Literature DB >> 20804226

Issues surrounding orphan disease and orphan drug policies in Europe.

Alain Denis1, Lut Mergaert, Christel Fostier, Irina Cleemput, Steven Simoens.   

Abstract

An orphan disease is a disease with a very low prevalence. Although there are 5000-7000 orphan diseases, only 50 orphan drugs (i.e. drugs developed to treat orphan diseases) were marketed in the EU by the end of 2008. In 2000, the EU implemented policies specifically designed to stimulate the development of orphan drugs. While decisions on orphan designation and the marketing authorization of orphan drugs are made at the EU level, decisions on drug reimbursement are made at the member state level. The specific features of orphan diseases and orphan drugs make them a high-priority issue for policy makers. The aim of this article is to identify and discuss several issues surrounding orphan disease and drug policies in Europe. The present system of orphan designation allows for drugs for non-orphan diseases to be designated as orphan drugs. The economic factors underlying orphan designation can be questioned in some cases, as a low prevalence of a certain indication does not equal a low return on investment for the drug across its indications. High-quality evidence about the clinical added value of orphan drugs is rarely available at the time of marketing authorization, due to the low number of patients. A balance must be struck between ethical and economic concerns. To this effect, there is a need to initiate a societal dialogue on this issue, to clarify what society wants and accepts in terms of ethical and economic consequences. The growing budgetary impact of orphan drugs puts pressure on drug expenditure. Indications can be extended for an orphan drug and the total prevalence across indications is not considered. Finally, cooperation needs to be fostered in the EU, particularly through a standardized approach to the creation and use of registries. These issues require further attention from researchers, policy makers, health professionals, patients, pharmaceutical companies and other stakeholders with a view to optimizing orphan disease and drug policies in Europe.

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Year:  2010        PMID: 20804226     DOI: 10.2165/11536990-000000000-00000

Source DB:  PubMed          Journal:  Appl Health Econ Health Policy        ISSN: 1175-5652            Impact factor:   2.561


  9 in total

1.  Orphan drugs for rare diseases: is it time to revisit their special market access status?

Authors:  Steven Simoens; David Cassiman; Marc Dooms; Eline Picavet
Journal:  Drugs       Date:  2012-07-30       Impact factor: 9.546

Review 2.  A systematic review of moral reasons on orphan drug reimbursement.

Authors:  Bettina M Zimmermann; Johanna Eichinger; Matthias R Baumgartner
Journal:  Orphanet J Rare Dis       Date:  2021-06-30       Impact factor: 4.123

3.  Principles for consistent value assessment and sustainable funding of orphan drugs in Europe.

Authors:  Laura Gutierrez; Julien Patris; Adam Hutchings; Warren Cowell
Journal:  Orphanet J Rare Dis       Date:  2015-05-03       Impact factor: 4.123

4.  Shining a light in the black box of orphan drug pricing.

Authors:  Eline Picavet; Thomas Morel; David Cassiman; Steven Simoens
Journal:  Orphanet J Rare Dis       Date:  2014-04-27       Impact factor: 4.123

5.  The role of globalization in drug development and access to orphan drugs: orphan drug legislation in the US/EU and in Latin America.

Authors:  Renée J G Arnold; Lida Bighash; Alejandro Bryón Nieto; Gabriela Tannus Branco de Araújo; Juan Gabriel Gay-Molina; Federico Augustovski
Journal:  F1000Res       Date:  2015-02-27

6.  The European challenges of funding orphan medicinal products.

Authors:  Márta Szegedi; Tamás Zelei; Francis Arickx; Anna Bucsics; Emanuelle Cohn-Zanchetta; Jurij Fürst; Maria Kamusheva; Pawel Kawalec; Guenka Petrova; Juraj Slaby; Ewa Stawowczyk; Milan Vocelka; Ingrid Zechmeister-Koss; Zoltán Kaló; Mária Judit Molnár
Journal:  Orphanet J Rare Dis       Date:  2018-11-06       Impact factor: 4.123

Review 7.  Access to Orphan Drugs: A Comprehensive Review of Legislations, Regulations and Policies in 35 Countries.

Authors:  Todd Gammie; Christine Y Lu; Zaheer Ud-Din Babar
Journal:  PLoS One       Date:  2015-10-09       Impact factor: 3.240

Review 8.  Systematic review on the evaluation criteria of orphan medicines in Central and Eastern European countries.

Authors:  Tamás Zelei; Mária J Molnár; Márta Szegedi; Zoltán Kaló
Journal:  Orphanet J Rare Dis       Date:  2016-06-04       Impact factor: 4.123

9.  Evaluating facts and facting evaluations: On the fact-value relationship in HTA.

Authors:  Bjørn Hofmann; Ken Bond; Lars Sandman
Journal:  J Eval Clin Pract       Date:  2018-04-03       Impact factor: 2.431

  9 in total

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