{
"info": {
"nct_id": "NCT00509782",
"official_title": "Phase I Trial of ZIO-101 in Patients With Solid Tumors",
"inclusion_criteria": "1. Patients with histological confirmation solid malignancy refractory to conventional standard therapies for their condition.\n2. Eligible subjects MUST have at least one measurable lesion as defined by RECIST guidelines. If the measurable disease is restricted to a solitary lesion, its neoplastic nature should be confirmed by cytology/histology. Measurable lesions MUST not have been in a previously irradiated field or injected with biological agents.\n3. Pediatric patients will be eligible at the discretion of the primary investigator.\n4. ECOG performance status score </= 2.\n5. Women of child-bearing potential (i.e., women who are pre-menopausal or not surgically sterile) must use acceptable contraceptive methods (abstinence, intrauterine device [IUD], oral contraceptive or double barrier device), and must have a negative blood or urine pregnancy test within 1 week before beginning treatment. Sexually active men must also use acceptable contraceptive methods.\n6. Patients must provide written informed consent prior to treatment.\n7. At least four weeks from completion of prior therapy to day 1 of study drug.\n8. Baseline toxicity assessment less than or equal to grade 1 except treatment induced alopecia (NCI Common Terminology Criteria for Adverse Events [CTCAE] version 3.0).\n9. Evidence of adequate multi-organ functional status as reflected by the following clinical laboratory values: - Serum creatinine </= 2 times the upper normal limit OR a calculated creatinine clearance </= 50 cc/min. - Total bilirubin </= 2 times the upper normal limit. - Alanine aminotransferase (ALT), OR aspartate aminotransferase (AST) </= 3 times the upper limit of normal.\n10. Granulocytes in peripheral blood greater than or equal to 1 x 10(9) per liter, hemoglobin greater than or equal to 8.5 g/dL, and platelets greater than or equal to 50,000 cells/microL.\nHealthy volunteers allowed",
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"miscellaneous_criteria": ""
},
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}
},
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}
}
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}
}
]
}
},
{
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{
"exact_snippets": "12 lead electrocardiogram with a corrected QT interval >/= 460 milliseconds.",
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"unit": "milliseconds"
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{
"identified_line": {
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},
{
"exact_snippets": "History of ... dementia",
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{
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}
},
{
"identified_line": {
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],
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},
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"exact_snippets": "must have a negative blood or urine pregnancy test within 1 week before beginning treatment",
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},
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"identified_line": {
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}