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NCT02394028 | 1:35:chronic_disease | human immunodeficiency virus (HIV) | 1 | [
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NCT02929069 | 1:4:chronic_disease,, | HIV sexual risk (≥1 act of condomless anal with a male partner of unknown status or HIV+ status, unless with HIV+ partner with known undetectable viral load) | 1 | [
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NCT02303977 | 110:119:treatment | Patients must be capable of giving informed consent and be willing and able to comply with scheduled visits, treatment plan and laboratory testing | 1 | [
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NCT03114319 | 8:16:chronic_disease | Active diarrhea | 1 | [
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NCT02592551 | 9:28:treatment,33:36:cancer,38:70:treatment,74:109:treatment | Planned resectional surgery for MPM [extrapleural pneumonectomy (EPP) or pleurectomy and decortication (P/D)] | 1 | [
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NCT01238120 | 63:75:treatment | Patients with a neutropenic episode during the first cycle of chemotherapy or at high risk for a neutropenic episode during future chemotherapy cycles at the treating physicians discretion | 1 | [
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NCT01849146 | ,18:90:treatment | 4 weeks from any investigational (not Food and Drug Administration [FDA]-approved) agents | 1 | [
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NCT01686373 | 12:25:treatment | History of brain surgery | 1 | [
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NCT02437370 | ,,,233:243:treatment, | Female subjects of childbearing potential should be willing to use 2 methods of birth control or be surgically sterile, or abstain from heterosexual activity for the course of the study through 120 days after the last dose of study medication; subjects of childbearing potential are those who have not been surgically sterilized or have not been free from menses for > 1 year | 1 | [
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NCT03144245 | 52:63:treatment | patients with excessive blasts may be treated with hydroxyurea to bring counts down | 1 | [
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NCT02562430 | 1:20:chronic_disease | psychotic disorders | 1 | [
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NCT01807897 | 19:27:chronic_disease,, | Poorly controlled diabetes (HbA1c > 9.0) | 1 | [
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NCT02793921 | 14:24:chronic_disease | uncontrolled arrhythmia | 1 | [
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NCT03116685 | 20:30:treatment, | Patients receiving vitamin B6 must be receiving a stable dose for at least 3 months prior to screening and must not change the dose during the study | 1 | [
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NCT02078102 | ,45:67:treatment,79:89:treatment,91:105:treatment,107:125:treatment,131:145:treatment,151:173:treatment,185:197:treatment,201:213:treatment,250:259:treatment | Patients must be at least 4 weeks from last cytotoxic chemotherapy (including alkylating, anthracyclines, epipodophylatoxins, and platinum drugs), or immunomodulatory drugs (including lenalidomide or pomalidomide, or related derivatives) at time of treatment on this protocol | 1 | [
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NCT03069716 | 16:26:chronic_disease,28:37:chronic_disease,54:79:chronic_disease,99:136:chronic_disease | Diagnosed with idiopathic, heritable, or associated (connective tissue disease, drugs, or toxins) pulmonary arterial hypertension (PAH) according to World Health Organization consensus recommendations | 1 | [
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NCT02603757 | 29:41:treatment | Patients who do not undergo chemotherapy | 1 | [
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NCT02451215 | 17:27:cancer | Other low-grade CNS tumors | 1 | [
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NCT02503722 | ,,,99:118:treatment | Women under 50 years must be postmenopausal for at least 12 months following the end of exogenous hormonal treatments and with LH and FSH levels in the post-menopausal range for the institution | 1 | [
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NCT02527421 | 1:34:treatment,42:63:treatment,65:78:treatment,80:93:treatment | systemic anti-inflammatory agents (e.g., mycophenolate mofetil, sulfasalazine, 6-thioguanine) | 1 | [
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NCT00492778 | 23:35:treatment | Patients who received chemotherapy directed at the present recurrence | 1 | [
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NCT02139436 | 27:30:treatment | leg muscles responsive to FES | 1 | [
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NCT02418195 | 12:24:chronic_disease | Autoimmune polymyositis | 1 | [
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NCT02085941 | 35:44:treatment,54:63:treatment,65:77:treatment,79:86:treatment | must have sustained all available treatment options (radiation, chemotherapy, surgery) as verified by the Dana Farber Cancer Institute's Head and Neck Tumor Board | 1 | [
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NCT01943851 | ,73:82:treatment | at least 28 days (whichever is longer) following the last dose of study treatment | 1 | [
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NCT01757418 | 25:44:chronic_disease,46:48:chronic_disease,52:76:chronic_disease | Documented diagnosis of sickle cell disease (SS or S-β thalassemia genotype) | 1 | [
