Bioequivalence of fluralaner-based veterinary medicinal products: VEPRIPAK® and BRAVECTO®

General information: fluralaner is a systemic ectoparasiticide that provides long-term control of fleas and ticks in dogs after a single oral administration. Based on this compound, VETSTEM LLC has developed a new veterinary medicinal product, VEPRIPAK®. Objective: to evaluate the pharmacokinetic bioequivalence of the test generic product VEPRIPAK® and the reference product BRAVECTO® in dogs. Results: analysis of serum fluralaner concentrations by HPLC–MS/MS demonstrated equivalence of key pharmacokinetic parameters: the mean time to maximum concentration (Tmax) was 48 h for both products; peak serum (or plasma, if per protocol) concentrations (Cmax) were 7,958.6 ng/mL for the test product and 7,987.0 ng/mL for the reference product. The 90% confidence intervals for the ratios CmaxT/CmaxR and AUC0–tT/AUC0–tR were within the bioequivalence acceptance range of 80.00–125.00 %. Conclusions: these data provide sufficient evidence to conclude that the test product is pharmacokinetically equivalent to the reference product in dogs.

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Publication Details

Journal
Russian veterinary journal
Published
2025-10-22
DOI
https://doi.org/10.32416/2500-4379-2025-5-54-59
Citations
1
Primary Topic
Nanoparticle-Based Drug Delivery
Type
article
Field-Weighted Citation Impact
0.60
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article

Bioequivalence of fluralaner-based veterinary medicinal products: VEPRIPAK® and BRAVECTO®

1 citations
Russian veterinary journal
Nanoparticle-Based Drug Delivery
0.60
article

Bioequivalence of fluralaner-based veterinary medicinal products: VEPRIPAK® and BRAVECTO®

article en
1 citations

Abstract

General information: fluralaner is a systemic ectoparasiticide that provides long-term control of fleas and ticks in dogs after a single oral administration. Based on this compound, VETSTEM LLC has developed a new veterinary medicinal product, VEPRIPAK®. Objective: to evaluate the pharmacokinetic bioequivalence of the test generic product VEPRIPAK® and the reference product BRAVECTO® in dogs. Results: analysis of serum fluralaner concentrations by HPLC–MS/MS demonstrated equivalence of key pharmacokinetic parameters: the mean time to maximum concentration (Tmax) was 48 h for both products; peak serum (or plasma, if per protocol) concentrations (Cmax) were 7,958.6 ng/mL for the test product and 7,987.0 ng/mL for the reference product. The 90% confidence intervals for the ratios CmaxT/CmaxR and AUC0–tT/AUC0–tR were within the bioequivalence acceptance range of 80.00–125.00 %. Conclusions: these data provide sufficient evidence to conclude that the test product is pharmacokinetically equivalent to the reference product in dogs.

Russian veterinary journalVol. 2025(5)
All-Russian Scientific Research Institute of Refrigeration Industry (RU)
Openalex Percentile: Top 26%
Nanoparticle-Based Drug Delivery
0.60
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