Clinical trial
A Study to Evaluate the Safety, Tolerability, and Efficacy of an Investigational…
NCT00092066 · Organon and Co, Industry · Completed
Key facts
| NCT number | NCT00092066 |
|---|---|
| Title | 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) |
| Official title | A 15-Week, Double-Blind, Randomized, Active-Controlled, Multi-Center Study With 24-Week Extension to Evaluate the Safety, Tolerability, Efficacy of Alendronate 70 mg Plus Vitamin D3 2800 IU Combination Tablet in Men and Postmenopausal Women With Osteoporosis |
| Lead sponsor | Organon and Co, Industry |
| Status | Completed |
| Phase | Phase 3 |
| Study type | Interventional |
| Conditions | Osteoporosis, Vitamin D Deficiency |
| Intervention type | Drug |
| Interventions | MK0217A, alendronate sodium (+) cholecalciferol / Duration of Treatment: 15 weeks |
| Enrollment | 717 |
| Start date | Sep 24, 2003 |
| Primary completion | May 1, 2004 |
| Completion | May 1, 2004 |
| First posted | Sep 24, 2004 |
| Last update posted | Aug 14, 2024 |
At a glance
- No Results posted
- None Linked FDA submissions
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
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Source: U.S. National Library of Medicine (NLM), ClinicalTrials.gov · Source date: