Clinical Trials · NCT00532545

Bone Marker Changes With Teriparatide/Postmenopausal Osteoporosis

CompletedPhase 4Teriparatide (Approved)
Phase
Phase 4
Recruitment status
Completed
Sponsor
Eli Lilly and Company
Enrollment
45
Start date
Apr 2003
Locations
7 sites, Puerto Rico
Primary endpoint
To test the hypothesis that Teriparatide injections given 20 micrograms/daily subcutaneously, for one month, is able to produce reliable changes in the bone marker in a severe osteoporotic population in Puerto Rico.
View Teriparatide compound reference