Viewing Study NCT00035256



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Last Modification Date: 2024-10-26 @ 9:07 AM
Study NCT ID: NCT00035256
Status: COMPLETED
Last Update Posted: 2007-05-15
First Post: 2002-05-02

Brief Title: Sequential Use of Teriparatide and Raloxifene HCl in the Treatment of Postmenopausal Women With Osteoporosis
Sponsor: Eli Lilly and Company
Organization: Eli Lilly and Company

Study Overview

Official Title: Sequential Use of Teriparatide and Raloxifene HCl in the Treatment of Postmenopausal Women With Osteoporosis
Status: COMPLETED
Status Verified Date: 2007-05
Last Known Status: None
Delayed Posting: No
If Stopped, Why?: Not Stopped
Has Expanded Access: No
If Expanded Access, NCT#: N/A
Has Expanded Access, NCT# Status: N/A
Acronym: None
Brief 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
Detailed Description: None

Study Oversight

Has Oversight DMC: None
Is a FDA Regulated Drug?: None
Is a FDA Regulated Device?: None
Is an Unapproved Device?: None
Is a PPSD?: None
Is a US Export?: None
Is an FDA AA801 Violation?: None
Secondary IDs
Secondary ID Type Domain Link
B3D-MC-GHBQ None None None