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pubmed-article:7740479pubmed:abstractTextThe pharmacokinetics of intravenously administered recombinant human factor IX (rhFIX) were studied in Sprague-Dawley rats and Beagle dogs. Rats received rhFIX (50 IU/kg once daily) for 28 days, and the plasma half-life was 5 h. Anti-Human Factor IX serum antibody levels were found in only 1 of 12 rats. The pharmacokinetic profiles of rhFIX or Mononine, a purified human plasma-derived factor IX, after single 100 IU/kg i.v. doses in dogs, were similar. Peak plasma concentrations of rhFIX and Mononine were 4-5 micrograms/ml. The mean plasma half-lives were 13.2 +/- 1.6 h for rhFIX and 13.3 +/- 1.6 h for Mononine. Dogs also received rhFIX (40 IU/kg i.v., daily) for 28 days or Mononine (40 IU/kg i.v. daily) for 14 days. Anti-human Factor IX serum antibody levels were determined for each compound. Pharmacokinetic half-lives decreased in these treated dogs which developed antihuman Factor IX antibodies. The antibody responses in 28 day rhFIX (40 IU/kg) dogs were similar to 14 day Mononine (40 IU/kg) dogs.lld:pubmed
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pubmed-article:7740479pubmed:articleTitleEvaluation of recombinant human factor IX: pharmacokinetic studies in the rat and the dog.lld:pubmed
pubmed-article:7740479pubmed:affiliationDepartment of Preclinical Research, Genetics Institute, Inc., Cambridge, MA 02140, USA.lld:pubmed
pubmed-article:7740479pubmed:publicationTypeJournal Articlelld:pubmed
pubmed-article:7740479pubmed:publicationTypeComparative Studylld:pubmed