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Study of PF-05212384 (Also Known as PKI-587)Administered Intravenously To Subjects With Solid Tumors Summary This is a two-part study of a compound called PF-05212384 (also known as PKI-587). The purpose of part 1 is to identify the Maximum Tolerated Dose (MTD) of PF-05212384 using a Continual Reassessment Method (CRM). Part 1 will include subjects with any solid tumor. In Part 2 two cohorts will be enrolled. One cohort will assess safety, tolerability and preliminary efficacy in 20 subjects at the MTD and will include subjects with breast cancer , ovarian cancer, endometrial cancer, colorectal cancer renal cancer or glioblastoma (a type of brain tumor). The other cohort will include 5 to 15 subjects with any type of tumor who consent to provide tumor biopsies while participating in the study.
View Eligibility Criteria Eligibility Criteria Inclusion Criteria: Pathologic diagnosis of any solid tumor Incurable cancer, with disease progression following at least 1 therapy with no further standard treatment available in the opinion of the investigator. At least 1 evaluable lesion per RECIST criteria Exclusion Criteria: Clinically unstable primary or metastatic CNS tumors Subjects with known diabetes QTc interval greater than 470 ms.
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There are 8 Locations for this study
Massachusetts General Hospital Boston Massachusetts, 02114, United States
Beth Israel Deaconess Medical Center Boston Massachusetts, 02215, United States
Dana-Farber Cancer Insitute Boston Massachusetts, 02215, United States
Mayo Clinic Rochester Minnesota, 55905, United States
Memorial Sloan-Kettering Cancer Center New York New York, 10022, United States
Memorial Sloan-Kettering Cancer Center New York New York, 10065, United States
Sarah Cannon Research Institute, Tennessee Oncology, PLLC Nashville Tennessee, 37203, United States
Hospital General Vall D'Hebron Barcelona , 08035, Spain
King's College London London England, SE1 9, United Kingdom
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