Clinical Trials · NCT00532207

Study of Teriparatide in the Treatment of Postmenopausal Women With Osteoporosis

CompletedPhase 3Teriparatide (Approved)
Phase
Phase 3
Recruitment status
Completed
Sponsor
Eli Lilly and Company
Enrollment
50
Start date
Nov 2003
Locations
1 site, Russia
Primary endpoint
To test the hypothesis that therapy for 12 months with once daily subcutaneous PTH 1-34 (teriparatide; TPTD) 20 micrograms will increase Bone Mineral Density (BMD) at the lumbar spine in postmenopausal women with osteoporosis
View Teriparatide compound reference