Dose accuracy of the follitropin alfa pen injector 2.0, the follitropin alfa:lutropin alfa 2:1 combination pen injector 2.0 and the choriogonadotropin alfa pen injector 1.0 used for fertility treatment.

Expert opinion on drug delivery Pub Date : 2024-02-01 Epub Date: 2024-02-02 DOI:10.1080/17425247.2024.2311127
Evelyn Cottell, Damien Michalet, Monica Lispi, Thiago Dantas Araujo, Ralf Gleixner, Salvatore Longobardi, Thomas D'Hooghe
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Abstract

Background: This study aimed to confirm that the incremental dose/clicks system dispenses accurate doses for the Merck family of fertility pen injectors.

Research design and methods: Set doses (Vset) for three dose dial settings (minimum dose [Vmin], midpoint dose [Vmid] and maximum dose [Vmax] for the follitropin alfa, choriogonadotropin alfa [D2 classification: single use/variable dose], and follitropin alfa:lutropin-alfa 2:1 combination pen injectors) or a single Vset for the choriogonadotropin alfa (D1 classification: single use/single dose) were assessed. Last dose administered by the multi-dose device was assessed for the 900 IU, 450 IU, 300 IU and 150 IU follitropin alfa, and the 900:450 IU, 450:225 IU and 300:150 IU follitropin alfa:lutropin-alfa 2:1 combination pen presentations.

Results: Dose accuracy tests for Vmin, Vmid and Vmax for the follitropin alfa and the follitropin alfa:lutropin-alfa 2:1 combination pen injectors, and last dose administered, were within acceptable limits according to ISO 11,608-1:2012/2014. Dose accuracy tests for the single use/single dose device classification and the single use/variable dose device classification of the choriogonadotropin alfa pen injector were also within the acceptable limits, according to ISO 11608-1:2000/2014.

Conclusions: The Merck family of fertility pen injectors functions reliably and the incremental dose/clicks system dispenses accurate doses.

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用于生育治疗的促性腺激素 alfa 笔式注射器 2.0、促性腺激素 alfa:促性腺激素 alfa 2:1 组合笔式注射器 2.0 和促性腺激素 alfa 笔式注射器 1.0 的剂量准确性。
背景:本研究旨在确认增量剂量/点击系统能为默克公司的生育笔系列注射器准确配药:评估了三种剂量刻度盘设置(最小剂量[Vmin]、中点剂量[Vmid]和最大剂量[Vmax],分别用于促性腺激素α、促性腺激素α[D2分类:单次使用/可变剂量]和促性腺激素α:卢托品-α 2:1组合笔式注射器)的设定剂量(Vset)或促性腺激素α(D1分类:单次使用/单剂量)的单一Vset。对900 IU、450 IU、300 IU和150 IU的促性腺激素α,以及900:450 IU、450:225 IU和300:150 IU的促性腺激素α:促性腺激素-α2:1组合笔注射器的多剂量装置最后给药剂量进行了评估:根据ISO 11,608-1:2012/2014标准,卵泡素α和卵泡素α:卢托品-阿法2:1混合笔注射器的Vmin、Vmid和Vmax剂量准确性测试以及最后给药剂量均在可接受范围内。根据 ISO 11,608-1:2000/2014,绒促性素α笔型注射器的单次使用/单剂量设备分类和单次使用/可变剂量设备分类的剂量准确性测试也在可接受范围内:默克公司的生育力笔式注射器系列功能可靠,增量剂量/点击系统配出的剂量准确。
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