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dc.contributor.authorOner, Ahmet F.
dc.contributor.authorKavakli, Kaan
dc.contributor.authorTimur, Cetin
dc.contributor.authorNorton, Miranda
dc.contributor.authorCelkan, Tiraje
dc.date.accessioned2021-03-03T17:58:15Z
dc.date.available2021-03-03T17:58:15Z
dc.date.issued2018
dc.identifier.citationOner A. F. , Celkan T., Timur C., Norton M., Kavakli K., "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", TURKISH JOURNAL OF HEMATOLOGY, cilt.35, sa.2, ss.129-133, 2018
dc.identifier.issn1300-7777
dc.identifier.otherav_4c87f784-de3a-4eec-8ed0-8d9c1dcadbb8
dc.identifier.othervv_1032021
dc.identifier.urihttp://hdl.handle.net/20.500.12627/54802
dc.identifier.urihttps://doi.org/10.4274/tjh.2017.0446
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.language.isoeng
dc.subjectSağlık Bilimleri
dc.subjectHematoloji
dc.subjectDahili Tıp Bilimleri
dc.subjectİç Hastalıkları
dc.subjectTıp
dc.subjectKlinik Tıp (MED)
dc.subjectKlinik Tıp
dc.subjectHEMATOLOJİ
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.typeMakale
dc.relation.journalTURKISH JOURNAL OF HEMATOLOGY
dc.contributor.departmentİstanbul Üniversitesi , ,
dc.identifier.volume35
dc.identifier.issue2
dc.identifier.startpage129
dc.identifier.endpage133
dc.contributor.firstauthorID250451


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