BackgroundConcerns about the high cost of orphan drugs has led to questions being asked about the generosity of the incentives for development, and associated company profits.MethodsWe conducted a retrospective, propensity score matched study of publicly-listed orphan companies. Cases were defined as holders of orphan drug market authorisation in Europe or the USA between 2000-12. Control companies were selected based on their propensity for being orphan drug market authorisation holders. We applied system General Method of Moments to test whether companies with orphan drug market authorization are valued higher, as measured by the Tobin's Q and market to book value ratios, and are more profitable based on return on assets, than non-orphan ...
Conventional cost-effectiveness analysis-i.e., assessing pharmaceuticals through a cost per quality-...
Orphan designated medicinal products benefit from regulatory and economic incentives for orphan drug...
International audienceBackground:Drug development for rare diseases has been limited mainly by the p...
Concerns about the high cost of orphan drugs has led to questions being asked about the generosity o...
After describing the intellectual property and regulatory environment for orphan drugs in the United...
BACKGROUND: The Orphan Drug Act is an important piece of legislation that uses financial incentives ...
This project carries out an analysis of market access of orphan drugs for rare diseases. In the Euro...
In principle, pharmaceutical producers lack the incentives to develop orphan drugs, i.e. medicines i...
This project carries out an analysis of market access of orphan drugs for rare diseases. In the Euro...
Background The Orphan Drug Act (1983) established several incentives to encourage the development...
Background More than 6,800 rare diseases and conditions have been identified in the US, which affect...
Since the early 80s, incentives have been introduced to stimulate R&D for rare diseases. We deve...
Since the early 80s, orphan drug regulations have been introduced to stimulate R&D for rare dis...
Since the early 80s, orphan drug regulations have been introduced to stimulate R&D for rare dise...
On the thirty-fifth anniversary of the adoption of the Orphan Drug Act (ODA), we describe the enormo...
Conventional cost-effectiveness analysis-i.e., assessing pharmaceuticals through a cost per quality-...
Orphan designated medicinal products benefit from regulatory and economic incentives for orphan drug...
International audienceBackground:Drug development for rare diseases has been limited mainly by the p...
Concerns about the high cost of orphan drugs has led to questions being asked about the generosity o...
After describing the intellectual property and regulatory environment for orphan drugs in the United...
BACKGROUND: The Orphan Drug Act is an important piece of legislation that uses financial incentives ...
This project carries out an analysis of market access of orphan drugs for rare diseases. In the Euro...
In principle, pharmaceutical producers lack the incentives to develop orphan drugs, i.e. medicines i...
This project carries out an analysis of market access of orphan drugs for rare diseases. In the Euro...
Background The Orphan Drug Act (1983) established several incentives to encourage the development...
Background More than 6,800 rare diseases and conditions have been identified in the US, which affect...
Since the early 80s, incentives have been introduced to stimulate R&D for rare diseases. We deve...
Since the early 80s, orphan drug regulations have been introduced to stimulate R&D for rare dis...
Since the early 80s, orphan drug regulations have been introduced to stimulate R&D for rare dise...
On the thirty-fifth anniversary of the adoption of the Orphan Drug Act (ODA), we describe the enormo...
Conventional cost-effectiveness analysis-i.e., assessing pharmaceuticals through a cost per quality-...
Orphan designated medicinal products benefit from regulatory and economic incentives for orphan drug...
International audienceBackground:Drug development for rare diseases has been limited mainly by the p...