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NCT02451553 | 1:31:treatment,33:42:treatment,46:81:treatment,83:92:treatment,97:108:treatment | Prior treatment with erlotinib, gefitinib or EGFR-blocking monoclonal antibodies (cetuximab and panitumumab) | 1 | [
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NCT02324582 | 12:46:chronic_disease, | history of Human Immunodeficiency Virus (HIV) (HIV 1/2 antibodies) | 1 | [
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NCT02624258 | 14:30:chronic_disease | Uncontrolled active infection | 1 | [
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NCT01931202 | 44:56:allergy_name | history of allergic or adverse reaction to escitalopram | 1 | [
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NCT02203695 | 25:35:cancer | Currently active second malignancy | 1 | [
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NCT01703949 | ,63:75:treatment | Patients must be anticipated to complete at least 2 cycles of chemotherapy on study | 1 | [
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NCT02606396 | 20:40:chronic_disease | Prior diagnosis of esophageal achalasia | 1 | [
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NCT02245841 | 44:52:chronic_disease | Patients with clear features of an overlap myositis | 1 | [
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NCT03104699 | 1:45:cancer | basal or squamous cell carcinoma of the skin | 1 | [
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NCT01389024 | 7:51:chronic_disease | Known human immunodeficiency virus (HIV) infection | 1 | [
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NCT02481245 | 19:33:treatment,35:42:treatment,48:62:treatment | Current use of of MAO Inhibitors, statins, and anticoagulants | 1 | [
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NCT02353728 | 1:44:treatment, | Treatment with other investigational agents within 30 days of Day 1 | 1 | [
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NCT02828618 | 1:17:cancer | liver metastasis or bulky lymph-nodes in the mediastinum in CT chest and abdomen/pelvis | 1 | [
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NCT02991651 | 25:55:treatment | Prior treatment with an EGFR tyrosine kinase inhibitor | 1 | [
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NCT02798458 | 14:22:chronic_disease,, | Uncontrolled diabetes with a hemoglobin A1C greater than 10 | 1 | [
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NCT02358187 | 58:78:chronic_disease,89:98:treatment,102:127:treatment | Patients must not have a history of, or currently active autoimmune disorders requiring cytotoxic or immunosuppressive therapy, or autoimmune disorders with visceral involvement | 1 | [
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NCT02977468 | ,,,176:186:treatment | Female subjects of childbearing potential must be willing to use an adequate method of contraception for the course of the study through 120 days after the last dose of study medication | 1 | [
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NCT02807272 | 1:19:chronic_disease,20:44:chronic_disease,56:60:cancer | Myeloproliferative/myelodysplastic syndrome other than CMML | 1 | [
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NCT02389309 | 36:51:treatment,55:75:treatment,127:139:chronic_disease | patients must not be receiving any anti-thrombotic or anti-platelet agents; patient cannot be on drugs that cause significant prolonged QT (category I drug) | 1 | [
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NCT00959140 | 1:4:cancer,20:29:treatment,34:49:treatment | ALL: Refractory to Induction and salvage therapy | 1 | [
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NCT02409888 | 47:80:treatment | individuals reporting current enrollment in a substance abuse treatment program | 1 | [
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NCT03158974 | 28:38:cancer, | Have evidence of an active malignancy or have been immunocompromised within the 60 days prior to Screening | 1 | [
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NCT01827384 | 29:38:treatment,48:62:treatment,83:95:treatment | Patients who have had prior treatment with any PARP inhibitor in combination with temozolomide | 1 | [
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NCT02067819 | 7:27:chronic_disease,110:119:chronic_disease,121:126:chronic_disease,128:138:chronic_disease,164:168:chronic_disease,170:176:chronic_disease,181:214:chronic_disease | Major psychiatric disorder at screening that would preclude full participation in study procedures including psychosis, mania, depression, untreated combined type ADHD, autism and pervasive developmental disorders | 1 | [
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NCT01967238 | 13:28:chronic_disease,30:42:treatment,46:67:treatment | (either the influenza virus, pneumococcal or meningococcal vaccine) | 1 | [
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NCT02913430 | 29:41:treatment | More than one prior line of chemotherapy in the metastatic setting | 1 | [
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NCT02274116 | 1:30:chronic_disease | cardiopulmonary complications | 1 | [
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NCT01676259 | 35:47:chronic_disease | History of clinically significant coagulopathy | 1 | [
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NCT01906385 | 33:45:chronic_disease, | History or clinical evidence of pancreatitis within 2 years | 1 | [
