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NCT02471911
|
21:24:chronic_disease,26:44:chronic_disease,46:64:chronic_disease
|
Patients with known HIV, active hepatitis B, active hepatitis C
| 3
|
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NCT02577731
|
14:32:chronic_disease
|
Blunt and/or penetrating trauma patient
| 3
|
[
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"penetrating",
"trauma",
"patient"
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[
0,
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NCT02004275
|
1:14:chronic_disease
|
Liver disease with history of positive serology
| 3
|
[
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NCT02133885
|
1:25:chronic_disease
|
unstable angina pectoris,
| 3
|
[
"unstable",
"angina",
"pectoris",
","
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[
2,
2,
2,
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NCT01950351
|
11:37:chronic_disease,42:72:chronic_disease,86:115:treatment,125:146:treatment
|
diagnosed connective tissue disorder, or congenital coagulation defects (patients on medical therapy with Coumadin or other blood thinning agents are eligible for participation)
| 3
|
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NCT03135171
|
1:44:treatment,
|
Immunization with a live/attenuated vaccine within 30 days of enrollment
| 3
|
[
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NCT02685605
|
12:19:cancer,,
|
History of cancers or other comorbidities that limit life expectancy to less than five years
| 3
|
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NCT02566304
|
35:45:cancer,62:73:cancer,99:108:treatment
|
Patients with evidence of another malignancy, exclusive of a skin cancer that requires only local treatment, should not be enrolled on this protocol
| 3
|
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NCT02048371
|
,,19:35:cancer
|
Age ≥ 5 years for Rhabdomyosarcoma cohorts
| 3
|
[
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NCT02516696
|
28:65:treatment,73:84:treatment,88:103:treatment,125:142:treatment
|
Patients may have received prior adjuvant antiresorptive therapy (i.e., pamidronate or zoledronic acid) as routine care, or radiation therapy as palliation for pain and/or spinal cord compression
| 3
|
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NCT02007239
|
7:32:chronic_disease
|
Known active herpetic infection
| 3
|
[
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"herpetic",
"infection"
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[
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NCT02252432
|
1:16:chronic_disease
|
Thyroid disease
| 3
|
[
"Thyroid",
"disease"
] |
[
2,
2
] |
NCT02484404
|
20:30:cancer,32:43:cancer,45:79:cancer
|
Patients must have metastatic, progressive, castrate resistant prostate cancer (mCRPC)
| 3
|
[
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NCT02549937
|
56:71:treatment
|
Subject is currently receiving or intending to receive anti-coagulants for therapeutic purposes
| 3
|
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NCT02517307
|
1:19:chronic_disease,28:36:chronic_disease,40:65:chronic_disease
|
endocrine disorder such as diabetes or untreated thyroid disease
| 3
|
[
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"thyroid",
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NCT03060564
|
10:35:treatment
|
previous acromioclavicular surgery
| 3
|
[
"previous",
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"surgery"
] |
[
0,
1,
1
] |
NCT01306019
|
29:51:chronic_disease
|
Any current or pre-existing hematologic malignancy
| 3
|
[
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"current",
"or",
"pre-existing",
"hematologic",
"malignancy"
] |
[
0,
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0,
0,
2,
2
] |
NCT02519322
|
120:130:treatment
|
