Carfilzomib, proteasome inhibitor; intravenous
Drugmultiple dose, single schedule
NCT Number: NCT01989325
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.
Looking for future studies?
Notify Me18 year and older
All sexes
Interventional
Phase 2
Genesis Cancer Center, Hot Springs, Arkansas, United States
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Key Inclusion Criteria:
Key Exclusion Criteria:
multiple dose, single schedule
multiple dose, single schedule
as indicated, per the carfilzomib prescribing information
standard of care
Time frame: 18 months
Time frame: 18 months
Time frame: 18 months
Time frame: 6 months
Time frame: 18 months
Time frame: 18 months
Time frame: 18 months
Pfizer
Industry
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
Published trials that share one or more normalized conditions with this study.
NCT02092922
Advanced Multiple Myeloma
Birmingham, Alabama, United States
View Trial Details