Evaluation of VELCADE Given as Retreatment to Multiple Myeloma Patients for Efficacy, Safety and Tolerability

Completed · Phase 4

Conditions studied: Multiple Myeloma

In brief

Multiple myeloma represents the second most common hematological malignancy.VELCADE is a small molecule to treat human malignancies. Its anti-neoplastic effect invovles several distinct mechanisms including inhibition of cell growth. Patients who have relapsed or are refractory to therapy, the standard of care is now VELCADE based on the results of previous clinical trials.

Key facts

Study ID

NCT00257114

Run by

Millennium Pharmaceuticals, Inc.

Last updated by the study team

2008-02-11

Who can join

Age: 18 and older. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• Voluntary written informed consent with the understanding that the consent may be w/d by the patient at any time w/o prejudice to future medical care.
• Patient previously diagnosed with Multiple Myeloma (MM).
• Patient previously tolerated 0.7, 1.0, or 1.3 mg/m2/dose of VELCADE alone or therapy combination and had at least a greater/equal 50% reduction in M-Protein upon completion of VELCADE therapy. The DOR prior to VELCADE greater/equal 4 months for the patient population.
• It has been greater/equal 2 months since the patient's last VELCADE dose and the patient meets certain Lab criteria as per protocol.
• Patient has a Karnosfsky performance status greater/equal 60%.
• Patient has a life-expectancy greater than 3 months.
• Patient has laboratory values (defined in protocol) within 14 days before enrollment.

You may not qualify if…

• Patients with a Hx of PD, minimal response, or stable disease (SD)on first exposure to VELCADE.
• Patient has received chemotherapy, radiotherapy, immunotherapy or experimental therapy to treat multiple myeloma since their last dose of VELCADE.
• Patients who achieved a CR or PR but relapsed while on therapy.
• Patient had major surgery w/in 2 wks before enrollment.
• Patient has a Hx of allergic reaction to compounds containing boron or mannitol.
• Patient has peripheral sensory neuropathy of Grade 2 w/pain or greater intensity.
• Patient has cardiac amyloidosis.
• Patient has poorly controlled hypertension, diabetes mellitus, or other serious medical or pysychiatric illness.
• Patient is known to be human immunodeficiency virus (HIV)+.
• Patient is known to be hepatitis B surface antigen-positive or has known active hepatitis C infection.
• Patient has an active systemic infection requiring treatment.
• Female patient is pregnant or breast-feeding. Confirmation must be established by a negative serum B-hCG.
• Patient is currently enrolled in another clinical research study.

Where it is running

• Sinai Hospital of Baltimore — Baltimore, Maryland, United States

Full record on ClinicalTrials.gov

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