Weekly 70 mg/m2 Carfilzomib for Multiple Myeloma Patients Refractory to 27 mg/m2 Carfilzomib

Inclusion Criteria: 1. Has a diagnosis of MM based on standard criteria as follows: Major criteria: * Plasmacytomas on tissue biopsy. * Bone marrow plasmacytosis (greater than 30% plasma cells). * Monoclonal immunoglobulin (Ig) spike on serum electrophoresis IgG greater than 3.5 g/dL or IgA greater than 2.0 g/dL; kappa or lambda light chain excretion greater than 1 g/day on 24-hour urine protein electrophoresis. Minor criteria: * bone marrow plasmacytosis (10% to 30% plasma cells) * monoclonal immunoglobulin present but of lesser magnitude than given under major criteria * lytic bone lesions * normal IgM less than 50 mg/dL, IgA less than 100 mg/dL, or IgG less than 600 mg/dL Any of the following sets of criteria will confirm the diagnosis of multiple myeloma: * any 2 of the major criteria * major criterion 1 plus minor criterion 2, 3, or 4 * major criterion 3 plus minor criterion 1 or 3 * minor criteria 1, 2, and 3, or 1, 2, and 4 2. Patient must meet one of the following: * Currently, patient has progressive MM that has progressed while receiving twice weekly carfilzomib 27mg/m2 alone or as part of their last carfilzomib-containing combination regimen * Currently, the patient is not in CR and plateaued (as defined by unchanged disease markers for at least 8 weeks) while treated with carfilzomib (twice weekly 27 mg/m2) and dexamethasone with or without lenalidomide or pomalidomide * Patients who were previously receiving a carfilzomib (twice weekly 27 mg/m2) containing regimen and are currently receiving carfilzomib (twice weekly 27mg/m2) and dexamethasone maintenance therapy with or without lenalidomide or pomalidomide and are not in CR and have plateaued 3. Patient must have received at least one full cycle of carfilzomib at a dose of twice weekly 27mg/m2 prior to showing evidence of PD or plateauing from their last carfilzomib-containing regimen. 4. Patient must have previously received treatment with an immunomodulatory agents lenalidomide or pomalidomide to be eligible for the study (applicable only for subjects who qualify via inclusion criteria 2B or 2C). 5. There is no limit to the number of prior lines of therapy that a patient may have received. 6. Measurable disease, as defined by one or more of the following (assessed within 14 days prior to first dose): * Serum M-protein ≥ 0.5 g/dL, or * Urine M-protein ≥ 200 mg/24 hours, or * Only in patients who do not meet a or b, then use serum free light chain (SFLC) \> 100 mg/L (involved light chain) and an abnormal κ/λ ratio 7. Age ≥ 18 years. 8. Life expectancy ≥ 6 months. 9. Eastern Cooperative Oncology Group (ECOG) performance status ≤ 2. 10. Adequate hepatic function within 14 days prior to first dose, with bilirubin \< 1.5 × the upper limit of normal (ULN), and aspartate aminotransferase (AST) and alanine aminotransferase (ALT) \< 3 × ULN. 11. LVEF ≥ 40%. 2-D transthoracic echocardiogram (ECHO) is the preferred method of evaluation. Multigated Acquisition Scan (MUGA) is acceptable if ECHO is not available. 12. Absolute neutrophil count (ANC) ≥ 1000/mm3 within 14 days prior to first dose. Screening ANC is to be independent of granulocyte colony stimulating factor support for ≥ 1 week and pegylated granulocyte colony stimulating factor for ≥ 2 weeks. 13. Hemoglobin ≥ 8.0 g/dL within 14 days prior to enrollment. Use of erythropoietic stimulating factors and red blood cell (RBC) transfusions per institutional guidelines is allowed; however, most recent RBC transfusion must have been at least 7 days prior to obtaining screening hemoglobin. 14. Platelet count ≥ 75,000/mm3 (≥ 50,000/mm3 if myeloma involvement in the bone marrow is \> 50%) within 14 days prior to first dose. Patients must not have received platelet transfusions for at least 7 days prior to obtaining the screening platelet count. 15. Calculated or measured creatinine clearance (CrCl) of ≥ 30 mL/min within 14 days prior to first dose. Calculations are based on a standard formula, such as the Cockcroft and Gault: \[(140 - Age) × Mass (kg) / (72 × Creatinine mg/ dL)\]; multiply result by 0.85 if female. 16. Written informed consent in accordance with federal, local, and institutional guidelines. 17. Women of childbearing potential (WOCBP) must have a negative serum pregnancy test within the 7 days prior to study drug administration and a negative urine pregnancy test within the 3 days prior to the first study drug administration 18. WOCBP and male subjects who are sexually active with WOCBP must agree to use 2 highly effective methods of contraception during the study and for 30 days following the last dose of study treatment including a male condom. Exclusion Criteria: 1. POEMS syndrome (polyneuropathy, organomegaly, endocrinopathy, monoclonal protein, and skin changes) 2. Plasma cell leukemia (\> 2.0 × 109/L circulating plasma cells by standard differential) 3. Waldenström's macroglobulinemia 4. Amyloidosis 5. Glucocorticoid therapy (prednisone \> 30 mg/day or equivalent) within 7 days prior to first dose 6. Cytotoxic chemotherapy with approved or investigational anticancer therapeutics within 28 days prior to first dose 7. Treatment with bortezomib (Velcade®), thalidomide, pomalidomide (Pomalyst®) or lenalidomide (Revlimid®) within 21 days prior to first dose 8. Focal radiation therapy within 7 days prior to first dose. Radiation therapy to an extended field involving a significant volume of bone marrow within 21 days prior to enrollment (i.e., prior radiation must have been to \< 30% of the bone marrow) 9. Immunotherapy within 21 days prior to first dose 10. Major surgery within 21 days prior to first dose 11. Active congestive heart failure (New York Heart Association \[NYHA\] Classes III to IV), symptomatic ischemia, or conduction abnormalities uncontrolled by conventional intervention. Myocardial infarction within 6 months prior to first dose. Echocardiogram or MUGA evidence of left ventricular ejecti…

Reproduced word-for-word from the public registry record — the study team can answer questions about it.