Baloxavir Marboxil 2% Granules in Japanese Children With Influenza: An Open-label Phase 3 Study

Pediatr Infect Dis J. 2020 Aug;39(8):706-712. doi: 10.1097/INF.0000000000002748.

Abstract

Background: A granule formulation of baloxavir marboxil, a selective inhibitor of influenza cap-dependent endonuclease, was newly developed for children with difficulty swallowing tablets.

Methods: A multicenter open-label study was conducted during the 2017-2018 influenza season to assess the safety, pharmacokinetics and clinical/virologic outcomes of single, oral, weight-based doses of baloxavir granules in Japanese children infected with influenza virus. The primary clinical endpoint was the time to illness alleviation of influenza.

Results: All 33 enrolled children completed the study and received baloxavir (1 mg/kg for 12 children weighing <10 kg, 10 mg for 21 children weighing 10 to <20 kg). Detected viruses were influenza B (36.4%), A(H1N1)pdm09 (33.3%) and A(H3N2) (27.3%). Adverse events (AEs) were reported in 54.5% of children. No deaths, serious AEs or AEs leading to discontinuation were reported. The mean (SD) plasma concentrations of baloxavir acid at 24 hours post-dose were 72.8 (24.0) and 51.3 (19.3) ng/mL in the 1-mg/kg and 10-mg dose groups, respectively. The median time to illness alleviation (95% confidence interval) was 45.3 (28.5-64.1) hours. A >4-log decrease in infectious viral titer occurred on day 2 and a temporary 2-log increase on day 4. Polymerase acidic protein/I38T/M-substituted viruses were detected in 5 children infected with influenza A, but none with influenza B.

Conclusions: Baloxavir granules and the weight-based dose regimen were considered to be well tolerated in children, with rapid influenza virus reduction and associated symptom alleviation. Evidence of baloxavir activity against influenza B was observed, but further data are required for confirmation.

Publication types

  • Clinical Trial, Phase III
  • Multicenter Study
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Administration, Oral
  • Antiviral Agents / administration & dosage
  • Antiviral Agents / chemistry*
  • Antiviral Agents / pharmacokinetics
  • Antiviral Agents / therapeutic use*
  • Child
  • Child, Preschool
  • Dibenzothiepins / administration & dosage
  • Dibenzothiepins / chemistry*
  • Dibenzothiepins / pharmacokinetics
  • Dibenzothiepins / therapeutic use*
  • Drug Compounding*
  • Drug Resistance, Viral
  • Female
  • Humans
  • Infant
  • Infant, Newborn
  • Influenza, Human / drug therapy*
  • Japan
  • Male
  • Morpholines / administration & dosage
  • Morpholines / chemistry*
  • Morpholines / pharmacokinetics
  • Morpholines / therapeutic use*
  • Pyridones / administration & dosage
  • Pyridones / chemistry*
  • Pyridones / pharmacokinetics
  • Pyridones / therapeutic use*
  • Tablets
  • Triazines / administration & dosage
  • Triazines / chemistry*
  • Triazines / pharmacokinetics
  • Triazines / therapeutic use*
  • Viral Load / drug effects*

Substances

  • Antiviral Agents
  • Dibenzothiepins
  • Morpholines
  • Pyridones
  • Tablets
  • Triazines
  • baloxavir