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NCT02351544 | 70:77:treatment,79:102:chronic_disease,117:134:chronic_disease | Patients with systemic conditions that make them poor candidates for surgery (coronary artery disease, uncontrolled diabetes mellitus, etc…) | 1 | [
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NCT02451423 | ,,16:26:chronic_disease | CTCAE Gr >/= 2 neuropathy | 1 | [
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NCT01659203 | 27:44:allergy_name | History of sensitivity to radiation therapy | 1 | [
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NCT02383927 | ,,25:35:chronic_disease | Non-tolerable > Grade 2 neuropathy | 1 | [
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NCT01389024 | ,24:27:treatment,24:35:treatment,,,72:93:treatment, | History of two or more TCD studies with a velocity ≥ 200 cm/sec by the non-imaging technique, or ≥185 cm/sec for the imaging technique or a indeterminate TCD | 1 | [
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NCT02150967 | 11:25:treatment | selective FGFR inhibitor (Cohorts 1 and 2 only) | 1 | [
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NCT02329327 | 1:15:chronic_disease | Acute bleeding in a critical area or organ such as intraspinal, pericardial, or intracranial | 1 | [
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NCT02527421 | 15:24:chronic_disease,, | Subjects with psoriasis involving ≥ 10% BSA | 1 | [
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NCT02339922 | ,65:74:treatment | Male patients, even if surgically sterilized (i.e., status post-vasectomy), must agree to one of the following | 1 | [
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NCT02877134 | ,,,,177:188:treatment,219:228:chronic_disease,,337:347:cancer | A participant who has had extensive colitis for greater than or equal to (>=) 8 years, or disease limited to the left side of the colon for >= 12 years, must either have had a colonoscopy to assess for the presence of dysplasia within 1 year before the first administration of study agent or a colonoscopy to assess for the presence of malignancy at the screening visit, with no evidence of malignancy | 1 | [
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NCT01554371 | 20:35:treatment | Concomitant use of bisphosphonates | 1 | [
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NCT02979366 | 11:31:chronic_disease | active or chronic pancreatitis | 1 | [
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NCT02923921 | 32:70:chronic_disease,79:97:chronic_disease,99:113:chronic_disease,117:147:chronic_disease | Participants with a history of immune-mediated neurological disorders such as multiple sclerosis, Guillain-Barré or inflammatory CNS/PNS disorders | 1 | [
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NCT02538198 | 15:27:treatment,55:62:treatment,,255:275:treatment | Refractory to lenalidomide in the most recent line of therapy, as defined by the International Myeloma Consensus Panel criteria [47]- as failure to achieve minimal response or development of progressive disease while on lenalidomide or within 30 days of lenalidomide therapy | 1 | [
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NCT02837510 | 5:20:chronic_disease | any Axis 1 disorder | 1 | [
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NCT02544880 | 29:34:cancer | Recurrent or second primary HNSCC arises within the previously irradiated field | 1 | [
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NCT03143894 | 1:11:chronic_disease,15:22:chronic_disease,52:77:treatment,82:92:chronic_disease, | Depression or anxiety as defined either by ongoing pharmacological treatment for depression or anxiety or a HADS score on initial screening | 1 | [
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NCT03088033 | ,,,107:135:chronic_disease,128:135:chronic_disease,137:146:chronic_disease, | NYHA class II with a history of > NYHA class II; OR NYHA class III, or ambulatory NYHA class IV symptoms (paroxysmal nocturnal dyspnea, orthopnea, dyspnea on mild or moderate exertion) at screening; or signs (any rales post cough, chest x-ray demonstrating pulmonary congestion,) within past 12 months | 1 | [
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NCT02524379 | 17:20:chronic_disease,,, | Non-penetrating SCI at neurologic level from C2 to C8 | 1 | [
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NCT02020018 | 1:8:treatment | Steroid-dependent patients | 1 | [
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NCT02977468 | 16:28:treatment, | Has received a live vaccine within 30 days of planned start of study therapy | 1 | [
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NCT02343549 | ,,,113:122:treatment | Participants of childbearing age must use effective contraception for at least 6 months following completion of treatment | 1 | [
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NCT02744391 | 21:46:chronic_disease,48:57:chronic_disease,62:72:chronic_disease | DSM 5 non-psychotic Major Depressive Disorder, Dysthymia, or Depression Not Otherwise Specified | 1 | [
