Approximately 1,200 women who meet the inclusion criteria will be enrolled in this double-blind, randomized, multicenter, two-year study to compare the safety and efficacy of daily oral alendronate 5 mg vs. 35 mg alendronate once weekly in increasing lumbar spine bone density in ambulatory postmenopausal women with normal or mild reduction in bone density. About 25 women will be required to participate at the University of Chicago site.

Project Start
1998-12-01
Project End
1999-11-30
Budget Start
1998-10-01
Budget End
1999-09-30
Support Year
38
Fiscal Year
1999
Total Cost
Indirect Cost
Name
University of Chicago
Department
Type
DUNS #
225410919
City
Chicago
State
IL
Country
United States
Zip Code
60637
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