Multiple Myeloma Clinical Trial
Official title:
An Open-Label Randomized Study of Subcutaneous and Intravenous VELCADE in Subjects With Previously Treated Multiple Myeloma
Randomized, open-label, international, multi-center, Phase 3 study in which patients are randomized to receive VELCADE administered by subcutaneous injection or intravenous infusion.
Status | Completed |
Enrollment | 222 |
Est. completion date | September 2010 |
Est. primary completion date | August 2010 |
Accepts healthy volunteers | No |
Gender | Both |
Age group | 18 Years and older |
Eligibility |
Inclusion Criteria: 1. Male or female subjects 18 years or older 2. Diagnosis of multiple myeloma 3. Measurable, secretory multiple myeloma defined as serum monoclonal IgG of =10 g/L, serum monoclonal IgA or IgE =5 g/L, or serum monoclonal IgD =0.5g/L; or urine M-protein of =200 mg/24 hr 4. Relapse or progression of myeloma following prior systemic antineoplastic therapy. Exclusion Criteria: 1. Previous treatment with VELCADE 2. More than 3 previous lines of therapy (separate lines of therapy are defined as single or combination therapies that are either separated by disease progression or by a greater than 6 month treatment-free interval) 3. Peripheral neuropathy or neuropathic pain of NCI CTCAE Grade =2 4. Any of the following within 3 weeks prior to randomization: antineoplastic or experimental therapy, corticosteroid use above 10mg a day (prednisone or equivalent), or plasmapheresis 5. Any of the following within 2 weeks prior to randomization: radiation therapy, major surgery (kyphoplasty is not considered major surgery) 6. Prior malignancy other than multiple myeloma diagnosed or treated within the last 2 years, with the exception of completely resected carcinoma in situ or basal/squamous carcinoma of the skin |
Allocation: Randomized, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Treatment
Country | Name | City | State |
---|---|---|---|
Belgium | UZ Brussel Department Medical Oncology Laarbeeklaan 101 | Brussel | |
France | Hôtel DIEU, Service D'Hématologie Place Alexis RICORDEAU | NANTES Cedex 01 | |
Germany | Universitätsklinikum Münster Onkologische Ambulanz West Albert-Schweitzer-Str. 33 | Münster |
Lead Sponsor | Collaborator |
---|---|
Millennium Pharmaceuticals, Inc. | Johnson & Johnson Pharmaceutical Research & Development, L.L.C. |
Belgium, France, Germany,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Number of Patients With Overall Response (Complete Response + Partial Response) | Disease response was measured according to European Group for Blood and Marrow Transplantation (EBMT) criteria with the addition of the response categories of nCR and VGPR. Complete response requires disappearance of monoclonal protein from the blood and urine and <5% plasma cells in the bone marrow on at least 2 determinations for a minimum of 6 weeks. Partial Response requires =50% reduction in serum m-protein for at least 2 determinations at least 6 weeks apart and if present, reduction in 24-hour urinary light chain excretion by either =90% or to <200 mg |
Over 4 cycles (prior to the addition of dexamethasone) | No |
Secondary | Number of Patients With Complete Response | Disease response was measured according to European Group for Blood and Marrow Transplantation (EBMT) criteria with the addition of the response categories of nCR and VGPR. Complete response requires disappearance of monoclonal protein from the blood and urine and <5% plasma cells in the bone marrow on at least 2 determinations for a minimum of 6 weeks. |
Over 4 cycles (prior to the addition of dexamethasone) | No |
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