{
"info": {
"nct_id": "NCT02065973",
"official_title": "An Open-Label, Phase I, Escalating Dose Study to Evaluate the Safety, Tolerability, and Pharmacodynamics of PDS0101 in Subjects With Cervical Intraepithelial Neoplasia (CIN) and High-risk Human Papillomavirus (HPV) Infection",
"inclusion_criteria": "1. Written informed consent prior to initiation of any study-related procedures;\n2. Nonlactating female between the ages of 21 to 65 years, inclusive;\n3. Non-childbearing potential (defined as surgically sterile or at least 2 years postmenopausal) or practicing effective contraception (defined as 2 concurrent methods of contraception, 1 of which is a barrier method) and agrees to continue using effective contraception throughout the duration of the study;\n4. Not pregnant based on a negative result on a serum human chorionic gonadotropin (HCG) test at screening Visit 1 and a negative urine pregnancy test prevaccination at Visit 2 (and at subsequent vaccination visits);\n5. Pap test documenting atypical squamous cells of undetermined significance (ASCUS)/HPV+, atypical squamous cells high grade (ASC-H), low-grade squamous intraepithelial lesion (LSIL), or high-grade squamous intraepithelial lesion (HSIL) within 4 months prior to screening Visit 1;\n6. History of pathologically confirmed CIN1 by colposcopically-directed punch biopsy, within 12 weeks prior to administration of first study vaccination (CIN 2/3 subjects will not be eligible);\n7. For the diagnosis of CIN1, has a documented satisfactory colposcopy, ie, the entire lesion as well as the entire squamocolumnar junction is visualizible by colposcopy;\n8. Confirmed high-risk HPV infection by a commercially available high-risk DNA assay (eg, Hybrid Capture II [Qiagen]);\n9. Good health with adequate hematologic, renal, hepatic, and cardiac function, as determined by the Investigator, based upon medical history, physical examination, and laboratory test results at the screening visit (Visit 1):\n\n * Bone marrow function: absolute neutrophil count ≥1,500/µL, and platelets ≥ 100,000/ µL;\n * Renal function: creatinine ≤ 1.5 x institutional upper limit of normal (ULN);\n * Hepatic function: total bilirubin ≤ 1.5 x ULN (Common Terminology Criteria for AEs [CTCAE] v4.0 grade 1) except patients with Gilbert's disease (up to 5.0 mg/dL). Aspartate aminotransferase (AST) and alkaline phosphatase ≤ 2.5 x ULN.\n * Normal Cardiac function: as assessed by history and physical exam.\nHealthy volunteers allowed\nMust be FEMALE\nMust have minimum age of 21 Years\nMust have maximum age of 65 Years",
"exclusion_criteria": "1. Atypical endometrial or glandular cells or evidence of invasive cervical carcinoma on cervical biopsy;\n2. Previous history of cancer, other than adequately treated basal cell or Stage 1 squamous cell carcinoma of the skin;\n3. Current recognized immunodeficiency disease, including infection with HIV, cellular immunodeficiencies, hypogammaglobulinemia, or dysgammaglobulinemia, or hereditary or congenital immunodeficiencies.\n4. Received immunotherapy (eg, IFNs, tumor necrosis factor, interleukins, or biological response modifiers [granulocyte-macrophage colony-stimulating factor, granulocyte colony-stimulating factor, macrophage colony-stimulating factor]) within 30 days prior to administration of the first study vaccination;\n5. Serious, concomitant disorder, including active systemic infection requiring treatment, in the opinion of the investigator;\n6. Currently receiving or has received treatment with systemic steroids in the following dosages within 30 days prior to administration of the first study vaccination.\n\n * Chronic or long-term corticosteroids: ≥0.5 mg/kg/day of oral prednisolone or equivalent\n * Sporadic corticosteroids: ≥1 mg/kg/day of oral prednisolone or equivalent for 2 or more short courses of > 3 days\n * Note: Current or recent use of intra-articular, topical or inhaled glucocorticoid therapy is acceptable;\n7. Other condition or prior therapy that, in the opinion of the Investigator, compromises the subject's welfare or may confound study results;\n8. Participation in another investigational study concurrently or use of another investigational drug within 6 months prior to administration of the first study vaccination;\n9. Previously enrolled in this study.",
"miscellaneous_criteria": ""
},
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"requirement": {
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}
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]
}
},
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}
},
{
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"criterion": "gender",
"requirement": {
