Literature DB >> 24629431

Safety evaluation of orally administered afoxolaner in 8-week-old dogs.

Marlene Drag1, Judith Saik2, Jay Harriman2, Diane Larsen2.   

Abstract

The safety profile of afoxolaner, a new isoxazoline molecule, was evaluated following the regulatory requirements when administered six times orally in a soft chewable formulation at a dose of at least 1×, 3× or 5× the maximum exposure dose (6.3mg/kg) in 8-week-old Beagle dogs. Thirty-two healthy puppies (16 males and 16 females) were enrolled and allocated randomly to one of four treatment groups. Treatments were administered at three, one-month dose intervals (Days 0, 28 and 56) followed by three, 2-week dose intervals (Days 84, 98 and 112). The study ended at Day 126. The groups were: Group 1: non-treated control; Group 2: afoxolaner chews administered at a dosage of at least 6.3mg/kg (1×); Group 3: afoxolaner chews administered at a dosage of at least 18.9 mg/kg (3×); and Group 4: afoxolaner chews administered at a dosage of at least 31.5mg/kg (5×). All dogs were examined for general health twice a day beginning on at least Day-14. Physical examinations, and blood collections for clinical pathology analysis and afoxolaner plasma concentrations, were performed throughout the study. On Day 126, 2 weeks following the last treatment, all dogs were humanely euthanized prior to the conduction of a full necropsy with tissue collection. No afoxolaner-related changes were observed in growth, physical variables, clinical pathology variables, or tissues examined histologically. No clinically or statistically significant health abnormalities related to the administration of afoxolaner were observed. Vomiting and diarrhea were observed sporadically across all groups including the controls. The kinetics of afoxolaner plasma concentrations was linear following 6 doses of 6.3, 18.9 and 31.5mg/kg and dose proportionality was demonstrated. There were no statistical differences (p<0.05) between samples taken on Days 55 and 83 when compared to Day 27. Based upon the results of this study, afoxolaner was shown to be safe when administered repeatedly in a soft chewable formulation at up to 5× the maximum exposure dose in dogs as young as 8 weeks of age.
Copyright © 2014 The Authors. Published by Elsevier B.V. All rights reserved.

Entities:  

Keywords:  Afoxolaner; Dogs; Oral treatment; Safety

Mesh:

Substances:

Year:  2014        PMID: 24629431     DOI: 10.1016/j.vetpar.2014.02.022

Source DB:  PubMed          Journal:  Vet Parasitol        ISSN: 0304-4017            Impact factor:   2.738


  9 in total

1.  Efficacy and Pharmacokinetics Evaluation of a Single Oral Dose of Afoxolaner against Sarcoptes scabiei in the Porcine Scabies Model for Human Infestation.

Authors:  Charlotte Bernigaud; Fang Fang; Olivier Chosidow; Jacques Guillot; Katja Fischer; Anne Lespine; Ludwig S Aho; Amanda J Mullins; Berhane Tecle; Andrew Kelly; Jean-François Sutra; Francis Moreau; Thomas Lilin; Frédéric Beugnet; Françoise Botterel
Journal:  Antimicrob Agents Chemother       Date:  2018-08-27       Impact factor: 5.191

2.  Efficacy of oral afoxolaner for the treatment of canine generalised demodicosis.

Authors:  Frédéric Beugnet; Lénaïg Halos; Diane Larsen; Christa de Vos
Journal:  Parasite       Date:  2016-03-24       Impact factor: 3.000

3.  Safety evaluation of lotilaner in dogs after oral administration as flavoured chewable tablets (Credelio™).

Authors:  Emmanuelle A Kuntz; Srinivas Kammanadiminti
Journal:  Parasit Vectors       Date:  2017-11-01       Impact factor: 3.876

4.  Target animal safety evaluation of a novel topical combination of esafoxolaner, eprinomectin and praziquantel for cats.

Authors:  Aradhana Gupta; Christine Baker; Hailun Wang; Norba Targa; Anthony Pfefferkorn; Eric Tielemans
Journal:  Parasite       Date:  2021-04-02       Impact factor: 3.000

5.  Efficacy of afoxolaner (NexGard®) against natural infestations with Trichodectes canis in dogs under field conditions.

Authors:  Andrei Daniel Mihalca; Georgiana Deak; Luciana Cătălina Panait; Ștefan Rabei; Frederic Beugnet
Journal:  Parasit Vectors       Date:  2022-09-07       Impact factor: 4.047

6.  Safety of oral afoxolaner formulated with or without milbemycin oxime in homozygous MDR1-deficient collie dogs.

Authors:  Marlene Drag; Eric Tielemans; Elizabeth Mitchell
Journal:  J Vet Pharmacol Ther       Date:  2022-05-10       Impact factor: 1.567

7.  Efficacy of afoxolaner in a clinical field study in dogs naturally infested with Sarcoptes scabiei.

Authors:  Frédéric Beugnet; Christa de Vos; Julian Liebenberg; Lénaïg Halos; Diane Larsen; Josephus Fourie
Journal:  Parasite       Date:  2016-06-17       Impact factor: 3.000

8.  Assessment of the insecticidal activity of afoxolaner against Aedes aegypti in dogs treated with NexGard®.

Authors:  Julian Liebenberg; Josephus Fourie; Wilfried Lebon; Diane Larsen; Lenaïg Halos; Frédéric Beugnet
Journal:  Parasite       Date:  2017-10-23       Impact factor: 3.000

9.  Survey of canine use and safety of isoxazoline parasiticides.

Authors:  Valerie Palmieri; W Jean Dodds; Judy Morgan; Elizabeth Carney; Herbert A Fritsche; Jaclyn Jeffrey; Rowan Bullock; Jon P Kimball
Journal:  Vet Med Sci       Date:  2020-06-02
  9 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.