Clinical Trials Directory

Trials / Completed

CompletedNCT00532545

Bone Marker Changes With Teriparatide/Postmenopausal Osteoporosis

Bone Marker Changes In One Month Treatment With TERIPARATIDE (LY333334) Injections (rDNA Origin) in Men and Postmenopausal Women With Severe Osteoporosis

Status
Completed
Phase
Phase 4
Study type
Interventional
Enrollment
45 (actual)
Sponsor
Eli Lilly and Company · Industry
Sex
All
Age
50 Years
Healthy volunteers
Not accepted

Summary

To test the hypothesis that Teriparatide injections given 20 micrograms/daily subcutaneously, for one month, are able to produce reliable changes in the bone marker in a severe osteoporotic population

Conditions

Interventions

TypeNameDescription
DRUGTeriparatideTeriparatide 20 micrograms/daily subcutaneously

Timeline

Start date
2003-04-01
Completion
2004-04-01
First posted
2007-09-20
Last updated
2007-09-20

Locations

7 sites across 1 country: Puerto Rico

Source: ClinicalTrials.gov record NCT00532545. Inclusion in this directory is not an endorsement.