Viewing Study NCT00104104



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Last Modification Date: 2024-10-26 @ 9:11 AM
Study NCT ID: NCT00104104
Status: COMPLETED
Last Update Posted: 2011-06-29
First Post: 2005-02-22

Brief Title: A Multiple Myeloma Trial in Patients With Bone Metastases
Sponsor: Novartis Pharmaceuticals
Organization: Novartis

Study Overview

Official Title: A MulticenterOpen Label Randomized Trial Evaluating the Duration of Infusion of Zoledronic Acid 4 mg IV in Multiple Myeloma Patients With Bone Metastases
Status: COMPLETED
Status Verified Date: 2011-06
Last Known Status: None
Delayed Posting: No
If Stopped, Why?: Not Stopped
Has Expanded Access: False
If Expanded Access, NCT#: N/A
Has Expanded Access, NCT# Status: N/A
Acronym: None
Brief Summary: The purpose of this trial is to study the safety of treating patients with multiple myeloma and at least one bone lesion with zoledronic acid 4mg intravenously IV every 3 - 4 weeks for 2 years Patients will receive a zoledronic acid infusion for 15 minutes or 30 minutes
Detailed Description: None

Study Oversight

Has Oversight DMC: None
Is a FDA Regulated Drug?: None
Is a FDA Regulated Device?: None
Is an Unapproved Device?: None
Is a PPSD?: None
Is a US Export?: None
Is an FDA AA801 Violation?: None
Secondary IDs
Secondary ID Type Domain Link
US97 None None None