drugset / Trial / NCT00239629

Teriparatide and Strontium Ranelate Head-To-Head Comparison Trial

NCT00239629

Phase 4 Completed 73 enrolled Eli Lilly and Company
RandomizedParallel-groupOpen-labelTreatment

Summary

The aim of this study is to directly compare the bone forming effects of 20 microg/day of teriparatide with those of 2 g/day strontium ranelate as measured by the histomorphometric variables and biochemical bone formation markers after 6 months of therapy in postmenopausal women with osteoporosis.

Timeline

Start
2005-09
Primary completion
Completion
2007-01

Drugs

EvaluationDrugModalityDoseRoute
Subject Strontium Ranelate Small molecule 2 g
Subject Teriparatide Protein / enzyme biologic 20 ug