Literature DB >> 26945941

Matched analysis on orphan drug designations and approvals: cross regional analysis in the United States, the European Union, and Japan.

Manabu Murakami1, Mamoru Narukawa2.   

Abstract

Orphan drugs have become a key area of focus in drug development for resolving unmet medical needs. The Orphan Drug Act in the USA and similar legislation in Japan, the European Union (EU), and several other countries has been enacted since 1983. This study provides a quantitative review of all orphan drug designations and approvals since the implementation of orphan drug legislation in key three regions. This study also identified and reviewed 'commonly designated' drugs across regions. Out of approximately 5000 designations, approximately 800 designations were common among the USA, EU, and/or Japan. Regional similarities, differences, and trends were identified. It is important to understand these aspects and the crucial role of orphan drug designation in global drug development.
Copyright © 2016 Elsevier Ltd. All rights reserved.

Mesh:

Year:  2016        PMID: 26945941     DOI: 10.1016/j.drudis.2016.02.016

Source DB:  PubMed          Journal:  Drug Discov Today        ISSN: 1359-6446            Impact factor:   7.851


  8 in total

1.  Using four decades of FDA orphan drug designations to describe trends in rare disease drug development: substantial growth seen in development of drugs for rare oncologic, neurologic, and pediatric-onset diseases.

Authors:  Kathleen L Miller; Lewis J Fermaglich; Janet Maynard
Journal:  Orphanet J Rare Dis       Date:  2021-06-09       Impact factor: 4.123

Review 2.  Evolving Acceptance and Use of RWE for Regulatory Decision Making on the Benefit/Risk Assessment of a Drug in Japan.

Authors:  Kinue Nishioka; Tomomi Makimura; Akihiro Ishiguro; Takahiro Nonaka; Mitsune Yamaguchi; Yoshiaki Uyama
Journal:  Clin Pharmacol Ther       Date:  2021-09-18       Impact factor: 6.903

3.  Points to consider: efficacy and safety evaluations in the clinical development of ultra-orphan drugs.

Authors:  Kojiro Maeda; Masayuki Kaneko; Mamoru Narukawa; Teruyo Arato
Journal:  Orphanet J Rare Dis       Date:  2017-08-23       Impact factor: 4.123

4.  Orphan medicinal products in Europe and United States to cover needs of patients with rare diseases: an increased common effort is to be foreseen.

Authors:  Viviana Giannuzzi; Rosa Conte; Annalisa Landi; Serena Antonella Ottomano; Donato Bonifazi; Paola Baiardi; Fedele Bonifazi; Adriana Ceci
Journal:  Orphanet J Rare Dis       Date:  2017-04-03       Impact factor: 4.123

5.  Application of orphan drug designation to cancer treatments (2008-2017): a comprehensive and comparative analysis of the USA and EU.

Authors:  Kerstin Noëlle Vokinger; Aaron S Kesselheim
Journal:  BMJ Open       Date:  2019-10-10       Impact factor: 2.692

6.  Survey of Japanese Orphan Drug Program: Factors Related to Successful Marketing Approval.

Authors:  Kenji Harada; Kazuki Toriyabe; Shunsuke Ono
Journal:  J Clin Pharmacol       Date:  2019-07-31       Impact factor: 3.126

7.  Effects of socio-economic factors on research over systemic sclerosis: an analysis based on long time series of bibliometric data.

Authors:  Wei Guo; Zeyu Zhou; Yinhe Liang; Chuanhui Xu; Lin Zeng; Zhiyong Dong; Rong Mu
Journal:  Orphanet J Rare Dis       Date:  2021-12-20       Impact factor: 4.123

8.  Nationwide incidence of central retinal artery occlusion in Japan: an exploratory descriptive study using the National Database of Health Insurance Claims (2011-2015).

Authors:  Ai Kido; Hiroshi Tamura; Hanako Ohashi Ikeda; Masahiro Miyake; Shusuke Hiragi; Akitaka Tsujikawa
Journal:  BMJ Open       Date:  2020-09-24       Impact factor: 2.692

  8 in total

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