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A Study to Evaluate and Compare the Effects of Two Approved Drugs in Women With Postmenopausal Osteoporosis

2014-08-27 03:54:04 | BioPortfolio

Summary

This study is to evaluate and compare the effects of two approved medications to treat women with postmenopausal osteoporosis.

Study Design

Allocation: Randomized, Control: Active Control, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Double Blind (Subject, Investigator), Primary Purpose: Treatment

Conditions

Postmenopausal Osteoporosis

Intervention

MK0217, alendronate sodium/Duration of Treatment: 12 mo, Comparator: risedronate/Duration of Treatment: 12 mo

Status

Completed

Source

Merck

Results (where available)

View Results

Links

Published on BioPortfolio: 2014-08-27T03:54:04-0400

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Medical and Biotech [MESH] Definitions

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