drugset / Trial / NCT00035256

Sequential Use of Teriparatide and Raloxifene HCl in the Treatment of Postmenopausal Women With Osteoporosis

NCT00035256

Phase 4 Completed 330 enrolled Eli Lilly and Company
RandomizedParallel-groupDouble-blindTreatment

Summary

The purpose of this study is to determine whether the increase in spine bone mineral density that has been generally observed in previous clinical studies involving the study drug can be maintained or even increased if followed with raloxifene HCl. All qualifying study participants will receive the study drug followed by treatment with raloxifene HCl or placebo. All study participants will receive raloxifene HCl in the third phase of the study.

Timeline

Start
2001-10
Primary completion
Completion
2005-07

Drugs

EvaluationDrugModalityDoseRoute
Subject Raloxifene Other / unclassified
Subject Teriparatide Protein / enzyme biologic