Literature DB >> 23506063

The impact of the Orphan Drug Act on drug discovery.

Marlene E Haffner1, Paul D Maher.   

Abstract

For nearly a quarter of a century the FDA Office of Orphan Products Development has administered the US Orphan Drug Act, which assists in bringing a wide variety of drug and biological (drug) products to treat rare diseases to market. Enthusiasm for rare disease product development has been sustained, seen throughout a wide spectrum of product types and disease conditions, and has resulted in clinically meaningful medical advances. Development of programmes for rare disease treatment worldwide, coupled with the development of drugs for diseases affecting developing countries, attests to the strength of this legislation. The marketing of almost 300 products in the US for rare diseases also testifies to the depth and intensity of scientific endeavour in this area.

Entities:  

Year:  2006        PMID: 23506063     DOI: 10.1517/17460441.1.6.521

Source DB:  PubMed          Journal:  Expert Opin Drug Discov        ISSN: 1746-0441            Impact factor:   6.098


  3 in total

Review 1.  Emptying the stores: lysosomal diseases and therapeutic strategies.

Authors:  Frances M Platt
Journal:  Nat Rev Drug Discov       Date:  2017-11-17       Impact factor: 84.694

2.  Predictors of orphan drug approval in the European Union.

Authors:  Harald E Heemstra; Remco L de Vrueh; Sonja van Weely; Hans A Büller; Hubert G M Leufkens
Journal:  Eur J Clin Pharmacol       Date:  2008-01-22       Impact factor: 2.953

3.  Genetically Modified Cell Transplantation Through Macroencapsulated Spheroids with Scaffolds to Treat Fabry Disease.

Authors:  Daisuke Kami; Yosuke Suzuki; Masashi Yamanami; Takahiro Tsukimura; Tadayasu Togawa; Hitoshi Sakuraba; Satoshi Gojo
Journal:  Cell Transplant       Date:  2021 Jan-Dec       Impact factor: 4.064

  3 in total

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