Clinical trial

Safety/Efficacy of Zoledronic Acid and Alendronate on Bone Metabolism in…

NCT00404820 · Novartis, Industry · Completed

Key facts

NCT number NCT00404820
Title Safety/Efficacy of Zoledronic Acid and Alendronate on Bone Metabolism in Postmenopausal Women With Osteoporosis
Official title A Multi-center, Randomized, Open-label, Controlled, One-year Trial to Measure the Effect of Zoledronic Acid and Alendronate on Bone Metabolism in Postmenopausal Women With Osteopenia and Osteoporosis
Acronym ROSE
Lead sponsor Novartis, Industry
Status Completed
Phase Phase 3
Study type Interventional
Conditions Osteoporosis
Intervention type Drug
Interventions Zoledronic acid 5 mg solution, Alendronate 70 mg tablets, Calcium/Vitamin D
Enrollment 604
Start date Oct 1, 2006
Primary completion Dec 1, 2008
Completion Dec 1, 2008
First posted Nov 29, 2006
Last update posted Jul 1, 2011
Countries Germany

At a glance

  • 1–9 Study sites
  • Yes 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:

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