drugset / Trial / NCT00048074

DIVA Study - A Study of Different Regimens of Intravenous Administration of Bonviva (Ibandronate) in Women With Post-Menopausal Osteoporosis

NCT00048074

Phase 3 Completed 1395 enrolled Hoffmann-La Roche
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

EvaluationDrugModalityDoseRoute
Subject Ibandronate Other / unclassified 2 mg Intravenous
Subject Ibandronate Other / unclassified 2.5 mg Intravenous
Subject Ibandronate Other / unclassified 3 mg Intravenous