[96a5a0]: / output / allTrials / logical / NCT04235101_logical.json

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{
"info": {
"nct_id": "NCT04235101",
"official_title": "A Two-part Phase I Study With the Antibody-drug Conjugate SYD985 in Combination With Niraparib to Evaluate Safety, Pharmacokinetics and Efficacy in Patients With HER2-expressing Locally Advanced or Metastatic Solid Tumors.",
"inclusion_criteria": "* Male or female, age ≥ 18 years at the time of signing first informed consent;\n* Patient with a histologically-confirmed, locally advanced or metastatic tumour who has progressed on standard therapy or for whom no standard therapy exists, with the following restriction:\n\n * Part 1: solid tumours of any origin;\n * Part 2: breast cancer, ovarian cancer or endometrial carcinoma/carcinosarcoma;\n* HER2 tumor status at least 1+ as assessed by immunohistochemistry (IHC) as determined by the local laboratory;\n* Presence of a tumor lesion accessible for biopsy and patient should be willing to undergo a fresh biopsy for central HER2 testing and genetic testing, unless adequate (biopsy) tumour material is available obtained < 6 months prior to signing the main informed consent;\n* At least one measurable cancer lesion as defined by the Response Evaluation Criteria for Solid Tumours (RECIST version 1.1);\n* Eastern Cooperative Oncology Group (ECOG) performance status ≤ 1;\n* Adequate organ function.\nHealthy volunteers allowed\nMust have minimum age of 18 Years",
"exclusion_criteria": "* Having been treated with:\n\n 1. DUBA-containing ADCs at any time;\n 2. Anthracycline treatment within 8 weeks prior to start of study treatment;\n 3. Other anticancer therapy including chemotherapy, immunotherapy, or investigational agents within 4 weeks prior to start of study treatment or 5 times the half-life of the therapy, whichever is shorter;\n 4. Radiotherapy within 4 weeks prior to start of study treatment or within 1 week for palliative care (as long as the lungs were not exposed);\n 5. Hormone therapy within 1 week prior to start of study treatment. The patient must have sufficiently recovered from any treatment-related toxicities to NCI CTCAE Grade ≤ 1 (except for toxicities not considered a safety risk for the patient at the investigator's discretion);\n* History or presence of keratitis;\n* Left ventricular ejection fraction (LVEF) < 50% as assessed by either echocardiography or multigated acquisition (MUGA) scan at screening, or a history of clinically significant decrease in LVEF during previous trastuzumab containing treatment leading to permanent discontinuation of treatment;\n* History (within 6 months prior to start of study treatment) or presence of clinically significant cardiovascular disease such as unstable angina, congestive heart failure, myocardial infarction, uncontrolled hypertension, or cardiac arrhythmia requiring medication;\n* History or presence of idiopathic pulmonary fibrosis, organizing pneumonia (e.g. bronchiolitis obliterans), drug-induced pneumonitis, or idiopathic pneumonitis, or evidence of active pneumonitis on screening chest CT scan;\n* Severe, uncontrolled systemic disease (e.g. clinically significant cardiovascular, pulmonary, or metabolic disease) at screening;\n* Symptomatic brain metastases, brain metastasis requiring steroids to manage symptoms or treatment for brain metastases within 8 weeks prior to start of study treatment.",
"miscellaneous_criteria": ""
},
"inclusion_lines": [
{
"identified_line": {
"line": "* Patient with a histologically-confirmed, locally advanced or metastatic tumour who has progressed on standard therapy or for whom no standard therapy exists, with the following restriction:",
"criterions": [
{
"exact_snippets": "histologically-confirmed, locally advanced or metastatic tumour",
"criterion": "tumour status",
"requirement": {
"requirement_type": "confirmation",
"expected_value": "histologically-confirmed"
}
},
{
"exact_snippets": "histologically-confirmed, locally advanced or metastatic tumour",
"criterion": "tumour status",
"requirement": {
"requirement_type": "stage",
"expected_value": [
"locally advanced",
"metastatic"
]
}
},
{
"exact_snippets": "progressed on standard therapy",
"criterion": "progression on standard therapy",
"requirement": {
"requirement_type": "progression",
"expected_value": true
}
},
{
"exact_snippets": "for whom no standard therapy exists",
"criterion": "availability of standard therapy",
"requirement": {
"requirement_type": "availability",
"expected_value": false
}
}
]
},
"logical_structure": {
"and_criteria": [
{
"and_criteria": [
{
"and_criteria": [
{
"exact_snippets": "histologically-confirmed, locally advanced or metastatic tumour",
"criterion": "tumour status",
"requirement": {
"requirement_type": "confirmation",
"expected_value": "histologically-confirmed"
}
},
{
"exact_snippets": "histologically-confirmed, locally advanced or metastatic tumour",
"criterion": "tumour status",
"requirement": {
"requirement_type": "stage",
"expected_value": [
"locally advanced",
"metastatic"
]
}
}
]
},
{
"or_criteria": [
{
"exact_snippets": "progressed on standard therapy",
"criterion": "progression on standard therapy",
"requirement": {
"requirement_type": "progression",
"expected_value": true
}
},
{
"exact_snippets": "for whom no standard therapy exists",
"criterion": "availability of standard therapy",
"requirement": {
"requirement_type": "availability",
"expected_value": false
}
}
]
}
]
}
]
}
},
{
"identified_line": {
"line": "* Part 1: solid tumours of any origin;",
"criterions": [
{
"exact_snippets": "solid tumours of any origin",
"criterion": "solid tumours",
"requirement": {
"requirement_type": "origin",
"expected_value": "any"
}
}
]
},
"logical_structure": {
"and_criteria": [
{
"exact_snippets": "solid tumours of any origin",
