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1.
Value Health ; 24(5): 625-631, 2021 05.
Artículo en Inglés | MEDLINE | ID: mdl-33933230

RESUMEN

The potential health and economic value of a vaccine for coronavirus disease (COVID-19) is self-evident given nearly 2 million deaths, "collateral" loss of life as other conditions go untreated, and massive economic damage. Results from the first licensed products are very encouraging; however, there are important reasons why we will likely need second and third generation vaccines. Dedicated incentives and funding focused explicitly on nurturing and advancing competing second and third generation vaccines are essential. This article proposes a collaborative, market-based financing mechanism for the world to incentivize and pay for the development of, and provide equitable access to, second and third generation COVID-19 vaccines. Specifically, we propose consideration of a Benefit-Based Advance Market Commitment (BBAMC). The BBAMC uses health technology assessment to determine value-based prices to guarantee overall market revenues, not revenue for any specific product or company. The poorest countries would not pay a value-based price but a discounted "tail-price." Innovators must agree to supply them at this tail price or to facilitate technology transfer to local licensees at low or zero cost to enable them to supply at this price. We expect these purchases to be paid for in full or large part by global donors. The BBAMC therefore sets prices in relation to value, protects intellectual property rights, encourages competition, and ensures all populations get access to vaccines, subject to agreed priority allocation rules.


Asunto(s)
COVID-19/prevención & control , Salud Global/economía , Programas de Inmunización/economía , COVID-19/economía , Vacunas contra la COVID-19/economía , Vacunas contra la COVID-19/uso terapéutico , Defensa Civil/métodos , Defensa Civil/tendencias , Competencia Económica/normas , Competencia Económica/tendencias , Salud Global/tendencias , Humanos , Programas de Inmunización/métodos , Tratamiento Farmacológico de COVID-19
3.
Health Aff (Millwood) ; 40(8): 1243-1251, 2021 08.
Artículo en Inglés | MEDLINE | ID: mdl-34339239

RESUMEN

The COVID-19 global pandemic has devastated lives and economies. It has served as a reminder of how critical it is to invest in preventing and treating infectious diseases. Until the COVID-19 pandemic, the largest US government-sponsored reward for infectious disease drug and vaccine development was the Tropical Disease Priority Review Voucher program. Under this program, the Food and Drug Administration awards a priority review voucher to the sponsor of a new drug or vaccine for tropical infectious diseases. The voucher then can be exchanged for the faster review of one drug. We provide case studies for tropical disease voucher recipients between 2007 and 2018, examine the effects of the voucher program on product innovation and access, and recommend that policy makers protect the voucher program while creating complementary incentives.


Asunto(s)
COVID-19 , Pandemias , Desarrollo de Medicamentos , Humanos , SARS-CoV-2 , Estados Unidos , United States Food and Drug Administration
4.
BMJ Glob Health ; 4(Suppl 2): e001179, 2019.
Artículo en Inglés | MEDLINE | ID: mdl-30815287

RESUMEN

Diagnostics are fundamental for successful outbreak containment. In this supplement, 'Diagnostic preparedness for WHO Blueprint pathogens', we describe specific diagnostic challenges presented by selected priority pathogens most likely to cause future epidemics. Some challenges to diagnostic preparedness are common to all outbreak situations, as highlighted by recent outbreaks of Ebola, Zika and yellow fever. In this article, we review these overarching challenges and explore potential solutions. Challenges include fragmented and unreliable funding pathways, limited access to specimens and reagents, inadequate diagnostic testing capacity at both national and community levels of healthcare and lack of incentives for companies to develop and manufacture diagnostics for priority pathogens during non-outbreak periods. Addressing these challenges in an efficient and effective way will require multiple stakeholders-public and private-coordinated in implementing a holistic approach to diagnostics preparedness. All require strengthening of healthcare system diagnostic capacity (including surveillance and education of healthcare workers), establishment of sustainable financing and market strategies and integration of diagnostics with existing mechanisms. Identifying overlaps in diagnostic development needs across different priority pathogens would allow more timely and cost-effective use of resources than a pathogen by pathogen approach; target product profiles for diagnostics should be refined accordingly. We recommend the establishment of a global forum to bring together representatives from all key stakeholders required for the response to develop a coordinated implementation plan. In addition, we should explore if and how existing mechanisms to address challenges to the vaccines sector, such as Coalition for Epidemic Preparedness Innovations and Gavi, could be expanded to cover diagnostics.

