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 | 0000-0001-7287-1276 | |
| 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 | 2025-05-10T19:59:11Z | |
| dc.date.issued | 2018 | |
| dc.department | İstanbul Medeniyet Üniversitesi | |
| 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 | |
| dc.description.sponsorship | Bio Products Laboratory (Elstree, UK) | |
| 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. | |
| dc.identifier.doi | 10.4274/tjh.2017.0446 | |
| dc.identifier.endpage | 133 | |
| dc.identifier.issn | 1300-7777 | |
| dc.identifier.issn | 1308-5263 | |
| dc.identifier.issue | 2 | |
| dc.identifier.pmid | 29545231 | |
| dc.identifier.scopus | 2-s2.0-85047784869 | |
| dc.identifier.scopusquality | Q3 | |
| dc.identifier.startpage | 129 | |
| dc.identifier.trdizinid | 289211 | |
| dc.identifier.uri | https://doi.org/10.4274/tjh.2017.0446 | |
| dc.identifier.uri | https://search.trdizin.gov.tr/tr/yayin/detay/289211 | |
| dc.identifier.uri | https://hdl.handle.net/20.500.14730/13778 | |
| dc.identifier.volume | 35 | |
| dc.identifier.wos | WOS:000433166100006 | |
| dc.identifier.wosquality | Q3 | |
| dc.indekslendigikaynak | Web of Science | |
| dc.indekslendigikaynak | Scopus | |
| dc.indekslendigikaynak | TR-Dizin | |
| dc.indekslendigikaynak | PubMed | |
| dc.language.iso | en | |
| dc.publisher | Galenos Yayincilik | |
| dc.relation.ispartof | Turkish Journal of Hematology | |
| dc.relation.publicationcategory | Makale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı | |
| dc.rights | info:eu-repo/semantics/openAccess | |
| dc.snmz | KA_WOS_20250302 | |
| dc.subject | Clinical trial | |
| dc.subject | Clotting factor concentrate | |
| dc.subject | Efficacy | |
| dc.subject | Factor X deficiency | |
| dc.subject | Orphan drug | |
| dc.subject | Safety | |
| 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 | |
| dc.type | Article |
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