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Safety, Pharmacokinetics, and Efficacy of 100, 150, and 200 mg Risedronate Administered to Women With Low BMD
This study has been completed.
Study NCT00577837   Information provided by Procter and Gamble
First Received: December 19, 2007   Last Updated: February 5, 2008   History of Changes
Related Studies can be found by searching for the Conditions, Interventions, and Sponsors found in this study:
Conditions listed in this trial
Postmenopausal
Interventions listed in this trial
risedronate
experimental
Additional drug interventions recognized in this trial
Etidronic Acid
Risedronic acid
More general drug interventions related to this trial
Bone Density Conservation Agents
Calcium Channel Blockers
Cardiovascular Agents
Membrane Transport Modulators
Molecular Mechanisms of Pharmacological Action
Pharmacologic Actions
Physiological Effects of Drugs
Therapeutic Uses
Sponsors listed in this trial
Procter and Gamble
Sanofi-Aventis


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