Pharmacokinetics‐Bridging Between Autoinjectors and Prefilled Syringes for Subcutaneous Injection: Case Examples Revealing a Knowledge Gap

Author:

Li Zhe1ORCID,Du Xiulian1,Huang Shiew Mei1ORCID,Wang Yow‐Ming C.1ORCID

Affiliation:

1. Office of Clinical Pharmacology, Office of Translational Sciences, Center for Drug Evaluation and Research US Food and Drug Administration (OCP/CDER/FDA) Silver Spring Maryland USA

Abstract

Comparative pharmacokinetics (PK) studies have efficiently served as the bridge between autoinjectors and prefilled syringes given the underlying principles that comparable exposure could translate to comparable efficacy and safety. This article discusses approaches used to address uncertainties associated with the observation of noncomparable PK leading to the successful introduction of new autoinjector devices for monoclonal antibody and Fc‐fusion protein products. Information from seven case examples suggests a knowledge gap that warrants attention in autoinjector development.

Publisher

Wiley

Reference4 articles.

1. Systematic Review of Device Parameters and Design of Studies Bridging Biologic-Device Combination Products Using Prefilled Syringes and Autoinjectors

2. US Food and Drug Administration.Purple Book Database of Licensed Biological Products. Accessed December 26 2021.

3. US Food and Drug Administration.Guidance for industry: bioavailability and bioequivalence studies submitted in NDAs or INDs — general considerations(2014). .

Cited by 1 articles. 订阅此论文施引文献 订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献

1. Subcutaneous Biologics: Clinical Pharmacology and Drug Development;Clinical Pharmacology & Therapeutics;2024-02-16

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