A known or underlying medical condition that, in the opinion of the Investigator, could make the administration of the study drug hazardous to the subject or could adversely affect the ability of the subject to comply with or tolerate the study
| 3
|
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NCT03154476
|
15:37:treatment
|
Subjects with implantable pacemakers
| 3
|
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"Subjects",
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"pacemakers"
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[
0,
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NCT02995330
|
8:30:chronic_disease,59:62:chronic_disease,63:67:chronic_disease,71:87:chronic_disease
|
Active uncontrolled infection, including known history of HIV/AIDS or hepatitis B or C
| 3
|
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NCT02564796
|
1:23:chronic_disease,48:53:treatment,126:149:treatment,151:188:treatment
|
Cyanotic heart disease who have had a surgical shunt or a catheterization intervention that is equivalent to a shunt (patent ductus arteriosus stent, right ventricular outflow tract stent)
| 3
|
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NCT02095808
|
37:53:allergy_name
|
Patients with a contraindication to MRI examinations
| 3
|
[
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NCT02568267
|
23:42:treatment,44:48:treatment,53:67:treatment,89:95:cancer
|
excluding approved or investigational Trk, ROS1, or ALK inhibitors in patients who have tumors that harbor those respective gene rearrangements
| 3
|
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NCT02543983
|
1:48:treatment,
|
Treatment with any other concomitant medication not allowed within 5 (Omega) half-lives prior to study Phase II
| 3
|
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NCT02374021
|
,33:43:treatment
|
Current use of >10mg per day of prednisone
| 3
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[
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NCT02105766
|
1:19:chronic_disease,,,,
|
Sickle hepatopathy defined as EITHER ferritin >1000mcg/L OR direct bilirubin >0.4 mg/dL at baseline
| 3
|
[
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"hepatopathy",
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NCT02304458
|
1:19:treatment
|
Stem cell infusion
| 3
|
[
"Stem",
"cell",
"infusion"
] |
[
1,
1,
1
] |
NCT01389024
|
33:36:treatment,,,
|
All screening procedures except MRI can be completed between 9 and 12 months of age, with the exception of the MRI, for which the child must have reached the age of 12 months
| 3
|
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NCT01966367
|
28:50:treatment,,,141:162:treatment,163:188:treatment
|
Patients who have received prior hematocrit (HCT) within three months of enrollment for reduced intensity regimen and within six months for myeloablative regimen/reduced toxicity regimens
| 3
|
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NCT02323880
|
,57:83:treatment
|
at least 42 days must have elapsed if other substantial bone marrow (BM) radiation
| 3
|
[
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NCT03114319
|
32:48:treatment
|
Must have progressed following standard therapy, or for whom, in the opinion of the Investigator
| 3
|
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NCT02588326
|
,96:115:treatment,117:135:treatment,140:148:treatment
|
Exposure to any medication/food that alters the CYP 3A4 activity within last 2 weeks (e.g. any grapefruit products, azole anti-fungals, or rifampin)
| 3
|
[
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NCT01730794
|
17:39:treatment
|
Need to provide controlled ventilation
| 3
|
[
"Need",
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"controlled",
"ventilation"
] |
[
0,
0,
0,
1,
1
] |
NCT01415752
|
15:18:chronic_disease,,
|
No history of CD4 prior to or at the time of lymphoma diagnosis < 300 cells/mm³
| 3
|
[
