.contributor.authorTimur, Cetin
dc.contributor.authorNorton, Miranda
dc.contributor.authorKavakli, Kaan
dc.date.accessioned2025-05-10T19:59:11Z
dc.date.issued2018
dc.departmentİstanbul Medeniyet Üniversitesi
dc.description.abstractHereditary 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
dc.description.sponsorshipBio Products Laboratory (Elstree, UK)
dc.description.sponsorshipBio 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.
dc.identifier.doi10.4274/tjh.2017.0446
dc.identifier.endpage133
dc.identifier.issn1300-7777
dc.identifier.issn1308-5263
dc.identifier.issue2
dc.identifier.pmid29545231
dc.identifier.scopus2-s2.0-85047784869
dc.identifier.scopusqualityQ3
dc.identifier.startpage129
dc.identifier.trdizinid289211
dc.identifier.urihttps://doi.org/10.4274/tjh.2017.0446
dc.identifier.urihttps://search.trdizin.gov.tr/tr/yayin/detay/289211
dc.identifier.urihttps://hdl.handle.net/20.500.14730/13778
dc.identifier.volume35
dc.identifier.wosWOS:000433166100006
dc.identifier.wosqualityQ3
dc.indekslendigikaynakWeb of Science
dc.indekslendigikaynakScopus
dc.indekslendigikaynakTR-Dizin
dc.indekslendigikaynakPubMed
dc.language.isoen
dc.publisherGalenos Yayincilik
dc.relation.ispartofTurkish Journal of Hematology
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı
dc.rightsinfo:eu-repo/semantics/openAccess
dc.snmzKA_WOS_20250302
dc.subjectClinical trial
dc.subjectClotting factor concentrate
dc.subjectEfficacy
dc.subjectFactor X deficiency
dc.subjectOrphan drug
dc.subjectSafety
dc.titleUse 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.typeArticle

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