"requirement_type": "gender",
"expected_value": "female"
}
},
{
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"requirement": {
"requirement_type": "range",
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"comparisons": [
{
"operator": ">=",
"value": 21,
"unit": "years"
},
{
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"value": 65,
"unit": "years"
}
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}
}
}
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}
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{
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{
"operator": ">=",
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"unit": "years"
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},
{
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"line": "4. Not pregnant based on a negative result on a serum human chorionic gonadotropin (HCG) test at screening Visit 1 and a negative urine pregnancy test prevaccination at Visit 2 (and at subsequent vaccination visits);",
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{
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"criterion": "pregnancy status",
"requirement": {
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"expected_value": "negative"
}
},
{
"exact_snippets": "a negative urine pregnancy test prevaccination at Visit 2 (and at subsequent vaccination visits)",
"criterion": "pregnancy status",
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"expected_value": "negative"
}
}
]
},
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"expected_value": "negative"
}
},
{
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{
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"line": "5. Pap test documenting atypical squamous cells of undetermined significance (ASCUS)/HPV+, atypical squamous cells high grade (ASC-H), low-grade squamous intraepithelial lesion (LSIL), or high-grade squamous intraepithelial lesion (HSIL) within 4 months prior to screening Visit 1;",
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"expected_value": true
}
},
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"expected_value": true
}
},
{
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"expected_value": true
}
},
{
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"expected_value": true
}
},
{
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"criterion": "time since Pap test",
"requirement": {
"requirement_type": "duration",
"expected_value": {
"comparisons": [
{
"operator": "<=",
"value": 4,
"unit": "months"
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{
"or_criteria": [
{
"and_criteria": [
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"operator": "<=",
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"unit": "months"
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"operator": "<=",
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"unit": "months"
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"criterion": "low-grade squamous intraepithelial lesion (LSIL)",
"requirement": {
"requirement_type": "presence",
"expected_value": true
}
},
{
"exact_snippets": "within 4 months prior to screening Visit 1",
"criterion": "time since Pap test",
"requirement": {
"requirement_type": "duration",
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"comparisons": [
{
"operator": "<=",
"value": 4,
"unit": "months"
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"and_criteria": [
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"exact_snippets": "Pap test documenting ... high-grade squamous intraepithelial lesion (HSIL)",
"criterion": "high-grade squamous intraepithelial lesion (HSIL)",
"requirement": {
"requirement_type": "presence",
"expected_value": true
}
},
{
"exact_snippets": "within 4 months prior to screening Visit 1",
"criterion": "time since Pap test",
"requirement": {
"requirement_type": "duration",
"expected_value": {
"comparisons": [
{
"operator": "<=",
"value": 4,
"unit": "months"
}
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]
}
},
{
"identified_line": {
"line": "6. History of pathologically confirmed CIN1 by colposcopically-directed punch biopsy, within 12 weeks prior to administration of first study vaccination (CIN 2/3 subjects will not be eligible);",
"criterions": [
{
"exact_snippets": "History of pathologically confirmed CIN1 by colposcopically-directed punch biopsy",
"criterion": "CIN1",
"requirement": {
"requirement_type": "confirmation",
"expected_value": true
}
},
{
"exact_snippets": "within 12 weeks prior to administration of first study vaccination",
"criterion": "time since biopsy",
"requirement": {
"requirement_type": "time since",