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NCT03080142
|
29:46:allergy_name
|
Patients with an allergy to local anesthetics
| 3
|
[
"Patients",
"with",
"an",
"allergy",
"to",
"local",
"anesthetics"
] |
[
0,
0,
0,
0,
0,
4,
4
] |
NCT03153410
|
48:71:allergy_name
|
History of severe hypersensitivity reaction to any monoclonal antibody
| 3
|
[
"History",
"of",
"severe",
"hypersensitivity",
"reaction",
"to",
"any",
"monoclonal",
"antibody"
] |
[
0,
0,
0,
0,
0,
0,
4,
4,
4
] |
NCT02091999
|
76:105:allergy_name
|
Known sensitivity to any of the ingredients of the investigational product enfortumab vedotin (ASG-22CE)
| 3
|
[
"Known",
"sensitivity",
"to",
"any",
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"the",
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"the",
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"vedotin",
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NCT01280994
|
25:58:treatment,74:79:treatment,,99:102:treatment
|
Subject has received an investigational medicinal product (not including 129Xe) within 30 days of MRI
| 3
|
[
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NCT01912612
|
21:28:chronic_disease
|
Significant risk of suicide based on the Investigator's judgment
| 3
|
[
"Significant",
"risk",
"of",
"suicide",
"based",
"on",
"the",
"Investigator",
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[
0,
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0,
2,
0,
0,
0,
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0,
0
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NCT02577731
|
10:37:treatment
|
Previous bone marrow transplantation
| 3
|
[
"Previous",
"bone",
"marrow",
"transplantation"
] |
[
0,
1,
1,
1
] |
NCT02554903
|
31:55:chronic_disease,,
|
Documented moderate to severe restrictive lung disease defined as: total lung capacity < 60% of predicted value
| 3
|
[
"Documented",
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"to",
"severe",
"restrictive",
"lung",
"disease",
"defined",
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NCT02423863
|
12:32:treatment
|
History of active immunotherapy in the previous month
| 3
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[
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NCT02213289
|
4:7:chronic_disease,
|
No CVA within 6 months
| 3
|
[
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[
0,
2,
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NCT02638454
|
1:15:treatment
|
ACE inhibitors
| 3
|
[
"ACE",
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[
1,
1
] |
NCT02946658
|
17:37:treatment,
|
Exposure to any investigational drug or procedure with 1 month prior to study entry or enrollment in concurrent study which may interfere with interpretation of study results
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NCT02349035
|
52:62:treatment
|
Significant new injury that would prevent use of a prosthesis: The ability to consistently wear a prosthesis and perform activities of daily living and specific performance tasks is necessary to evaluate the relative benefits of the interventions
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NCT02524379
|
,105:119:treatment
|
Breast-feeding women who do not agree to stop breast-feeding during and for 7 days following the end of oral glyburide administration
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[
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NCT02334579
|
17:29:treatment
|
Prior high-dose radiotherapy to the prostate or lower pelvis
| 3
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[
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NCT01415752
|
35:57:treatment
|
Must be willing to take effective antiretroviral therapy, if indicated
| 3
|
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NCT02474667
|
1:27:chronic_disease,,71:83:treatment,87:106:treatment,,144:159:treatment
|
