Literature DB >> 27527064

[Orphan drugs : New opportunities for the treatment of rare diseases].

M Beck1,2.   

Abstract

Not only in Europe and USA, but also in many other countries rare disorders-so-called orphan diseases-have attracted more and more attention. The formation of specialized centers for rare disorders has enabled the diagnosis of diseases that have been widely unknown before. In addition, pharmaceutical companies have recognized orphan diseases as a profitable source of revenue. The development and marketing of new drugs for rare diseases-so-called orphan diseases-means a great challenge for all who participate in the health care system: Because the number of patients who are available for a clinical study is mostly very small, it is often very difficult or even impossible to show statistically firm evidence of efficacy. The standard placebo-controlled, double-blind clinical trial is often inappropriate for the approval procedure of an orphan drug; thus other study designs or other parameters (e.g. biomarkers) have to be used to prove clinical efficacy of the study drug. Only relatively small amounts of drugs can be sold to the generally few patients affected by an orphan disease and clinical trials require an high amount of financial investment; therefore orphan drugs have in general extremely high prices. How long these high expenses can be borne by the health care system in view of the great number of rare diseases remains questionable.

Entities:  

Keywords:  Clinical trials; Drug approval; Public health; Rare diseases, economics; Self-help groups

Mesh:

Year:  2016        PMID: 27527064     DOI: 10.1007/s00108-016-0114-y

Source DB:  PubMed          Journal:  Internist (Berl)        ISSN: 0020-9554            Impact factor:   0.743


  16 in total

Review 1.  Two decades of orphan product development.

Authors:  Marlene E Haffner; Janet Whitley; Marie Moses
Journal:  Nat Rev Drug Discov       Date:  2002-10       Impact factor: 84.694

2.  Rare disease policies to improve care for patients in Europe.

Authors:  Charlotte Rodwell; Ségolène Aymé
Journal:  Biochim Biophys Acta       Date:  2015-02-25

3.  Adopting orphan drugs--two dozen years of treating rare diseases.

Authors:  Marlene E Haffner
Journal:  N Engl J Med       Date:  2006-02-02       Impact factor: 91.245

Review 4.  Adaptive licensing: taking the next step in the evolution of drug approval.

Authors:  H-G Eichler; K Oye; L G Baird; E Abadie; J Brown; C L Drum; J Ferguson; S Garner; P Honig; M Hukkelhoven; J C W Lim; R Lim; M M Lumpkin; G Neil; B O'Rourke; E Pezalla; D Shoda; V Seyfert-Margolis; E V Sigal; J Sobotka; D Tan; T F Unger; G Hirsch
Journal:  Clin Pharmacol Ther       Date:  2012-02-15       Impact factor: 6.875

5.  Enzyme-replacement therapy in mucopolysaccharidosis I.

Authors:  E D Kakkis; J Muenzer; G E Tiller; L Waber; J Belmont; M Passage; B Izykowski; J Phillips; R Doroshow; I Walot; R Hoft; E F Neufeld
Journal:  N Engl J Med       Date:  2001-01-18       Impact factor: 91.245

6.  Multifaceted roles of ultra-rare and rare disease patients/parents in drug discovery.

Authors:  Jill Wood; Lori Sames; Allison Moore; Sean Ekins
Journal:  Drug Discov Today       Date:  2013-08-19       Impact factor: 7.851

7.  Pricing and reimbursement of orphan drugs: the need for more transparency.

Authors:  Steven Simoens
Journal:  Orphanet J Rare Dis       Date:  2011-06-17       Impact factor: 4.123

8.  A methodological framework for drug development in rare diseases.

Authors:  Patrice Nony; Polina Kurbatova; Agathe Bajard; Salma Malik; Charlotte Castellan; Sylvie Chabaud; Vitaly Volpert; Nathalie Eymard; Behrouz Kassai; Catherine Cornu
Journal:  Orphanet J Rare Dis       Date:  2014-11-18       Impact factor: 4.123

Review 9.  Adaptive design methods in clinical trials - a review.

Authors:  Shein-Chung Chow; Mark Chang
Journal:  Orphanet J Rare Dis       Date:  2008-05-02       Impact factor: 4.123

10.  Comparative Effectiveness of Biosimilar, Reference Product and Other Erythropoiesis-Stimulating Agents (ESAs) Still Covered by Patent in Chronic Kidney Disease and Cancer Patients: An Italian Population-Based Study.

Authors:  Ylenia Ingrasciotta; Francesco Giorgianni; Ilaria Marcianò; Jenny Bolcato; Roberta Pirolo; Alessandro Chinellato; Valentina Ientile; Domenico Santoro; Armando A Genazzani; Angela Alibrandi; Andrea Fontana; Achille P Caputi; Gianluca Trifirò
Journal:  PLoS One       Date:  2016-05-17       Impact factor: 3.240

View more
  2 in total

1.  [Orphan drugs].

Authors:  Jürgen R Schäfer; Claus F Vogelmeier
Journal:  Internist (Berl)       Date:  2019-04       Impact factor: 0.743

Review 2.  From promising molecules to orphan drugs: Early clinical drug development.

Authors:  Marc Dooms
Journal:  Intractable Rare Dis Res       Date:  2017-02
  2 in total

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