[HTML][HTML] Qualitative analysis of the design and implementation of benefit-sharing programs for biologics across Europe

T Barcina Lacosta, AG Vulto, A Turcu-Stiolica, I Huys… - BioDrugs, 2022 - Springer
Background To encourage the rational prescribing of biologics, payers across Europe have
experimented with the implementation of benefit-sharing programs. Benefit-sharing …

[HTML][HTML] The economic impact of originator-to-biosimilar non-medical switching in the real-world setting: a systematic literature review

E Hillhouse, K Mathurin, J Bibeau, D Parison… - Advances in …, 2022 - Springer
Introduction To save costs to the healthcare system, forced non-medical switch (NMS)
policies that cut drug coverage for originator biologics and fund only less expensive …

[HTML][HTML] European stakeholder learnings regarding biosimilars: part II—improving biosimilar use in clinical practice

L Barbier, S Simoens, AG Vulto, I Huys - BioDrugs, 2020 - Springer
Background Despite the benefits biosimilars offer in terms of cost savings and patient
access, healthcare professionals and patients have been reluctant to use them. Next to …

Potential cost implications of mandatory non‐medical switching policies for biologics for rheumatic conditions and inflammatory bowel disease in Canada

M Crosby, M Tadrous, T Gomes - Clinical Pharmacology & …, 2021 - Wiley Online Library
In 2018, TNFα inhibitors were the highest cost drug class for Canadian public drug
programs. In 2019, two Canadian provinces announced mandatory nonmedical switching …

[HTML][HTML] Uptake of biosimilar trastuzumab in Denmark compared with other European countries: a comparative study and discussion of factors influencing …

S Azuz, M Newton, D Bartels, BK Poulsen - European Journal of Clinical …, 2021 - Springer
Purpose The aim of this study was to describe the implementation and uptake of biosimilar
trastuzumab in Denmark compared with other European countries. Methods European data …

The mode of delivery and content of communication strategies used in mandatory and non-mandatory biosimilar transitions: a systematic review with meta-analysis

C Gasteiger, AA Den Broeder, S Stewart… - Health psychology …, 2023 - Taylor & Francis
Effective patient-provider communication is crucial to promote shared decision-making.
However, it is unclear how to explain treatment changes to ensure patient acceptance, such …

Switching from biologic to biosimilar products: insight from an integrated health care system

B Bhardwaja, S Klocke, E Ekinci, A Jackson, S Kono… - BioDrugs, 2022 - Springer
Biologics are indicated for the treatment of a wide range of conditions and have transformed
care in several therapeutic areas; however, they are expensive for both health care systems …

Real-world budget impact of the adoption of insulin glargine biosimilars in primary care in England (2015–2018)

I Agirrezabal, E Sánchez-Iriso, K Mandar… - Diabetes …, 2020 - Am Diabetes Assoc
BACKGROUND Lantus, the reference insulin glargine used for the treatment of diabetes,
lost its patent protection in 2014, opening the market to biosimilar competitors. OBJECTIVE …

[HTML][HTML] Barriers to biosimilar prescribing incentives in the context of clinical governance in Spain

F Lobo, I Río-Álvarez - Pharmaceuticals, 2021 - mdpi.com
Incentives contribute to the proper functioning of the broader contracts that regulate the
relationships between health systems and professionals. Likewise, incentives are an …

Biosimilars in rheumatology

FC Araujo, J Goncalves, JE Fonseca - Pharmacological Research, 2019 - Elsevier
Biotechnologicals are an invaluable resource in the treatment of patients with inflammatory
rheumatic diseases (IRD) non-responsive or intolerant to conventional therapies. However …