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1.
PLoS Negl Trop Dis ; 14(6): e0008398, 2020 06.
Artículo en Inglés | MEDLINE | ID: mdl-32569280

RESUMEN

Approximately 300,000 persons in the United States (US) are infected with Trypanosoma cruzi, the protozoan that causes Chagas disease, but less than 1% are estimated to have received antiparasitic treatment. Benznidazole was approved by the US Food and Drug Administration (FDA) for treatment of T. cruzi infection in 2017 and commercialized in May 2018. This paper analyzes factors that affect access to benznidazole following commercialization and suggests directions for future actions to expand access. We applied an access framework to identify barriers, facilitators, and key actors that influence the ability of people with Chagas disease to receive appropriate treatment with benznidazole. Data were collected from the published literature, key informants, and commercial databases. We found that the mean number of persons who obtained benznidazole increased from just under 5 when distributed by the CDC to 13 per month after the commercial launch (from May 2018 to February 2019). Nine key barriers to access were identified: lack of multi-sector coordination, failure of health care providers to use a specific order form, lack of an emergency delivery system, high medical costs for uninsured patients, narrow indications for use of benznidazole, lack of treatment guidelines, limited number of qualified treaters, difficulties for patients to make medical appointments, and inadequate evaluation by providers to determine eligibility for treatment. Our analysis shows that access to benznidazole is still limited after FDA approval. We suggest six areas for strategic action for the pharmaceutical company that markets benznidazole and its allied private foundation to expand access to benznidazole in the US. In addition, we recommend expanding the existing researcher-clinician network by including government agencies, companies and others. This paper's approach could be applied to access programs for benznidazole in other countries or for other health products that target neglected populations throughout the world.


Asunto(s)
Enfermedad de Chagas/tratamiento farmacológico , Nitroimidazoles/provisión & distribución , Nitroimidazoles/uso terapéutico , Tripanocidas/provisión & distribución , Tripanocidas/uso terapéutico , Factores de Edad , Centers for Disease Control and Prevention, U.S. , Costos de los Medicamentos , Drogas en Investigación , Humanos , Nitroimidazoles/economía , Tripanocidas/economía , Trypanosoma cruzi , Estados Unidos , United States Food and Drug Administration
2.
Expert Rev Anti Infect Ther ; 17(3): 145-157, 2019 03.
Artículo en Inglés | MEDLINE | ID: mdl-30712412

RESUMEN

INTRODUCTION: Chagas disease, caused by infection with the parasite Trypanosoma cruzi, represents a huge public health problem in the Americas, where millions of people are affected. Despite the availability of two drugs against the infection (benznidazole and nifurtimox), multiple factors impede their effective usage: (1) gaps in patient and healthcare provider awareness; (2) lack of access to diagnosis; (3) drug toxicity and absence of treatment algorithms to address adverse effects; (4) failures in drug supply and distribution; and (5) inconsistent drug efficacy against the symptomatic chronic stage. Areas covered: We review new approaches and technologies to enhance access to diagnosis and treatment to reduce the disease burden. We also provide an updated picture of recently published and ongoing anti-T. cruzi drug clinical trials. Although there has been progress improving the research and development (R&D) landscape, it is unclear whether any new treatments will emerge soon. Literature search methodologies included multiple queries to public databases and the use of own-built libraries. Expert opinion: Besides R&D, there is a major need to continue awareness and advocacy efforts by patient associations, local and national governments, and international agencies. Overall, health systems strengthening is essential to ensure vector control commitments, as well as patient access to diagnosis and treatment.


Asunto(s)
Enfermedad de Chagas/tratamiento farmacológico , Accesibilidad a los Servicios de Salud , Tripanocidas/uso terapéutico , Enfermedad de Chagas/diagnóstico , Enfermedad de Chagas/epidemiología , Humanos , América Latina/epidemiología , Nifurtimox/efectos adversos , Nifurtimox/provisión & distribución , Nifurtimox/uso terapéutico , Nitroimidazoles/efectos adversos , Nitroimidazoles/provisión & distribución , Nitroimidazoles/uso terapéutico , Tripanocidas/efectos adversos , Tripanocidas/provisión & distribución , Trypanosoma cruzi/aislamiento & purificación
3.
Int J Tuberc Lung Dis ; 22(4): 407-412, 2018 04 01.
Artículo en Inglés | MEDLINE | ID: mdl-29562988

RESUMEN

SETTING: The World Health Organization recommended two new drugs, bedaquiline (BDQ) and delamanid (DLM), for the treatment of multidrug-resistant tuberculosis (MDR-TB) in 2013 and 2014, respectively. An estimated one third of patients with MDR-TB would benefit from the inclusion of these drugs in their treatment regimens. DESIGN: A convenience sample of 36 countries voluntarily reported monthly data on cumulative programmatic use of new drugs to the Drug-Resistant TB Scale-Up Treatment Action Team between 1 July 2015 and 31 June 2017. Programmatic use was defined as treatment for MDR-TB with newer drugs outside of clinical trials or compassionate use. RESULTS: A total of 10 164 persons were started on BDQ and 688 started on DLM during the reporting period. Only 15.7% of the 69 213 persons estimated to need newer drugs over the study period were reported to have received them. CONCLUSION: While there has been significant progress in some countries, uptake of the newer drugs has not kept pace with a conservative estimate of need; fewer than 20% of persons likely to benefit from either BDQ or DLM have received them. Concerted efforts are needed to ensure that the newer drugs are made available more widely for persons with MDR-TB in need of these therapeutic options.


