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Eur J Pharm Sci ; 114: 24-29, 2018 Mar 01.
Artículo en Inglés | MEDLINE | ID: mdl-29191521

RESUMEN

BACKGROUND: 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. METHODS: 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. RESULTS: 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. CONCLUSIONS: 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.


Asunto(s)
4-Aminopiridina/análogos & derivados , Composición de Medicamentos/métodos , Síndrome Miasténico de Lambert-Eaton/tratamiento farmacológico , Mercadotecnía/métodos , Producción de Medicamentos sin Interés Comercial/métodos , 4-Aminopiridina/economía , 4-Aminopiridina/uso terapéutico , Amifampridina , Publicidad Directa al Consumidor/economía , Publicidad Directa al Consumidor/legislación & jurisprudencia , Publicidad Directa al Consumidor/métodos , Composición de Medicamentos/economía , Humanos , Síndrome Miasténico de Lambert-Eaton/economía , Mercadotecnía/economía , Mercadotecnía/legislación & jurisprudencia , Producción de Medicamentos sin Interés Comercial/economía , Producción de Medicamentos sin Interés Comercial/legislación & jurisprudencia , Bloqueadores de los Canales de Potasio/economía , Bloqueadores de los Canales de Potasio/uso terapéutico , Investigación Cualitativa , Estudios Retrospectivos
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