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Pharmacokinetic interactions of CEP-1347 and atazanavir in HIV-infected patients

  • Qing Ma
  • , Harris A. Gelbard
  • , Sanjay B. Maggirwar
  • , Stephen Dewhurst
  • , Howard E. Gendelman
  • , Derick R. Peterson
  • , Robin Difrancesco
  • , Jill S. Hochreiter
  • , Gene D. Morse
  • , Giovanni Schifitto
  • University of Rochester
  • University of Nebraska Medical Center
  • SUNY Buffalo
  • Clinical Trials Coordination Center

Research output: Contribution to journalArticlepeer-review

15 Scopus citations

Abstract

CEP-1347 is a potent inhibitor of mixed lineage kinase (MLK), which was investigated for ameliorating HIV-associated neurocognitive disorders. CEP-1347 and atazanavir pharmacokinetics were determined when CEP-1347 50 mg twice daily was administered to HIV-infected patients (n = 20) receiving combination antiretroviral therapy including atazanavir and ritonavir (ATV/RTV, 300/100 mg) once daily continuously. Co-administration of CEP-1347 and ATV/RTV resulted with significant changes in pharmacokinetics of ATV but not RTV. Specifically, an increase in ATV accumulation ratio of 15 % (p = 0.007) and a prolongation of T 1/2 from 12.7 to 15.9 h (p = 0.002) were observed. The results suggested that co-administration of CEP-1347 with ATV/RTV in HIV-infected patients might result in limited impact on ATV but not on RTV pharmacokinetics.

Original languageEnglish
Pages (from-to)254-260
Number of pages7
JournalJournal of NeuroVirology
Volume19
Issue number3
DOIs
StatePublished - Jun 2013

Keywords

  • Atazanavir
  • CEP-1347
  • Drug interactions
  • HIV
  • Mixed lineage kinases
  • Ritonavir

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