"expected_value": {
"comparisons": [
{
"operator": "<=",
"value": 12,
"unit": "weeks"
}
]
}
}
},
{
"exact_snippets": "CIN 2/3 subjects will not be eligible",
"criterion": "CIN 2/3",
"requirement": {
"requirement_type": "eligibility",
"expected_value": false
}
}
]
},
"logical_structure": {
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"and_criteria": [
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"requirement": {
"requirement_type": "confirmation",
"expected_value": true
}
},
{
"exact_snippets": "within 12 weeks prior to administration of first study vaccination",
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"requirement": {
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"operator": "<=",
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"unit": "weeks"
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"criterion": "CIN 2/3",
"requirement": {
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"expected_value": false
}
}
}
]
}
},
{
"identified_line": {
"line": "7. For the diagnosis of CIN1, has a documented satisfactory colposcopy, ie, the entire lesion as well as the entire squamocolumnar junction is visualizible by colposcopy;",
"criterions": [
{
"exact_snippets": "diagnosis of CIN1",
"criterion": "CIN1 diagnosis",
"requirement": {
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"expected_value": true
}
},
{
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"criterion": "satisfactory colposcopy",
"requirement": {
"requirement_type": "documentation",
"expected_value": true
}
},
{
"exact_snippets": "entire lesion ... is visualizible by colposcopy",
"criterion": "lesion visualization",
"requirement": {
"requirement_type": "completeness",
"expected_value": true
}
},
{
"exact_snippets": "entire squamocolumnar junction is visualizible by colposcopy",
"criterion": "squamocolumnar junction visualization",
"requirement": {
"requirement_type": "completeness",
"expected_value": true
}
}
]
},
"logical_structure": {
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{
"and_criteria": [
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"expected_value": true
}
},
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"requirement_type": "documentation",
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}
}
]
},
{
"and_criteria": [
{
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"criterion": "lesion visualization",
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"expected_value": true
}
},
{
"exact_snippets": "entire squamocolumnar junction is visualizible by colposcopy",
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"expected_value": true
}
}
]
}
]
}
},
{
"identified_line": {
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"criterions": [
{
"exact_snippets": "Confirmed high-risk HPV infection by a commercially available high-risk DNA assay",
"criterion": "high-risk HPV infection",
"requirement": {
"requirement_type": "confirmation",
"expected_value": true
}
},
{
"exact_snippets": "commercially available high-risk DNA assay (eg, Hybrid Capture II [Qiagen])",
"criterion": "high-risk DNA assay",
"requirement": {
"requirement_type": "availability",
"expected_value": true
}
}
]
},
"logical_structure": {
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{
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"expected_value": true
}
},
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"expected_value": true
}
}
]
}
},
{
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"criterions": [
{
"exact_snippets": "Good health",
"criterion": "general health",
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}
},
{
"exact_snippets": "adequate hematologic ... function",
"criterion": "hematologic function",
"requirement": {
"requirement_type": "adequacy",
"expected_value": true
}
},
{
"exact_snippets": "adequate ... renal ... function",
"criterion": "renal function",
"requirement": {
"requirement_type": "adequacy",
"expected_value": true
}
},
{
"exact_snippets": "adequate ... hepatic ... function",
"criterion": "hepatic function",
"requirement": {
"requirement_type": "adequacy",
"expected_value": true
}
},
{
"exact_snippets": "adequate ... cardiac function",
"criterion": "cardiac function",
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}
]
},
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"expected_value": true
}
},
{
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"expected_value": true
}
},
{
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"expected_value": true
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},
{
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{
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"criterion": "absolute neutrophil count",