Oligo-anuric renal failure (less than 200 mL of UO per day) requiring hemodialysis or peritoneal dialysis initiated at least 3 months prior to transplantation
| 3
|
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NCT02692651
|
,44:54:treatment,59:68:treatment,96:99:chronic_disease,
|
Patients receiving ≥ 1 high or medium risk antibiotic for treatment of an infection other than CDI, for an anticipated duration of ≥ 5 days from the time of enrollment
| 3
|
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NCT01976169
|
24:75:cancer
|
All subjects must have recurrent or metastatic HER2-positive breast cancer
| 3
|
[
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NCT02431897
|
37:47:treatment
|
Physically able to apply/insert the study drug
| 3
|
[
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[
0,
0,
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0,
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1,
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NCT02533674
|
1:38:cancer
|
Gastrointestinal stromal tumor (GIST)
| 3
|
[
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[
3,
3,
3,
3,
0,
0
] |
NCT02347891
|
17:25:treatment,
|
Discontinuation IS agent < 3 months prior to Screening
| 3
|
[
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[
0,
1,
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0,
0,
0,
0,
0,
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NCT02964182
|
1:14:treatment
|
nitroglycerin
| 3
|
[
"nitroglycerin"
] |
[
1
] |
NCT02494869
|
11:30:chronic_disease
|
Suspected dissecting aneurysm
| 3
|
[
"Suspected",
"dissecting",
"aneurysm"
] |
[
0,
2,
2
] |
NCT02391987
|
23:32:allergy_name,34:46:allergy_name,48:56:allergy_name,58:65:allergy_name
|
Known skin allergy to adhesives (hydrocolloid, silicone, acrylic)
| 3
|
[
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NCT03034564
|
24:49:chronic_disease
|
Significant history of Gastro Intestinal disease that may interfere with absorption
| 3
|
[
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NCT02796391
|
1:20:treatment
|
Erlotinib (Tarceva)
| 3
|
[
"Erlotinib",
"(",
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")"
] |
[
1,
1,
0,
0
] |
NCT03021486
|
14:29:cancer
|
Diagnosis of advanced cancer (defined as locally advanced, metastatic recurrent, or incurable disease)
| 3
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NCT01925573
|
29:42:treatment,49:63:treatment,65:80:treatment,84:96:treatment,99:110:treatment,126:142:chronic_disease,,171:181:treatment,239:247:treatment,264:286:treatment,
|
Patients who have undergone major surgery (e.g. intra-thoracic, intra-abdominal or intra-pelvic), open biopsy or significant traumatic injury ≤ 4 weeks prior to starting study drug, or patients who have had minor procedures, percutaneous biopsies or placement of vascular access device ≤ 1 week prior to starting study drug, or who have not recovered from side effects of such procedure or injury
| 3
|
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NCT01989585
|
35:45:treatment,64:70:treatment,77:105:treatment,116:142:treatment,188:198:treatment,251:308:treatment,317:334:treatment,343:353:treatment,355:362:treatment,368:378:treatment,388:423:treatment,483:494:treatment,528:584:treatment,,621:645:treatment
|
Preclinical studies indicate that navitoclax is metabolized by CYP3A4, is a moderate inhibitor of CYP2C8, and is a strong inhibitor of CYP2C9; there is also evidence of interactions with dabrafenib; therefore, caution should be exercised when dosing navitoclax concurrently with CYP2C8 and CYP2C9 substrates; common CYP2C8 substrates include paclitaxel, statins, and glitazones, whereas CYP2C9 substrates include phenytoin; when possible, investigators should switch to alternative medications or monitor the patients closely; CYP3A inhibitors such as ketoconazole and clarithromycin are not allowed 7 days prior to the first dose of navitoclax or during navitoclax administration
| 3
