Key drivers for market penetration of biosimilars in Europe.

scientific article published on 30 January 2017

Key drivers for market penetration of biosimilars in Europe. is …
instance of (P31):
scholarly articleQ13442814

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P356DOI10.1080/20016689.2016.1272308
P932PMC publication ID5328350
P698PubMed publication ID28265349

P50authorOlivier CristeauQ61697281
P2093author name stringMondher Toumi
Cécile Rémuzat
Dan Ionescu
Julie Dorey
Guerric Radière
P2860cites workBiosimilar competition: lessons from EuropeQ87133468
Biosimilar granulocyte colony-stimulating factor uptakes in the EU-5 markets: a descriptive analysisQ87375385
Are biosimilars the next tool to guarantee cost-containment for pharmaceutical expenditures?Q26863707
Biosimilars: How Can Payers Get Long-Term Savings?Q28834400
Biological therapy in inflammatory bowel diseases: access in Central and Eastern EuropeQ35069447
How Much Are Biosimilars Used in Clinical Practice? A Retrospective Italian Population-Based Study of Erythropoiesis-Stimulating Agents in the Years 2009-2013.Q36034344
Barriers to the uptake of biosimilars and possible solutions: a Belgian case study.Q38209872
Incentives for market penetration of biosimilars in Belgium and in five European countriesQ38308835
Use of biologics for psoriasis in Central and Eastern European countriesQ38586836
Postmarket policy considerations for biosimilar oncology drugsQ38693911
Biosimilars: A Multidisciplinary PerspectiveQ38778909
Supply-side and demand-side policies for biosimilars: an overview in 10 European member states.Q39455869
Biosimilar versus patented erythropoietins: learning from 5 years of European and Japanese experienceQ46086372
P275copyright licenseCreative Commons Attribution 4.0 InternationalQ20007257
P6216copyright statuscopyrightedQ50423863
P433issue1
P304page(s)1272308
P577publication date2017-01-30
P1433published inJournal of market access & health policyQ27727071
P1476titleKey drivers for market penetration of biosimilars in Europe
P478volume5

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cites work (P2860)
Q48250617A randomised trial comparing the pharmacokinetics and safety of the biosimilar CT-P6 with reference trastuzumab.
Q52447008An overview of biosimilars and non-biologic complex drugs in Europe, the United States, and Canada and their relevance to multiple sclerosis.
Q64106987Biological Therapies in Immune-Mediated Inflammatory Diseases: Can Biosimilars Reduce Access Inequities?
Q52651099Biosimilar Drugs for Psoriasis: Principles, Present, and Near Future.
Q61810432Biosimilars: Considerations for Payers
Q57191804Comparative Price Analysis of Biological Products for Treatment of Rheumatoid Arthritis
Q64899490Different Policy Measures and Practices between Swedish Counties Influence Market Dynamics: Part 1-Biosimilar and Originator Infliximab in the Hospital Setting.
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Q55212098Patient Access, Unmet Medical Need, Expected Benefits, and Concerns Related to the Utilisation of Biosimilars in Eastern European Countries: A Survey of Experts.
Q47173303Policies for biosimilar uptake in Europe: An overview.
Q33775526Pricing and Reimbursement of Biosimilars in Central and Eastern European Countries
Q92177218Regulatory and Clinical Experiences with Biosimilar Filgrastim in the U.S., the European Union, Japan, and Canada
Q39455869Supply-side and demand-side policies for biosimilars: an overview in 10 European member states.
Q93139736The arrival of biosimilar monoclonal antibodies in oncology: clinical studies for trastuzumab biosimilars
Q98177418Uptake of Biosimilar Infliximab in the UK, France, Japan, and Korea: Budget Savings or Market Expansion Across Countries?

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