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2.
Clin Pharmacol Ther ; 100(6): 685-698, 2016 12.
Artigo em Inglês | MEDLINE | ID: mdl-27626610

RESUMO

The current system of biomedical innovation is unable to keep pace with scientific advancements. We propose to address this gap by reengineering innovation processes to accelerate reliable delivery of products that address unmet medical needs. Adaptive biomedical innovation (ABI) provides an integrative, strategic approach for process innovation. Although the term "ABI" is new, it encompasses fragmented "tools" that have been developed across the global pharmaceutical industry, and could accelerate the evolution of the system through more coordinated application. ABI involves bringing stakeholders together to set shared objectives, foster trust, structure decision-making, and manage expectations through rapid-cycle feedback loops that maximize product knowledge and reduce uncertainty in a continuous, adaptive, and sustainable learning healthcare system. Adaptive decision-making, a core element of ABI, provides a framework for structuring decision-making designed to manage two types of uncertainty - the maturity of scientific and clinical knowledge, and the behaviors of other critical stakeholders.


Assuntos
Pesquisa Biomédica/organização & administração , Tomada de Decisões , Atenção à Saúde/organização & administração , Difusão de Inovações , Indústria Farmacêutica/organização & administração , Retroalimentação , Necessidades e Demandas de Serviços de Saúde , Humanos , Incerteza
4.
Clin Pharmacol Ther ; 97(3): 234-46, 2015 Mar.
Artigo em Inglês | MEDLINE | ID: mdl-25669457

RESUMO

The concept of adaptive licensing (AL) has met with considerable interest. Yet some remain skeptical about its feasibility. Others argue that the focus and name of AL should be broadened. Against this background of ongoing debate, we examine the environmental changes that will likely make adaptive pathways the preferred approach in the future. The key drivers include: growing patient demand for timely access to promising therapies, emerging science leading to fragmentation of treatment populations, rising payer influence on product accessibility, and pressure on pharma/investors to ensure sustainability of drug development. We also discuss a number of environmental changes that will enable an adaptive paradigm. A life-span approach to bringing innovation to patients is expected to help address the perceived access vs. evidence trade-off, help de-risk drug development, and lead to better outcomes for patients.


Assuntos
Aprovação de Drogas/legislação & jurisprudência , Aprovação de Drogas/métodos , Descoberta de Drogas/legislação & jurisprudência , Licenciamento , Humanos
5.
Clin Pharmacol Ther ; 96(5): 559-71, 2014 Nov.
Artigo em Inglês | MEDLINE | ID: mdl-25006877

RESUMO

There is broad agreement among health-care stakeholders that more must be done to ensure that patients have timely access to new and innovative medicines. Assuming that industry will continue to develop such medicines at a sustainable rate, regulators and payers become the gatekeepers. Regulators, starting in the late 1980s/early 1990s, and, more recently, payers have implemented a variety of early-access pathways or initiatives, and this practice is continuing even today. This article describes the specific approaches that have been taken in four economically developed regions, reviews their success rates, and suggests possible new directions.


Assuntos
Acessibilidade aos Serviços de Saúde , Necessidades e Demandas de Serviços de Saúde , Preparações Farmacêuticas/provisão & distribuição , Tecnologia Biomédica , Canadá , Humanos , Mecanismo de Reembolso , Singapura , Estados Unidos , United States Food and Drug Administration
6.
Clin Pharmacol Ther ; 91(3): 426-37, 2012 Mar.
Artigo em Inglês | MEDLINE | ID: mdl-22336591

RESUMO

Traditional drug licensing approaches are based on binary decisions. At the moment of licensing, an experimental therapy is presumptively transformed into a fully vetted, safe, efficacious therapy. By contrast, adaptive licensing (AL) approaches are based on stepwise learning under conditions of acknowledged uncertainty, with iterative phases of data gathering and regulatory evaluation. This approach allows approval to align more closely with patient needs for timely access to new technologies and for data to inform medical decisions. The concept of AL embraces a range of perspectives. Some see AL as an evolutionary step, extending elements that are now in place. Others envision a transformative framework that may require legislative action before implementation. This article summarizes recent AL proposals; discusses how proposals might be translated into practice, with illustrations in different therapeutic areas; and identifies unresolved issues to inform decisions on the design and implementation of AL.


Assuntos
Aprovação de Drogas/legislação & jurisprudência , Aprovação de Drogas/métodos , Necessidades e Demandas de Serviços de Saúde/legislação & jurisprudência , Necessidades e Demandas de Serviços de Saúde/organização & administração , Licenciamento/legislação & jurisprudência , Animais , Tomada de Decisões , União Europeia , Humanos , Estados Unidos
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