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NCT01631617
|
19:45:chronic_disease
|
Family history of toxic epidermal necrolysis
| 3
|
[
"Family",
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"toxic",
"epidermal",
"necrolysis"
] |
[
0,
0,
0,
2,
2,
2
] |
NCT02905591
|
1:9:treatment
|
warfarin
| 3
|
[
"warfarin"
] |
[
1
] |
NCT02912572
|
59:77:cancer
|
This test is now done routinely for every newly diagnosed endometrial cancer patient in most centers in the US
| 3
|
[
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NCT02484404
|
52:69:cancer
|
Histologically or cytologically confirmed advanced colorectal cancer
| 3
|
[
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"cancer"
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[
0,
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NCT02960113
|
9:32:chronic_disease,34:43:chronic_disease,48:60:chronic_disease
|
Current urinary tract infection, pneumonia, or otitis media
| 3
|
[
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[
0,
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NCT02446457
|
26:45:cancer,,93:117:treatment,138:156:treatment,180:185:cancer
|
with histologic proof of follicular lymphoma grade 1, 2, or 3a relapsing after at least two prior systemic therapies, which must include CAR T cell therapy or histologic proof of DLBCL relapsing after at least two prior systemic therapies, which must include CAR T cell therapy
| 3
|
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NCT03011307
|
48:63:treatment
|
Currently Workman's Comp litigation related to hip replacement
| 3
|
[
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0,
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NCT02627495
|
210:227:treatment
|
Presence of the following contraindication to transcranial direct current stimulation Ferromagnetic metal in the head (e.g., plates or pins, bullets, shrapnel) Implanted head electronic medical devices (e.g., cochlear implants)
| 3
|
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NCT01822522
|
,115:137:treatment,139:151:treatment,153:177:treatment,182:204:treatment
|
women of childbearing potential include women who have experienced menarche and who have not undergone successful surgical sterilization (hysterectomy, bilateral tubal ligation, or bilateral oophorectomy) or are not postmenopausal
| 3
|
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NCT02465268
|
28:40:allergy_name,42:48:allergy_name,52:54:allergy_name
|
Prior allergic reaction to temozolomide, GM-CSF or Td
| 3
|
[
"Prior",
"allergic",
"reaction",
"to",
"temozolomide",
",",
"GM-CSF",
"or",
"Td"
] |
[
0,
0,
0,
0,
4,
0,
4,
0,
4
] |
NCT01360606
|
10:22:treatment
|
No prior radiotherapy to the upper abdomen
| 3
|
[
"No",
"prior",
"radiotherapy",
"to",
"the",
"upper",
"abdomen"
] |
[
0,
0,
1,
0,
0,
0,
0
] |
NCT02423525
|
25:37:cancer
|
Previous or concomitant malignancies at other sites
| 3
|
[
"Previous",
"or",
"concomitant",
"malignancies",
"at",
"other",
"sites"
] |
[
0,
0,
0,
3,
0,
0,
0
] |
NCT02950233
|
18:42:treatment
|
Planned elective VATS pulmonary lobectomy
| 3
|
[
"Planned",
"elective",
"VATS",
"pulmonary",
"lobectomy"
] |
[
0,
0,
1,
1,
1
] |
NCT01773694
|
10:28:treatment,32:57:treatment,63:87:treatment
|
standard excisional surgery or Mohs micrographic surgery with immediate reconstruction
| 3
|
[
"standard",
"excisional",
"surgery",
"or",
"Mohs",
"micrographic",
"surgery",
"with",
"immediate",
"reconstruction"
] |
[
0,
1,
1,
0,
1,
1,
1,
0,
1,
1
] |
NCT01130077
|
5:43:treatment
|
Any investigational therapeutic medication
| 3
|
[
"Any",
"investigational",
"therapeutic",
"medication"
] |
[
0,
1,
1,
1
] |
NCT03059355
|
1:27:chronic_disease
|
Advanced pulmonary disease
| 3
|
[
"Advanced",
"pulmonary",
"disease"
] |
[
2,
2,
2
] |
NCT01280994
|
52:55:treatment
|
Subject does not fit into 129Xe vest coil used for MRI
| 3
|
[
"Subject",
"does",
"not",
"fit",
