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STA-9090 for Treatment of AML, CML, MDS and Myeloproliferative Disorders Summary The purpose of this study is to characterize the safety and efficacy of STA-9090 (ganetespib) in subjects with hematologic malignancies.
View Eligibility Criteria Eligibility Criteria Inclusion Criteria Males and females 18 years or older Eligible subjects must have one of the following relapsed or refractory hematologic malignancies: AML, MDS, leukemia -cml/" >CML, or myeloproliferative disorders as defined in the protocol Must have acceptable organ function during screening as defined in the protocol Exclusion Criteria Pregnant or breast-feeding women Patients must meet the washout periods for prior chemotherapies and radiation History of stroke within 6 months of treatment Poor venous access for study drug administration Treatment with chronic immunosuppressants Other severe acute/chronic medical or psychiatric condition, or laboratory abnormality that may increase the risk associated with study participation
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There are 3 Locations for this study
Boston Massachusetts, 02115, United States
New York New York, 10065, United States
San Antonio Texas, 78229, United States
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