Last updated on February 2020

A Study to Determine Dose Safety Tolerability and Efficacy of CC-220 Monotherapy and in Combination With Other Treatments in Subjects With Multiple Myeloma

Are you eligible to participate in this study?

You may be eligible for this study if you meet the following criteria:

  • Conditions: Lymphoproliferative disorders | Multiple Myeloma | Lymphoproliferative Disorder
  • Age: Between 18 - 100 Years
  • Gender: Male or Female

Inclusion Criteria:

  1. All subjects in RRMM cohorts must have a documented diagnosis of Multiple Myeloma and have measurable disease defined as:
  2. M-protein (serum and/or urine protein electrophoresis (sPEP or uPEP)): sPEP 0.5 g/dL or uPEP 200 mg/24 hours and/or
  3. Light chain Multiple Myeloma without measurable disease in the serum or urine: serum immunoglobulin free light chain 10 mg/dL (100 mg/L) and abnormal serum immunoglobulin kappa lambda free light chain ratio 2. All subjects in RRMM cohorts must have documented disease progression on or within 60 days from the last dose of their last myeloma therapy. Subjects who had CAR T therapy as their last myeloma therapy must have documented disease progression.
  4. Eastern Cooperative Oncology Group (ECOG) performance status score of 0, 1 or 2 3. Subject must have documented diagnosis with previously untreated symptomatic MM as defined by the criteria below (Rajkumar, 2016): MM diagnostic criteria;
    • Clonal bone marrow plasma cells 10% or biopsy-proven bony or extramedullary plasmacytoma
    • Any one or more of the following myeloma defining events:
    • One or more of the following myeloma-related organ dysfunction (at least one of the following);

[C] Calcium elevation (serum calcium > 0.25 mmol/L [> 1 mg/dL] higher than the upper limit of laboratory normal or > 2.75 mmol/L [> 11 mg/dL])

[R] Renal insufficiency (serum creatinine > 2 mg/dl [> 177 mol/L] or creatinine clearance < 40 ml/min)

  • [A] Anemia (hemoglobin < 10 g/dl or > 2 g/dL below the lower limit of laboratory normal)
  • [B] Bone lesions (lytic or osteopenic) one or more bone lesions on skeletal radiography, computed tomography (CT), or positron emission tomography (PET)/CT
  • One or more of the following biomarkers of malignancy:
  • Clonal bone marrow plasma cell percentage* 60%
  • Abnormal serum free light-chain (FLC) ratio 100 (involved kappa) or <0.01 (involved lambda) and involved FLC level must be 100 mg/L
  • >1 focal lesion detected by magnetic resonance imaging (MRI) (at least 5 mm in size)

AND have measurable disease, as assessed by central laboratory, defined by any of the

  • Immunoglobulin (Ig)G myeloma: serum M-protein level 1.0 g/dL or urine M-protein level 200 mg/24 hours; or
  • IgA, IgM, IgD, or IgE multiple myeloma: serum M-protein level 0.5 g/dL or urine M-protein level 200 mg/24 hours; or
  • Light chain multiple myeloma without measurable disease in serum or urine: serum FLC 100 mg/L and abnormal kappa lambda (/) ratio 4. Subjects in Cohort J1 are not considered by the investigator as eligible for high-dose chemotherapy and autologous stem cell transplantation due to:
  • Age 65 years, OR
  • In subjects <65 years: presence of important comorbid condition(s) likely to have a negative impact on tolerability of high-dose chemotherapy with autologous stem cell transplantation. 5. Subjects in Cohort J2 are considered by the investigator as eligible for high-dose chemotherapy and autologous stem cell transplantation according to the institution's criteria based on age, medical history, cardiac and pulmonary status, overall health and condition, co-morbid condition(s), physical examination, and laboratory data.

Exclusion Criteria:

  1. Subject has nonsecretory or oligosecretory multiple myeloma 2. Subjects with Plasma Cell leukemia or amyloidosis 3. Any of the following laboratory abnormalities

Absolute neutrophil count (ANC) <1,000/L

Platelet count < 75,000/L for Part 1. For Part 2; platelet count < 75,000/L for subjects in whom < 50% of bone marrow nucleated cells are plasma cells; otherwise platelet count < 50,000/L (transfusions are not permitted to achieve minimum platelet counts

Corrected serum calcium >13.5 mg/dL (>3.4 mmol/L)

  • Serum glutamic oxaloacetic transaminase (SGOT)/aspartate aminotransferase (AST) or serum glutamic pyruvic transaminase (SGPT)/alanine aminotransferase (ALT)2.0 x upper limit of normal (ULN)
  • Serum total bilirubin and alkaline phosphatase >1.5 x ULN
  • Subjects with serious renal impairment creatinine clearance ([CrCl] <45 mL/min) or requiring dialysis would be excluded 4. Subjects with peripheral neuropathy Grade 2

Recruitment Status: Open

Brief Description Eligibility Contact Research Team

Volunteer Sign-up

Sign up for our FREE service to receive email notifications when clinical trials are posted in the medical category of interest to you.