The increasing cost of originator biologicals, combined with consequences of the COVID-19 pandemic, have burdened the healthcare system. Unfortunately, the biosimilar uptake in Saudi Arabia has not reached an optimal level despite the approval of several agents. Therefore, physicians are essential stakeholders in the process and acceptance of biosimilars.
Biosimilars and non-medical switching among Saudi rheumatologists. The knowledge gap
Biosimilars/Research | Posted 25/02/2022 0 Post your comment
A previous pilot study that was conducted in the pre-COVID period on Arab rheumatologists showed a low level of understanding of the manufacturing process and approval requirements of biosimilars [1]. The current cross-sectional study aimed to assess the perception toward biosimilars and non-medical switching in members of the Saudi Society for Rheumatology (SSR) through an online survey, which was carried out between 1‒30 November 2020 [2].
A total of 143 of the 249 adult and paediatric rheumatologists registered in the SSR database (57.4%) completed the questionnaire. Of these, only 30.07% and 18.18% reported previous experience of prescribing a biosimilar and performing non-medical switching, respectively.
An adequate level of knowledge about biosimilars was reported by 69 respondents (48.25%). In addition, 69 (48.3%) of participants thought that the current published evidence is adequate to allow extrapolation of biosimilars to all indications approved for the originator biological. However, an adequate understanding of the concept of totality-of-evidence was reported by only 37% of participants. Despite this lack of understanding, 87 participants (60.8%) answered that they are willing to prescribe a biosimilar to an eligible patient.
Paediatric rheumatologists were less likely to agree on the adequacy of data generated in biosimilar programmes to grant extrapolation for non-studied populations, such as children (27% vs. 53% p = 0.014). Almost two thirds (60.1%) of participants believed that non-medical switching can be harmful. On the other hand, 88 (61.5%) believe that non-medical switching can lead to significant cost savings to the healthcare system.
Educational activities are believed by the majority (96.5%) to be best organized by societies rather than pharmaceutical companies due to the high risk of bias. In fact, 112 (78.3%) participants believed that educational activities about biosimilars sponsored by a single pharmaceutical company are biased.
The authors concluded that ‘this initiative has identified critical knowledge gaps regarding the biosimilar approval process and other barriers that likely affect their use by rheumatologists in Saudi Arabia’. They added that it ‘also identified negative views on non-medical switching, which should be the target of future educational activities’.
Conflict of interest
The authors of the research paper [2] reported conflicts of interest, including having received speaker’s honoraria from pharmaceutical companies. For full details of the authors’ conflicts of interest, see the research paper [1].
Abstracted by Mohammed A Omair, Rheumatology Unit, Department of Medicine, King Saud University, Riyadh, Saudi Arabia.
Readers interested to learn more about biosimilars in Saudi Arabia are invited to visit www.gabi-journal.net to view the following manuscript published in GaBI Journal:
Biosimilars in Saudi Arabia: a single-centre, open-label case series examining infliximab switching
Pricing of biosimilars in Saudi Arabia
GaBI Journal is indexed in Embase, Scopus, Emerging Sources Citation Index and more.
Readers interested in contributing a research or perspective paper to GaBI Journal – an independent, peer reviewed academic journal – please send us your submission here.
GaBI Journal Citation Impact
1.9 – CiteScore 2020 (calculated on 5 May 2021)
2.2 – CiteScoreTracker 2021 (Last updated on 7 February 2022)
Submit a manuscript to GaBI Journal
Related articles
Questions over DANBIO relevance for non-medical switching
Saudi Arabian guidelines for biosimilars
LATIN AMERICAN FORUM The new section of the ‘Latin American Forum’ on GaBI has been launched. The objective of this new section is to provide you with all the latest news and updates on developments of generic and biosimilar medicines in Latin America in Spanish. View this week’s headline article: Nomenclatura de biológicos y biosimilares en Brasil Browse the news in the Latin American Forum! Register to receive the GaBI Latin American Forum newsletter. Inform colleagues and friends of this new initiative. LATIN AMERICAN FORUM Se ha lanzado la nueva sección del ‘Foro Latinoamericano’ sobre GaBI. El objetivo de esta nueva sección es brindarle las últimas noticias y actualizaciones sobre desarrollos de medicamentos genéricos y biosimilares en América Latina en español. Vea el artículo principal de esta semana: Nomenclatura de biológicos y biosimilares en Brasil !Explore las noticias en el Foro Latinoamericano! Regístrese para recibir el boletín informativo GaBI Foro Latinoamericano. Informe a colegas y amigos sobre esta nueva iniciativa. |
References
1. Omair MA, Al Wahshi H, Al Saleh J, et al. Perception toward biosimilars and nonmedical switching: a cross-sectional survey among Arab rheumatologists. Dr Sulaiman Al Habib Medical Journal. 2020;2(4):179-85.
2. Omair MA, Almadany R, Omair MA, et al. Perception of biosimilar biologics and non-medical prescription switching among rheumatologists: a Saudi Society for Rheumatology initiative. Saudi Pharm J. 2022;30(1):39-44.
Permission granted to reproduce for personal and non-commercial use only. All other reproduction, copy or reprinting of all or part of any ‘Content’ found on this website is strictly prohibited without the prior consent of the publisher. Contact the publisher to obtain permission before redistributing.
Copyright – Unless otherwise stated all contents of this website are © 2022 Pro Pharma Communications International. All Rights Reserved.
General
Biosimilar medicines on the Pharmaceutical Benefits Scheme in Australia
SBR issues consensus on interchangeability of reference products and biosimilars
Most viewed articles
The best selling biotechnology drugs of 2008: the next biosimilars targets
Global biosimilars guideline development – EGA’s perspective
Related content
Long-term real-world safety experience of biosimilars confirms concept of biosimilarity
Budget impact analysis of Rixathon introduction in Chile for non-Hodgkin lymphoma
Biosimilars in inflammatory bowel disease: are we ready for multiple switches
Topline results from clinical development programme for candidate biosimilar AVT05 golimumab
Comments (0)
Post your comment