"requirement": {
"requirement_type": "quantity",
"expected_value": {
"operator": ">=",
"value": 1500,
"unit": "µL"
}
}
},
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"operator": ">=",
"value": 100000,
"unit": "µL"
}
}
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"value": 1500,
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"criterions": [
{
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},
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}
]
}
},
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"exact_snippets": "Healthy volunteers allowed",
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}
]
}
},
{
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{
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"expected_value": "female"
}
}
]
},
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}
}
]
}
},
{
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"line": "Must have minimum age of 21 Years",
"criterions": [
{
"exact_snippets": "minimum age of 21 Years",
"criterion": "age",
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"value": 21,
"unit": "Years"
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}
]
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"exact_snippets": "minimum age of 21 Years",
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"unit": "Years"
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},
{
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"line": "Must have maximum age of 65 Years",
"criterions": [
{
"exact_snippets": "maximum age of 65 Years",
"criterion": "age",
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"operator": "<=",
"value": 65,
"unit": "Years"
}
}
}
]
},
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{
"exact_snippets": "maximum age of 65 Years",
"criterion": "age",
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"operator": "<=",
"value": 65,
"unit": "Years"
}
}
}
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}
],
"exclusion_lines": [
{
"identified_line": {
"line": "1. Atypical endometrial or glandular cells or evidence of invasive cervical carcinoma on cervical biopsy;",
"criterions": [
{
"exact_snippets": "Atypical endometrial or glandular cells",
"criterion": "atypical endometrial or glandular cells",
"requirement": {
"requirement_type": "presence",
"expected_value": true
}
},
{
"exact_snippets": "evidence of invasive cervical carcinoma on cervical biopsy",
"criterion": "invasive cervical carcinoma",
"requirement": {
"requirement_type": "evidence",
"expected_value": true
}
}
]
},
"logical_structure": {
"or_criteria": [
{
"exact_snippets": "Atypical endometrial or glandular cells",
"criterion": "atypical endometrial or glandular cells",
"requirement": {
"requirement_type": "presence",
"expected_value": true
}
},
{
"exact_snippets": "evidence of invasive cervical carcinoma on cervical biopsy",
"criterion": "invasive cervical carcinoma",
"requirement": {
"requirement_type": "evidence",
"expected_value": true
}
}
]
}
},
{
"identified_line": {
"line": "3. Current recognized immunodeficiency disease, including infection with HIV, cellular immunodeficiencies, hypogammaglobulinemia, or dysgammaglobulinemia, or hereditary or congenital immunodeficiencies.",
"criterions": [
{
"exact_snippets": "Current recognized immunodeficiency disease",
"criterion": "immunodeficiency disease",
"requirement": {
"requirement_type": "presence",
"expected_value": true
}
},
{
"exact_snippets": "infection with HIV",
"criterion": "HIV infection",
"requirement": {
"requirement_type": "presence",
"expected_value": true
}
},
{
"exact_snippets": "cellular immunodeficiencies",
"criterion": "cellular immunodeficiencies",
"requirement": {
"requirement_type": "presence",
"expected_value": true
}
},
{
"exact_snippets": "hypogammaglobulinemia",
"criterion": "hypogammaglobulinemia",
"requirement": {
"requirement_type": "presence",
"expected_value": true
}
},
{
"exact_snippets": "dysgammaglobulinemia",
"criterion": "dysgammaglobulinemia",
"requirement": {
"requirement_type": "presence",
"expected_value": true
}
},
{
"exact_snippets": "hereditary or congenital immunodeficiencies",
"criterion": "hereditary or congenital immunodeficiencies",
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"requirement_type": "presence",
"expected_value": true
}
}
]
},
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"or_criteria": [
{
"exact_snippets": "Current recognized immunodeficiency disease",
"criterion": "immunodeficiency disease",
"requirement": {
"requirement_type": "presence",
"expected_value": true
}
},
{
"exact_snippets": "infection with HIV",
"criterion": "HIV infection",
"requirement": {
