Polak Yasmin, Jacobs Bart A W, Kemper E Marleen
Department of Pharmacy and Clinical Pharmacology, University of Amsterdam, Amsterdam, Netherlands.
Platform Medicine for Society, Amsterdam, Netherlands.
Front Pharmacol. 2021 Sep 28;12:758210. doi: 10.3389/fphar.2021.758210. eCollection 2021.
Patients with rare diseases are often confronted with the fact that effective medicines are unavailable or simply not being developed. This situation jeopardizes the health of a large population of vulnerable patients with rare diseases. Pharmacy compounded formulations can provide a safe alternative when authorized treatments are unavailable or unsuitable. Practical guidelines on how to develop and implement pharmacy compounded formulations for patients with rare diseases are limited. The aim of this article is to provide guidance for when and how to apply pharmacy compounded formulations for patients with rare diseases. This is illustrated with two challenging examples: the development and implementation of pharmacy compounding of 1) chenodeoxycholic acid (CDCA) capsules for patients with cerebrotendinous xanthomatosis (CTX) and 2) cholic acid (CA) capsules for patients with rare bile acid synthesis defects (BASD). All critical steps of the development of CDCA and CA capsules are explained and summarized in a practical guideline.
罕见病患者常常面临有效药物无法获取或根本未被研发的情况。这种状况危及大量患有罕见病的脆弱患者的健康。当授权治疗不可用或不合适时,药房配制制剂可提供一种安全的替代方案。关于如何为罕见病患者研发和实施药房配制制剂的实用指南有限。本文旨在为何时以及如何为罕见病患者应用药房配制制剂提供指导。通过两个具有挑战性的例子进行说明:1)为脑腱性黄瘤病(CTX)患者配制鹅去氧胆酸(CDCA)胶囊以及2)为罕见胆汁酸合成缺陷(BASD)患者配制胆酸(CA)胶囊的研发和实施。CDCA和CA胶囊研发的所有关键步骤在一份实用指南中进行了解释和总结。