Reynaud Lucie, Marsden Edward
Ricerca Biosciences, Saint-Germain sur l'Arbresle, France.
Methods Mol Biol. 2013;947:125-37. doi: 10.1007/978-1-62703-131-8_11.
Under normal circumstances, fertility and embryotoxicity studies are run separately according to the ICH S5(R2) guideline for the detection of toxicity to reproduction of medicinal products (1). However, the flexible approach of the S5(R2) guideline also allows the reproduction stages covered in the fertility and embryo-fetal development studies (stages A to D) to be combined into a single study design. The administration period covers the pre-mating and gestation phases through to closure of the hard palate. The principal advantages of the combined study include reductions in the number of animals required and cost. Although the rat is the routine species of choice, the mouse may also be used.
在正常情况下,根据国际人用药品注册技术协调会(ICH)S5(R2) 指导原则(1),生殖毒性和胚胎毒性研究是分开进行的,以检测药品对生殖的毒性。然而,S5(R2) 指导原则的灵活方法也允许将生殖毒性研究和胚胎-胎儿发育研究涵盖的生殖阶段(A至D阶段)合并为单一研究设计。给药期涵盖从交配前和妊娠期直至硬腭闭合。联合研究的主要优点包括所需动物数量减少和成本降低。虽然大鼠是常规的首选物种,但也可以使用小鼠。