"requirement_type": "presence",
"expected_value": true
}
},
{
"exact_snippets": "cellular immunodeficiencies",
"criterion": "cellular immunodeficiencies",
"requirement": {
"requirement_type": "presence",
"expected_value": true
}
},
{
"exact_snippets": "hypogammaglobulinemia",
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"requirement_type": "presence",
"expected_value": true
}
},
{
"exact_snippets": "dysgammaglobulinemia",
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"requirement_type": "presence",
"expected_value": true
}
},
{
"exact_snippets": "hereditary or congenital immunodeficiencies",
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"requirement_type": "presence",
"expected_value": true
}
}
]
}
},
{
"identified_line": {
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{
"exact_snippets": "Received immunotherapy (eg, IFNs, tumor necrosis factor, interleukins, or biological response modifiers [granulocyte-macrophage colony-stimulating factor, granulocyte colony-stimulating factor, macrophage colony-stimulating factor])",
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"requirement_type": "receipt",
"expected_value": true
}
},
{
"exact_snippets": "within 30 days prior to administration of the first study vaccination",
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"requirement_type": "time since last treatment",
"expected_value": {
"operator": "<=",
"value": 30,
"unit": "days"
}
}
}
]
},
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{
"exact_snippets": "Received immunotherapy (eg, IFNs, tumor necrosis factor, interleukins, or biological response modifiers [granulocyte-macrophage colony-stimulating factor, granulocyte colony-stimulating factor, macrophage colony-stimulating factor])",
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"requirement_type": "receipt",
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}
},
{
"exact_snippets": "within 30 days prior to administration of the first study vaccination",
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"expected_value": {
"operator": "<=",
"value": 30,
"unit": "days"
}
}
}
]
}
},
{
"identified_line": {
"line": "5. Serious, concomitant disorder, including active systemic infection requiring treatment, in the opinion of the investigator;",
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{
"exact_snippets": "Serious, concomitant disorder",
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}
},
{
"exact_snippets": "active systemic infection requiring treatment",
"criterion": "systemic infection",
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"requirement_type": "activity",
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}
},
{
"exact_snippets": "active systemic infection requiring treatment",
"criterion": "systemic infection",
"requirement": {
"requirement_type": "treatment requirement",
"expected_value": true
}
}
]
},
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"and_criteria": [
{
"and_criteria": [
{
"exact_snippets": "Serious, concomitant disorder",
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"requirement_type": "severity",
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}
},
{
"exact_snippets": "active systemic infection requiring treatment",
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"requirement": {
"requirement_type": "activity",
"expected_value": "active"
}
},
{
"exact_snippets": "active systemic infection requiring treatment",
"criterion": "systemic infection",
"requirement": {
"requirement_type": "treatment requirement",
"expected_value": true
}
}
]
}
]
}
},
{
"identified_line": {
"line": "6. Currently receiving or has received treatment with systemic steroids in the following dosages within 30 days prior to administration of the first study vaccination.",
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{
"exact_snippets": "Currently receiving or has received treatment with systemic steroids",
"criterion": "systemic steroid treatment",
"requirement": {
"requirement_type": "presence",
"expected_value": true
}
},
{
"exact_snippets": "dosages within 30 days prior to administration of the first study vaccination",
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}
}
]
},
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"and_criteria": [
{
"and_criteria": [
{
"exact_snippets": "Currently receiving or has received treatment with systemic steroids",
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"requirement_type": "presence",
"expected_value": true
}
},
{
"exact_snippets": "dosages within 30 days prior to administration of the first study vaccination",
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}
}
]
}
]
}
},
{