"criterion": "solid tumours",
"requirement": {
"requirement_type": "origin",
"expected_value": "any"
}
}
]
}
},
{
"identified_line": {
"line": "* Part 2: breast cancer, ovarian cancer or endometrial carcinoma/carcinosarcoma;",
"criterions": [
{
"exact_snippets": "breast cancer",
"criterion": "breast cancer",
"requirement": {
"requirement_type": "presence",
"expected_value": true
}
},
{
"exact_snippets": "ovarian cancer",
"criterion": "ovarian cancer",
"requirement": {
"requirement_type": "presence",
"expected_value": true
}
},
{
"exact_snippets": "endometrial carcinoma/carcinosarcoma",
"criterion": "endometrial carcinoma/carcinosarcoma",
"requirement": {
"requirement_type": "presence",
"expected_value": true
}
}
]
},
"logical_structure": {
"or_criteria": [
{
"exact_snippets": "breast cancer",
"criterion": "breast cancer",
"requirement": {
"requirement_type": "presence",
"expected_value": true
}
},
{
"exact_snippets": "ovarian cancer",
"criterion": "ovarian cancer",
"requirement": {
"requirement_type": "presence",
"expected_value": true
}
},
{
"exact_snippets": "endometrial carcinoma/carcinosarcoma",
"criterion": "endometrial carcinoma/carcinosarcoma",
"requirement": {
"requirement_type": "presence",
"expected_value": true
}
}
]
}
},
{
"identified_line": {
"line": "* HER2 tumor status at least 1+ as assessed by immunohistochemistry (IHC) as determined by the local laboratory;",
"criterions": [
{
"exact_snippets": "HER2 tumor status at least 1+ ... as assessed by immunohistochemistry (IHC)",
"criterion": "HER2 tumor status",
"requirement": {
"requirement_type": "assessment method",
"expected_value": "immunohistochemistry (IHC)"
}
},
{
"exact_snippets": "HER2 tumor status at least 1+ ... as assessed by immunohistochemistry (IHC)",
"criterion": "HER2 tumor status",
"requirement": {
"requirement_type": "value",
"expected_value": {
"operator": ">=",
"value": 1,
"unit": "+"
}
}
}
]
},
"logical_structure": {
"and_criteria": [
{
"exact_snippets": "HER2 tumor status at least 1+ ... as assessed by immunohistochemistry (IHC)",
"criterion": "HER2 tumor status",
"requirement": {
"requirement_type": "assessment method",
"expected_value": "immunohistochemistry (IHC)"
}
},
{
"exact_snippets": "HER2 tumor status at least 1+ ... as assessed by immunohistochemistry (IHC)",
"criterion": "HER2 tumor status",
"requirement": {
"requirement_type": "value",
"expected_value": {
"operator": ">=",
"value": 1,
"unit": "+"
}
}
}
]
}
},
{
"identified_line": {
"line": "* Presence of a tumor lesion accessible for biopsy and patient should be willing to undergo a fresh biopsy for central HER2 testing and genetic testing, unless adequate (biopsy) tumour material is available obtained < 6 months prior to signing the main informed consent;",
"criterions": [
{
"exact_snippets": "Presence of a tumor lesion accessible for biopsy",
"criterion": "tumor lesion",
"requirement": {
"requirement_type": "presence",
"expected_value": true
}
},
{
"exact_snippets": "Presence of a tumor lesion accessible for biopsy",
"criterion": "tumor lesion",
"requirement": {
"requirement_type": "accessibility for biopsy",
"expected_value": true
}
},
{
"exact_snippets": "patient should be willing to undergo a fresh biopsy",
"criterion": "willingness to undergo fresh biopsy",
"requirement": {
"requirement_type": "willingness",
"expected_value": true
}
},
{
"exact_snippets": "adequate (biopsy) tumour material is available obtained < 6 months prior to signing the main informed consent",
"criterion": "biopsy tumour material",
"requirement": {
"requirement_type": "availability",
"expected_value": true
}
},
{
"exact_snippets": "adequate (biopsy) tumour material is available obtained < 6 months prior to signing the main informed consent",
"criterion": "biopsy tumour material",
"requirement": {
"requirement_type": "recency",
"expected_value": {
"operator": "<",
"value": 6,
"unit": "months"
}
}
}
]
},
"logical_structure": {
"condition": {
"and_criteria": [
{
"and_criteria": [
{
"and_criteria": [
{
"and_criteria": [
{
"and_criteria": [
{
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},
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},
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}
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}
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}
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},
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{
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}
},
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}
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}
}
},
{
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"line": "* At least one measurable cancer lesion as defined by the Response Evaluation Criteria for Solid Tumours (RECIST version 1.1);",
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}
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"identified_line": {
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{
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}
}
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},
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}
}
]
}
},
{
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}
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},
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{
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}
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{
"identified_line": {
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{
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]
},
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}
]
}
},
{
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"line": "Must have minimum age of 18 Years",
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{
"exact_snippets": "minimum age of 18 Years",
