drugset / Trial / NCT00092066
A Study to Evaluate the Safety, Tolerability, and Efficacy of an Investigational Drug and Dietary Supplement in Men and Postmenopausal Women With Osteoporosis (0217A-227)
RandomizedParallel-groupDouble-blindTreatment
Summary
The purpose of this study is to test the safety, tolerability and effectiveness of an investigational drug and dietary supplement to reduce the risk of vitamin D insufficiency and deficiency during the treatment of osteoporosis in men and postmenopausal women.
Timeline
- Start
- 2003-09-24
- Primary completion
- 2004-05-01
- Completion
- 2004-05-01
Drugs
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Subject | Alendronic Acid | Small molecule | 70 mg | — |
| Subject | Cholecalciferol | Other / unclassified | 2800 iu | — |