Search Results - "Norton, Miranda"
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A New Liquid 10% Intravenous Immunoglobulin (IVIG) Administered with 15-Minute Titration Periods Allows Shorter Infusion Durations and Tolerability Similar to a 5% Formulation
Published in Journal of allergy and clinical immunology (01-02-2017)“…Methods GMX07 (NCT01963143) was a phase 3, multicenter, open-label, randomized, 2-period, crossover bioequivalence trial that evaluated the pharmacokinetics,…”
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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
Published in Turkish journal of haematology (25-05-2018)“…Hereditary factor X (FX) deficiency is a rare bleeding disorder more prevalent in countries with high rates of consanguineous marriage. In a prospective,…”
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Plasma Derived Factor X Concentrate Has Not Induced Inhibitor Development in the Clinical Setting
Published in Blood (15-11-2022)Get full text
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Analysis of trough levels of total IgG, IgG subclasses, measles neutralizing antibodies and IgG antibodies to encapsulated pathogens after infusion of a 5% or 10% intravenous immunoglobulin
Published in Clinical immunology (Orlando, Fla.) (01-05-2023)“…Patients with primary immunodeficiency (PI) are at risk of infection due to low IgG levels. We report trough levels of total IgG, IgG subclasses, measles…”
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Genotype Analysis of Patients with Hereditary Factor X Deficiency Enrolled in 2 Phase 3 Studies of Pdfx, a New High-Purity Factor X Concentrate
Published in Blood (03-12-2015)“…Introduction: Hereditary factor X (FX) deficiency is a rare, autosomal recessive bleeding disorder of variable severity, with an estimated prevalence of…”
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Genotype analysis and identification of novel mutations in a multicentre cohort of patients with hereditary factor X deficiency
Published in Blood coagulation & fibrinolysis (01-01-2019)“…The objective was to examine the genotypic and phenotypic characteristics of individuals with hereditary factor X deficiency (FXD), a rare autosomal recessive…”
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Evaluation of the Safety, Tolerability, and Pharmacokinetics of Gammaplex^sup ^ 10% Versus Gammaplex^sup ^ 5% in Subjects with Primary Immunodeficiency
Published in Journal of clinical immunology (01-04-2017)“…Purpose This phase 3, multicenter, open-label, randomized, two-period, crossover bioequivalence trial evaluated the safety, tolerability, and pharmacokinetics…”
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Evaluation of the Safety, Tolerability, and Pharmacokinetics of Gammaplex® 10% Versus Gammaplex® 5% in Subjects with Primary Immunodeficiency
Published in Journal of clinical immunology (01-04-2017)“…Purpose This phase 3, multicenter, open-label, randomized, two-period, crossover bioequivalence trial evaluated the safety, tolerability, and pharmacokinetics…”
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