Study of ABT-888 in Combination With Bortezomib and Dexamethasone in Patients With Relapsed Refractory Myeloma

Inclusion Criteria:

• Confirmed diagnosis of multiple myeloma.
• Measurable disease, according to the International Myeloma Working Group criteria.
• ECOG performance status 0, 1 or 2.
• Patients must have received prior treatment for MM and have relapsed or progressed on prior therapy; no limit on number of prior treatment regimens, but prior treatment must be completed 2 weeks prior to registration. Prior exposure to Bortezomib is not an exclusion criteria as long as patients did not progress or relapse while receiving or within 3 months of completing trt with bortezomib
• Prior radiation, completed at least 4 weeks prior to registration, is permitted.
• Adequate marrow reserve, liver and renal function

Exclusion Criteria:

• patients with a history of other malignancies, except: adequately treated nonmelanoma skin cancer, curatively treated in-situ cancer of the cervix, prostate cancer with stable PSA for > 3 years, or other solid tumours curatively treated with no evidence of disease for > 5 years.
• Patients with preexisting grade 2 (or higher) sensory neuropathy or grade 1 sensory neuropathy with neuropathic pain.
• Pregnant or lactating women
• Patients receiving concurrent treatment with other anti-cancer therapy any other investigational agents.
• Active or uncontrolled infections
• Patient with known documented congenital or acquired risk factor for thromboembolic event
• Patients with known brain metastases should be excluded from this clinical trial because of their poor prognosis and because they often develop progressive