Multicenter Study of CPX-351(Cytarabine:Daunorubicin) Liposome Injection in Patients With Advanced Hematologic Cancer.
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|ClinicalTrials.gov Identifier: NCT00389428|
Recruitment Status : Completed
First Posted : October 18, 2006
Last Update Posted : May 17, 2012
|Condition or disease||Intervention/treatment||Phase|
|Hematologic Neoplasms||Drug: CPX-351 (Cytarabine:Daunorubicin) Liposome Injection||Phase 1|
CPX-351 is a liposomal formulation of a fixed combination of the antineoplastic drugs cytarabine and daunorubicin. The two drugs are present inside the liposome in a 5:1 molar ratio. The development of CPX-351 (cytarabine:daunorubicin) Liposome Injection was based on 1) defining a synergistic ratio of the two active moieties, cytarabine and daunorubicin, using cell-based screening assays and 2) designing a liposomal drug carrier to maintain this ratio after intravenous administration. CPX-351 was found to be more active in in vivo models of cancer than combinations of conventional cytarabine and daunorubicin. Both cytarabine and daunorubicin are active chemotherapeutic agents, each approved for clinical use in the United States for the treatment of hematological neoplasms.
CPX-351 is being developed with the hypothesis that it is superior to the currently used regimen of cytarabine and daunorubicin in the treatment of acute leukemia. This phase I study will determine the dose to carry forward into phase II trials.
|Study Type :||Interventional (Clinical Trial)|
|Actual Enrollment :||48 participants|
|Intervention Model:||Single Group Assignment|
|Masking:||None (Open Label)|
|Official Title:||Phase 1 Study of CPX-351(Cytarabine:Daunorubicin) Liposome Injection in Patients With Advanced Hematologic Malignancies.|
|Study Start Date :||September 2006|
|Actual Primary Completion Date :||December 2008|
|Actual Study Completion Date :||December 2009|
- To determine the maximum tolerated dose (MTD) for use in phase 2
- To evaluate the safety and dose-limiting toxicities (DLT) of CPX-351.
- To determine the pharmacokinetic parameters of CPX-351 administered in this schedule.
- To assess preliminary efficacy information of CPX-351 administered in this schedule in patients with advanced leukemias.
To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.
Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT00389428
|United States, District of Columbia|
|Georgetown University Medical Center|
|Washington, District of Columbia, United States, 20007|
|United States, Florida|
|H. Lee Moffit Cancer Center & Research Institute at the University of S. Florida|
|Tampa, Florida, United States, 33612-9497|
|United States, New York|
|North Shore University Hospital|
|Manhasset, New York, United States, 11030|
|New York Presbyterian Hospital Weill Medical College of Cornell University|
|New York, New York, United States, 10021|
|Study Director:||Arthur Louie, M.D.||Jazz Pharmaceuticals|
|Principal Investigator:||Jonathan Kolitz, M.D.||New York School of Medicine at North Shore University Hospital|