A health economic guide to market access of biosimilars

S Simoens, AG Vulto - Expert opinion on biological therapy, 2021 - Taylor & Francis
Introduction: Little is known about market access to biosimilars from a health economic
perspective, except for studies that compute the budget impact of biosimilar use. Areas …

[图书][B] Access to high-priced medicines in lower-income countries in the WHO European Region

B Németh, M Csanádi, A Inotai, D Ameyaw, Z Kaló - 2022 - apps.who.int
Lower-income countries (‎ LICs)‎ in the WHO European Region generally have poorer health
status and more limited resources than higher-income countries. This creates pressing …

Maximizing the benefits of using biosimilars in Egypt

AN Fasseeh, B Elezbawy, KA El-Fass, M GamaI… - … of Pharmaceutical Policy …, 2023 - Springer
Background Biosimilars constitute a pathway for sustainable financing of healthcare systems
in the era of expensive biologics. However, such a pathway is not free of challenges. Since …

The impact of reimbursement practices on the pharmaceutical market for off-patent medicines in Slovakia

T Tesar, P Golias, L Masarykova, P Kawalec… - Frontiers in …, 2021 - frontiersin.org
Background: The aim of this study was to investigate the impact of selected legislative
initiatives and their implementation for off-patent medicinal products in Slovakia compared …

Utilisation Trend of Long‐Acting Insulin Analogues including Biosimilars across Europe: Findings and Implications

B Godman, M Wladysiuk, S McTaggart… - BioMed research …, 2021 - Wiley Online Library
Background. Diabetes mellitus rates and associated costs continue to rise across Europe
enhancing health authority focus on its management. The risk of complications is enhanced …

How to solve financing gap to ensure patient access to patented pharmaceuticals in CEE countries?–the good, the bad, and the ugly ways

A Inotai, Z Kaló - Expert Review of Pharmacoeconomics & …, 2019 - Taylor & Francis
Introduction: There is significant difference in utilization of patented medicines in the EU, as
pharmaceuticals at Western European price levels are usually not cost-effective in Central …

Safety and effectiveness of multiple switching between originators and biosimilars: literature review and status report on interchangeability

R Lasala, P Abrate, A Zovi, F Santoleri - Therapeutic Innovation & …, 2023 - Springer
To date, numerous biosimilars are available in Europe and the practice of switching
between originator and biosimilar or between two different biosimilars has become very …

Policy measures and instruments used in European countries to increase biosimilar uptake: a systematic review

S Machado, A Cruz, PL Ferreira, C Morais… - Frontiers in Public …, 2024 - frontiersin.org
Introduction While biosimilar medicines can contribute to the sustainability of healthcare
systems, their utilization rate varies across European countries. This study aims to identify …

Monitoring a Mandatory Nonmedical Switching Policy from Originator to Biosimilar Infliximab in Patients with Inflammatory Bowel Diseases: A Population‐Based …

A Fisher, JD Kim, CR Dormuth - … Research and Practice, 2023 - Wiley Online Library
Background. On September 5, 2019, British Columbia announced a new policy (the
Biosimilars Initiative) to switch from originator to biosimilar infliximab for patients with …

Biosimilar development and review process in the BRICS-TM countries: Proposal for a standardized model to improve regulatory performance

H Rahalkar, A Sheppard, S Salek - Expert Review of Clinical …, 2022 - Taylor & Francis
Objectives The current study is aimed at proposing a standardized regulatory model for
biosimilar development and approval for adoption by BRICS-TM agencies, based on …