"into",
"129Xe",
"vest",
"coil",
"used",
"for",
"MRI"
] |
[
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
1
] |
NCT02650206
|
1:14:cancer
|
MEN2 Syndrome
| 3
|
[
"MEN2",
"Syndrome"
] |
[
3,
3
] |
NCT01851369
|
31:43:cancer
|
Phase II only: No other prior malignancies are allowed
| 3
|
[
"Phase",
"II",
"only",
":",
"No",
"other",
"prior",
"malignancies",
"are",
"allowed"
] |
[
0,
0,
0,
0,
0,
0,
0,
3,
0,
0
] |
NCT03037879
|
1:16:chronic_disease
|
Vision impaired
| 3
|
[
"Vision",
"impaired"
] |
[
2,
2
] |
NCT01829958
|
31:63:treatment
|
patients being treated with a single agent monoclonal antibody
| 3
|
[
"patients",
"being",
"treated",
"with",
"a",
"single",
"agent",
"monoclonal",
"antibody"
] |
[
0,
0,
0,
0,
0,
1,
1,
1,
1
] |
NCT02310399
|
24:36:chronic_disease
|
Group 1: Prelinguistic hearing loss
| 3
|
[
"Group",
"1",
":",
"Prelinguistic",
"hearing",
"loss"
] |
[
0,
0,
0,
0,
2,
2
] |
NCT02578901
|
29:46:chronic_disease
|
Known inherited or acquired bleeding disorder
| 3
|
[
"Known",
"inherited",
"or",
"acquired",
"bleeding",
"disorder"
] |
[
0,
0,
0,
0,
2,
2
] |
NCT02516241
|
1:17:cancer,21:44:chronic_disease,94:102:treatment,,146:161:treatment,196:212:cancer,241:244:treatment
|
Brain metastases or spinal cord compression unless the patient's condition is stable and off steroids for at least 14 days prior to the start of study treatment. Patients with suspected or known brain metastases at screening should have an MRI (preferred)/CT, preferably with IV contrast to access baseline disease status
| 3
|
[
"Brain",
"metastases",
"or",
"spinal",
"cord",
"compression",
"unless",
"the",
"patient",
"'s",
"condition",
"is",
"stable",
"and",
"off",
"steroids",
"for",
"at",
"least",
"14",
"days",
"prior",
"to",
"the",
"start",
"of",
"study",
"treatment",
".",
"Patients",
"with",
"suspected",
"or",
"known",
"brain",
"metastases",
"at",
"screening",
"should",
"have",
"an",
"MRI",
"(",
"preferred",
")",
"/CT",
",",
"preferably",
"with",
"IV",
"contrast",
"to",
"access",
"baseline",
"disease",
"status"
] |
[
3,
3,
0,
2,
2,
2,
0,
0,
0,
0,
0,
0,
0,
0,
0,
1,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
1,
1,
0,
0,
0,
0,
0,
0,
3,
3,
0,
0,
0,
0,
0,
1,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0
] |
NCT01703949
|
16:35:treatment
|
Intolerance to brentuximab vedotin
| 3
|
[
"Intolerance",
"to",
"brentuximab",
"vedotin"
] |
[
0,
0,
1,
1
] |
NCT03122691
|
11:33:treatment,35:62:treatment,64:84:treatment,89:99:treatment,
|
Use of an Over-the-Counter (OTC), systemic or topical drug(s), herbal supplement(s), or vitamin(s) within 14 days of experimental sessions; which, in the opinion of the investigator or sponsor, will interfere with the study result or the safety of the subject
| 3
|
[
"Use",
"of",
"an",
"Over-the-Counter",
"(",
"OTC",
")",
",",
"systemic",
"or",
"topical",
"drug",
"(",
"s",
")",
",",
"herbal",
"supplement",
"(",
"s",
")",
",",
"or",
"vitamin",
"(",
"s",
")",
"within",
"14",
"days",
"of",
"experimental",
"sessions",
";",
"which",
",",
"in",
"the",
"opinion",
"of",
"the",
"investigator",
"or",
"sponsor",
",",
"will",
"interfere",
"with",
"the",
"study",
"result",
"or",
"the",
"safety",
"of",
"the",
"subject"
] |
[
1,
1,
1,
1,
1,
1,
1,
1,
1,
1,
1,
1,
1,
1,
1,
1,
1,
1,
1,
1,
1,
1,
1,
1,
1,
1,
1,
1,
1,
1,
1,
1,
1,
1,
1,
1,
1,
1,
1,
1,
1,
1,
1,
1,
1,
1,
1,
1,
1,
1,
1,
1,
1,
1,
1,
1,
1
] |
NCT02262806
|
35:73:treatment
|
Documented metabolic benefit from prior or current metreleptin treatment
| 3
|
[
"Documented",
"metabolic",
"benefit",
"from",
"prior",
"or",
"current",
"metreleptin",
"treatment"
] |
[
0,
0,
0,
0,
1,
1,
1,
1,
1
] |
NCT02359253
|
1:8:chronic_disease
|
Apraxia
| 3
|
[
"Apraxia"
] |
[
2
] |
NCT02501096
|
1:17:chronic_disease,8:17:chronic_disease,43:61:treatment
|
Active infection (any infection requiring systemic treatment)
| 3
|
[
"Active",
"infection",
"(",
"any",
"infection",
"requiring",
"systemic",
"treatment",
