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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.
- 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
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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.)
- Subjects :
- Adolescent
Adult
Antiviral Agents adverse effects
Antiviral Agents pharmacokinetics
Area Under Curve
Cross-Over Studies
Diarrhea chemically induced
Diarrhea epidemiology
Double-Blind Method
Drug Interactions
Female
Humans
Male
Middle Aged
Oseltamivir administration & dosage
Oseltamivir pharmacokinetics
Pyridines adverse effects
Pyridines pharmacokinetics
Pyrimidines adverse effects
Pyrimidines pharmacokinetics
Pyrroles adverse effects
Pyrroles pharmacokinetics
Time Factors
Young Adult
Antiviral Agents administration & dosage
Oseltamivir analogs & derivatives
Pyridines administration & dosage
Pyrimidines administration & dosage
Pyrroles administration & dosage
Subjects
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