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A Phase I Study of CYC140, a PLK-1 Inhibitor, in Advanced Leukemias or MDS Summary A Phase I Pharmacologic Study of CYC140, a polo-like kinase 1 inhibitor, in Patients with Advanced Leukemias or Myelodysplastic Syndromes
View Full Description Full Description This is a First in Human, open-label, single arm, dose escalation study in patients with advanced leukemias or myelodysplastic syndrome s. Patients will receive CYC140 as a 1 hr infusion once a week for 2 weeks followed by 1 week of rest on an outpatient basis. One treatment cycle is 3 weeks.
View Eligibility Criteria Eligibility Criteria Inclusion Criteria: Diagnosis of relapsed or refractory advanced leukemias or MDS ECOG 0-2 Adequate renal function Adequate liver function ≥ 2 weeks from prior chemotherapy, radiation therapy or major surgery ≥ 4 weeks from other investigational anticancer therapy Agree to practice effective contraception Exclusion Criteria: Known CNS involvement by leukemia Currently receiving radiotherapy, biological therapy, or any other investigational agents Uncontrolled intercurrent illness Pregnant or lactating Known to be HIV-positive Known active hepatitis B and/ or hepatitis C infection
Check Your Eligibility
Let’s see if you might be eligible for this study.
What is your age and gender ?
There is 1 Location for this study
MD Anderson Cancer Center Houston Texas, 77030, United States
More Info How clear is this clinincal trial information?
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