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Orphan medicines and therapeutic innovation

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Resumo:Rare diseases are by definition a disease that affects a small amount of people. However, adding up all the small number of rare diseases, the total number of patients will become significant, affecting millions of people around the world. The lack of interest in the development of orphan medicines and the patients' urgent medical need led the government and agencies to take action in order to promote and incentive the development of orphan medicines firstly in 1983 by the Food and Drug Administration and then followed by the European Union and several countries around the globe. These incentives not only enabled a growing knowledge pool on rare diseases but also the non rare diseases. During the last decade the concern about orphan medicines development has steadily increased to pharmaceutical and biopharmaceutical industry. This growth had obviously to do with the incentives, but also because industry saw the great opportunity that this underdeveloped market was and the vast income that could result from it. However, the access to these medicines is not equal to all the rare diseases' patients within different countries around the world and this is still a struggle that agencies are trying to find the best way to overcome. Therefore, most countries are trying to find a balance between the sustainability of the National Health Services and the equitable access of orphan medicines to patients with rare diseases.
Autores principais:Silva, Fábio da Costa
Assunto:Mestrado Integrado - 2014
Ano:2014
País:Portugal
Tipo de documento:dissertação de mestrado
Tipo de acesso:acesso restrito
Instituição associada:Universidade de Lisboa
Idioma:português
Origem:Repositório da Universidade de Lisboa
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author Silva, Fábio da Costa
author_facet Silva, Fábio da Costa
author_role author
contributor_name_str_mv Sepodes, Bruno Miguel Nogueira
Repositório Científico de Acesso Aberto da ULisboa
country_str PT
creators_json_txt [{\"Person.name\":\"Silva, Fábio da Costa\"}]
datacite.contributors.contributor.contributorName.fl_str_mv Sepodes, Bruno Miguel Nogueira
Repositório Científico de Acesso Aberto da ULisboa
datacite.creators.creator.creatorName.fl_str_mv Silva, Fábio da Costa
datacite.date.Accepted.fl_str_mv 2014-01-01T00:00:00Z
datacite.date.available.fl_str_mv 2017-03-06T19:25:05Z
datacite.date.embargoed.fl_str_mv 2017-03-06T19:25:05Z
datacite.rights.fl_str_mv http://purl.org/coar/access_right/c_16ec
datacite.subjects.subject.fl_str_mv Mestrado Integrado - 2014
datacite.titles.title.fl_str_mv Orphan medicines and therapeutic innovation
dc.contributor.none.fl_str_mv Sepodes, Bruno Miguel Nogueira
Repositório Científico de Acesso Aberto da ULisboa
dc.creator.none.fl_str_mv Silva, Fábio da Costa
dc.date.Accepted.fl_str_mv 2014-01-01T00:00:00Z
dc.date.available.fl_str_mv 2017-03-06T19:25:05Z
dc.date.embargoed.fl_str_mv 2017-03-06T19:25:05Z
dc.format.none.fl_str_mv application/pdf
dc.identifier.none.fl_str_mv http://hdl.handle.net/10451/26906
dc.language.none.fl_str_mv por
dc.rights.none.fl_str_mv http://purl.org/coar/access_right/c_16ec
dc.subject.none.fl_str_mv Mestrado Integrado - 2014
dc.title.fl_str_mv Orphan medicines and therapeutic innovation
dc.type.none.fl_str_mv http://purl.org/coar/resource_type/c_bdcc
description Rare diseases are by definition a disease that affects a small amount of people. However, adding up all the small number of rare diseases, the total number of patients will become significant, affecting millions of people around the world. The lack of interest in the development of orphan medicines and the patients' urgent medical need led the government and agencies to take action in order to promote and incentive the development of orphan medicines firstly in 1983 by the Food and Drug Administration and then followed by the European Union and several countries around the globe. These incentives not only enabled a growing knowledge pool on rare diseases but also the non rare diseases. During the last decade the concern about orphan medicines development has steadily increased to pharmaceutical and biopharmaceutical industry. This growth had obviously to do with the incentives, but also because industry saw the great opportunity that this underdeveloped market was and the vast income that could result from it. However, the access to these medicines is not equal to all the rare diseases' patients within different countries around the world and this is still a struggle that agencies are trying to find the best way to overcome. Therefore, most countries are trying to find a balance between the sustainability of the National Health Services and the equitable access of orphan medicines to patients with rare diseases.
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spelling porRare diseases are by definition a disease that affects a small amount of people. However, adding up all the small number of rare diseases, the total number of patients will become significant, affecting millions of people around the world. The lack of interest in the development of orphan medicines and the patients' urgent medical need led the government and agencies to take action in order to promote and incentive the development of orphan medicines firstly in 1983 by the Food and Drug Administration and then followed by the European Union and several countries around the globe. These incentives not only enabled a growing knowledge pool on rare diseases but also the non rare diseases. During the last decade the concern about orphan medicines development has steadily increased to pharmaceutical and biopharmaceutical industry. This growth had obviously to do with the incentives, but also because industry saw the great opportunity that this underdeveloped market was and the vast income that could result from it. However, the access to these medicines is not equal to all the rare diseases' patients within different countries around the world and this is still a struggle that agencies are trying to find the best way to overcome. Therefore, most countries are trying to find a balance between the sustainability of the National Health Services and the equitable access of orphan medicines to patients with rare diseases.application/pdfOrphan medicines and therapeutic innovationSilva, Fábio da CostaSepodes, Bruno Miguel NogueiraHostingInstitutionOrganizationalRepositório Científico de Acesso Aberto da ULisboae-mailmailto:repositorio@reitoria.ulisboa.ptrepositorio@reitoria.ulisboa.pt2017-03-06T19:25:05Z201420162014-01-01T00:00:00ZHandlehttp://hdl.handle.net/10451/26906http://purl.org/coar/access_right/c_16ecrestricted accessMestrado Integrado - 2014427669 bytesliteraturehttp://purl.org/coar/resource_type/c_bdccmaster thesishttp://purl.org/coar/access_right/c_16ecapplication/pdffulltexthttps://repositorio.ulisboa.pt/bitstreams/da34f142-9ea7-42b9-8161-39dece29b13f/download
spellingShingle Orphan medicines and therapeutic innovation
Silva, Fábio da Costa
Mestrado Integrado - 2014
status SINGLETON
subject.fl_str_mv Mestrado Integrado - 2014
title Orphan medicines and therapeutic innovation
title_full Orphan medicines and therapeutic innovation
title_fullStr Orphan medicines and therapeutic innovation
title_full_unstemmed Orphan medicines and therapeutic innovation
title_short Orphan medicines and therapeutic innovation
title_sort Orphan medicines and therapeutic innovation
topic Mestrado Integrado - 2014
topic_facet Mestrado Integrado - 2014
url http://hdl.handle.net/10451/26906
visible 1