drugset / Trial / NCT00622505

Zoledronic Acid Treatment (Every 4 or 12 Weeks) to Prevent Skeletal Complications in Advanced Multiple Myeloma Participants

NCT00622505

Phase 4 Completed 121 enrolled Novartis Pharmaceuticals
NaSingle-groupOpen-labelPrevention

Summary

This study evaluated the effectiveness and safety of a dosing method for zoledronic acid in preventing skeletal complications in multiple myeloma participants who have been on an intravenous (IV) bisphosphonate for about one to two years.

Timeline

Start
2007-11-07
Primary completion
2012-04-03
Completion
2012-04-03

Drugs

EvaluationDrugModalityDoseRoute
Subject Zoledronic acid Other / unclassified 3 mg Intravenous
Subject Zoledronic acid Other / unclassified 3.3 mg Intravenous
Subject Zoledronic acid Other / unclassified 3.5 mg Intravenous
Subject Zoledronic acid Other / unclassified 4 mg Intravenous

Indications