Status:
WITHDRAWN
CPX-351 in Patients Treated for Higher-risk Myelodysplastic Syndromes Experiencing Hypomethylating Agent Failure.
Lead Sponsor:
Yale University
Conditions:
MDS
Eligibility:
All Genders
18-78 years
Phase:
PHASE1
PHASE2
Brief Summary
The proposed study is of a Liposomal formulation of cytarabine and daunorubicin (CPX-351) in patients treated for higher-risk myelodysplastic syndromes (MDS) experiencing hypomethylating agent failure...
Detailed Description
Proposed is a two-phase study. The Phase I portion will confirm the tolerability and safety of CPX-351 chemotherapy. Patients who meet eligibility criteria will receive dose level 1 of CPX-351 (44mg/m...
Eligibility Criteria
Inclusion
- Patients with a diagnosis of MDS o (according to World Health Organization 2016 classification) made prior to administration off HMA
- Eastern Cooperative Oncology Group (ECOG) Performance Status 0 to 2
- Patient must have recovered from toxicities of any prior treatment regimen (no CTCAE grading over 1 for non-hematological toxicities and a return to baseline for hematological values)
- Patient is considered eligible for chemotherapy (at discretion of local investigator)
- Patient must have been treated with a hypomethylating agent (+/- other agents) and
- be treated for at least 4 cycles (16 weeks) and have a stable marrow disease (no response) or
- progressed without prior response based on MDS International Working Group (IWG) 2006 response criteria or
- relapsed after an initial response based on MDS IWG 2006 response criteria.
- Adequate liver and renal function:
- Estimated creatinine clearance above 40 ml/min
- Total bilirubin ≤ 1.5 x the Upper Limit of Normal (ULN) or ≤ 3.0 x the ULN unless considered due to Gilbert's syndrome,
- Alanine aminotransferase (ALT) (SGPT), and aspartate aminotransferase (AST) (SGOT) ≤ 2.5 x the ULN. For patients with hepatic leukemic involvement Alanine aminotransferase (ALT) (SGPT), and aspartate aminotransferase (AST) (SGOT) ≤ 5.0 x the ULN t
- Able to understand and sign the written informed consent
- Serum or urine pregnancy test (for female patients of childbearing potential) with a minimum sensitivity of 25 IU/L or equivalent units of human chorionic gonadotropin (HCG) negative at screening.
- Males and female patients both of childbearing potential and at risk for pregnancy must agree to use two highly effective method(s) of contraception throughout the study and for 180 days after the last dose of CPX-351 whichever occurs later.
- Female patients who are not of childbearing potential (i.e. meet at least 1 of the following criteria):
- Have undergone a documented hysterectomy and/or bilateral oophorectomy;
- Have medically confirmed ovarian failure;
- Have achieved postmenopausal status, defined as follows: cessation of regular menses for at least 12 consecutive months with no alternative pathological or physiological cause; status may be confirmed by having a serum follicle stimulating hormone (FSH) level within the laboratory's reference range for postmenopausal women.
Exclusion
- Any prior induction chemotherapy (defined as treatment with standard or high dose cytarabine in combination with an anthracycline and/or other agents)
- Any investigational agent administered within a month prior to inclusion or within 5 half-lives of the investigational agent whichever is longer.
- Promyelocytic acute leukemia and core binding factor acute leukemia.
- Active Central nervous system (CNS) disease
- Any severe chronic disease potentially interfering with the protocol including HIV infection, active or chronic hepatitis B or C. Testing will be completed during screening period.
- Any significant social condition that could limit the understanding of the study or the compliance to the protocol including but not limited to severe or uncontrolled psychiatric illness.
- Any sign of active uncontrolled disease including but not restricted to cardiac disease, infections and platelet refractoriness.
- Any other malignancy with active treatment within the past 1 year other than basal cell skin cancer or carcinoma in situ of the cervix.
- New York Heart Association (NYHA) grade 3 or 4 cardiac failure, or left ventricular ejection fraction (LVEF) below 50%
- Patients who have received a cumulative dose of anthracyclines superior to a total of 300mg/m2 of daunorubicin in the absence of prior mediastinal radiation or 150mg/m2 if the patient had a prior mediastinal radiation
- Oxygen dependency as defined by a chronic need of oxygen at least 2l/min for at least 6h a day.
- Women who are pregnant, planning to become pregnant, or who are currently breastfeeding
- Persistence of any clinically relevant (CTCAE grade 2 or above) toxicities from previous therapy
- Any other condition that, according to the investigator, may forbid the administration of CPX-351
- Hypersensitivity to cytarabine, daunorubicin or liposomal products
- History of Wilson's disease or another copper-metabolism disorder
- Major injuries and/or surgery within the past 4 weeks prior to start of study treatment with incomplete wound healing and/or planned surgery during the on-treatment study period.
Key Trial Info
Start Date :
December 30 2019
Trial Type :
INTERVENTIONAL
Allocation :
ACTUAL
End Date :
July 27 2021
Estimated Enrollment :
Patients enrolled
Trial Details
Trial ID
NCT04109690
Start Date
December 30 2019
End Date
July 27 2021
Last Update
January 24 2022
Active Locations (1)
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1
Yale University; Smilow Cancer Center
New Haven, Connecticut, United States, 06519