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NCT02793921 | 28:41:cancer | Medical clearance by their breast cancer surgeon | 1 | [
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NCT02532543 | 25:35:treatment | Use of any substance or medication that will influence bone metabolism | 1 | [
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NCT00929006 | 1:8:chronic_disease,39:53:chronic_disease,57:73:chronic_disease | Obesity resulting from a well-defined endocrinopathy or genetic syndrome | 1 | [
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NCT02954185 | 1:20:treatment | Cortisone injection | 1 | [
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NCT02471430 | 25:47:chronic_disease | No evidence of clinical coronary heart disease | 1 | [
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NCT02131597 | 16:31:cancer,169:185:treatment,210:231:treatment | organ-confined prostate cancer with no evidence of recurrent or progressive disease based on prostate-specific antigen (PSA) values are also eligible for this study if hormonal therapy has been initiated or a radical prostatectomy has been performed | 1 | [
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NCT03137082 | 26:54:chronic_disease | Having any other current Axis I psychiatric disorders or medical conditions requiring treatment or medication | 1 | [
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NCT01306019 | 30:63:treatment,,, | demonstrated requirement for intravenous gamma globulin (IVIG) (significant drop over 3 to 6 weeks between peak and trough IgG levels) | 1 | [
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NCT01925131 | 75:106:allergy_name | Patients with a history of a serious allergic or anaphylactic reaction to humanized monoclonal antibodies are not eligible | 1 | [
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NCT03089125 | 1:36:chronic_disease | Cognitive or psychiatric conditions prohibiting study consent or participation | 1 | [
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NCT02519322 | ,,87:111:cancer | Patients must have histologically or cytologically confirmed stage IIIB/C or stage IV oligometastatic melanoma | 1 | [
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NCT02347891 | 17:51:treatment,, | Have received a non-biologic investigational agent within 30 days or 5 half-lives of the agent (whichever is longer) prior to Screening | 1 | [
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NCT00739362 | 12:25:chronic_disease,37:54:chronic_disease,64:76:chronic_disease | History of HIV infection or ongoing chronic infection (such as tuberculosis) | 1 | [
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NCT02514083 | 1:10:treatment,17:20:cancer,34:56:treatment,58:74:treatment,84:98:treatment,100:121:treatment,127:199:treatment | Treatment-naive CLL indicates no prior anti-CLL therapy. Anti-CLL therapy includes chemotherapies, monoclonal antibodies, and targeted agents with known or reasonably expected anti-leukemic activity | 1 | [
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NCT02159495 | 139:185:treatment | In the case of a related donor: The identified donor must be the original donor whose stem cells were used for the research participant's allogeneic stem cell transplantation (alloSCT) | 1 | [
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NCT02639065 | ,,,,216:225:treatment | Females of childbearing potential and males must be willing to use an effective method of contraception (hormonal or barrier method of birth control; abstinence) from the time consent is signed until 12 weeks after treatment discontinuation | 1 | [
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NCT02515110 | 1:13:treatment,,55:67:treatment,72:85:cancer,106:127:treatment | Radiotherapy must begin within 10 weeks following the last surgery for breast cancer or the last dose of adjuvant chemotherapy | 1 | [
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NCT02762006 | 8:26:chronic_disease,84:103:chronic_disease,105:116:chronic_disease,137:171:chronic_disease | active bleeding diathesis including any subject known to have evidence of acute or chronic hepatitis B, hepatitis C (detectable RNA) or human immunodeficiency virus (HIV) | 1 | [
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NCT01648751 | 10:41:treatment, | Previous bilateral salpingo-oophorectomy (women with 1 ovary will be eligible) | 1 | [
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NCT02442102 | ,49:59:treatment | Patient is not expected to require ≥48 hours of intubation | 1 | [
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NCT02535312 | 92:98:treatment | No studies have been performed to assess potential metabolic and transport interactions of TRC102 | 1 | [
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NCT02332668 | ,110:120:treatment | abstain from heterosexual activity for the course of the study through 120 days after the last dose of study medication | 1 | [
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NCT00107289 | 1:24:chronic_disease | grade 3 hearing deficit is acceptable | 1 | [
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NCT02442635 | 11:23:treatment | Receiving Chemotherapy | 1 | [
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NCT02309580 | 1:25:treatment | Systemic corticosteroids are permissible in the following circumstances | 1 | [
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