Clinical Trials · NCT00543023

A Study of the Treatment of Postmenopausal Women With Osteoporosis

CompletedPhase 3Teriparatide (Approved)
Phase
Phase 3
Recruitment status
Completed
Sponsor
Eli Lilly and Company
Enrollment
104
Start date
Jun 2003
Locations
2 sites, China
Primary endpoint
to compare the effect of treatment with teriparatide 20 micrograms/day subcutaneous with that of salmon calcitonin 100 IU/day subcutaneous on change in lumbar spine BMD in postmenopausal women with established osteoporosis.
View Teriparatide compound reference