Harmonization of Activity Determination Requirements for Recombinant Blood Clotting Factor rFVIIa


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Abstract

The interchangeability of coagulation methods for determining the activity of recombinant blood clotting factor rFVIIa was assessed. Single-factor analysis of variance (ANOVA) and comparison of the metrological characteristics of the methods led to the conclusion that results obtained by reproducing the methods of the European Pharmacopoeia and Generium were comparable and interchangeable. One method could be used to confirm that a drug conformed to regulations established using another method. The Generium method was chosen for introduction into national pharmacopoeial practice because it was more economical.

About the authors

O. B. Ustinnikova

Scientific Centre for Expert Evaluation of Medicinal Products, Ministry of Public Health of the Russian Federation; Generium Inc.

Author for correspondence.
Email: Ustinnikova@expmed.ru
Russian Federation, 8/2 Petrovskii Blvd., Moscow, 127051; Moscow

E. V. Novikova

Scientific Centre for Expert Evaluation of Medicinal Products, Ministry of Public Health of the Russian Federation

Email: Ustinnikova@expmed.ru
Russian Federation, 8/2 Petrovskii Blvd., Moscow, 127051

O. B. Runova

Scientific Centre for Expert Evaluation of Medicinal Products, Ministry of Public Health of the Russian Federation

Email: Ustinnikova@expmed.ru
Russian Federation, 8/2 Petrovskii Blvd., Moscow, 127051

D. V. Shvedov

Scientific Centre for Expert Evaluation of Medicinal Products, Ministry of Public Health of the Russian Federation

Email: Ustinnikova@expmed.ru
Russian Federation, 8/2 Petrovskii Blvd., Moscow, 127051

M. V. Zhilyaeva

Generium International Biotechnology Center

Email: Ustinnikova@expmed.ru
Russian Federation, Moscow, 123317

D. A. Kudlai

Generium Inc.

Email: Ustinnikova@expmed.ru
Russian Federation, Moscow

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