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1.
Drug News Perspect ; 22(1): 53-8, 2009.
Artigo em Inglês | MEDLINE | ID: mdl-19209299

RESUMO

The U.S. Food and Drug Administration's (FDA) Fast Track program, created in 1997, was designed to facilitate the development and expedite the review of drugs and biologics intended to treat serious or life-threatening conditions, and that demonstrate the potential to address unmet medical needs. Although the intent is laudable, the significance of designations and effectiveness of the program have recently come into question. Tufts Center for the Study of Drug Development has collected data on fast track candidates since 1998. We analyzed the current dataset of 344 fast track candidates granted nearly 400 designations, representing approximately 70% of the fast track designations granted by FDA, to address questions regarding common metrics. We found that fast track candidates were widely diverse in characteristics and development histories. The complexity and limitations of the data introduced biases in metrics such as clinical phase lengths and phase transition probabilities, although these could be determined for subsets of the candidates. Our results suggest that evaluation of the Fast Track program requires a nuanced approach, and estimates of the program's value should include assessment of the resulting marketed products.


Assuntos
Ensaios Clínicos como Assunto/legislação & jurisprudência , Aprovação de Drogas/legislação & jurisprudência , Desenho de Fármacos , Ensaios Clínicos como Assunto/métodos , Aprovação de Drogas/métodos , Indústria Farmacêutica/legislação & jurisprudência , Drogas em Investigação/normas , Humanos , Estados Unidos , United States Food and Drug Administration
2.
IDrugs ; 12(12): 779-84, 2009 Dec.
Artigo em Inglês | MEDLINE | ID: mdl-19943221

RESUMO

The development of peptides as drugs is attracting increasing attention from the pharmaceutical industry. This interest is at least partially a consequence of the widespread acceptance of therapeutic proteins by physicians and patients, and because of improvements to problems such as a short half-life and delivery issues. The markets for peptide-based compounds can be substantial, with six peptide drugs attaining global sales of more than US $750 million in 2008. To track trends in the clinical development and marketing approval of peptides, Tufts Center for the Study of Drug Development and Ferring Research Institute compiled publically available data for peptides that entered clinical trials sponsored by commercial firms, with a focus on peptide therapeutics, but also including peptide vaccines and diagnostics. The results provide an historical overview of the development of peptide therapeutics, and may inform strategic planning in this area.


Assuntos
Desenho de Fármacos , Indústria Farmacêutica/tendências , Peptídeos/uso terapêutico , Atitude do Pessoal de Saúde , Ensaios Clínicos como Assunto , Comércio/tendências , Aprovação de Drogas , Indústria Farmacêutica/economia , Humanos , Aceitação pelo Paciente de Cuidados de Saúde , Peptídeos/economia , Vacinas de Subunidades Antigênicas/imunologia
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