An overview of FDA-approved biologics medicines

Drug Discov Today. 2015 Apr;20(4):393-8. doi: 10.1016/j.drudis.2014.09.003. Epub 2014 Sep 16.

Abstract

Recombinant DNA technologies revolutionized medicine. Herein, the approvals and mechanistic basis of biologics-based medicines are analyzed. The overall and relative rate of FDA approvals for recombinant proteins grew from the 1980s through the first half-decade of the new millennium. Over time, the number of biologics gaining approval for an orphan indication has climbed to more than 50% in the current decade. The field has been dynamic in terms of the types of biologics, indications targeted and the mechanistic basis of drug activity. Despite impressive increases in recombinant-protein-based medicine, the rate of new biologics approvals could have leveled out.

Publication types

  • Review

MeSH terms

  • Animals
  • Antibodies, Monoclonal / therapeutic use
  • Biological Products / adverse effects
  • Biological Products / therapeutic use*
  • Drug Approval*
  • Enzyme Therapy
  • Humans
  • Patient Safety
  • Receptors, Cell Surface / drug effects
  • Receptors, Cytoplasmic and Nuclear / drug effects
  • Risk Assessment
  • Risk Factors
  • Treatment Outcome
  • United States
  • United States Food and Drug Administration*

Substances

  • Antibodies, Monoclonal
  • Biological Products
  • Receptors, Cell Surface
  • Receptors, Cytoplasmic and Nuclear