Monoclonal antibody and protein therapeutic formulations for subcutaneous delivery: high-concentration, low-volume vs. low-concentration, high-volume

被引:12
|
作者
Desai, M. [1 ,5 ]
Kundu, A. [2 ]
Hageman, M. [3 ]
Lou, H. [4 ]
Boisvert, D.
机构
[1] Enable Inject Inc, Med Affairs, Cincinnati, OH USA
[2] Takeda Pharmaceut, Mfg Sci, Brooklyn Pk, MN USA
[3] Univ Kansas, Dept Pharmaceut Chem, Lawrence, KS USA
[4] Univ Kansas, Biopharmaceut Innovat & Optimizat Ctr, Lawrence, KS USA
[5] Enable Inject, Med Affairs, 2863 East Sharon Rd, Cincinnati, OH 45241 USA
关键词
Monoclonal antibodies; protein therapeutics; subcutaneous; high-volume; high-concentration; REVERSIBLE SELF-ASSOCIATION; RHEUMATOID-ARTHRITIS; MULTIPLE-MYELOMA; PREDICTING BIOAVAILABILITY; NON-INFERIORITY; OPEN-LABEL; INJECTION; PATIENT; PAIN; IMMUNOGENICITY;
D O I
10.1080/19420862.2023.2285277
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
Biologic drugs are used to treat a variety of cancers and chronic diseases. While most of these treatments are administered intravenously by trained healthcare professionals, a noticeable trend has emerged favoring subcutaneous (SC) administration. SC administration of biologics poses several challenges. Biologic drugs often require higher doses for optimal efficacy, surpassing the low volume capacity of traditional SC delivery methods like autoinjectors. Consequently, high concentrations of active ingredients are needed, creating time-consuming formulation obstacles. Alternatives to traditional SC delivery systems are therefore needed to support higher-volume biologic formulations and to reduce development time and other risks associated with high-concentration biologic formulations. Here, we outline key considerations for SC biologic drug formulations and delivery and explore a paradigm shift: the flexibility afforded by low-to-moderate-concentration drugs in high-volume formulations as an alternative to the traditionally difficult approach of high-concentration, low-volume SC formulation delivery.
引用
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页数:19
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