Literature DB >> 25343087

Access to orphan drugs in the Middle East: Challenge and perspective.

Ziyad S Almalki1, Abdullah K Alahmari1, Jeff J Guo1, Christina M L Kelton2.   

Abstract

An orphan drug is a drug developed specifically to treat a rare medical condition. With a combined population of less than 400 million, about 2.8 million patients are estimated to be suffering from a rare disease in the Middle East. Some disorders such as hemoglobinopathy, glucose-6-phosphate dehydrogenase deficiency, autosomal recessive syndromes, and several metabolic disorders have a presence throughout the Middle East. In order to promote the treatment of these diseases, Middle Eastern governments need to facilitate education and training of healthcare personnel; develop and execute a method for obtaining and paying for orphan drugs; and, finally, provide tax, marketing, and other incentives to domestic and international firms to develop drugs specifically for the diseases of most importance to Middle Eastern patients.

Entities:  

Keywords:  Middle East; Orphan drug; genetic disorder; rare disease

Year:  2012        PMID: 25343087      PMCID: PMC4204565          DOI: 10.5582/irdr.2012.v1.4.139

Source DB:  PubMed          Journal:  Intractable Rare Dis Res        ISSN: 2186-3644


  14 in total

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3.  Glutaric aciduria type I in the Arab and Jewish communities in Israel.

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Review 5.  Rare diseases, orphan drugs, and their regulation in Asia: Current status and future perspectives.

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6.  Intractable and rare diseases research.

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7.  Orphan drug pricing and payer management in the United States: are we approaching the tipping point?

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Journal:  Am Health Drug Benefits       Date:  2010-01

8.  Orphan drug: Development trends and strategies.

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Journal:  J Pharm Bioallied Sci       Date:  2010-10

9.  Recommendations for genetic variation data capture in developing countries to ensure a comprehensive worldwide data collection.

Authors:  George P Patrinos; Jumana Al Aama; Aida Al Aqeel; Fahd Al-Mulla; Joseph Borg; Andrew Devereux; Alex E Felice; Finlay Macrae; Makia J Marafie; Michael B Petersen; Ming Qi; Rajkumar S Ramesar; Joel Zlotogora; Richard G H Cotton
Journal:  Hum Mutat       Date:  2011-01       Impact factor: 4.878

10.  CTGA: the database for genetic disorders in Arab populations.

Authors:  Ghazi O Tadmouri; Mahmoud Taleb Al Ali; Sarah Al-Haj Ali; Najib Al Khaja
Journal:  Nucleic Acids Res       Date:  2006-01-01       Impact factor: 16.971

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  2 in total

1.  Analysis of patient access to orphan drugs in Turkey.

Authors:  Güvenç Koçkaya; Sibel Atalay; Gülpembe Oğuzhan; Mustafa Kurnaz; Selin Ökçün; Çiğdem Sar Gedik; Mete Şaylan; Nazlı Şencan
Journal:  Orphanet J Rare Dis       Date:  2021-02-06       Impact factor: 4.123

2.  Rare disease in Malaysia: Challenges and solutions.

Authors:  Asrul Akmal Shafie; Azuwana Supian; Mohamed Azmi Ahmad Hassali; Lock-Hock Ngu; Meow-Keong Thong; Hatijah Ayob; Nathorn Chaiyakunapruk
Journal:  PLoS One       Date:  2020-04-02       Impact factor: 3.752

  2 in total

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