Department of Clinical Pharmacy and Toxicology, Leiden University Medical Center, Leiden, The Netherlands.
Utrecht Institute for Pharmaceutical Sciences, Utrecht University, The Netherlands.
Eur J Pharm Sci. 2018 Mar 1;114:24-29. doi: 10.1016/j.ejps.2017.11.025. Epub 2017 Nov 28.
Pharmaceutical compounding preparations, produced by (hospital) pharmacies, usually do not have marketing authorization. As a consequence, some of these pharmaceutical compounding preparations can be picked-up by a pharmaceutical company to obtain marketing authorization, often leading to price increases. An example is the 3,4-diaminopyridine slow release (3,4-DAP SR) tablets for Lambert-Eaton Myasthenic Syndrome (LEMS). In 2009 marketing authorization was given for the commercial immediate release phosphate salt of the drug, including a fifty-fold price increase compared to the pharmaceutical compounding preparation. Obtaining marketing authorization for 3,4-DAP SR by academia might have been a solution to prevent this price increase. To determine whether the available data of a pharmaceutical compounding preparation with long-term experience in regular care are adequate to obtain marketing authorization, 3,4-DAP SR is used as a case study.
A retrospective qualitative case-study was performed. Initially, document analysis was executed by collecting the required data for marketing authorization in general and whether data of Firdapse® and 3,4-DAP SR met these requirements. Secondly, the (non-) available data of the two formulations were compared with each other to determine the differences in availability.
At the time of approval, almost all data were available for both Firdapse® and 3,4-DAP SR. Conversely, much of the data used for the approval of Firdapse® originated from the 3,4-DAP immediate release (3,4-DAP IR) formulation. Only two bioequivalence studies and one pharmacology safety study was performed with Firdapse® before marketing authorization application.
In conclusion, at time Firdapse® obtained approval, the data available did not differ substantially from 3,4-DAP SR, indicating that approval with 3,4-DAP SR would have been possible. We make a plea for approval of orphan medicinal products developed and manufactured by academic institutions as to keep utilization of these products affordable.
医院药房配制的药物制剂通常没有营销许可。因此,一些药物制剂可能会被制药公司拿走以获得营销许可,这通常会导致价格上涨。一个例子是用于 Lambert-Eaton 肌无力综合征(LEMS)的 3,4-二氨基吡啶缓释(3,4-DAP SR)片。2009 年,该药物的商业即时释放磷酸盐盐获得了营销许可,价格与药物制剂相比上涨了五十倍。学术界获得 3,4-DAP SR 的营销许可可能是防止这种价格上涨的一种解决方案。为了确定长期在常规护理中使用的药物制剂的现有数据是否足以获得营销许可,以 3,4-DAP SR 作为案例研究。
进行了回顾性定性案例研究。最初,通过收集一般营销许可所需的数据以及 Firdapse®和 3,4-DAP SR 是否满足这些要求,进行了文件分析。其次,比较了两种制剂的(可用)和(不可用)数据,以确定可用性的差异。
在批准时,几乎所有数据都可用于 Firdapse®和 3,4-DAP SR。相反,Firdapse®批准所使用的许多数据都源自 3,4-DAP 即时释放(3,4-DAP IR)制剂。在申请营销许可之前,仅对 Firdapse®进行了两项生物等效性研究和一项药理学安全性研究。
总之,在 Firdapse®获得批准时,可用的数据与 3,4-DAP SR 没有实质性差异,表明 3,4-DAP SR 的批准是可能的。我们呼吁批准由学术机构开发和制造的孤儿药物,以保持这些产品的使用负担得起。