Clinical trial
Switching Osteoporosis Patients Currently on Oral Bisphosphonate to Zoledronic…
NCT00097812 · Novartis Pharmaceuticals, Industry · Completed
Key facts
| NCT number | NCT00097812 |
|---|---|
| Title | Switching Osteoporosis Patients Currently on Oral Bisphosphonate to Zoledronic Acid |
| Official title | A Study to Assess the Safety, Tolerability, and Efficacy of Switching Patients Currently on Oral Bisphosphonate to Zoledronic Acid |
| Lead sponsor | Novartis Pharmaceuticals, Industry |
| Status | Completed |
| Phase | Phase 3 |
| Study type | Interventional |
| Conditions | Osteoporosis |
| Intervention type | Drug |
| Interventions | zoledronic acid |
| Enrollment | 220 |
| Start date | May 1, 2004 |
| Primary completion | Dec 1, 2005 |
| Completion | Dec 1, 2005 |
| First posted | Dec 1, 2004 |
| Last update posted | Apr 27, 2012 |
| Countries | Germany, United States |
At a glance
- 10–99 Study sites
- 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: