{
"info": {
"nct_id": "NCT06832982",
"official_title": "A Single-arm, Open Phase I Clinical Trial Evaluating the Safety, Tolerability, Pharmacokinetics, Pharmacokinetics, and Preliminary Efficacy of FS-8002 in Patients With Advanced Solid Tumors",
"inclusion_criteria": "1. Patients with advanced solid tumors confirmed by histology or cytology who have failed or become intolerant to previous standard treatments, or who do not have a standard treatment regimen;\n2. At least one measurable lesion according to the RECIST V1.1 assessment criteria ;\n3. The subject has sufficient organ and bone marrow function;\nHealthy volunteers allowed\nMust have minimum age of 18 Years",
"exclusion_criteria": "1. Patients who have previously received TGF-β inhibitor therapy;\n2. Have received any experimental drug treatment within 4 weeks prior to the first administration of the investigational drug;\n3. Have used any systemic anti-tumor therapy within 4 weeks or 5 half-lives (whichever is shorter) before the first administration of the study drug, including systemic chemotherapy, radiotherapy, immunotherapy, hormone therapy, targeted therapy (small molecule targeted drugs are within 2 weeks before the first administration), systemic immunomodulators (including but not limited to IFN, IL-2 and tumor necrosis factor [TNF]). Received Chinese herbal or proprietary Chinese medicines with anti-tumor effects within 2 weeks before the first administration;\n4. Have used or are currently using aspirin (≥ 325 mg/day) or other anti-platelet aggregation drugs such as clopidogrel, dipyridamole, ticlopidine, and cilostazole, or full-dose anticoagulants or thrombolytics within 2 weeks prior to the first administration of the study drug;\n5. Those who have received major surgical treatment or significant traumatic injury within 4 weeks before the first administration of the study drug, or those who have a history of fistula, gastrointestinal perforation, or tumor invasion of large blood vessels within 6 months before the first administration; or those who have intestinal obstruction during the screening period;",
"miscellaneous_criteria": ""
},
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{
"identified_line": {
"line": "1. Patients with advanced solid tumors confirmed by histology or cytology who have failed or become intolerant to previous standard treatments, or who do not have a standard treatment regimen;",
"criterions": [
{
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"criterion": "solid tumors",
"requirement": {
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"expected_value": "advanced"
}
},
{
"exact_snippets": "advanced solid tumors confirmed by histology or cytology",
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"requirement": {
"requirement_type": "confirmation method",
"expected_value": [
"histology",
"cytology"
]
}
},
{
"exact_snippets": "failed or become intolerant to previous standard treatments",
"criterion": "response to previous standard treatments",
"requirement": {
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},
{
"exact_snippets": "do not have a standard treatment regimen",
"criterion": "availability of standard treatment regimen",
"requirement": {
"requirement_type": "availability",
"expected_value": false
}
}
]
},
"logical_structure": {
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{
"and_criteria": [
{
"and_criteria": [
{
"exact_snippets": "advanced solid tumors confirmed by histology or cytology",
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"exact_snippets": "advanced solid tumors confirmed by histology or cytology",
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"exact_snippets": "At least one measurable lesion according to the RECIST V1.1 assessment criteria",
"criterion": "measurable lesion",
"requirement": {
"requirement_type": "quantity",
"expected_value": {
"operator": ">=",
"value": 1,
"unit": "N/A"
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"exact_snippets": "At least one measurable lesion according to the RECIST V1.1 assessment criteria",
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"requirement": {
"requirement_type": "assessment criteria",
"expected_value": "RECIST V1.1"
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"expected_value": {
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"value": 1,
"unit": "N/A"
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"exact_snippets": "At least one measurable lesion according to the RECIST V1.1 assessment criteria",
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"line": "3. The subject has sufficient organ and bone marrow function;",
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"exact_snippets": "sufficient organ and bone marrow function",
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"requirement": {
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"expected_value": true
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"exact_snippets": "sufficient organ and bone marrow function",
"criterion": "bone marrow function",
"requirement": {
"requirement_type": "sufficiency",
"expected_value": true
}
}
