Literature DB >> 20065635

Guardians at the gate: Biosimilar and patent reform legislation could fundamentally change the guards for therapeutic monoclonal antibodies--Part 2.

Kevin W McCabe1.   

Abstract

Patent protection and FDA exclusivities are the two principal forms of protection available to companies that develop therapeutic monoclonal antibodies. Propo-sed changes to both forms of protection are currently being debated in the United States Congress. Specifically, Congress is presently debating both biosimilar and patent reform legislations. Although no bill has yet passed, it is expected that patent reform legislation should pass this year. It is less likely that a biosimilar bill will pass this year. However, when legislations are enacted, the changes will significantly impact the business of therapeutic monoclonal antibodies.

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Year:  2009        PMID: 20065635      PMCID: PMC2759490          DOI: 10.4161/mabs.1.5.9493

Source DB:  PubMed          Journal:  MAbs        ISSN: 1942-0862            Impact factor:   5.857


  1 in total

1.  Rapidly rising clinical trial costs worry researchers.

Authors:  Roger Collier
Journal:  CMAJ       Date:  2009-02-03       Impact factor: 8.262

  1 in total
  2 in total

1.  European Medicines Agency workshop on biosimilar monoclonal antibodies: July 2, 2009, London, UK.

Authors:  Janice M Reichert; Alain Beck; Harish Iyer
Journal:  MAbs       Date:  2009-09-25       Impact factor: 5.857

2.  Guardians at the gate: patent protection of therapeutic monoclonal antibodies through product life cycle management--Part 3.

Authors:  Kevin W McCabe; Paul A Calvo
Journal:  MAbs       Date:  2009-11-14       Impact factor: 5.857

  2 in total

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