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NCT03131960 | 1:27:chronic_disease,, | Severe or worse depression (Beck Depression Scale > 29) | 1 | [
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NCT03004807 | 1:10:chronic_disease | Dysphagia or difficulty swallowing | 1 | [
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NCT03101566 | 26:38:treatment, | Must not have received a live vaccine within 30 days of planned start of the study therapy | 1 | [
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NCT02583893 | 13:37:chronic_disease | symptomatic congestive heart failure | 1 | [
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NCT03135171 | ,,127:138:treatment,140:151:treatment,156:166:treatment | must use two forms of effective contraception during the duration of the trial and for minimum of 7 months after last dose of tocilizumab, trastuzumab, or pertuzumab | 1 | [
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NCT03118973 | 1:30:treatment,36:60:treatment,62:89:treatment | Complex post-surgical anatomy e.g. Billroth type II anatomy, Roux-en-Y-gastrojejunostomy | 1 | [
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NCT03143985 | 13:22:chronic_disease | Presence of aneurisms of the ascending aorta or aortic stress | 1 | [
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NCT02091141 | 32:59:treatment,41:59:treatment,52:59:treatment,75:81:cancer,98:104:cancer,218:227:treatment,284:293:treatment | Participants who have received standard first-line therapy for metastatic cancer (except for the tumors for which no first-line therapy exists) and in whom a trial of targeted therapy is considered the best available treatment option. Eligible participants should not have available therapies that will convey clinical benefit and/or are not suitable options per the treating physician's judgment | 1 | [
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NCT02474927 | 1:12:chronic_disease | Neutropenia | 1 | [
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NCT02781519 | 8:28:treatment,, | taking estrogen supplements or oral contraceptive pills (for women) | 1 | [
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NCT02047474 | 16:39:chronic_disease,43:66:treatment,68:76:treatment,81:92:treatment,171:181:cancer | No evidence of extrapancreatic disease by cross sectional imaging, PET scan, or laparoscopy, including nodal involvement beyond the peripancreatic tissues and/or distant metastases | 1 | [
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NCT02403193 | ,,,,174:183:treatment, | Women of child-bearing potential, defined as all women physiologically capable of becoming pregnant, must use 2 highly effective methods of contraception while taking study treatment and for 90 days after the last dose of study treatment | 1 | [
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NCT02188745 | 1:19:chronic_disease | pulmonary embolism | 1 | [
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NCT03116685 | 54:77:treatment,79:87:treatment,,154:157:treatment,198:223:treatment | Participation in any interventional study of another investigational product, biologic, device, or other agent within 60 days prior to the first dose of OC5 or not willing to forego other forms of investigational treatment during this study | 1 | [
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NCT01983462 | 12:34:chronic_disease,43:60:treatment,61:84:treatment,86:107:chronic_disease,109:115:chronic_disease,117:130:chronic_disease,,,188:202:chronic_disease,204:226:chronic_disease,244:265:treatment,267:293:chronic_disease | History of cardiovascular disease such as heart angioplasty/stent or bypass surgery, myocardial infarction, stroke, heart failure with or without left ventricular ejection fraction <40%, cardiomyopathy, valvular heart disease, cardiomyopathy, heart transplantation, Type 2 and Type 1 diabetes | 1 | [
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NCT02338232 | 17:31:treatment,33:54:treatment,59:73:treatment,88:115:treatment,200:219:treatment | Subjects taking ACE inhibitors, potassium supplements, or spironolactone (or any other potassium-sparing diuretics) who cannot discontinue use prior to initiation of study treatment OR who require a high-potassium diet | 1 | [
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NCT02273375 | 33:42:treatment | Patients must be accessible for treatment and follow-up | 1 | [
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NCT01419561 | 33:37:chronic_disease,, | Immunohistochemical evidence of KSHV in tissues (for example by staining for LANA or vIL-6). Confirmed in the Laboratory of Pathology, CCR, NCI | 1 | [
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NCT03188042 | 21:38:allergy_name | Photosensitivity to flickering lights | 1 | [
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NCT02148796 | 1:13:chronic_disease | tuberculosis | 1 | [
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NCT02570854 | 20:35:chronic_disease,37:59:cancer,61:81:cancer,85:109:cancer | Known diagnosis of hemochromatosis, bone marrow malignancy, lymphatic malignancy or myelodysplastic syndrome | 1 | [
