MedPath

Comparative Trial inMultiple Myeloma Patients of Oral Ibandronic Acid versus Intravenous Zoledronate: a phase III study

Conditions
Multiple Myeloma
Registration Number
EUCTR2005-003770-23-AT
Lead Sponsor
F. Hoffmann-La Roche Ltd
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
ot Recruiting
Sex
All
Target Recruitment
424
Inclusion Criteria

•Patients with multiple myeloma & confirmation of bone lesions
•Age > 18 years
•Patient’s written informed consent
•WHO performance status 0-2
•Life expectancy of ? 6 months
•Adequate renal function (defined by a creatinine clearance >60 ml/min)
•No history of brain metastases
Are the trial subjects under 18? no
Number of subjects for this age range:
F.1.2 Adults (18-64 years) yes
F.1.2.1 Number of subjects for this age range
F.1.3 Elderly (>=65 years) yes
F.1.3.1 Number of subjects for this age range

Exclusion Criteria

•Any circumstance liable to compromise follow-up and compliance
•Pregnant or lactating period
•Participation in a clinical trial with any investigational drug within 4 weeks preceding the first dose of the study drug
•History of other concomitant cancer in evolution
•Prior bisphosphonate treatment with the exception of bisphosphonate treatment for hypercalcemia and osteoporosis
•Pre-scheduled radiotherapy that would fall within the study period

Study & Design

Study Type
Interventional clinical trial of medicinal product
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Secondary Outcome Measures
NameTimeMethod
© Copyright 2025. All Rights Reserved by MedPath