# Oseltamivir and baloxavir monotherapy and combination therapy efficacy against clade 2.3.4.4b A(H5N1) influenza virus infection in ferrets

**Authors:** Jessica A. Belser, Nicole Brock, Xiangjie Sun, Troy J. Kieran, Joanna A. Pulit-Penaloza, Claudia Pappas, Hui Zeng, Larisa V. Gubareva, Timothy M. Uyeki, Taronna R. Maines

PMC · DOI: 10.1038/s42003-026-09607-w · Communications Biology · 2026-01-26

## TL;DR

Combining oseltamivir and baloxavir reduces H5N1 flu virus replication and disease severity in ferrets, whether given before or after symptoms start.

## Contribution

Demonstrates combination antiviral therapy efficacy against clade 2.3.4.4b A(H5N1) influenza in ferrets.

## Key findings

- Baloxavir monotherapy reduced clinical signs and viral levels in ferrets compared to untreated controls.
- Combination OST/BXA treatment improved outcomes more than oseltamivir alone.
- Efficacy was observed whether treatment started before or after symptom onset.

## Abstract

Neuraminidase inhibitors (NAIs) and cap-dependent endonuclease inhibitors (CENIs) represent two classes of antiviral drugs recommended for early treatment of patients with seasonal influenza A virus (IAV) infections. However, only limited human data, particularly on combination antiviral treatment, are available to inform optimal dosing regimens against novel IAVs, including highly pathogenic avian influenza A(H5N1) virus, associated with severe disease. Clade 2.3.4.4b A(H5N1) viruses have caused outbreaks in avian and mammalian species worldwide, highlighting the need to assess antiviral drug efficacy against these strains. We challenged ferrets with a D1.1 genotype A(H5N1) virus and treated infected animals with the NAI oseltamivir phosphate (OST) and the CENI baloxavir acid (BXA), alone or in combination, with treatment onset commencing pre- or post-symptom onset (24- or 48-hours post-inoculation (p.i.), respectively). When administered pre- or post-illness onset, BXA, but not OST, monotherapy provided significant reduction of clinical signs and significantly decreased infectious viral levels (in both respiratory and extrapulmonary specimens) compared with mock-treated animals. Combination OST/BXA treatment, when administered pre- or post-symptom onset, resulted in significant improvements in both metrics versus OST monotherapy. These data support continued investigation of antiviral treatment modalities that include both NAI and CENI for patients with mild and severe A(H5N1) disease.

Combination treatment with two antiviral drugs (oseltamivir and baloxavir) effectively limits clade 2.3.4.4b A(H5N1) influenza virus replication and disease severity in ferrets.

## Linked entities

- **Chemicals:** oseltamivir phosphate (PubChem CID 65028), baloxavir acid (PubChem CID 124081876)

## Full-text entities

- **Diseases:** A(H5N1) disease (MESH:D004194), influenza virus infection (MESH:D007251)
- **Chemicals:** baloxavir (MESH:C000628402), BXA (-), OST (MESH:D053139)
- **Species:** Mustela putorius furo (black ferret, subspecies) [taxon 9669], H5N1 subtype (serotype) [taxon 102793], Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

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## References

14 references — full list in the complete paper: https://tomesphere.com/paper/PMC12946176/full.md

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Source: https://tomesphere.com/paper/PMC12946176