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New drugs for the treatment of osteogenesis imperfecta: Research advances

  • Fang Lv
  • , Mei Li*
  • *Corresponding author for this work
  • Chinese Academy of Medical Sciences

Research output: Contribution to journalArticlepeer-review

Abstract

Osteogenesis imperfecta(OI)is a genetic bone disease characterized by increased bone fragility and recurrent bone fractures. It belongs to orphan diseases of which the diagnosis and treatment are facing challenges. The effective treatments targeting at the underlying causes are still unavailable. Recently, many agents have been demonstrated to increase bone mineral density, improve bone microstructures, and reduce the incidence of fractures. Herein, we review the progress in new drugs for the treatment of OI.

Original languageEnglish
Pages (from-to)173-177
Number of pages5
JournalJournal of International Pharmaceutical Research
Volume44
Issue number2
DOIs
Publication statusPublished - 28 Feb 2017
Externally publishedYes

Keywords

  • Orphan drug
  • Osteogenesis imperfect
  • Rare disease

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