Acute Myeloid Leukemia Clinical Trial
Study of IMC-EB10 in Participant With Leukemia
The purpose of this study is to determine if IMC-EB10 is safe for participants with leukemia, and also to determine the best dose of IMC-EB10 to give to participants.
The purpose of this study is to define the maximum tolerated dose (MTD) and the pharmacokinetic (PK) profile of the anti-FMS-like tyrosine kinase 3 (FLT3) monoclonal antibody IMC-EB10, administered weekly in participant with acute lymphoblastic leukemia (AML) who have failed to achieve complete remission to a standard induction regimen, relapsed after response to previous antileukemia therapy, or are not eligible for potentially curative or approved salvage options.
The participant has acute myeloid leukemia in the bone marrow or blood that has relapsed with or without a prior complete remission
The participant is not regarded to be a candidate for a potentially curative, higher priority treatment for acute myeloid leukemia
The participant has resolution of all clinically significant toxic effects of any prior antitumor therapy and any other study-specific clinical or laboratory parameter specified in the entry criteria
The participant has not had major surgery, an open biopsy, a significant injury, and/or prior antitumor therapy (except antileukemia therapy) within 21 days prior to the first infusion of IMC-EB10
The participant has an Eastern Cooperative Oncology Group (ECOG)performance status of 0, 1, or 2 at study entry.
The participant is age 18 years or older
The participant has a life expectancy of >3 months
The participant has adequate liver and kidney function, as defined in the entry criteria
The participant is using an effective contraception (per the institutional standard), if procreative potential exists
The participant is able to give written informed consent
The participant is willing and able to comply with study procedures, scheduled visits, and treatment plans
The participant has had prior allogenic or autologous stem cell transplant within <3 months of the first infusion of IMC-EB10
The participant has had an organ transplant (nonhematologic) within 3 years of study entry
The participant has active central nervous system leukemia
The participant has extramedullary disease without peripheral/and or bone marrow involvement
The participant is disease-free from a previous or concurrent malignancy for a period ≤ 1 year. A participant who has basal cell carcinoma or carcinoma in situ of the cervix will not be excluded from the study
The participant is currently receiving antileukemia therapy. Concurrent treatment with hydroxyurea is permitted
The participant has uncontrolled intercurrent illness as specified in the study entry criteria
The participant is receiving chronic steroid or other immunosuppressive medications. Occasional use of steroid-containing medications for, for example (e.g.), asthma exacerbation or for skin lesions, is permitted
The participant is receiving full-dose heparin (including low molecular weight heparin) or warfarin. [The participant is permitted to use low-dose warfarin to maintain patency of preexisting, permanent, indwelling intravenous (I.V.) catheters.]
The participant is pregnant (confirmed by urine or serum pregnancy test) or breast feeding
The participant has received treatment with monoclonal antibodies within 6 weeks prior to first infusion of IMC-EB10
The participant has a history of clinically significant allergic reactions to monoclonal antibodies or other therapeutic proteins
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There are 2 Locations for this study
Columbus Ohio, 43210, United States
Houston Texas, 77030, United States
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