")"
] |
[
2,
2,
0,
0,
0,
0,
1,
1,
0
] |
NCT01500551
|
25:28:chronic_disease
|
Pediatric subjects with JIA
| 3
|
[
"Pediatric",
"subjects",
"with",
"JIA"
] |
[
0,
0,
0,
2
] |
NCT02506192
|
1:13:chronic_disease
|
Pericarditis
| 3
|
[
"Pericarditis"
] |
[
2
] |
NCT01570816
|
1:19:chronic_disease
|
cardiac arrythmias
| 3
|
[
"cardiac",
"arrythmias"
] |
[
2,
2
] |
NCT02171104
|
14:23:chronic_disease,25:31:chronic_disease,35:51:chronic_disease,62:65:chronic_disease,77:93:chronic_disease,99:110:chronic_disease,
|
Uncontrolled bacterial, fungal or viral infections including HIV (including active infection with Aspergillus or other mold within 30 days)
| 3
|
[
"Uncontrolled",
"bacterial",
",",
"fungal",
"or",
"viral",
"infections",
"including",
"HIV",
"(",
"including",
"active",
"infection",
"with",
"Aspergillus",
"or",
"other",
"mold",
"within",
"30",
"days",
")"
] |
[
0,
2,
0,
2,
0,
2,
2,
0,
2,
0,
0,
2,
2,
0,
2,
0,
0,
0,
0,
0,
0,
0
] |
NCT02319369
|
14:60:treatment,,97:105:treatment,113:148:treatment,205:209:chronic_disease,218:234:treatment,,,374:410:treatment
|
Has received Hematopoietic Stem Cell Transplantation (HSCT) within 60 days of the first dose of DS-3032b, is on immunosuppressive therapy post-HSCT at the time of screening, or has clinically significant GVHD (use of topical steroids for ongoing skin GVHD will be permitted). Has a washout period of ≥ 2 weeks or at least 4 half-lives (whichever is longer) from their last systemic immunosuppressive treatment for GVHD
| 3
|
[
"Has",
"received",
"Hematopoietic",
"Stem",
"Cell",
"Transplantation",
"(",
"HSCT",
")",
"within",
"60",
"days",
"of",
"the",
"first",
"dose",
"of",
"DS-3032b",
",",
"is",
"on",
"immunosuppressive",
"therapy",
"post-HSCT",
"at",
"the",
"time",
"of",
"screening",
",",
"or",
"has",
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"significant",
"GVHD",
"(",
"use",
"of",
"topical",
"steroids",
"for",
"ongoing",
"skin",
"GVHD",
"will",
"be",
"permitted",
")",
".",
"Has",
"a",
"washout",
"period",
"of",
"≥",
"2",
"weeks",
"or",
"at",
"least",
"4",
"half-lives",
"(",
"whichever",
"is",
"longer",
")",
"from",
"their",
"last",
"systemic",
"immunosuppressive",
"treatment",
"for",
"GVHD"
] |
[
0,
0,
1,
1,
1,
1,
1,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
1,
0,
0,
0,
1,
1,
1,
0,
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0,
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0,
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0,
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0,
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0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
1,
1,
1,
0,
0
] |
NCT01896999
|
6:32:chronic_disease
|
have primary refractory disease
| 3
|
[
"have",
"primary",
"refractory",
"disease"
] |
[
0,
2,
2,
2
] |
NCT03104699
|
12:32:treatment,
|
use of any investigational drug within 28 days before start of trial treatment
| 3
|
[
"use",
"of",
"any",
"investigational",
"drug",
"within",
"28",
"days",
"before",
"start",
"of",
"trial",
"treatment"
] |
[
0,
0,
0,
1,
1,
0,
0,
0,
0,
0,
0,
0,
0
] |
NCT03058679
|
55:76:treatment,78:97:treatment,99:126:treatment,128:147:treatment,151:162:treatment,
|
Start or change*** dose of anti-TNF agents (including infliximab (Remicade), adalimumab (Humira), certolizumab pegol (Cimzia), golimumab (Simponi) or ustekinumab within 8 weeks prior to screening
| 3
|
[
"Start",
"or",
"change",
"*",
"*",
"*",
"dose",
"of",
"anti-TNF",
"agents",
"(",
"including",
"infliximab",
"(",
"Remicade",
")",
",",
"adalimumab",
"(",
"Humira",
")",
",",
"certolizumab",
"pegol",
"(",
"Cimzia",
")",
",",
"golimumab",
"(",
"Simponi",
")",
"or",
"ustekinumab",
"within",
"8",
"weeks",
"prior",
"to",
"screening"
] |
[
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
1,
1,
0,
0,
0,
1,
1,
0,
0,
0,
1,
1,
1,
0,
0,
0,
1,
1,
0,
0,
0,
1,
0,
0,
0,
0,
0,
0
] |
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