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What impact does ‘conventional’ economic evaluation have on patient access to new orphan medicines? A comparative study of their reimbursement in Australia (2005–2012)

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Kentaro Kogushi, Toshio Ogawa & Shunya Ikeda. (2020) An impact analysis of the implementation of health technology assessment for new treatment of orphan diseases in Japan. Expert Review of Pharmacoeconomics & Outcomes Research 20:5, pages 455-471.
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Mohammad M. Haque, Mutsa Gumbie, Megan Gu & Gnanadarsha Dissanayake. (2022) Factors associated with Pharmaceutical Benefits Advisory Committee decisions for listing medicines for diabetes and its associated complications. Australian Health Review 47:2, pages 139-147.
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Yu-Jun Huang, Wan-Yu Chao, Chi-Chuan Wang & Lin-Chau Chang. (2022) Orphan drug development: The impact of regulatory and reimbursement frameworks. Drug Discovery Today 27:6, pages 1724-1732.
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Olga A. Belousova, Aard J. Groen & Aniek M. Ouendag. (2020) Opportunities and barriers for innovation and entrepreneurship in orphan drug development. Technological Forecasting and Social Change 161, pages 120333.
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Yen Hoang Le Phan, Richard De Abreu Lourenco, Marion Haas & Naomi van der Linden. (2018) Key considerations in reimbursement decision-making for multiple sclerosis drugs in Australia. Multiple Sclerosis and Related Disorders 25, pages 144-149.
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Agnes Isabelle Vitry & Russell Shute. 2018. Equitable Access to High-Cost Pharmaceuticals. Equitable Access to High-Cost Pharmaceuticals 165 181 .
Irina Degtiar. (2017) A review of international coverage and pricing strategies for personalized medicine and orphan drugs. Health Policy 121:12, pages 1240-1248.
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Michael Wonder. (2016) Registration and Reimbursement of New Cancer Medicines in Australia. Value in Health Regional Issues 9, pages 63-64.
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