Study of Sapacitabine in Acute Myeloid Leukemia (AML)
Status: | Active, not recruiting |
---|---|
Conditions: | Blood Cancer, Hematology |
Therapuetic Areas: | Hematology, Oncology |
Healthy: | No |
Age Range: | 70 - Any |
Updated: | 11/2/2018 |
Start Date: | June 2010 |
End Date: | June 2020 |
A Phase I/II Combination Study of Sapacitabine in Acute Myeloid Leukemia
This is an open label, phase I/II study to evaluate the safety and efficacy of sapacitabine
administered in alternating cycles with decitabine in elderly patients with newly diagnosed
Acute Myeloid Leukemia (AML).
administered in alternating cycles with decitabine in elderly patients with newly diagnosed
Acute Myeloid Leukemia (AML).
Inclusion Criteria:
- Newly diagnosed AML based on WHO classification
- Age 70 years or older for whom the treatment of choice is low-intensity therapy by
investigator assessment or who has refused intensive induction therapy recommended by
investigator
- ECOG performance status 0-2
- Adequate renal function
- Adequate liver function
- Able to swallow capsules
- Ability to understand and willingness to sign the informed consent form
Exclusion Criteria:
- AML is of the sub-type of acute promyelocytic leukemia or extramedullary myeloid tumor
without bone marrow involvement
- Having received any systemic anti-cancer therapy for AML or received treatment with
hypomethylating agents or cytotoxic chemotherapy for the preceding MDS or MPD
- Known central nervous system (CNS) involvement by leukemia
- Uncontrolled intercurrent illness including
- Known hypersensitivity to decitabine
- Known to be HIV-positive
We found this trial at
3
sites
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Roswell Park Cancer Institute Welcome to Roswell Park Cancer Institute (RPCI), America's first cancer center...
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Rush University Medical Center Rush University Medical Center encompasses a 664-bed hospital serving adults and...
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