Use of Model-Informed Drug Development to Streamline Development of Long-Acting Products: Can These Successes Be Translated to Long-Acting Hormonal Contraceptives?

被引:6
|
作者
Li, Li [1 ]
Tran, Doanh [1 ]
Zhu, Hao [1 ]
Balimane, Praveen [1 ]
Willett, Gerald [2 ]
Zhao, Ping [3 ]
Gerrard, Stephen E. [3 ]
Vogelsong, Kirsten M. [3 ]
Wang, Yaning [1 ]
Seo, Shirley K. [1 ]
机构
[1] US FDA, Off Clin Pharmacol, Off Translat Sci, Ctr Drug Evaluat & Res, Silver Spring, MD 20993 USA
[2] US FDA, Off New Drugs, Ctr Drug Evaluat & Res, Silver Spring, MD 20993 USA
[3] Bill & Melinda Gates Fdn, Seattle, WA 98109 USA
来源
ANNUAL REVIEW OF PHARMACOLOGY AND TOXICOLOGY, VOL 61, 2021 | 2021年 / 61卷
关键词
long-acting contraceptive; long-acting injectable antipsychotics; modeling and simulation; exposure-response; drug development; SUSTAINED-RELEASE; ETHINYL ESTRADIOL; OVARIAN ACTIVITY; POPULATION; PILL;
D O I
10.1146/annurev-pharmtox-031120-015212
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Long-acting contraceptives are the most effective reversible contraceptive methods. Increasing patients' access to these contraceptives may translate into fewer unintended pregnancies and lead to substantial individual and public health benefits. However, development of long-acting products can be complex and challenging. This review provides (a) an overview of representative development programs for long-acting antipsychotics as cases for conceptual translation to long-acting contraceptives, (b) several case examples on how modeling and simulation have been used to streamline the development of long-acting products, and (c) examples of challenges and opportunities in developing long-acting contraceptives and information on how exposure-response relationships of commonly used progestins may enable regulators and developers to rely on prior findings of effectiveness and safety from an approved contraceptive to streamline the development of long-acting contraceptives. The US Food and Drug Administration is seeking assistance from stakeholders to provide data from studies in which pharmacokinetic and pharmacodynamic or clinical outcomes of hormonal contraceptives were evaluated and not previously submitted.
引用
收藏
页码:745 / 756
页数:12
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