"identified_line": {
"line": "* Chronic or long-term corticosteroids: ≥0.5 mg/kg/day of oral prednisolone or equivalent",
"criterions": [
{
"exact_snippets": "Chronic or long-term corticosteroids: ≥0.5 mg/kg/day of oral prednisolone or equivalent",
"criterion": "corticosteroid dosage",
"requirement": {
"requirement_type": "dosage",
"expected_value": {
"operator": ">=",
"value": 0.5,
"unit": "mg/kg/day"
}
}
}
]
},
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"and_criteria": [
{
"exact_snippets": "Chronic or long-term corticosteroids: ≥0.5 mg/kg/day of oral prednisolone or equivalent",
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"requirement_type": "dosage",
"expected_value": {
"operator": ">=",
"value": 0.5,
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}
}
}
]
}
},
{
"identified_line": {
"line": "* Sporadic corticosteroids: ≥1 mg/kg/day of oral prednisolone or equivalent for 2 or more short courses of > 3 days",
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{
"exact_snippets": "Sporadic corticosteroids: ≥1 mg/kg/day of oral prednisolone or equivalent",
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"requirement_type": "dosage",
"expected_value": {
"operator": ">=",
"value": 1,
"unit": "mg/kg/day"
}
}
},
{
"exact_snippets": "2 or more short courses of > 3 days",
"criterion": "corticosteroid course duration",
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"requirement_type": "number of courses",
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"operator": ">=",
"value": 2,
"unit": "courses"
}
}
},
{
"exact_snippets": "2 or more short courses of > 3 days",
"criterion": "corticosteroid course duration",
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"requirement_type": "duration per course",
"expected_value": {
"operator": ">",
"value": 3,
"unit": "days"
}
}
}
]
},
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"and_criteria": [
{
"and_criteria": [
{
"exact_snippets": "Sporadic corticosteroids: ≥1 mg/kg/day of oral prednisolone or equivalent",
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}
}
},
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"value": 2,
"unit": "courses"
}
}
}
]
},
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"operator": ">",
"value": 3,
"unit": "days"
}
}
}
]
}
},
{
"identified_line": {
"line": "* Note: Current or recent use of intra-articular, topical or inhaled glucocorticoid therapy is acceptable;",
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{
"exact_snippets": "Current or recent use of intra-articular, topical or inhaled glucocorticoid therapy is acceptable",
"criterion": "glucocorticoid therapy",
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"requirement_type": "route of administration",
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]
}
},
{
"exact_snippets": "Current or recent use of intra-articular, topical or inhaled glucocorticoid therapy is acceptable",
"criterion": "glucocorticoid therapy",
"requirement": {
"requirement_type": "acceptability",
"expected_value": true
}
}
]
},
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{
"not_criteria": {
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{
"exact_snippets": "Current or recent use of intra-articular, topical or inhaled glucocorticoid therapy is acceptable",
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"requirement_type": "route of administration",
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"topical",
"inhaled"
]
}
},
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"exact_snippets": "Current or recent use of intra-articular, topical or inhaled glucocorticoid therapy is acceptable",
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"requirement_type": "acceptability",
"expected_value": true
}
}
]
}
}
]
}
},
{
"identified_line": {
"line": "7. Other condition or prior therapy that, in the opinion of the Investigator, compromises the subject's welfare or may confound study results;",
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{
"exact_snippets": "Other condition or prior therapy ... compromises the subject's welfare",
"criterion": "condition or prior therapy",
"requirement": {
"requirement_type": "impact on welfare",
"expected_value": "compromises"
}
},
{
"exact_snippets": "Other condition or prior therapy ... may confound study results",
"criterion": "condition or prior therapy",
"requirement": {
"requirement_type": "impact on study results",
"expected_value": "may confound"
}
}
]
},
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"and_criteria": [
{
"and_criteria": [
{
"exact_snippets": "Other condition or prior therapy ... compromises the subject's welfare",
