Peer-reviewed veterinary case report
Remdesivir drug levels and treatment results in cats with feline
By Coggins, S J et al.·Published in The Journal of small animal practice·2025·Faculty of Science, United Kingdom·View original on PubMed →
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Original publication title: Pharmacokinetics of GS-441524 following intravenous remdesivir in six cats and results of therapeutic drug monitoring during treatment of feline infectious peritonitis: 22 cases (2021-2024).
- Species:
- cat
Plain-English summary
Six cats with feline infectious peritonitis (FIP) were treated with an intravenous dose of remdesivir to see how it affected the levels of a drug called GS-441524 in their bodies. The treatment showed that GS-441524 reached its highest concentration in the blood about an hour after administration and was also found in body fluids and urine. While the study aimed to see if the levels of GS-441524 could predict recovery or survival, it did not find a significant link. Overall, the findings support the use of remdesivir and GS-441524 as effective treatments for FIP in cats.
People also search for: cat FIP treatment · remdesivir for cats · GS-441524 dosage in cats
Abstract
OBJECTIVES: This study aimed to: (1) characterise the pharmacokinetics of GS-441524 following intravenous (iv) administration of 15 mg/kg remdesivir (RDV) in client-owned cats with feline infectious peritonitis (FIP); (2) document plasma protein binding of GS-441524 in cats; (3) determine whether trough GS-441524 plasma concentrations predict 'simple remission' or survival to 18 months; (4) measure GS-441524 concentration in effusions relative to plasma; and (5) qualitatively assess excretion of GS-441524 in urine. MATERIALS AND METHODS: Six cats with FIP were administered 15 mg/kg iv RDV. Serial plasma GS-441524 concentrations were measured using high-performance liquid chromatography (HPLC). Twenty-two cats with FIP had trough plasma concentrations monitored over a 12-week treatment period. Simultaneous effusion and plasma GS-441524 concentrations were compared, and urine was assessed for GS-441524 excretion. RESULTS: The mean peak plasma concentration of GS-441524 (C) after a single 15 mg/kg iv dose of RDV was 2632 ng/mL (SD 862); time to reach C(T) was 1 hour (SD 0); and elimination half-life (t) was 5.14 hours (SD 0.81). GS-441524 was present in effusions (n = 3 cats) and eliminated in urine following treatment (n = 6 cats). Assessment of the predictive relationship between median GSand achieving 'simple remission' failed to demonstrate a significant correlation. CLINICAL SIGNIFICANCE: This study supports the use of RDV and GS-441524 for FIP treatment and suggests that population pharmacokinetic modelling is required to better explore the utility of therapeutic drug monitoring of GS-441524.
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Search related cases →Original publication on PubMed: https://pubmed.ncbi.nlm.nih.gov/40097914/