Clinical trial

Study of Teriparatide (FORTEO) to Treat Adults With Osteogenesis Imperfecta

NCT00131469 · Oregon Health and Science University, Other · Completed

Key facts

NCT number NCT00131469
Title Study of Teriparatide (FORTEO) to Treat Adults With Osteogenesis Imperfecta
Official title A Study to Assess the Effectiveness of Teriparatide (FORTEO) for Increasing Bone Mass and Improving Bone Strength in Adults Affected With Osteogenesis Imperfecta (OI)
Acronym OI
Lead sponsor Oregon Health and Science University, Other
Collaborators Eli Lilly and Company Industry Osteogenesis Imperfecta Foundation National Institutes of Health (NIH) NIH National Center for Research Resources (NCRR)
Status Completed
Phase Phase 4
Study type Interventional
Conditions Osteogenesis Imperfecta
Intervention type Drug
Interventions Teriparatide (FORTEO), Placebos
Enrollment 79
Start date Jun 1, 2005
Primary completion Jan 1, 2011
Completion Jan 1, 2011
First posted Aug 18, 2005
Last update posted Apr 24, 2019
Countries United States

At a glance

  • 1–9 Study sites
  • Yes Results posted
  • None Linked FDA submissions

Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.

About ClinicalTrials.gov studies

ClinicalTrials.gov is the U.S. National Library of Medicine's registry of clinical studies conducted around the world. Contact and investigator details are not shown here.

Source: U.S. National Library of Medicine (NLM), ClinicalTrials.gov · Source date:

Browse all ClinicalTrials.gov studies