A multiple-dose toxicity study of tanezumab in cynomolgus monkeys

Regul Toxicol Pharmacol. 2011 Mar;59(2):334-42. doi: 10.1016/j.yrtph.2010.11.005. Epub 2010 Dec 3.


Nerve growth factor (NGF) is an important mediator of pain and hyperalgesia and has become a target of novel analgesic therapeutics. Tanezumab is a humanized IgG(2) antibody that binds NGF with high affinity and specificity. In a study to assess the toxicity and pharmacokinetic properties of tanezumab in adult, male and female, cynomolgus monkeys following weekly intravenous administration of 1, 10, or 30 mg/kg for up to 26 weeks (followed by an 8-week recovery period), tanezumab was well tolerated with no macroscopic or microscopic effects on those brain, spinal cord, nerve, or ganglia sections evaluated. One fifth of tanezumab-treated monkeys developed an antibody response to tanezumab that prevented maintenance of tanezumab exposure between dosing. In the antibody-negative animals, accumulation of tanezumab was observed; steady state was achieved approximately 8 weeks after the first dose of study drug, and exposure to tanezumab was approximately dose proportional with no observed difference between male and female animals. One monkey died during the study; this monkey had findings suggestive of hypersensitivity reaction. The favorable toxicity and pharmacokinetic profile of tanezumab seen in this study supports its further evaluation for the treatment of pain in clinical practice.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Antibodies, Monoclonal / administration & dosage
  • Antibodies, Monoclonal / pharmacokinetics
  • Antibodies, Monoclonal / toxicity*
  • Antibodies, Monoclonal, Humanized
  • Dose-Response Relationship, Drug
  • Female
  • Injections, Intravenous
  • Macaca fascicularis
  • Male
  • Nervous System / drug effects*
  • Nervous System / metabolism
  • Pain / drug therapy
  • Pain / metabolism
  • Toxicity Tests / methods


  • Antibodies, Monoclonal
  • Antibodies, Monoclonal, Humanized
  • tanezumab