Published October 1, 2014 | Version v1
Journal article

Analysis of the safety and pharmacodynamics of human fibrinogen concentrate in animals

  • 1. CSL Behring GmbH, Preclinical Research and Development, Marburg (Germany)
  • 2. Department of Anaesthesiology, Perioperative Medicine and General Intensive Care, Paracelsus Medical University, Salzburg (Austria)
  • 3. CSL Behring GmbH, Medical Affairs, Marburg (Germany)

Description

Fibrinogen, a soluble 340 kDa plasma glycoprotein, is critical in achieving and maintaining hemostasis. Reduced fibrinogen levels are associated with an increased risk of bleeding and recent research has investigated the efficacy of fibrinogen concentrate for controlling perioperative bleeding. European guidelines on the management of perioperative bleeding recommend the use of fibrinogen concentrate if significant bleeding is accompanied by plasma fibrinogen levels less than 1.5–2.0 g/l. Plasma-derived human fibrinogen concentrate has been available for therapeutic use since 1956. The overall aim of the comprehensive series of non-clinical investigations presented was to evaluate i) the pharmacodynamic and pharmacokinetic characteristics and ii) the safety and tolerability profile of human fibrinogen concentrate Haemocomplettan P® (RiaSTAP®). Pharmacodynamic characteristics were assessed in rabbits, pharmacokinetic parameters were determined in rabbits and rats and a safety pharmacology study was performed in beagle dogs. Additional toxicology tests included: single-dose toxicity tests in mice and rats; local tolerance tests in rabbits; and neoantigenicity tests in rabbits and guinea pigs following the introduction of pasteurization in the manufacturing process. Human fibrinogen concentrate was shown to be pharmacodynamically active in rabbits and dogs and well tolerated, with no adverse events and no influence on circulation, respiration or hematological parameters in rabbits, mice, rats and dogs. In these non-clinical investigations, human fibrinogen concentrate showed a good safety profile. This data adds to the safety information available to date, strengthening the current body of knowledge regarding this hemostatic agent. - Highlights: • A comprehensive series of pre-clinical investigations of human fibrinogen concentrate. • Human fibrinogen concentrate was shown to be pharmacodynamically active. • Human fibrinogen concentrate was well tolerated, with no adverse events. • Overall, human fibrinogen concentrate demonstrated a good safety profile. • This data adds to the safety information available to date on this hemostatic agent

Availability note (English)

Available from http://dx.doi.org/10.1016/j.taap.2014.07.019

Additional details

Identifiers

DOI
10.1016/j.taap.2014.07.019;
PII
S0041-008X(14)00279-8;

Publishing Information

Journal Title
Toxicology and Applied Pharmacology
Journal Volume
280
Journal Issue
1
Journal Page Range
p. 70-77
ISSN
0041-008X
CODEN
TXAPA9

INIS

Country of Publication
United States
Country of Input or Organization
International Atomic Energy Agency (IAEA)
INIS RN
47009387
Subject category
S60: APPLIED LIFE SCIENCES;
Descriptors DEI
BEAGLES; FIBRINOGEN; GLYCOPROTEINS; GUINEA PIGS; HAZARDS; MICE; PASTEURIZATION; PHARMACOLOGY; RABBITS; RATS; RESPIRATION; THERAPEUTIC USES; TOXICITY
Descriptors DEC
ANIMALS; BLOOD COAGULATION FACTORS; CARBOHYDRATES; DOGS; FOOD PROCESSING; GLOBULINS; MAMMALS; ORGANIC COMPOUNDS; PROCESSING; PROTEINS; RODENTS; SACCHARIDES; USES; VERTEBRATES

Optional Information

Copyright
Copyright (c) 2014 Elsevier Science B.V., Amsterdam, The Netherlands, All rights reserved.