Clinical pharmacology of tyrosine kinase inhibitors becoming generic drugs: the regulatory perspective

J Exp Clin Cancer Res. 2014 Feb 7;33(1):15. doi: 10.1186/1756-9966-33-15.

Abstract

Over the last decades, billions have been spent and huge efforts have been taken in basic and clinical cancer research [CA Cancer J Clin63:11-30]. About a decade ago, the arms race between drugs and cancer cells reached a new level by introduction of tyrosine kinase inhibitors (TKI) into pharmacological anti-cancer therapy. According to their molecular mechanism of action, TKI in contrast to so-called "classic" or "conventional" cytostatics belong to the group of targeted cancer medicines, characterized by accurately fitting with biological structures (i.e. active centers of kinases). Numerous (partly orphan) indications are covered by this new class of substances. Approximately ten years after the first substances of this class of medicines were authorized, patent protection will end within the next years. The following article covers clinical meaning and regulatory status of anti-cancer TKI and gives an outlook to what is expected from the introduction of generic anti-cancer TKI.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Antineoplastic Agents / adverse effects
  • Antineoplastic Agents / pharmacology*
  • Antineoplastic Agents / therapeutic use
  • Area Under Curve
  • Drug and Narcotic Control
  • Drugs, Generic / adverse effects
  • Drugs, Generic / pharmacology*
  • Drugs, Generic / therapeutic use
  • Humans
  • Molecular Targeted Therapy
  • Neoplasms / drug therapy*
  • Protein Kinase Inhibitors / adverse effects
  • Protein Kinase Inhibitors / pharmacology*
  • Protein Kinase Inhibitors / therapeutic use
  • Protein-Tyrosine Kinases / antagonists & inhibitors
  • Protein-Tyrosine Kinases / metabolism
  • Signal Transduction

Substances

  • Antineoplastic Agents
  • Drugs, Generic
  • Protein Kinase Inhibitors
  • Protein-Tyrosine Kinases