[96a5a0]: / output / allTrials / identified / NCT02538666_identified.json

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{
"info": {
"nct_id": "NCT02538666",
"official_title": "A Randomized, Multicenter, Double-Blind, Phase 3 Study of Nivolumab, Nivolumab in Combination With Ipilimumab, or Placebo as Maintenance Therapy in Subjects With Extensive-Stage Disease Small Cell Lung Cancer (ED-SCLC) After Completion of Platinum-based First Line Chemotherapy (CheckMate 451: CHECKpoint Pathway and nivoluMAb Clinical Trial Evaluation 451)",
"inclusion_criteria": "* Subjects with histologically or cytologically confirmed extensive stage disease SCLC\n* Ongoing response of stable disease or better following 4 cycles of platinum-based first line chemotherapy\n* Eastern Cooperative Oncology Group (ECOG) performance status of 0 or 1\nHealthy volunteers allowed\nMust have minimum age of 18 Years",
"exclusion_criteria": "* Subjects with symptomatic Central Nervous System (CNS) metastases\n* Subjects receiving consolidative chest radiation\n* Subjects with active, known, or suspected autoimmune disease are excluded\n* All side effects attributed to prior anti-cancer therapy must have resolved to Grade 1 or baseline\n\nOther protocol-defined inclusion/exclusion criteria apply",
"miscellaneous_criteria": ""
},
"inclusion_lines": [
{
"line": "* Subjects with histologically or cytologically confirmed extensive stage disease SCLC",
"criterions": [
{
"exact_snippets": "histologically or cytologically confirmed extensive stage disease SCLC",
"criterion": "extensive stage disease SCLC",
"requirements": [
{
"requirement_type": "confirmation method",
"expected_value": [
"histologically",
"cytologically"
]
}
]
}
]
},
{
"line": "* Ongoing response of stable disease or better following 4 cycles of platinum-based first line chemotherapy",
"criterions": [
{
"exact_snippets": "Ongoing response of stable disease or better",
"criterion": "disease response",
"requirements": [
{
"requirement_type": "response level",
"expected_value": [
"stable disease",
"better"
]
}
]
},
{
"exact_snippets": "following 4 cycles of platinum-based first line chemotherapy",
"criterion": "platinum-based first line chemotherapy",
"requirements": [
{
"requirement_type": "completion",
"expected_value": "4 cycles"
}
]
}
]
},
{
"line": "* Eastern Cooperative Oncology Group (ECOG) performance status of 0 or 1",
"criterions": [
{
"exact_snippets": "Eastern Cooperative Oncology Group (ECOG) performance status of 0 or 1",
"criterion": "ECOG performance status",
"requirements": [
{
"requirement_type": "value",
"expected_value": [
"0",
"1"
]
}
]
}
]
},
{
"line": "Healthy volunteers allowed",
"criterions": [
{
"exact_snippets": "Healthy volunteers allowed",
"criterion": "volunteer health status",
"requirements": [
{
"requirement_type": "status",
"expected_value": "healthy"
}
]
}
]
},
{
"line": "Must have minimum age of 18 Years",
"criterions": [
{
"exact_snippets": "minimum age of 18 Years",
"criterion": "age",
"requirements": [
{
"requirement_type": "minimum",
"expected_value": {
"operator": ">=",
"value": 18,
"unit": "Years"
}
}
]
}
]
}
],
"exclusion_lines": [
{
"line": "* Subjects with symptomatic Central Nervous System (CNS) metastases",
"criterions": [
{
"exact_snippets": "symptomatic Central Nervous System (CNS) metastases",
"criterion": "Central Nervous System (CNS) metastases",
"requirements": [
{
"requirement_type": "symptomatic",
"expected_value": true
}
]
}
]
},
{
"line": "* Subjects receiving consolidative chest radiation",
"criterions": [
{
"exact_snippets": "Subjects receiving consolidative chest radiation",
"criterion": "consolidative chest radiation",
"requirements": [
{
"requirement_type": "presence",
"expected_value": true
}
]
}
]
},
{
"line": "* Subjects with active, known, or suspected autoimmune disease are excluded",
"criterions": [
{
"exact_snippets": "active, known, or suspected autoimmune disease",
"criterion": "autoimmune disease",
"requirements": [
{
"requirement_type": "status",
"expected_value": [
"active",
"known",
"suspected"
]
}
]
}
]
},
{
"line": "* All side effects attributed to prior anti-cancer therapy must have resolved to Grade 1 or baseline",
"criterions": [
{
"exact_snippets": "All side effects attributed to prior anti-cancer therapy must have resolved to Grade 1 or baseline",
"criterion": "side effects from prior anti-cancer therapy",
"requirements": [
{
"requirement_type": "severity",
"expected_value": "Grade 1 or baseline"
}
]
}
]
},
{
"line": "Other protocol-defined inclusion/exclusion criteria apply",
"criterions": [
{
"exact_snippets": "Other protocol-defined inclusion/exclusion criteria apply",
"criterion": "protocol-defined inclusion/exclusion criteria",
"requirements": [
{
"requirement_type": "application",
"expected_value": true
}
]
}
]
}
],
"miscellaneous_lines": [],
"failed_inclusion": [],
"failed_exclusion": [],
"failed_miscellaneous": []
}