Follow-on biologics: data exclusivity and the balance between innovation and competition.
Nat Rev Drug Discov
; 7(6): 479-88, 2008 06.
Article
en En
| MEDLINE
| ID: mdl-18469828
Legislation to create a regulatory pathway for follow-on biologics is currently being considered by the United States Congress. A critical issue in this respect is the period of data exclusivity for innovator companies before a follow-on competitor can rely in part on data obtained for an original biologic for an abbreviated approval. Given the nature of patents on biologics, the period of data exclusivity is anticipated to have a key role in determining how quickly follow-on competitors emerge, and consequently also on the time available for originator companies to recoup their investment. With this issue in mind, this article discusses factors influencing return on investment on biologic research and development. A break-even analysis for a representative portfolio of biologics provides support for a substantial data exclusivity period.
Texto completo:
1
Base de datos:
MEDLINE
Asunto principal:
Biotecnología
/
Medicamentos Genéricos
/
Aprobación de Drogas
/
Difusión de Innovaciones
/
Industria Farmacéutica
/
Competencia Económica
Tipo de estudio:
Prognostic_studies
/
Sysrev_observational_studies
País/Región como asunto:
America do norte
Idioma:
En
Revista:
Nat Rev Drug Discov
Asunto de la revista:
FARMACOLOGIA
/
TERAPIA POR MEDICAMENTOS
Año:
2008
Tipo del documento:
Article
País de afiliación:
Estados Unidos