Patent disclosure requirements for therapeutic antibody patents

Expert Opin Ther Pat. 2017 Aug;27(8):867-875. doi: 10.1080/13543776.2017.1296950. Epub 2017 Mar 9.

Abstract

Therapeutic antibodies have grown to become an important product class within the biopharmaceutical market. A prerequisite to their commercialization is adequate patent protection. Disclosure requirements and the types of claims available in different jurisdictions can impact the scope of protection available for antibodies. Areas covered: A comparative review of statutory bases, patent office practices and selected decisions in Canada, the United States and the United Kingdom related to disclosure requirements is provided. Expert opinion: Differences in disclosure requirements exist in different jurisdictions which can impact the type of claims obtained and their survival when attacked in litigation. Including a wide variety of claim types is a key strategy to ensuring therapeutic antibodies are adequately protected. Method of use claims may provide advantages and broader protection in some circumstances and should also be considered.

Keywords: Canada; Therapeutic antibodies; United States and United Kingdom; disclosure requirements; patent protection; sufficiency; support requirements.

Publication types

  • Comparative Study
  • Review

MeSH terms

  • Animals
  • Antibodies / therapeutic use*
  • Canada
  • Disclosure
  • Humans
  • Legislation, Drug*
  • Patents as Topic / legislation & jurisprudence*
  • United Kingdom
  • United States

Substances

  • Antibodies