Obesity drugs in clinical development

Curr Opin Investig Drugs. 2006 Apr;7(4):312-8.

Abstract

A number of anti-obesity drugs are currently undergoing clinical development. These include: (i) centrally-acting drugs, such as the noradrenergic and dopaminergic reuptake inhibitor radafaxine, the endocannabinoid antagonist rimonabant, the selective serotonin 5-HT2c agonist APD-356, and oleoyl-estrone; (ii) drugs that target peripheral episodic satiety signals, such as glucagon-like peptide-1 (exenatide, exenatide-LAR and liraglutide), peptide YY (intranasal PYY3-36 and AC-162325) and amylin (pramlintide); (iii) drugs that block fat absorption, such as the novel lipase inhibitors cetilistat and GT-389255; and (iv) a human growth hormone fragment (AOD-9604) that increases adipose tissue breakdown. Of these, only rimonabant has got as far as completing phase III clinical trials. This review will provide an overview of the most prominent drugs currently undergoing clinical development as potential anti-obesity therapies.

Publication types

  • Review

MeSH terms

  • Amyloid / therapeutic use
  • Animals
  • Anti-Obesity Agents / pharmacology
  • Anti-Obesity Agents / therapeutic use*
  • Appetite Depressants / pharmacology
  • Appetite Depressants / therapeutic use
  • Energy Metabolism / drug effects
  • Glucagon-Like Peptide 1 / therapeutic use
  • Humans
  • Islet Amyloid Polypeptide
  • Obesity / drug therapy*
  • Peptide Fragments / therapeutic use
  • Peptide YY / therapeutic use
  • Receptor, Cannabinoid, CB1 / antagonists & inhibitors
  • Selective Serotonin Reuptake Inhibitors / therapeutic use
  • Somatostatin / therapeutic use

Substances

  • AOD 9604
  • Amyloid
  • Anti-Obesity Agents
  • Appetite Depressants
  • Islet Amyloid Polypeptide
  • Peptide Fragments
  • Receptor, Cannabinoid, CB1
  • Serotonin Uptake Inhibitors
  • Peptide YY
  • Somatostatin
  • Glucagon-Like Peptide 1
  • pramlintide