drugset / Trial / NCT00048074
DIVA Study - A Study of Different Regimens of Intravenous Administration of Bonviva (Ibandronate) in Women With Post-Menopausal Osteoporosis
RandomizedParallel-groupDouble-blindTreatment
Summary
This study will assess the efficacy and safety of intravenous administration of Bonviva regimens in women with post-menopausal osteoporosis, compared to oral daily administration. Patients will also receive daily supplementation with vitamin D and calcium. The anticipated time of study treatment is 2+ years, and the target sample size is 500+ individuals.
Timeline
- Start
- 2002-06
- Primary completion
- 2005-05
- Completion
- 2005-05
Drugs
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Subject | Ibandronate | Other / unclassified | 2 mg | Intravenous |
| Subject | Ibandronate | Other / unclassified | 2.5 mg | Intravenous |
| Subject | Ibandronate | Other / unclassified | 3 mg | Intravenous |