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"exact_snippets": "sufficient organ and bone marrow function",
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"exact_snippets": "sufficient organ and bone marrow function",
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"exact_snippets": "Healthy volunteers allowed",
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{
"exact_snippets": "minimum age of 18 Years",
"criterion": "age",
"requirement": {
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"expected_value": {
"operator": ">=",
"value": 18,
"unit": "Years"
}
}
}
]
},
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"exact_snippets": "minimum age of 18 Years",
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"operator": ">=",
"value": 18,
"unit": "Years"
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"exact_snippets": "Patients who have previously received TGF-β inhibitor therapy",
"criterion": "TGF-β inhibitor therapy",
"requirement": {
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"expected_value": true
}
}
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"exact_snippets": "Patients who have previously received TGF-β inhibitor therapy",
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"expected_value": true
}
}
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"identified_line": {
"line": "2. Have received any experimental drug treatment within 4 weeks prior to the first administration of the investigational drug;",
"criterions": [
{
"exact_snippets": "Have received any experimental drug treatment within 4 weeks prior to the first administration of the investigational drug",
"criterion": "experimental drug treatment",
"requirement": {
"requirement_type": "time since last treatment",
"expected_value": {
"comparisons": [
{
"operator": "<=",
"value": 4,
"unit": "weeks"
}
]
}
}
}
]
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"exact_snippets": "Have received any experimental drug treatment within 4 weeks prior to the first administration of the investigational drug",
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"expected_value": {
"comparisons": [
{
"operator": "<=",
"value": 4,
"unit": "weeks"
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]
}
}
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},
{
"identified_line": {
"line": "3. Have used any systemic anti-tumor therapy within 4 weeks or 5 half-lives (whichever is shorter) before the first administration of the study drug, including systemic chemotherapy, radiotherapy, immunotherapy, hormone therapy, targeted therapy (small molecule targeted drugs are within 2 weeks before the first administration), systemic immunomodulators (including but not limited to IFN, IL-2 and tumor necrosis factor [TNF]). Received Chinese herbal or proprietary Chinese medicines with anti-tumor effects within 2 weeks before the first administration;",
"criterions": [
{
"exact_snippets": "Have used any systemic anti-tumor therapy within 4 weeks or 5 half-lives (whichever is shorter) before the first administration of the study drug",
"criterion": "systemic anti-tumor therapy",
"requirement": {
"requirement_type": "usage",
"expected_value": false
}
},
{
"exact_snippets": "systemic chemotherapy",
"criterion": "systemic chemotherapy",
"requirement": {
"requirement_type": "usage",
"expected_value": false
}
},
{
"exact_snippets": "radiotherapy",
"criterion": "radiotherapy",
"requirement": {
"requirement_type": "usage",
"expected_value": false
}
},
{
"exact_snippets": "immunotherapy",
"criterion": "immunotherapy",
"requirement": {
"requirement_type": "usage",
"expected_value": false
}
},
{
"exact_snippets": "hormone therapy",
"criterion": "hormone therapy",
"requirement": {
"requirement_type": "usage",
"expected_value": false
}
},
{
"exact_snippets": "targeted therapy (small molecule targeted drugs are within 2 weeks before the first administration)",
"criterion": "targeted therapy",
"requirement": {
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"expected_value": false
}
},
{
"exact_snippets": "systemic immunomodulators (including but not limited to IFN, IL-2 and tumor necrosis factor [TNF])",
"criterion": "systemic immunomodulators",
"requirement": {
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"expected_value": false
}
},
{
"exact_snippets": "Received Chinese herbal or proprietary Chinese medicines with anti-tumor effects within 2 weeks before the first administration",
"criterion": "Chinese herbal or proprietary Chinese medicines with anti-tumor effects",
"requirement": {
"requirement_type": "usage",
"expected_value": false
}
}
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"exact_snippets": "systemic immunomodulators (including but not limited to IFN, IL-2 and tumor necrosis factor [TNF])",
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"exact_snippets": "Received Chinese herbal or proprietary Chinese medicines with anti-tumor effects within 2 weeks before the first administration",
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{
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"requirement": {
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{
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}