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ORPHAN DRUGS
被引:0
|作者:
Fontanet Sacristan, Juan Manuel
[1
]
Torrent-Farnell, Josep
[1
]
机构:
[1] Univ Autonoma Barcelona, Hosp Santa Creu & St Pau, Barcelona, Spain
关键词:
Rare disease;
orphan drug;
designation;
incentives;
investigation;
CLINICAL-TRIALS;
D O I:
10.3989/arbor.2018.789n3008
中图分类号:
C [社会科学总论];
学科分类号:
03 ;
0303 ;
摘要:
Orphan drugs are intended for the treatment of diseases of low prevalence, also known as rare diseases. Research and development into new therapies for this heterogeneous group of diseases presents a number of well-recognized difficulties. One of these is that the small number of patients affected jeopardizes the economic return on the investment made by the pharmaceutical industry. For this reason, in the year 2000 the European Union brought out a specific European Regulation to promote and encourage the development of these therapies. After more than a decade, the results reveal a positive effect of the approval of that regulation. Currently, more than 1300 compounds have been designated orphan drugs, of which over 90 have already obtained marketing authorization. The voice of the patient has been key to producing this change and programs and research consortia promoted by the EU promise an even brighter future.
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