subject: Aarkstore Enterprise--- Orphan Drugs In Asia-pacific: From Designation To Pricing, Funding & Marke [print this page] A major new report Orphan Drugs in Asia-Pacific: From designation to pricing, funding and market access focuses on five developed markets in the region: Japan, South Korea, Taiwan, Singapore and Australia. Each has passed specific measures to promote the development, registration and/or commercialisation of rare disease treatments. Singapores Medicines (Orphan Drug) Exemption Order of 1991 was the first legislation anywhere to follow the US Orphan Drug Act, with the other four Asia-Pacific countries also implementing orphan-promoting measures ahead of the EU.
Rare diseases are collectively not that rare, indeed 6-10% of people will suffer from one at some point in life. Asia-Pacific contains nearly two-thirds of the worlds population, and should offer great potential to companies developing orphan drugs. But clinical need alone does not mean that adequate money for diagnosis and treatment will be made available.
The report describes the processes for obtaining orphan product designation, what can be omitted from the standard dossier to obtain marketing authorisation, and provides full details of the regulatory bodies and timelines involved. The main emphasis though is not on registration but on market access, which for products like orphan drugs that often carry premium prices, means eligibility for reimbursement or other sources of public funds.
Based on extensive research, including fieldwork in Tokyo and Seoul in November 2009 to capture detail, understanding and all the latest trends, the report includes:
The incentives on offer to orphan drug sponsors.
How P&R processes work specifically for orphan drugs.
The role of HTA and risk sharing as levers to obtain reimbursement.
Where special funding schemes operate and how to access them.
13 case studies on the P&R history of 12 different orphan drugs in 5 countries.
How much patients are expected to contribute to the cost of their treatment.
Listings of designated and approved orphan drugs.
Comparisons between countries with orphan drug policies and those without.
Contact details of the main rare disease patient organisations.
