[Eldecalcitol (ED-71)]

Clin Calcium. 2011 Jan;21(1):53-8.
[Article in Japanese]

Abstract

ED-71 is a new vitamin D receptor ligand, bearing a hydroxypropoxy substituent at the 2β-position of 1α, 25 (OH) (2)D(3). In ovariectomized rats, ED-71 increased vertebral bone mass and bone strength by inhibiting bone resorption and maintaining bone formation. In randomized, placebo-controlled, double-blinded clinical trial for osteoporotic subjects, ED-71 increased lumber vertebral and hip bone mineral density independently vitamin D status. Furthermore, ED-71 may have a better osteoprotective effect than alfacalcidol and suggest that ED-71 may serve as a new generation of active vitamin D with anti-fracture efficacy in osteiporotic subjects.

Publication types

  • Review

MeSH terms

  • Animals
  • Bone Density / drug effects
  • Bone Resorption / drug therapy
  • Dose-Response Relationship, Drug
  • Female
  • Fractures, Bone / etiology
  • Fractures, Bone / prevention & control*
  • Humans
  • Lumbar Vertebrae / metabolism
  • Osteogenesis / drug effects
  • Osteoporosis / complications
  • Osteoporosis / drug therapy*
  • Osteoporosis / metabolism
  • Randomized Controlled Trials as Topic
  • Rats
  • Stimulation, Chemical
  • Vitamin D / administration & dosage
  • Vitamin D / analogs & derivatives*
  • Vitamin D / pharmacology

Substances

  • Vitamin D
  • eldecalcitol