5.
Health Syst Reform ; 4(3): 188-193, 2018.
Artículo en Inglés | MEDLINE | ID: mdl-30060703

RESUMEN

The pharmaceutical industry has confirmed its commitment to partnering with other actors to achieve the Sustainable Development Goals. There is a unique opportunity for the industry, academia, and other global health stakeholders to come together and strengthen institutions for measuring industry-led access-to-medicines (IL-AtM) programs. We propose five critical elements of the institutional context for measurement of IL-AtM programs that should be strengthened: (1) standards for measurement; (2) platforms for learning; (3) systems for transparency; (4) mechanisms for accountability; and (5) investments for sustainability. Evidence about what works would help direct future investments toward more effective programs, to the benefit of industry and society.


Asunto(s)
Conducta Cooperativa , Industria Farmacéutica , Salud Global , Accesibilidad a los Servicios de Salud , Evaluación de Programas y Proyectos de Salud , Revelación , Humanos , Difusión de la Información , Liderazgo , Responsabilidad Social
7.
Health Aff (Millwood) ; 27(4): 1029-41, 2008.
Artículo en Inglés | MEDLINE | ID: mdl-18607038

RESUMEN

India and China have made major progress toward establishing research- and innovation-based health biotechnology sectors. Local health needs, including diseases that predominantly affect the poor, have driven much of this success. We argue that emerging domestic firms can play an important role as reliable and high-quality suppliers of existing products and as innovators for global health needs. Indeed, these firms' participation may make existing global health approaches more sustainable. However, global health stakeholders, including international donors and the Indian and Chinese governments, will need to fashion incentives for these companies to retain a strategic focus on the global poor.


Asunto(s)
Industria Farmacéutica/organización & administración , Salud Global , Biotecnología , China , Industria Farmacéutica/tendencias , India
8.
Bull World Health Organ ; 83(4): 301-7, 2005 Apr.
Artículo en Inglés | MEDLINE | ID: mdl-15868022

RESUMEN

New drugs and vaccines are needed for tackling diseases of poverty in low- and middle-income countries. The lack of effective demand or market for these products translates into insufficient investment being made in research and development to meet the need for them. Many have advocated cost-reducing (push) and market-enhancing (pull) incentives to tackle this problem. Advance price or purchase commitments (APPCs) funded by international agencies and governments offer one way forward. This paper looks at design issues for APPCs for drugs and vaccines for diseases of poverty drawing on experience and lessons from three case studies: the introduction of the meningitis C vaccine in the United Kingdom; the Orphan Drug Act (ODA) in the United States of America (US); and the newly legislated US Project BioShield for bioterrorist interventions. Our key conclusion is that that APPCs have the potential to be a powerful tool and should be tried. The correct structure and design may only be determined through the process of taking action to set one up.


Asunto(s)
Drogas en Investigación/economía , Sector de Atención de Salud , Política de Salud , Pobreza , Apoyo a la Investigación como Asunto/economía , Bioterrorismo/prevención & control , Servicios Contratados , Países en Desarrollo , Costos de los Medicamentos , Humanos , Vacunas Meningococicas/economía , Estudios de Casos Organizacionales , Producción de Medicamentos sin Interés Comercial/economía , Producción de Medicamentos sin Interés Comercial/legislación & jurisprudencia , Reembolso de Incentivo , Apoyo a la Investigación como Asunto/métodos , Reino Unido , Estados Unidos
9.
Science ; 309(5733): 401-4, 2005 Jul 15.
Artículo en Inglés | MEDLINE | ID: mdl-16020723

RESUMEN

Gross inequities in disease burden between developed and developing countries are now the subject of intense global attention. Public and private donors have marshaled resources and created organizational structures to accelerate the development of new health products and to procure and distribute drugs and vaccines for the poor. Despite these encouraging efforts directed primarily from and funded by industrialized countries, sufficiency and sustainability remain enormous challenges because of the sheer magnitude of the problem. Here we highlight a complementary and increasingly important means to improve health equity: the growing ability of some developing countries to undertake health innovation.


Asunto(s)
Investigación Biomédica , Atención a la Salud , Países en Desarrollo , Difusión de Innovaciones , Investigación Biomédica/economía , Biotecnología , Atención a la Salud/organización & administración , Países Desarrollados , Industria Farmacéutica , Política de Salud , Humanos , Cooperación Internacional , Patentes como Asunto , Sector Privado , Sector Público , Edición , Transferencia de Tecnología
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