Clinical update on teriparatide

Curr Rheumatol Rep. 2009 Jul;11(3):169-76. doi: 10.1007/s11926-009-0023-3.

Abstract

Teriparatide (recombinant human parathyroid hormone ) is an anabolic agent approved for the treatment of patients at high risk for fracture. The Fracture Prevention Trial administered teriparatide to treatment-naïve patients, leading to its US Food and Drug Administration approval in 2002. Clinical trial data using antiresorptive agents administered before, during, and after any parathyroid hormone (PTH) therapy, as well as alternative PTH dosing, have provided additional insight yet raise fundamental questions about the most appropriate use of teriparatide. This article provides an update on teriparatide, focusing on its mechanism of action compared with other antiresorptive agents, indications, adverse effects, therapy duration, combination therapy, contraindications, and cost effectiveness.

Publication types

  • Research Support, Non-U.S. Gov't
  • Review

MeSH terms

  • Bone Density Conservation Agents / therapeutic use*
  • Bone and Bones / drug effects
  • Bone and Bones / physiopathology
  • Clinical Trials as Topic
  • Compressive Strength / drug effects
  • Compressive Strength / physiology
  • Female
  • Fractures, Bone / etiology
  • Fractures, Bone / physiopathology
  • Fractures, Bone / prevention & control*
  • Humans
  • Male
  • Osteoporosis / complications
  • Osteoporosis / drug therapy*
  • Osteoporosis / physiopathology
  • Recombinant Proteins / therapeutic use
  • Risk Factors
  • Teriparatide / therapeutic use*

Substances

  • Bone Density Conservation Agents
  • Recombinant Proteins
  • Teriparatide