This is a double-blind, randomized, stratified, parallel-group study to compare the safety, tolerability, and clinical and biochemical efficacy of daily oral alendronate 40 mg with that of daily oral etidronate 400 mg in approximately 80 patients with Paget's disease of bone.

Project Start
Project End
Budget Start
Budget End
Support Year
33
Fiscal Year
1994
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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