Asunto(s)
Antituberculosos/uso terapéutico , Diarilquinolinas/uso terapéutico , Nitroimidazoles/uso terapéutico , Oxazoles/uso terapéutico , Tuberculosis Resistente a Múltiples Medicamentos/tratamiento farmacológico , Antituberculosos/provisión & distribución , Diarilquinolinas/provisión & distribución , Humanos , Internacionalidad , Nitroimidazoles/provisión & distribución , Oxazoles/provisión & distribución
4.
PLoS Negl Trop Dis ; 11(9): e0005794, 2017 Sep.
Artículo en Inglés | MEDLINE | ID: mdl-28910299

RESUMEN

Drugs for neglected tropical diseases (NTD) are being excessively priced in the United States. Benznidazole, the first-line drug for Chagas disease, may become approved by the Food and Drug Administration (FDA) and manufactured by a private company in the US, thus placing it at risk of similar pricing. Chagas disease is an NTD caused by Trypanosoma cruzi; it is endemic to Latin America, infecting 8 million individuals. Human migration has changed the epidemiology causing nonendemic countries to face increased challenges in diagnosing and managing patients with Chagas disease. Only 2 drugs exist with proven efficacy: benznidazole and nifurtimox. Benznidazole has historically faced supply problems and drug shortages, limiting accessibility. In the US, it is currently only available under an investigational new drug (IND) protocol from the CDC and is provided free of charge to patients. However, 2 companies have stated that they intend to submit a New Drug Application (NDA) for FDA approval. Based on recent history of companies acquiring licensing rights for NTD drugs in the US with limited availability, it is likely that benznidazole will become excessively priced by the manufacturer-paradoxically making it less accessible. However, if the companies can be taken at their word, there may be reason for optimism.


Asunto(s)
Enfermedad de Chagas/tratamiento farmacológico , Nitroimidazoles/economía , Nitroimidazoles/provisión & distribución , Tripanocidas/economía , Tripanocidas/provisión & distribución , Centers for Disease Control and Prevention, U.S. , Enfermedad de Chagas/epidemiología , Costos de los Medicamentos , Drogas en Investigación/economía , Humanos , Nifurtimox/uso terapéutico , Nitroimidazoles/uso terapéutico , Tripanocidas/uso terapéutico , Estados Unidos , United States Food and Drug Administration
5.
Rev Panam Salud Publica ; 41: e45, 2017 Jun 08.
Artículo en Español | MEDLINE | ID: mdl-28614468

RESUMEN

OBJECTIVE: Describe a tool to estimate demand for benznidazole and nifurtimox to treat Chagas disease, and report on its implementation in a group of Latin American countries. METHODS: The project was carried out in the following stages: 1) development of a tool to estimate demand, and definition of the evaluation and decision variables to estimate demand 2) data collection via a questionnaire completed by representatives of control programs, complemented with data from the literature; 3) presentation of the tool, followed by validation, and adaptation by representatives of the control programs in order to plan drug procurement for 2012 and 2013; and 4) further analysis of the obtained data, especially regarding benznidazole, and comparison of country estimates. RESULTS: Fourteen endemic countries of Latin America took part in the third stage, and a consolidated estimate was made. The number of estimated treatments, based on the number of tablets per treatment established in the regimen of reference was: 867 in the group under 1 year of age; 2 042 835 in the group from 1 to 15 years old; 2 028 in the group from 15 to 20 years old; and 10 248 in adults over 20. This means that it is possible to provide benznidazole to less than 1% of people for whom treatment is indicated. CONCLUSIONS: The development and systematic use of demand management tools can play a key role in helping to provide access to the anti-Chagas drugs. There is a significant gap between the projected demand for drugs and current estimates of prevalence rates.


Asunto(s)
Enfermedad de Chagas/tratamiento farmacológico , Nifurtimox/provisión & distribución , Nifurtimox/uso terapéutico , Nitroimidazoles/provisión & distribución , Nitroimidazoles/uso terapéutico , Tripanocidas/provisión & distribución , Tripanocidas/uso terapéutico , Adolescente , Adulto , Niño , Preescolar , Humanos , Lactante , América Latina , Adulto Joven
6.
Am J Trop Med Hyg ; 87(3): 489-90, 2012 Sep.
Artículo en Inglés | MEDLINE | ID: mdl-22826485

RESUMEN

Chagas disease is a neglected tropical disease endemic in Latin America. The first-line treatment option is benznidazole, but stocks are expected to run out in the coming months. Spain would need around 5 million benznidazole tablets. This drug shortage could make Chagas disease a neglected tropical disease also in developed countries.


Asunto(s)
Enfermedad de Chagas/tratamiento farmacológico , Países Desarrollados , Nitroimidazoles/provisión & distribución , Tripanocidas/provisión & distribución , Enfermedad de Chagas/epidemiología , Humanos , Nitroimidazoles/uso terapéutico , España/epidemiología , Tripanocidas/uso terapéutico , Trypanosoma cruzi/efectos de los fármacos
8.
Rev. Soc. Bras. Med. Trop ; 30(3): 251-251, maio-jun. 1997.
Artículo en Portugués | LILACS | ID: lil-464376
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