Pharmacokinetics of Subcutaneous Itepekimab Injection With an Autoinjector Device and Prefilled Syringe in Healthy Participants

被引:0
|
作者
Xu, Christine [1 ]
Xin, Kong [2 ]
Kosloski, Matthew P. [3 ]
Butler, Allison [1 ]
Goulaouic, Helene [4 ]
Nivens, Michael C. [3 ]
Kanamaluru, Vanaja [1 ]
机构
[1] Sanofi, 55 Corp Dr, Bridgewater, NJ 08807 USA
[2] Sanofi, Beijing, Peoples R China
[3] Regeneron Pharmaceut Inc, Tarrytown, NY USA
[4] Sanofi, Chilly Mazarin, France
关键词
autoinjector; itepekimab; pharmacokinetics; Phase; 1; prefilled syringe; EFFICACY; SUPPORT; SAFETY; IMPACT;
D O I
10.1002/cpdd.1466
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Itepekimab, a monoclonal antibody against interleukin-33, has demonstrated clinical utility in previous studies in patients with asthma and chronic obstructive pulmonary disease. An autoinjector (AI) has been developed for administering itepekimab to facilitate further development. This study compared pharmacokinetics of single 300-mg itepekimab subcutaneous administration via an AI versus a prefilled syringe (PFS). Of 90 healthy volunteers enrolled in this Phase 1, parallel-design, randomized study and stratified by body weight (50 to <70 kg, >= 70 to <80 kg, >= 80 to 100 kg) and injection site (abdomen, thigh, or arm), 84 completed the study. Systemic exposure of itepekimab was similar for both groups. Point estimates for geometric mean ratios of pharmacokinetic parameters for AI versus PFS groups were 1.01 for maximum serum concentration, 1.06 for area under the serum concentration-time curve to the last quantifiable concentration, and 1.04 for area under the serum concentration-time curve extrapolated to infinity. The exposure was similar for both devices in each body weight and injection site subgroup. Overall, systemic exposure of 300-mg single-dose itepekimab in healthy participants was comparable when administered subcutaneously via an AI device and PFS, with an acceptable safety profile in both device groups.
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页数:8
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