Literature DB >> 22249657

Biosimilars and market access: a question of comparability and costs?

Steven Simoens1, Gilbert Verbeken, Isabelle Huys.   

Abstract

This article discusses specific issues related to the market access of biosimilars. Biopharmaceuticals are complex molecules produced by living cells. Copies of these medicines, called biosimilars, are not identical to their reference medicine and therefore specific regulatory requirements apply. When considering the use of biosimilars, the question of the degree of comparability between a biosimilar and the reference biopharmaceutical needs to be considered for registration, pricing and reimbursement purposes in addition to the cost issue. To date, many key concepts (like clinically meaningful differences) remain undefined and the question of the degree of comparability is not yet resolved.

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Year:  2012        PMID: 22249657     DOI: 10.1007/s11523-011-0192-7

Source DB:  PubMed          Journal:  Target Oncol        ISSN: 1776-2596            Impact factor:   4.493


  9 in total

Review 1.  Encouraging the use of generic medicines: implications for transition economies.

Authors:  Derek R King; Panos Kanavos
Journal:  Croat Med J       Date:  2002-08       Impact factor: 1.351

2.  Addressing the health technology assessment of biosimilar pharmaceuticals.

Authors:  Alan Stewart; Philip Aubrey; Jonathan Belsey
Journal:  Curr Med Res Opin       Date:  2010-09       Impact factor: 2.580

Review 3.  Biosimilars: current status and future directions.

Authors:  Simon D Roger
Journal:  Expert Opin Biol Ther       Date:  2010-07       Impact factor: 4.388

Review 4.  Biosimilars: controversies as illustrated by rhGH.

Authors:  Paul J Declerck; Feyza Darendeliler; Miklós Góth; Stanislava Kolouskova; Ioana Micle; Cees Noordam; Valentina Peterkova; Natalia N Volevodz; Jirina Zapletalová; Michael B Ranke
Journal:  Curr Med Res Opin       Date:  2010-05       Impact factor: 2.580

Review 5.  Biosimilars: evidential standards for health technology assessment.

Authors:  D A Hughes
Journal:  Clin Pharmacol Ther       Date:  2010-03       Impact factor: 6.875

6.  The market for follow-on biologics: how will it evolve?

Authors:  Henry Grabowski; Iain Cockburn; Genia Long
Journal:  Health Aff (Millwood)       Date:  2006 Sep-Oct       Impact factor: 6.301

7.  Biosimilars approval process.

Authors:  Leyre Zuñiga; Begoña Calvo
Journal:  Regul Toxicol Pharmacol       Date:  2009-11-17       Impact factor: 3.271

8.  A combined analysis of two pivotal randomized trials of a single dose of pegfilgrastim per chemotherapy cycle and daily Filgrastim in patients with stage II-IV breast cancer.

Authors:  Salvatore Siena; Martine J Piccart; Frankie A Holmes; John Glaspy; James Hackett; Jennifer J Renwick
Journal:  Oncol Rep       Date:  2003 May-Jun       Impact factor: 3.906

9.  Biosimilar therapeutics-what do we need to consider?

Authors:  Huub Schellekens
Journal:  NDT Plus       Date:  2009-01
  9 in total
  10 in total

1.  Evaluation of Biosimilars for Formulary Inclusion: Factors for Consideration by P&T Committees.

Authors:  C Lee Ventola
Journal:  P T       Date:  2015-10

2.  Biosimilars: part 2: potential concerns and challenges for p&t committees.

Authors:  C Lee Ventola
Journal:  P T       Date:  2013-06

3.  Biosimilars: part 1: proposed regulatory criteria for FDA approval.

Authors:  C Lee Ventola
Journal:  P T       Date:  2013-05

4.  Cost-Effectiveness Analysis of Tyrosine Kinase Inhibitors for Patients with Advanced Gastrointestinal Stromal Tumors.

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Journal:  Clin Drug Investig       Date:  2017-01       Impact factor: 2.859

5.  Barriers to the uptake of biosimilars and possible solutions: a Belgian case study.

Authors:  Pieter Dylst; Arnold Vulto; Steven Simoens
Journal:  Pharmacoeconomics       Date:  2014-07       Impact factor: 4.981

6.  The economic burden of fragile x syndrome: healthcare resource utilization in the United States.

Authors:  Patricia Sacco; Gorana Capkun-Niggli; Xin Zhang; Rosemary Jose
Journal:  Am Health Drug Benefits       Date:  2013-03

Review 7.  Epoetin zeta in the management of anemia associated with chronic kidney disease, differential pharmacology and clinical utility.

Authors:  Mary Lynn Davis-Ajami; Jun Wu; Katherine Downton; Emilie Ludeman; Virginia Noxon
Journal:  Biologics       Date:  2014-04-16

8.  Adoption of Biosimilar Infliximab for Rheumatoid Arthritis, Ankylosing Spondylitis, and Inflammatory Bowel Diseases in the EU5: A Budget Impact Analysis Using a Delphi Panel.

Authors:  Tim A Kanters; Jelena Stevanovic; Isabelle Huys; Arnold G Vulto; Steven Simoens
Journal:  Front Pharmacol       Date:  2017-05-31       Impact factor: 5.810

9.  Aptamers as quality control tool for production, storage and biosimilarity of the anti-CD20 biopharmaceutical rituximab.

Authors:  Sabrina Wildner; Sara Huber; Christof Regl; Christian G Huber; Urs Lohrig; Gabriele Gadermaier
Journal:  Sci Rep       Date:  2019-02-01       Impact factor: 4.379

Review 10.  Are biosimilars the next tool to guarantee cost-containment for pharmaceutical expenditures?

Authors:  María-Isabel Farfan-Portet; Sophie Gerkens; Isabelle Lepage-Nefkens; Irmgard Vinck; Frank Hulstaert
Journal:  Eur J Health Econ       Date:  2013-11-23
  10 in total

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