Multiple Myeloma Clinical Trial

A Study of Filanesib (ARRY-520) and Carfilzomib in Patients With Advanced Multiple Myeloma

Summary

This is a Phase 2 study during which patients with advanced multiple myeloma will receive either carfilzomib alone (single-agent) or carfilzomib in combination with investigational study drug filanesib (ARRY-520). Patients will be followed to determine the effectiveness of both single-agent carfilzomib and carfilzomib + filanesib in treating myeloma. Patients will be allowed to crossover from single-agent carfilzomib to carfilzomib + filanesib if disease progression occurs. Approximately 75 patients from the US will be enrolled in this study.

View Eligibility Criteria

Eligibility Criteria

Key Inclusion Criteria:

Confirmed multiple myeloma with measurable disease.
Disease refractory to last myeloma regimen.
Patients must have received at least 2 prior treatment regimens, including bortezomib and an IMiD (e.g., lenalidomide, thalidomide, pomalidomide). Induction therapy and stem cell transplant ± maintenance are to be considered as a single regimen.
Eastern Cooperative Oncology Group (ECOG) performance status of 0, 1 or 2 within 14 days prior to first dose of study treatment.
Adequate hematology, liver and renal function laboratory values within 14 days prior to first dose of study treatment.
Additional criteria exist.

Key Exclusion Criteria:

Prior treatment with carfilzomib, filanesib, or any other KSP inhibitor.
Past or current plasma cell leukemia.
Primary amyloidosis (amyloidosis associated with multiple myeloma is allowed).
POEMS syndrome (polyneuropathy, organomegaly, endocrinopathy, monoclonal protein and skin changes).
Ongoing Grade 3 or Grade 4 peripheral neuropathy, or Grade 2 peripheral neuropathy with pain despite appropriate interventions, within 28 days prior to first dose of study treatment.
Autologous or allogeneic stem cell or bone marrow transplant within 3 months prior to first dose of study treatment.
Concomitant malignancies or previous malignancies (other than multiple myeloma) with less than a 2-year disease-free interval at the time of first dose of study treatment. Patients with adequately resected basal or squamous cell carcinoma of the skin, carcinoma in situ of the cervix or breast, or Stage 1 prostate cancer are eligible irrespective of the time of diagnosis.
Known pulmonary hypertension of any severity.
Concurrent cardiac disease that, in the judgment of the Investigator, would make the patient inappropriate for study participation.
Known positive serology for the human immunodeficiency virus (HIV), active hepatitis B and/or hepatitis C.
Acute active infection requiring treatment.
Additional criteria exist.

Study is for people with:

Multiple Myeloma

Phase:

Phase 2

Estimated Enrollment:

77

Study ID:

NCT01989325

Recruitment Status:

Completed

Sponsor:

Pfizer

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There are 22 Locations for this study

See Locations Near You

Genesis Cancer Center
Hot Springs Arkansas, 71913, United States
UCLA
Los Angeles California, 90095, United States
St. Joseph Heritage Healthcare
Santa Rosa California, 95403, United States
Florida Cancer Specialists
Fort Myers Florida, 33905, United States
Robert H. Lurie Comprehensive Cancer Center of Northwestern University
Chicago Illinois, 60611, United States
Crescent City Research Consortium
Marrero Louisiana, 70072, United States
Massachusetts General Hospital
Boston Massachusetts, 02114, United States
Karmanos Cancer Institute
Detroit Michigan, 48201, United States
Forrest General Cancer Center
Hattiesburg Mississippi, 39401, United States
Nebraska Cancer Specialists
Omaha Nebraska, 68130, United States
Memorial Sloan Kettering
New York New York, 10065, United States
Levine Cancer Institute
Charlotte North Carolina, 28204, United States
Oncology Hematology Care - Blue Ash
Cincinnati Ohio, 45242, United States
Cleveland Clinic
Cleveland Ohio, 44195, United States
Ohio State University
Columbus Ohio, 43210, United States
Knight Cancer Institute at Oregon Health & Science University
Portland Oregon, 97239, United States
Prairie Lakes Health Care System
Watertown South Dakota, 57201, United States
Sarah Cannon Research Institute
Nashville Tennessee, 37203, United States
Simmons Cancer Center - UT Southwestern Medical Center
Dallas Texas, 75390, United States
Virginia Cancer Specialists
Fairfax Virginia, 22031, United States
WVU - Mary Babb Randolph Cancer Center
Morgantown West Virginia, 26506, United States
Medical College of Wisconsin Cancer Center
Milwaukee Wisconsin, 53226, United States

How clear is this clinincal trial information?

Study is for people with:

Multiple Myeloma

Phase:

Phase 2

Estimated Enrollment:

77

Study ID:

NCT01989325

Recruitment Status:

Completed

Sponsor:


Pfizer

How clear is this clinincal trial information?

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