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. © 2012, International Research and Cooperation Association for Bio & Socio-Sciences Advancement. All rights reserved.
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Almalki1, Z. S., Alahmari, A. K., Guo, J. J., & Kelton, C. M. L. (2012). Access to orphan drugs in the Middle East: Challenge and perspective. Intractable and Rare Diseases Research, 1(4), 139–143. https://doi.org/10.5582/irdr.2012.v1.4.139
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