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To Assess Prevention of Bone Loss in Women With Lupus Receiving Treatment With Glucocorticoids

Lupus Clinical Trial

Official title:
A Randomized, Double-Blind, Multi-Center, Placebo- Controlled Study to Assess Prevention of Bone Loss by Treatment With GL701 (Prestara) in Women With Systemic Lupus Erythematosus Receiving Treatment With Glucocorticoids

Clinical Trial Summary

The purpose of this clinical trial is to study the effects of GL701 on bone mineral density in women with active systemic lupus erythematosus (SLE) who are also receiving treatment with glucocorticoids (e.g., prednisone).

Clinical Trial Description

n/a

Study Design

Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Double-Blind, Primary Purpose: Prevention

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT00053560
Study type Interventional
Source Genelabs Technologies
Contact
Status Active, not recruiting
Phase Phase 3
Start date December 2002
Completion date August 2004
View Details
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