Bioequivalence study between two formulations of ciclosporin A (Cyclavance® oral solution and Atopica® soft capsules) following a single oral administration to dogs

被引:10
|
作者
Navarro, C. [1 ]
Seguy, L.
Vila, M. [2 ]
Birckel, P. [2 ]
机构
[1] Virbac, Dept Med, Carros, France
[2] AmatsiAvogadro, Bioserv Dept, Fontenilles, France
关键词
Dog; Ciclosporin; Cyclosporine A; Bioequivalence; Pharmacokinetics; Substitution; Interchangeability; HPLC; DERMATITIS; EFFICACY; SAFETY;
D O I
10.1186/s12917-016-0669-9
中图分类号
S85 [动物医学(兽医学)];
学科分类号
0906 ;
摘要
Background: Ciclosporin is a selective immunomodulator used for the treatment of atopic dermatitis in dogs. A new 100 mg/ml oral solution formulation (Cyclavance (R), Virbac) was developed as a pharmaceutical equivalent to the marketed capsule formulations (Atopica (R), Novartis Animal Health) containing 25, 50 mg, or 100 mg of ciclosporin A. The aim of this study was to assess and compare the pharmacokinetic profiles and bioequivalence of the two formulations following a single oral administration to dogs. This randomised, two-period, two-sequence, crossover bioequivalence study was conducted in 40 healthy dogs under fasting conditions. Each dog received either one 50 mg capsule of Atopica (R) or 0.5 ml of Cyclavance (R). After dosing, blood samples were collected during a 48-h time period at 0, 0.5, 1, 2, 4, 6, 12, 24, 36 and 48 h. Blood ciclosporin A concentrations were measured by using an HPLC-MS/MS method. Cmax, Tmax, t1/2, AUC0-t, AUC0-infinity and Kel were determined for the two ciclosporin formulations. Bioequivalence was to be concluded if the 90 % confidence intervals were within the range of 80 % to 125 % for Cmax and AUC0-t. Dogs were monitored once daily throughout the study period for adverse effects. Results: The 90 % confidence intervals for Cyclavance (R)/Atopica (R) mean ratios of the log-transformed pharmacokinetic variables Cmax and AUC0-t were within the conventional bioequivalence range of 80 % to 125 % (Point estimate: 101.2 % and 101.4 % respectively). Except for salivation reported after administration of both products, or vomiting and diarrhoea reported after Atopica (R) administration, both formulations were well tolerated in the 40 healthy dogs over the 48-h study period. Conclusions: The two ciclosporin oral formulations demonstrated similar pharmacokinetic profiles and were found to be bioequivalent, and therefore, interchangeable.
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页数:6
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