Comparison of the recovery and half‐life of a high‐purity factor IX concentrate with those of a factor IX complex concentrate. Factor IX Study Group
- 1 April 1995
- journal article
- clinical trial
- Published by Wiley in Transfusion
- Vol. 35 (4) , 319-323
- https://doi.org/10.1046/j.1537-2995.1995.35495216081.x
Abstract
Recovery and half-life estimations were carried out to compare a high-purity factor IX concentrate with an established factor IX complex concentrate. Two high-purity factor IX concentrates, which are identical except for the presence or absence of heparin (Immuninehep-plus and Immuninehep-minus), were evaluated in two independent crossover studies using an intermediate-purity factor IX complex concentrate (Bebulin) as reference drug. In the Immuninehep-plus crossover study (n = 27), Immuninehep-plus and Bebulin had, respectively, a recovery of 0.90 +/- 0.26 and 0.84 +/- 0.23 IU per dL per IU per kg, a compartmental half-life of 17.11 +/- 6.18 and 15.94 +/- 4.69 hours, and an effective half-life of 16.51 +/- 3.48 and 16.48 +/- 4.26 hours. In the Immuninehep-minus crossover study (n = 26), Immuninehep-minus and Bebulin had, respectively, a recovery of 0.92 +/- 0.31 and 1.02 +/- 0.36 IU per dL per IU per kg, a compartmental half-life of 17.42 +/- 5.60 and 18.77 +/- 6.27 hours, and an effective half-life of 16.39 +/- 4.44 and 16.48 +/- 4.28 hours. Equivalence tests indicated that the recovery and half-life of Immunine, with or without heparin, are equivalent to those of Bebulin. The equivalence in pharmacokinetics and bioavailability indicates that the dosage schedule for Immunine should be the same as or very similar to that of Bebulin. The high specific activity of the former, however, allows administration at lower volumes.Keywords
This publication has 13 references indexed in Scilit:
- Low risk of viral infection after administration of vapor‐heated factor VII concentrate or factor IX complex in first‐time recipients of blood components. International Factor Safety Study GroupTransfusion, 1995
- Clinical Evaluation of Viral Safety of Coagulation Factor VIII and IX ConcentratesVox Sanguinis, 1993
- Viral Safety of Clotting Factor ConcentratesSeminars in Thrombosis and Hemostasis, 1993
- Factor IX Concentrates for Clinical UseSeminars in Thrombosis and Hemostasis, 1993
- Low risk of viral infection after administration of vapor-heated factor VIII concentrate. International Investigator GroupTransfusion, 1992
- A comparison of the Two One-Sided Tests Procedure and the Power Approach for assessing the equivalence of average bioavailabilityJournal of Pharmacokinetics and Biopharmaceutics, 1987
- Kinetic evaluation of four Factor VIII concentrates by model‐independent methodsScandinavian Journal of Haematology, 1985
- A new statistical procedure for testing equivalence in two-group comparative bioavailability trialsJournal of Pharmacokinetics and Biopharmaceutics, 1984
- Algorithm AS 183: An Efficient and Portable Pseudo-Random Number GeneratorJournal of the Royal Statistical Society Series C: Applied Statistics, 1982
- In vitro and in vivo Characterization of Factor VIII PreparationsVox Sanguinis, 1980