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"expected_value": "compromises"
}
},
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}
}
]
}
]
}
}
],
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{
"identified_line": {
"line": "3. Non-childbearing potential (defined as surgically sterile or at least 2 years postmenopausal) or practicing effective contraception (defined as 2 concurrent methods of contraception, 1 of which is a barrier method) and agrees to continue using effective contraception throughout the duration of the study;",
"criterions": [
{
"exact_snippets": "Non-childbearing potential (defined as surgically sterile or at least 2 years postmenopausal)",
"criterion": "childbearing potential",
"requirement": {
"requirement_type": "status",
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}
},
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"at least 2 years postmenopausal"
]
}
},
{
"exact_snippets": "practicing effective contraception (defined as 2 concurrent methods of contraception, 1 of which is a barrier method)",
"criterion": "contraception practice",
"requirement": {
"requirement_type": "status",
"expected_value": "practicing effective contraception"
}
},
{
"exact_snippets": "practicing effective contraception (defined as 2 concurrent methods of contraception, 1 of which is a barrier method)",
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"requirement": {
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}
},
{
"exact_snippets": "agrees to continue using effective contraception throughout the duration of the study",
"criterion": "contraception agreement",
"requirement": {
"requirement_type": "agreement",
"expected_value": "continue using effective contraception throughout the duration of the study"
}
}
]
},
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"or_criteria": [
{
"and_criteria": [
{
"and_criteria": [
{
"exact_snippets": "Non-childbearing potential (defined as surgically sterile or at least 2 years postmenopausal)",
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"requirement_type": "status",
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}
},
{
"or_criteria": [
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"requirement_type": "definition",
"expected_value": "surgically sterile"
}
},
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}
]
}
]
}
]
},
{
"and_criteria": [
{
"and_criteria": [
{
"exact_snippets": "practicing effective contraception (defined as 2 concurrent methods of contraception, 1 of which is a barrier method)",
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"requirement": {
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}
},
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}
}
]
},
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"criterion": "contraception agreement",
"requirement": {
"requirement_type": "agreement",
"expected_value": "continue using effective contraception throughout the duration of the study"
}
}
]
}
]
}
},
{
"identified_line": {
"line": "* Renal function: creatinine ≤ 1.5 x institutional upper limit of normal (ULN);",
"criterions": [
{
"exact_snippets": "Renal function: creatinine ≤ 1.5 x institutional upper limit of normal (ULN);",
"criterion": "creatinine level",
"requirement": {
"requirement_type": "comparison",
"expected_value": {
"operator": "<=",
"value": 1.5,
"unit": "x institutional upper limit of normal (ULN)"
}
}
}
]
},
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"and_criteria": [
{
"exact_snippets": "Renal function: creatinine \u0010.5 x institutional upper limit of normal (ULN);",
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"requirement": {
"requirement_type": "comparison",
"expected_value": {
"operator": "<=",
"value": 1.5,
"unit": "x institutional upper limit of normal (ULN)"
}
}
}
]
}
},
{
"identified_line": {
"line": "* Hepatic function: total bilirubin ≤ 1.5 x ULN (Common Terminology Criteria for AEs [CTCAE] v4.0 grade 1) except patients with Gilbert's disease (up to 5.0 mg/dL). Aspartate aminotransferase (AST) and alkaline phosphatase ≤ 2.5 x ULN.",
"criterions": [
{
"exact_snippets": "Hepatic function: total bilirubin ≤ 1.5 x ULN",
"criterion": "total bilirubin",
"requirement": {
"requirement_type": "level",
"expected_value": {
"operator": "<=",
"value": 1.5,
"unit": "x ULN"
}
}
},
{
"exact_snippets": "patients with Gilbert's disease (up to 5.0 mg/dL)",
"criterion": "total bilirubin in patients with Gilbert's disease",
"requirement": {
"requirement_type": "level",
"expected_value": {
"operator": "<=",
"value": 5.0,
"unit": "mg/dL"
}
}
},
{
"exact_snippets": "Aspartate aminotransferase (AST) ... ≤ 2.5 x ULN",
"criterion": "Aspartate aminotransferase (AST)",
