Literature DB >> 23946620

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

C Lee Ventola1.   

Abstract

Biosimilars, although not identical to their originator product, are expected to become essential in reducing health care costs and improving access to lifesaving drugs. The FDA must find a way to balance rigorous testing to ensure quality, as is done for generic chemical drugs, with providing a cost-efficient way to expedite approvals of these products.

Year:  2013        PMID: 23946620      PMCID: PMC3737980     

Source DB:  PubMed          Journal:  P T        ISSN: 1052-1372


  13 in total

Review 1.  Biosimilars and market access: a question of comparability and costs?

Authors:  Steven Simoens; Gilbert Verbeken; Isabelle Huys
Journal:  Target Oncol       Date:  2012-01-17       Impact factor: 4.493

Review 2.  Comparability and biosimilarity: considerations for the healthcare provider.

Authors:  Jaymi F Lee; Jason B Litten; Gustavo Grampp
Journal:  Curr Med Res Opin       Date:  2012-06-06       Impact factor: 2.580

3.  Innovation and Competition: Will Biosimilars Succeed?: The creation of an FDA approval pathway for biosimilars is complex and fraught with hazard. Yes, innovation and market competition are at stake. But so are efficacy and patient safety.

Authors:  Erwin A Blackstone; Joseph P Fuhr
Journal:  Biotechnol Healthc       Date:  2012

4.  The state of the art in the development of biosimilars.

Authors:  Mark McCamish; Gillian Woollett
Journal:  Clin Pharmacol Ther       Date:  2012-02-08       Impact factor: 6.875

5.  Biosimilars: are they ready for primetime in the United States?

Authors:  Bradford R Hirsch; Gary H Lyman
Journal:  J Natl Compr Canc Netw       Date:  2011-08-01       Impact factor: 11.908

6.  President obama reopens debate on patented biologics: will the FDA quickly define an abbreviated pathway for biosimilars?

Authors:  Stephen Barlas
Journal:  P T       Date:  2011-04

7.  The US approach to biosimilars: the long-awaited FDA approval pathway.

Authors:  Begoña Calvo; Leyre Zuñiga
Journal:  BioDrugs       Date:  2012-12-01       Impact factor: 5.807

8.  FDA Readies New Guidance and User Fee Program for Biosimilars: Drug interchangeability and user fees are contentious issues the FDA must resolve. Is the FDA up to the task?

Authors:  Stephen Barlas
Journal:  Biotechnol Healthc       Date:  2012

9.  Biosimilars might not measure up to health plan expectations.

Authors:  Tom Reinke
Journal:  Manag Care       Date:  2012-10

10.  Biosimilars: company strategies to capture value from the biologics market.

Authors:  Bruno Calo-Fernández; Juan Leonardo Martínez-Hurtado
Journal:  Pharmaceuticals (Basel)       Date:  2012-12-12
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  8 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.  Improving the power to establish clinical similarity in a Phase 3 efficacy trial by incorporating prior evidence of analytical and pharmacokinetic similarity.

Authors:  Donglin Zeng; Jean Pan; Kuolung Hu; Eric Chi; D Y Lin
Journal:  J Biopharm Stat       Date:  2017-11-27       Impact factor: 1.051

3.  Zarxio (Filgrastim-sndz): First Biosimilar Approved in the United States.

Authors:  Lisa A Raedler
Journal:  Am Health Drug Benefits       Date:  2016-03

4.  How Much Are Biosimilars Used in Clinical Practice? A Retrospective Italian Population-Based Study of Erythropoiesis-Stimulating Agents in the Years 2009-2013.

Authors:  Ylenia Ingrasciotta; Francesco Giorgianni; Jenny Bolcato; Alessandro Chinellato; Roberta Pirolo; Daniele Ugo Tari; Chiara Troncone; Andrea Fontana; Valentina Ientile; Rosa Gini; Domenico Santoro; Mariacarmela Santarpia; Armando Genazzani; Ilaria Uomo; Maurizio Pastorello; Walter Sebastiano Pollina Addario; Salvatore Scondotto; Pasquale Cananzi; Achille Patrizio Caputi; Gianluca Trifirò
Journal:  BioDrugs       Date:  2015-08       Impact factor: 5.807

5.  Biosimilars: new promise for reducing healthcare costs.

Authors:  Julia Munsch
Journal:  J Biomed Res       Date:  2014-03-20

6.  A bibliometric analysis of the global research on biosimilars.

Authors:  Akram Hernández-Vásquez; Christoper A Alarcon-Ruiz; Guido Bendezu-Quispe; Daniel Comandé; Diego Rosselli
Journal:  J Pharm Policy Pract       Date:  2018-03-27

7.  A randomised, single-blind, single-dose, three-arm, parallel-group study in healthy subjects to demonstrate pharmacokinetic equivalence of ABP 501 and adalimumab.

Authors:  Primal Kaur; Vincent Chow; Nan Zhang; Michael Moxness; Arunan Kaliyaperumal; Richard Markus
Journal:  Ann Rheum Dis       Date:  2016-07-27       Impact factor: 19.103

Review 8.  The process defines the product: what really matters in biosimilar design and production?

Authors:  Arnold G Vulto; Orlando A Jaquez
Journal:  Rheumatology (Oxford)       Date:  2017-08-01       Impact factor: 7.580

  8 in total

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