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Medicina is published by MDPI from Volume 54 Issue 1 (2018). Articles in this Issue were published by another publisher in Open Access under a CC-BY (or CC-BY-NC-ND) licence. Articles are hosted by MDPI on as a courtesy and upon agreement with Lithuanian Medical Association, Lithuanian University of Health Sciences, and Vilnius University.
Open AccessArticle

Access to information supporting availability of medicines for patients suffering from rare diseases looking for possible treatments: the EuOrphan Service

Mykolas Romeris University, Vilnius, Lithuania
Institute of Oncology, Vilnius University, Vilnius, Lithuania
University of Pavia and S. Maugeri Foundation, Pavia, Italy
Author to whom correspondence should be addressed.
EuOrphan Project – eTEN 510774-2003/C. Partners: Consorzio per Valutazioni Biologiche e Farmacologiche, Italy (Paola Baiardi); Softeco Sismat S.p.A, Italy (Enrico Morten); Istituto Superiore di Sanità, Italy (Domenica Taruscio); Fundación para la Cooperación y Salud Internacional Carlos III, Spain (Manuel Posada); Universidad de Barcellona, Spain (Elvira Bel Prieto), Karolinska Institutet, Sweden (Lars Savendahl); Fondazione Italiana “L. Giambrone” per la Guarigione dalla Thalassemia, Italy (Angela Iacono); Società di Scienze Farmacologiche Applicate, Italy (Domenico Criscuolo); Scuola Europea di Medicina Generale, Italy (Roberto Nardi); Vilnius University, Lithuania (Donatas Stakišaitis); Confederation of European Specialists in Paediatrics, Belgium (José Ramet); SC Sviluppo Chimica S.p.A, Italy (Leonardo Vingiani); Federazione Italiana Malattie Rare (UNIAMO), Italy (Flavio Minelli).
Medicina 2007, 43(6), 441;
Received: 2 April 2007 / Accepted: 11 June 2007 / Published: 16 June 2007
Currently in Europe, approximately 30 million people suffer from rare diseases, and a major problem is that many patients do not have access to quality healthcare for their disorders. Moreover, there is also a lack of quality information and a networking system aimed at supporting interaction among patients, clinicians, researchers, pharmaceutical industries, and governmental bodies. The purpose of this article is to inform physicians, public health care professionals, and other health care providers about EuOrphan service, the aim of which is to ensure easier access to quality information on rare diseases and their treatment. A set of web-based services is available at where information for target-users on treatments and products available worldwide for rare disease care as well as indications about healthcare centers are provided. Moreover, the service aims at providing consultancies for pharmaceutical companies to ultimately support the European legislation in bringing new drugs of a high ethical standard to the market and to exert a positive impact on the large population of patients suffering from rare diseases in Europe. The services provided by EuOrphan can facilitate concrete networking among patients, patient associations, doctors, and companies and also support the organization of clinical trials. In this perspective, EuOrphan could become a very valuable tool for globalizing the information about the availability of treatment (authorized or under development) of orphan patients.
Keywords: rare diseases; orphan drugs; health orphan; information; legislation rare diseases; orphan drugs; health orphan; information; legislation
MDPI and ACS Style

Stakišaitis, D.; Špokienė, I.; Juškevičius, J.; Valuckas, K.P.; Baiardi, P. Access to information supporting availability of medicines for patients suffering from rare diseases looking for possible treatments: the EuOrphan Service. Medicina 2007, 43, 441.

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