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NCT01925573 | 58:70:treatment | 6 weeks since the completion of a nitrosourea-containing chemotherapy regimen | 1 | [
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NCT02516969 | 1:37:treatment,30:37:treatment,95:101:treatment,105:115:treatment | Macroscopic complete salvage surgery with curative intent (surgery was not performed only for biopsy or palliation) | 1 | [
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NCT02796391 | 1:21:treatment | Clopidogrel (Plavix) | 1 | [
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NCT02434809 | 16:27:cancer | Patients whose lung tumors are being monitored by MR imaging as part of standard clinical care | 1 | [
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NCT02741791 | 51:76:treatment | History of inadequate response to 1 or 2 adequate antidepressant treatments | 1 | [
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NCT02115295 | 26:60:treatment,65:73:treatment,75:88:treatment,94:105:treatment,107:135:treatment,137:148:treatment,150:160:treatment,162:166:treatment,,,271:284:cancer,316:343:cancer,379:392:cancer | For Frontline cohort: No prior potentially-curative therapy for leukemia. Prior therapy with hydroxyurea, hematopoietic growth factors, azacytidine, decitabine, ATRA, or a total dose of cytarabine up to 2g (for emergency use for stabilization) is allowed. Patients with secondary AMLwho have been treated for their antecedent myeloid neoplasm will be enrolled into the separate Secondary AML cohort | 1 | [
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NCT01734512 | 29:71:treatment, | Patients should not receive immunization with attenuated live vaccines within one week of study entry or during study period | 1 | [
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NCT02303977 | ,,109:118:treatment | Women of childbearing potential and sexually active males must use an effective contraception method during treatment and for three months after completing treatment | 1 | [
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NCT02551679 | 1:7:chronic_disease | Anemia | 1 | [
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NCT02466685 | 12:18:chronic_disease,20:32:cancer,33:71:chronic_disease,105:127:chronic_disease, | History of stroke, brain tumor, head trauma with loss of consciousness, or other clinically significant neurological condition within 12 months before screening | 1 | [
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NCT02541565 | ,,88:96:cancer | Absolute neutrophil count (ANC) >= 1,500/mcL except in cases of marrow infiltration by lymphoma | 1 | [
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NCT03134274 | 6:14:chronic_disease | Have dementia | 1 | [
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NCT02392572 | 19:34:treatment,,103:119:treatment,,149:168:treatment | The interval from prior treatment to time of study drug administration should be at least 2 weeks for cytotoxic agents or at least 5 half-lives for noncytotoxic agents | 1 | [
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NCT02762006 | 12:41:chronic_disease | History of leptomeningeal carcinomatosis | 1 | [
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NCT02342782 | 67:77:treatment | Bone marrow (BM) harvest required to reach adequate cell dose for transplant | 1 | [
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NCT02394535 | 17:25:treatment | low dose (1 mg) Coumadin is allowed | 1 | [
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NCT02472834 | 1:4:chronic_disease | HIV positive | 1 | [
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NCT02461927 | 1:7:treatment,,54:75:treatment,90:96:treatment | Opioid use within 10 days prior to study medication (injectable naltrexone) or risks for opioid use during the study | 1 | [
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NCT02389309 | 1:15:treatment,16:30:treatment,44:90:treatment,97:105:treatment,107:135:treatment | Anticoagulants/anti-platelets: patients on therapeutic (treatment) dose of anticoagulants (e.g. warfarin, low molecular-weight heparin) | 1 | [
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NCT02315612 | 15:26:chronic_disease | Subjects with CNS disease | 1 | [
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NCT02120222 | 69:92:chronic_disease,96:111:treatment,129:167:chronic_disease,184:221:chronic_disease,222:254:chronic_disease | Uncontrolled clinically significant conduction abnormalities (e.g.: ventricular tachycardia on antiarrhythmics are excluded and 1st degree atrioventricular (AV) block or asymptomatic left anterior fascicular block [LAFB]/right bundle branch block [RBBB] | 1 | [
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NCT00632853 | 115:127:treatment | patients also must have met all of the eligibility criteria in the protocol prior to receiving the first cycle of chemotherapy | 1 | [
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NCT03032705 | 5:26:treatment, | Any restorative treatment of the teeth involved in the study in the last 12 months | 1 | [
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