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"operator": ">=",
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}
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]
},
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{
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}
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}
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],
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{
"identified_line": {
"line": "* Having been treated with:",
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{
"exact_snippets": "Having been treated with",
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},
{
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},
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}
},
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}
}
]
},
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}
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},
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},
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}
},
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}
},
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}
},
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}
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},
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"expected_value": false
}
},
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"expected_value": true
}
},
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"exact_snippets": "clinically significant ... pulmonary ... disease",
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}
},
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},
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}
},
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}
}
]
}
]
}
},
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"identified_line": {
"line": "* Symptomatic brain metastases, brain metastasis requiring steroids to manage symptoms or treatment for brain metastases within 8 weeks prior to start of study treatment.",
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"criterion": "brain metastases",
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"requirement_type": "symptomatic",
"expected_value": true
}
},
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"expected_value": true
}
},
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"exact_snippets": "treatment for brain metastases within 8 weeks prior to start of study treatment",
"criterion": "brain metastases",
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"value": 8,
"unit": "weeks"
}
}
}
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},
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}
},
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"unit": "weeks"
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}
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],
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"failed_inclusion": [
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},
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"unit": "years"
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}
}
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],
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{
"identified_line": {
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}
},
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"value": 4,
"unit": "weeks"
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]
}
}
},
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"criterion": "anticancer therapy",
"requirement": {
"requirement_type": "presence",
"expected_value": true
}
},
{
"or_criteria": [
{
"exact_snippets": "within 4 weeks prior to start of study treatment or 5 times the half-life of the therapy, whichever is shorter",
"criterion": "time since last anticancer therapy",
"requirement": {
"requirement_type": "duration",
"expected_value": {
"comparisons": [
{
"operator": "<=",
"value": 4,
"unit": "weeks"
}
]
}
}
},
{
"exact_snippets": "within 4 weeks prior to start of study treatment or 5 times the half-life of the therapy, whichever is shorter",
"criterion": "time since last anticancer therapy",
"requirement": {
"requirement_type": "duration",
"expected_value": {
"comparisons": [
{
"operator": "<=",
"value": 5,
"unit": "times the half-life of the therapy"
}
]
}
}
}
]
}
]
}
]
}
},
{
"identified_line": {
"line": "* History or presence of idiopathic pulmonary fibrosis, organizing pneumonia (e.g. bronchiolitis obliterans), drug-induced pneumonitis, or idiopathic pneumonitis, or evidence of active pneumonitis on screening chest CT scan;",
"criterions": [
{
"exact_snippets": "History or presence of idiopathic pulmonary fibrosis",
"criterion": "idiopathic pulmonary fibrosis",
"requirement": {
"requirement_type": "presence",
"expected_value": true
}
},
{
"exact_snippets": "History or presence of ... organizing pneumonia (e.g. bronchiolitis obliterans)",
"criterion": "organizing pneumonia",
"requirement": {
"requirement_type": "presence",
"expected_value": true
}
},
{
"exact_snippets": "History or presence of ... drug-induced pneumonitis",
"criterion": "drug-induced pneumonitis",
"requirement": {
"requirement_type": "presence",
"expected_value": true
}
},
{
"exact_snippets": "History or presence of ... idiopathic pneumonitis",
"criterion": "idiopathic pneumonitis",
"requirement": {
"requirement_type": "presence",
"expected_value": true
}
},
{
"exact_snippets": "evidence of active pneumonitis on screening chest CT scan",
"criterion": "active pneumonitis",
"requirement": {
"requirement_type": "evidence",
"expected_value": true
}
}
]
},
"logical_structure": {
"exact_snippets": "failed",
"criterion": "failed",
"requirement": {
"requirement_type": "failed",
"expected_value": "failed"
}
}
}
],
"failed_miscellaneous": []
}