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| Sponsor: | Merck |
|---|---|
| Information provided by: | Merck |
| ClinicalTrials.gov Identifier: | NCT00092053 |
Purpose
The purpose of this study is to evaluate the efficacy and safety of an investigational drug in postmenopausal women with osteoporosis.
| Condition | Intervention | Phase |
|---|---|---|
|
Postmenopausal Osteoporosis |
Drug: MK0217, alendronate sodium/Duration of Treatment: 3 months Drug: Comparator: placebo / Duration of Treatment: 3 months |
Phase III |
| Study Type: | Interventional |
| Study Design: | Randomized, Double Blind (Subject, Investigator), Safety/Efficacy Study |
| Official Title: | A Randomized, Double-Blind, Placebo-Controlled Study to Evaluate the Persistence of the Effect of Oral Monthly Ibandronate on Bone Reception in Postmenopausal Women in Osteoporosis |
Eligibility| Ages Eligible for Study: | 50 Years and older |
| Genders Eligible for Study: | Female |
| Accepts Healthy Volunteers: | No |
Inclusion Criteria:
Contacts and Locations
More Information
| Responsible Party: | Merck Sharp & Dohme Corp ( Executive Vice President, Clinical and Quantitative Sciences ) |
| Study ID Numbers: | 2004_007, MK0217-908 |
| Study First Received: | September 21, 2004 |
| Last Updated: | January 21, 2010 |
| ClinicalTrials.gov Identifier: | NCT00092053 History of Changes |
| Health Authority: | Germany: Federal Institute for Drugs and Medical Devices |
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Postmenopausal Osteoporosis |
|
Musculoskeletal Diseases Alendronate Physiological Effects of Drugs Osteoporosis, Postmenopausal Osteoporosis |
Bone Density Conservation Agents Bone Diseases, Metabolic Bone Diseases Pharmacologic Actions |