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Pharmaceutical policies and regulations of oral antiviral drugs for treatment of hepatitis C in Egypt—case study
BACKGROUND: There are limited studies on the role of efficient regulatory mechanisms in facilitating greater access to Hepatitis C virus (HCV) treatment. Evidence to support the importance of effective pharmaceutical policies and regulations in improving access to oral viral drugs towards the elimin...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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BioMed Central
2021
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8674831/ https://www.ncbi.nlm.nih.gov/pubmed/34915937 http://dx.doi.org/10.1186/s40545-021-00389-6 |
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author | Teaima, Mahmoud H. Al-Nuseirat, Adi Abouhussein, Dalia Badary, Osama A. El-Nabarawi, Mohamed A. |
author_facet | Teaima, Mahmoud H. Al-Nuseirat, Adi Abouhussein, Dalia Badary, Osama A. El-Nabarawi, Mohamed A. |
author_sort | Teaima, Mahmoud H. |
collection | PubMed |
description | BACKGROUND: There are limited studies on the role of efficient regulatory mechanisms in facilitating greater access to Hepatitis C virus (HCV) treatment. Evidence to support the importance of effective pharmaceutical policies and regulations in improving access to oral viral drugs towards the elimination of HCV is needed. This study aims to explore the adequacy of the implemented pharmaceutical policies and regulations in Egypt and their role to improve the availability and affordability of direct-acting antivirals (DAAs) to achieve universal access to the treatment of HCV. METHODS: The study adopts a qualitative methodology using desk review of regulatory and legislative information, literature review, and semi-structured interviews with key experts from the concerned governmental regulatory agencies, pharmaceutical industries, academic organizations, professional associations, civil society organizations, and clinicians who are working in researching treatments for hepatitis C. FINDINGS: The common DAAs available in the market are Daclatasvir, Sofosbuvir, and Sofosbuvir-based direct-acting antiviral combinations. Fast-track medicines registration pathway for marketing authorization of DAAs is used to reduce market access time frames. The pricing policies are supplemented using price negotiation to set up affordable prices that led to a reasonable price for DAAs. Using Trade-Related Aspects of Intellectual Property Rights (TRIPs) flexibility and local production of quality generics DAAs at lower prices. In addition, political will and collaboration between the government, civil society, and pharmaceutical companies improved patients' access to affordable DAAs and succeeding hepatitis C treatment in Egypt. CONCLUSIONS: The study findings indicated that the implemented pharmaceutical policies and regulations have an immense role in enhancing access to medicines towards the elimination of hepatitis C in Egypt. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s40545-021-00389-6. |
format | Online Article Text |
id | pubmed-8674831 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-86748312021-12-16 Pharmaceutical policies and regulations of oral antiviral drugs for treatment of hepatitis C in Egypt—case study Teaima, Mahmoud H. Al-Nuseirat, Adi Abouhussein, Dalia Badary, Osama A. El-Nabarawi, Mohamed A. J Pharm Policy Pract Review BACKGROUND: There are limited studies on the role of efficient regulatory mechanisms in facilitating greater access to Hepatitis C virus (HCV) treatment. Evidence to support the importance of effective pharmaceutical policies and regulations in improving access to oral viral drugs towards the elimination of HCV is needed. This study aims to explore the adequacy of the implemented pharmaceutical policies and regulations in Egypt and their role to improve the availability and affordability of direct-acting antivirals (DAAs) to achieve universal access to the treatment of HCV. METHODS: The study adopts a qualitative methodology using desk review of regulatory and legislative information, literature review, and semi-structured interviews with key experts from the concerned governmental regulatory agencies, pharmaceutical industries, academic organizations, professional associations, civil society organizations, and clinicians who are working in researching treatments for hepatitis C. FINDINGS: The common DAAs available in the market are Daclatasvir, Sofosbuvir, and Sofosbuvir-based direct-acting antiviral combinations. Fast-track medicines registration pathway for marketing authorization of DAAs is used to reduce market access time frames. The pricing policies are supplemented using price negotiation to set up affordable prices that led to a reasonable price for DAAs. Using Trade-Related Aspects of Intellectual Property Rights (TRIPs) flexibility and local production of quality generics DAAs at lower prices. In addition, political will and collaboration between the government, civil society, and pharmaceutical companies improved patients' access to affordable DAAs and succeeding hepatitis C treatment in Egypt. CONCLUSIONS: The study findings indicated that the implemented pharmaceutical policies and regulations have an immense role in enhancing access to medicines towards the elimination of hepatitis C in Egypt. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s40545-021-00389-6. BioMed Central 2021-12-16 /pmc/articles/PMC8674831/ /pubmed/34915937 http://dx.doi.org/10.1186/s40545-021-00389-6 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data. |
spellingShingle | Review Teaima, Mahmoud H. Al-Nuseirat, Adi Abouhussein, Dalia Badary, Osama A. El-Nabarawi, Mohamed A. Pharmaceutical policies and regulations of oral antiviral drugs for treatment of hepatitis C in Egypt—case study |
title | Pharmaceutical policies and regulations of oral antiviral drugs for treatment of hepatitis C in Egypt—case study |
title_full | Pharmaceutical policies and regulations of oral antiviral drugs for treatment of hepatitis C in Egypt—case study |
title_fullStr | Pharmaceutical policies and regulations of oral antiviral drugs for treatment of hepatitis C in Egypt—case study |
title_full_unstemmed | Pharmaceutical policies and regulations of oral antiviral drugs for treatment of hepatitis C in Egypt—case study |
title_short | Pharmaceutical policies and regulations of oral antiviral drugs for treatment of hepatitis C in Egypt—case study |
title_sort | pharmaceutical policies and regulations of oral antiviral drugs for treatment of hepatitis c in egypt—case study |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8674831/ https://www.ncbi.nlm.nih.gov/pubmed/34915937 http://dx.doi.org/10.1186/s40545-021-00389-6 |
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