Phase IB/II of CPX-351 for Relapse Prevention in AML

Launched by GEORGETOWN UNIVERSITY · Jul 26, 2021

Keywords

ClinConnect Summary

This clinical trial is investigating a treatment called CPX-351 for patients with Acute Myeloid Leukemia (AML) who are currently in remission. The goal is to see how well this treatment works in preventing the return of the disease. Participants in the trial will receive CPX-351 for six cycles, with doses given on specific days every 28 days, depending on how well they tolerate the medication. The study is designed to find the highest dose that patients can safely handle, which will be used in the later phase of the trial.

To be eligible for this trial, patients need to be over 18 years old and must have recently been diagnosed with AML, showing signs of remission. They should have completed initial treatment and be unable to undergo a stem cell transplant for various reasons. Participants will be screened for their overall health, including heart and kidney function, and must agree to use effective birth control during the study. If you or a family member is considering participation, you can expect close monitoring during the treatment and support from the research team throughout the trial.

Gender

ALL

Eligibility criteria

• Inclusion Criteria:
• • Newly diagnosed patients \> 18 years of age
• • Patients must be in CR or CRh (complete remission with partial count recovery).
• • Must have received ANY induction treatment with standard consolidation or hypomethylating agent (HMA) + venetoclax, for up to 6 cycles or no more than one year of treatment.
• • Must be able to start therapy within 3 months of last documented CR
• • De novo or secondary AML/treatment related AML (non-M3) including AML with myelodysplasia-related changes (MRC), histologically confirmed
• • Patients must be ineligible for allogeneic BMT (for any reason including poor performance status, patient's preference, favorable AML not a candidate for transplant, or comorbidities and age precluding from transplant etc)
• • Cardiac ejection fraction ≥ 50% by transthoracic echocardiography or MUGA scan
• * Adequate hepatic and renal function defined as:
• • Serum aspartate transaminase (AST) or alanine transaminase (ALT) ≤ 3 x upper limit of normal (ULN)
• • Serum aspartate transaminase (AST) or alanine transaminase (ALT) ≤ 3 is permissible if due to disease.
• • Bilirubin ≤3 x ULN (unless bilirubin rise is due to Gilbert's syndrome or of non-hepatic origin)
• • Estimated Creatinine Clearance ≥30 ml/min (Cockcroft-Gault based on actual weight) (See Appendix A)
• • Eastern Cooperative Oncology Group (ECOG) performance status of ≤ 3 (Appendix A)
• • Female subjects who are of non-reproductive potential (i.e., post-menopausal by history - no menses for ≥1 year; OR history of hysterectomy; OR history of bilateral tubal ligation; OR history of bilateral oophorectomy). Female subjects of childbearing potential must have a negative serum pregnancy test upon study entry.
• • Male and female subjects who agree to use highly effective methods of birth control (e.g., condoms, implants, injectables, combined oral contraceptives, some intrauterine devices \[IUDs\], sexual abstinence, or sterilized partner) during the period of therapy and for at least 6 months after the last dose of study drug
• Exclusion Criteria:
• • Prior allogeneic transplant
• • Previous cumulative anthracycline (doxorubicin equivalent) dose equal to or greater than 345 mg/m2, and for patients with prior mediastinal XRT, anthracycline dose equal to or greater than 295 mg/m2
• • Acute promyelocytic leukemia \[t(15;17)\]
• • If patient is unable to sign informed consent due to any serious medical condition, laboratory abnormality or psychiatric illness
• • Patients with evidence of uncontrolled current myocardial impairment (e.g. unstable ischemic heart disease, uncontrolled arrhythmia, symptomatic valvular dysfunction not controlled on medical therapy, uncontrolled hypertensive heart disease, and uncontrolled congestive heart failure)
• • History of Wilson's disease or other copper-related disorders
• • History of allergic reactions attributed to compounds of similar composition to cytarabine and daunorubicin or liposomal products
• * History of other malignancies, except:
• • Malignancy treated with curative intent and with no known active disease present for ≥ 3 years before the first dose of study drug and felt to be at low risk for recurrence by treating physician.
• • Adequately treated non-melanoma skin cancer or lentigo maligna without evidence of disease.
• • Adequately treated carcinoma in situ without evidence of disease.
• • Unresolved toxicities from prior anti-cancer therapy, defined as having not resolved to Common Terminology Criteria for Adverse Event (CTCAE, version 4.03), grade ≤1, or to the levels dictated in the inclusion/exclusion criteria with the exception of alopecia.
• • Known bleeding disorders (e.g., von Willebrand's disease) or hemophilia
• • Known active infection with hepatitis C virus (HCV) or hepatitis B virus (HBV).
• • Subjects who are positive for hepatitis B core antibody, hepatitis B surface antigen, hepatitis C antibody, must have a negative polymerase chain reaction (PCR) result for the respective disease before enrollment. Those who are PCR positive will be excluded.
• • Any uncontrolled active systemic infection.
• • Any life-threatening illness, medical condition, or organ system dysfunction that, in the investigator's opinion, could compromise the subject's safety or put the study outcomes at undue risk.
• • Currently active, clinically significant cardiovascular disease, such as uncontrolled arrhythmia or Class 3 or 4 congestive heart failure as defined by the New York Heart Association Functional Classification; or a history of myocardial infarction, unstable angina, or acute coronary syndrome within 6 months prior to randomization.
• • Known CNS involvement by leukemia
• • Erythema multiforme, toxic epidermal necrolysis, or Stevens-Johnson syndrome
• • Lactating or pregnant.
• • Unwilling or unable to participate in all required study evaluations and procedures.
• • Unable to understand the purpose and risks of the study and to provide a signed and dated informed consent form (ICF) and authorization to use protected health information (in accordance with national and local subject privacy regulations).
• • Currently active, clinically significant hepatic impairment (≥ moderate hepatic impairment according to the Child Pugh classification (class B or C))