"requirement": {
"requirement_type": "level",
"expected_value": {
"operator": "<=",
"value": 2.5,
"unit": "x ULN"
}
}
},
{
"exact_snippets": "alkaline phosphatase ≤ 2.5 x ULN",
"criterion": "alkaline phosphatase",
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"requirement_type": "level",
"expected_value": {
"operator": "<=",
"value": 2.5,
"unit": "x ULN"
}
}
}
]
},
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"and_criteria": [
{
"condition": {
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{
"exact_snippets": "Hepatic function: total bilirubin \u0010.5 x ULN",
"criterion": "total bilirubin",
"requirement": {
"requirement_type": "level",
"expected_value": {
"operator": "<=",
"value": 1.5,
"unit": "x ULN"
}
}
},
{
"not_criteria": {
"exact_snippets": "patients with Gilbert's disease (up to 5.0 mg/dL)",
"criterion": "total bilirubin in patients with Gilbert's disease",
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"requirement_type": "level",
"expected_value": {
"operator": "<=",
"value": 5.0,
"unit": "mg/dL"
}
}
}
}
]
},
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"else_criteria": {
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"value": 5.0,
"unit": "mg/dL"
}
}
}
},
{
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"criterion": "Aspartate aminotransferase (AST)",
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"requirement_type": "level",
"expected_value": {
"operator": "<=",
"value": 2.5,
"unit": "x ULN"
}
}
},
{
"exact_snippets": "alkaline phosphatase \u0010.5 x ULN",
"criterion": "alkaline phosphatase",
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"requirement_type": "level",
"expected_value": {
"operator": "<=",
"value": 2.5,
"unit": "x ULN"
}
}
}
]
}
}
],
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{
"identified_line": {
"line": "2. Previous history of cancer, other than adequately treated basal cell or Stage 1 squamous cell carcinoma of the skin;",
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{
"exact_snippets": "Previous history of cancer",
"criterion": "previous history of cancer",
"requirement": {
"requirement_type": "presence",
"expected_value": false
}
},
{
"exact_snippets": "adequately treated basal cell or Stage 1 squamous cell carcinoma of the skin",
"criterion": "adequately treated basal cell or Stage 1 squamous cell carcinoma of the skin",
"requirement": {
"requirement_type": "presence",
"expected_value": true
}
}
]
},
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"condition": {
"exact_snippets": "Previous history of cancer",
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"expected_value": true
}
},
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"expected_value": true
}
}
]
}
},
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}
},
{
"identified_line": {
"line": "8. Participation in another investigational study concurrently or use of another investigational drug within 6 months prior to administration of the first study vaccination;",
"criterions": [
{
"exact_snippets": "Participation in another investigational study concurrently",
"criterion": "participation in another investigational study",
"requirement": {
"requirement_type": "presence",
"expected_value": false
}
},
{
"exact_snippets": "use of another investigational drug within 6 months prior to administration of the first study vaccination",
"criterion": "use of another investigational drug",
"requirement": {
"requirement_type": "time frame",
"expected_value": {
"comparisons": [
{
"operator": "<=",
"value": 6,
"unit": "months"
}
]
}
}
}
]
},
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"or_criteria": [
{
"exact_snippets": "Participation in another investigational study concurrently",
"criterion": "participation in another investigational study",
"requirement": {
"requirement_type": "presence",
"expected_value": true
}
},
{
"exact_snippets": "use of another investigational drug within 6 months prior to administration of the first study vaccination",
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{
"operator": "<=",
"value": 6,
"unit": "months"
}
]
}
}
}
]
}
},
{
"identified_line": {
"line": "9. Previously enrolled in this study.",
"criterions": [
{
"exact_snippets": "Previously enrolled in this study.",
"criterion": "previous enrollment in this study",
"requirement": {
"requirement_type": "presence",
"expected_value": false
}
}
]
},
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"and_criteria": [
{
"exact_snippets": "Previously enrolled in this study.",
"criterion": "previous enrollment in this study",
"requirement": {
"requirement_type": "presence",
"expected_value": true
}
}
]
}
}
],
"failed_miscellaneous": []
}