Off-Patent Biological and Biosimilar Medicines in Belgium: A Market Landscape Analysis

被引:15
|
作者
Vandenplas, Yannick [1 ]
Simoens, Steven [1 ]
Van Wilder, Philippe [2 ]
Vulto, Arnold G. [1 ,3 ]
Huys, Isabelle [1 ]
机构
[1] Katholieke Univ Leuven, Dept Pharmaceut & Pharmacol Sci, Clin Pharmacol & Pharmacotherapy, Leuven, Belgium
[2] Univ Libre Bruxelles ULB, Ecole Sante Publ, Brussels, Belgium
[3] Erasmus MC, Hosp Pharm, Rotterdam, Netherlands
来源
FRONTIERS IN PHARMACOLOGY | 2021年 / 12卷
关键词
biological; medicine; competition; sustainability; market access; affordability; Belgium; biosimilar; ERYTHROPOIESIS-STIMULATING AGENTS; EULAR RECOMMENDATIONS; PSORIATIC-ARTHRITIS; MANAGEMENT; UPDATE; ANEMIA; IMPACT; GUIDE;
D O I
10.3389/fphar.2021.644187
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Background and objective: Best-value biological medicines may generate competition in the off-patent biologicals market, resulting in having more resources available to provide patients with access to necessary medicines while maintaining high-quality care. Belgium is a country known to have low biosimilar market shares, suggesting a malfunctioning market for off-patent biologicals. This study aims to gain an in-depth understanding of the Belgian off-patent biologicals market, by looking at the evolution in volumes and costs of the relevant products in the market. Methods: This study included a combination of quantitative and qualitative research methods. The quantitative part of this study consisted of the analysis of market data obtained by the National Institute for Health and Disability Insurance (NIHDI) for all relevant products in the Belgian off-patent biologicals market (i.e. TNF-inhibitors, insulins, granulocyte colony-stimulating factors, epoetins, rituximab, trastuzumab). In addition, for the qualitative part of this study, semi-structured interviews with Belgian stakeholders were conducted between December 2019 and March 2020. Results: Belgian market data and stakeholder perceptions suggest a suboptimal market environment for off-patent biological and biosimilar medicines. Shifts are observed after loss of exclusivities of originator biologicals toward second-generation products or new therapeutic class products, at a higher cost and often limited added value. Moreover, cost reductions for off-patent biologicals after biosimilar market entry are mainly determined by mandatory price reductions applicable to both originator and biosimilar products, and not by lower prices induced by competition. For products used in the retail setting, significant mandatory price reductions for both originator and reference products with low biosimilar volumes were pointed out as the main reasons for the lack of price competition. For products dispensed in hospitals, the hospital financing system is important. First, it does not always encourage the use of lower cost alternatives. Second, competition mainly takes place at the level of confidential discounts in tenders. Most interviewees acknowledged the lack of a competitive environment, which is not supportive of a sustainable Belgian off-patent biologicals market. Conclusion: Market data and stakeholder perceptions indicate that the sustainability of the Belgian market for off-patent biologicals is challenged. A sustainable market ensures access to biological therapies now and in the future.
引用
收藏
页数:19
相关论文
共 50 条
  • [21] Charting the Etanercept Journey: Tracing Cost Dynamics in Poland's Off-Patent Market from Reference Drug Rivalry to Biosimilar Monopoly
    Stajszczyk, Marcin
    Batko, Krzysztof
    Zuber, Zbigniew Michal
    Kwiatkowska, Brygida
    Krajewska-Wlodarczyk, Magdalena
    Batko, Bogdan
    BIODRUGS, 2024, 38 (04) : 557 - 569
  • [22] What pricing and reimbursement policies to use for off-patent biologicals? - Results from the EBE 2014 biological medicines policy survey
    Acha, Virginia
    Allin, Piers
    Bergunde, Stefan
    Bisordi, Fabio
    Roediger, Alexander
    GABI JOURNAL-GENERICS AND BIOSIMILARS INITIATIVE JOURNAL, 2015, 4 (01): : 17 - 24
  • [23] Market diffusion of biosimilars in off-patent biologic drug markets across Europe
    Boehm, Anna-Katharina
    Steiner, Isa Maria
    Stargardt, Tom
    HEALTH POLICY, 2023, 132
  • [24] Evaluating AE Reporting of Two Off-Patent Biologics to Inform Future Biosimilar Naming and Reporting Practices
    Stergiopoulos, Stella
    Getz, Kenneth
    DRUG SAFETY, 2015, 38 (08) : 687 - 692
  • [25] The extent to which off-patent registered prescription medicines are used for off-label indications in Australia: A scoping review
    Howe, Katrina
    Bourke, Siobhan
    Sansom, Lloyd
    PLOS ONE, 2021, 16 (12):
  • [26] OFF-PATENT BRAND ANTIDEPRESSANTS UTILIZATION: A NATIONALLY REPRESENTATIVE SAMPLE ANALYSIS
    Alruthia, Y. S.
    VALUE IN HEALTH, 2013, 16 (03) : A66 - A66
  • [27] Successful private–public funding of paediatric medicines research: lessons from the EU programme to fund research into off-patent medicines
    L. Ruggieri
    V. Giannuzzi
    P. Baiardi
    F. Bonifazi
    E. H. Davies
    C. Giaquinto
    D. Bonifazi
    M. Felisi
    C. Chiron
    R. Pressler
    H. Rabe
    M. J. Whitaker
    A. Neubert
    E. Jacqz-Aigrain
    I. Eichler
    M. A. Turner
    A. Ceci
    European Journal of Pediatrics, 2015, 174 : 481 - 491
  • [28] Competition in the off-patent medicine market in Spain: The national reference pricing system versus the regional system of tendering for outpatient prescription medicines in Andalusia
    Casanova-Juanes, Julieta
    Mestre-Ferrandiz, Jorge
    Espin-Balbino, Jaime
    HEALTH POLICY, 2018, 122 (12) : 1310 - 1315
  • [29] Successful private-public funding of paediatric medicines research: lessons from the EU programme to fund research into off-patent medicines
    Ruggieri, L.
    Giannuzzi, V.
    Baiardi, P.
    Bonifazi, F.
    Davies, E. H.
    Giaquinto, C.
    Bonifazi, D.
    Felisi, M.
    Chiron, C.
    Pressler, R.
    Rabe, H.
    Whitaker, M. J.
    Neubert, A.
    Jacqz-Aigrain, E.
    Eichler, I.
    Turner, M. A.
    Ceci, A.
    EUROPEAN JOURNAL OF PEDIATRICS, 2015, 174 (04) : 481 - 491
  • [30] Off-label despite high-level evidence: a clinical practice review of commonly used off-patent cancer medicines
    Zarkavelis, G.
    Amylidi, A. L.
    Verbaanderd, C.
    Cherny, N. I.
    Metaxas, Y.
    Vries, E. G. E. de
    Zygoura, P.
    Amaral, T.
    Jordan, K.
    Strijbos, M.
    Dafni, U.
    Latino, N.
    Galotti, M.
    Lordick, F.
    Giuliani, R.
    Pignatti, F.
    Pentheroudakis, G.
    ESMO OPEN, 2023, 8 (01)