# Assessment of a baloxavir marboxil treatment protocol for high pathogenicity avian influenza in Okinawa Rails, an endangered species endemic to Japan

**Authors:** Mariko Miki, Yo Shimazu, Ryo Daniel Obara, Takashi Nagamine, Yumiko Nakaya, Yoshinori Ikenaka, Hiromi Osaki, Takashi Kimura, Takahiro Hiono, Norikazu Isoda, Takao Shishido, Yoshihiro Sakoda

PMC · DOI: 10.1371/journal.pone.0345055 · PLOS One · 2026-03-23

## TL;DR

This study explores the best way to administer a drug to treat bird flu in endangered Okinawa rails, finding that subcutaneous injection works better than oral administration.

## Contribution

The study proposes a subcutaneous administration protocol for baloxavir marboxil in Okinawa rails to combat avian influenza.

## Key findings

- Oral administration of BXM did not achieve sufficient plasma concentrations for therapeutic efficacy.
- Subcutaneous administration of BXM at 7.5 mg/kg maintained therapeutic plasma levels for up to 24 hours.
- Subcutaneous BXM administration caused mild and reversible injection site irritation as the main adverse effect.

## Abstract

High pathogenicity avian influenza (HPAI) is a highly infectious and lethal disease of birds that causes systemic symptoms and has been spreading globally, including in Japan. The Okinawa rail (Hypotaenidia okinawae), a flightless bird endemic to Japan, is classified as an endangered species on the Red List. In 2004, the Ministry of the Environment of Japan began implementing a conservation breeding program for Okinawa rails, focusing on maintaining the species’ genetic diversity, captive breeding, and reintroduction to the wild. Given the potential for significant losses due to HPAI in Okinawa rails, the establishment of a treatment protocol as a preparedness measure is essential. The aim of this study was to determine an appropriate treatment method for HPAI in Okinawa rails using baloxavir marboxil (BXM), a drug shown to be effective in an avian laboratory model of HPAI virus infection. Single oral administration of BXM at 2.5 or 12.5 mg/kg did not produce plasma concentrations sufficient to achieve the expected therapeutic efficacy. Therefore, oral administration was deemed inadequate for generating the desired pharmacological effects. Consequently, subcutaneous administration of BXM to Okinawa rails at a dose of 2.5 or 7.5 mg/kg was explored as an alternative protocol, which resulted in higher systemic exposure compared with oral administration. Furthermore, plasma concentrations were maintained at therapeutically relevant levels up to 24 hours after subcutaneous administration at 7.5 mg/kg, with mild and reversible injection site irritation the main adverse effect. Based on these results, subcutaneous administration of BXM is proposed as a viable treatment protocol for HPAI in the conservation of endangered Okinawa rails.

## Linked entities

- **Chemicals:** baloxavir marboxil (PubChem CID 124081896)
- **Species:** Hypotaenidia okinawae (taxon 2861861)

## Full-text entities

- **Diseases:** granulomas (MESH:D006099), abnormalities (MESH:D000014), inflammation (MESH:D007249), necrosis (MESH:D009336), influenza (MESH:D007251), irritation (MESH:D001523), abrasions (MESH:D065306), HPAI (MESH:D005585), gait-related abnormalities (MESH:D020233), NC (OMIM:617025), fibrosis (MESH:D005355), viral infection (MESH:D014777), overdose (MESH:D062787), infection (MESH:D007239)
- **Chemicals:** saline (MESH:D012965), itraconazole (MESH:D017964), dichlorvos (MESH:D004006), eosin (MESH:D004801), sodium heparin (MESH:D006493), carboplatin (MESH:D016190), hematoxylin (MESH:D006416), lactic acid (MESH:D019344), formalin (MESH:D005557), thiopental (MESH:D013874), BLQ (-), paraffin (MESH:D010232), BXM (MESH:C000628402)
- **Species:** Hypotaenidia okinawae (Okinawa rail, species) [taxon 2861861], Homo sapiens (human, species) [taxon 9606], H5N1 subtype (serotype) [taxon 102793], Gallus gallus (bantam, species) [taxon 9031], Orthomyxoviridae (family) [taxon 11308], Mustela putorius furo (black ferret, subspecies) [taxon 9669], Mus musculus (house mouse, species) [taxon 10090], H7N9 subtype (serotype) [taxon 333278]

## Full text

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## Figures

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## References

38 references — full list in the complete paper: https://tomesphere.com/paper/PMC13008105/full.md

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Source: https://tomesphere.com/paper/PMC13008105