Literature DB >> 22318617

The state of the art in the development of biosimilars.

Mark McCamish1, Gillian Woollett.   

Abstract

The development of biologic therapeutics using advanced technology to copy and improve on nature's design of complex peptides, proteins, and glycoproteins has enabled the treatment of diseases in entirely new ways and brought unique and lifesaving treatments to many people. However, at least in part because of cost pressures, access to these truly amazing products has not been uniformly available; many patients do not qualify for these treatments, or the treatment is postponed until disabilities accumulate. The development of biosimilars--essentially copies of the original biologic drugs after patent expiration--allows for wider and, as important, earlier access to these agents because of their lower cost and consequently greater affordability. The development and commercialization of biosimilars can help address unmet medical needs by improving access to well-established therapeutic interventions while improving health-care affordability.

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Year:  2012        PMID: 22318617     DOI: 10.1038/clpt.2011.343

Source DB:  PubMed          Journal:  Clin Pharmacol Ther        ISSN: 0009-9236            Impact factor:   6.875


  37 in total

Review 1.  Biosimilarity Versus Manufacturing Change: Two Distinct Concepts.

Authors:  Paul Declerck; Mourad Farouk-Rezk; Pauline M Rudd
Journal:  Pharm Res       Date:  2015-09-17       Impact factor: 4.200

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

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

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

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

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

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

5.  Biosimilars: Implications for health-system pharmacists.

Authors:  Steven D Lucio; James G Stevenson; James M Hoffman
Journal:  Am J Health Syst Pharm       Date:  2013-11-15       Impact factor: 2.637

6.  Using Clinical PK/PD Studies to Support No Clinically Meaningful Differences Between a Proposed Biosimilar and the Reference Product.

Authors:  Peijuan Zhu; Ping Ji; Yaning Wang
Journal:  AAPS J       Date:  2018-08-09       Impact factor: 4.009

7.  The approval process for biosimilar erythropoiesis-stimulating agents.

Authors:  Jay B Wish
Journal:  Clin J Am Soc Nephrol       Date:  2014-06-26       Impact factor: 8.237

8.  Clinical Trial Design in Juvenile Idiopathic Arthritis.

Authors:  Stephen J Balevic; Mara L Becker; Michael Cohen-Wolkowiez; Laura E Schanberg
Journal:  Paediatr Drugs       Date:  2017-10       Impact factor: 3.930

Review 9.  Biosimilar insulins: a European perspective.

Authors:  J H DeVries; S C L Gough; J Kiljanski; L Heinemann
Journal:  Diabetes Obes Metab       Date:  2014-11-27       Impact factor: 6.577

10.  Update on the safety and bioequivalence of biosimilars - focus on enoxaparin.

Authors:  Walter Jeske; Jeanine M Walenga; Debra Hoppensteadt; Jawed Fareed
Journal:  Drug Healthc Patient Saf       Date:  2013-06-10
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