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Single- and multiple-dose pharmacokinetics and safety of pimodivir, a novel, non-nucleoside polymerase basic protein 2 subunit inhibitor of the influenza A virus polymerase complex, and interaction with oseltamivir: a Phase 1 open-label study in healthy volunteers.

Authors :
Deleu S
Kakuda TN
Spittaels K
Vercauteren JJ
Hillewaert V
Lwin A
Leopold L
Hoetelmans RMW
Source :
British journal of clinical pharmacology [Br J Clin Pharmacol] 2018 Nov; Vol. 84 (11), pp. 2663-2672. Date of Electronic Publication: 2018 Sep 14.
Publication Year :
2018

Abstract

Aims: The aim of this study was to evaluate the drug-drug interaction between pimodivir, a novel, non-nucleoside polymerase basic protein 2 (PB2) subunit inhibitor of the influenza A virus polymerase complex, and oseltamivir, to assess the feasibility of this combination therapy. Furthermore, single- and multiple-dose pharmacokinetics and safety of pimodivir in healthy volunteers were assessed.<br />Methods: In Part 1 of this open-label Phase 1 study, healthy volunteers (n = 18) were randomized to one of six cross-over treatment sequences, each comprising administration of oseltamivir 75 mg or pimodivir 600 mg or combination thereof twice daily on Days 1-4, followed by a single morning dose on Day 5. Between each treatment session, there was a minimum 5-day washout period. In Part 2, healthy volunteers (n = 16) randomly received pimodivir 600 mg or placebo (3:1) twice daily on Days 1-9, followed by a single morning dose on Day 10. Pharmacokinetics of pimodivir, oseltamivir and oseltamivir carboxylate, and safety were assessed.<br />Results: In Part 1, co-administration of pimodivir with oseltamivir increased the C <subscript>max</subscript> of pimodivir by 31% (90% CI: 0.92-1.85) with no change in C <subscript>min</subscript> or AUC <subscript>12h</subscript> . Pimodivir had no effect on oseltamivir or oseltamivir carboxylate pharmacokinetics. In Part 2, after single- and multiple-dose administration of pimodivir, there was a 1.2- and 1.8-fold increase in C <subscript>max</subscript> and AUC <subscript>12h</subscript> , respectively, between Day 1 and Day 10. The most frequently reported treatment-emergent adverse event was diarrhoea (n = 7 each in Part 1 and 2).<br />Conclusion: Combination treatment with pimodivir and oseltamivir in healthy volunteers showed no clinically relevant drug-drug interactions. No safety concerns were identified with pimodivir 600 mg twice daily alone or in combination with oseltamivir 75 mg twice daily.<br /> (© 2018 The British Pharmacological Society.)

Details

Language :
English
ISSN :
1365-2125
Volume :
84
Issue :
11
Database :
MEDLINE
Journal :
British journal of clinical pharmacology
Publication Type :
Academic Journal
Accession number :
30098042
Full Text :
https://doi.org/10.1111/bcp.13733