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NCT02315196 | ,,58:71:cancer | Life expectancy >= 52 weeks excluding their diagnosis of breast cancer | 1 | [
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NCT02204098 | 51:64:cancer | Newly diagnosed histologically confirmed invasive breast cancer | 1 | [
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NCT02106598 | 1:14:cancer | breast cancer patients in whom SLN mapping is indicated | 1 | [
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NCT02095184 | 21:34:cancer,,,, | Unresected operable breast cancer stage I-III with primary tumor ≥ 2.0 cm | 1 | [
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NCT02068092 | 183:196:cancer | A known deleterious mutation in BRCA1, BRCA2, PTEN, or TP53. (Note: The participant must be a documented carrier to meet this criterion. If there is a known mutation in a hereditary breast cancer susceptibility gene in a participant's family member, the participant herself must have undergone genetic testing as per National Comprehensive Cancer Network guidelines to be eligible per this criterion.) | 1 | [
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NCT01953588 | 10:23:cancer,,,,,, | Invasive breast cancer is estrogen receptor positive with an Allred score of 6, 7 or 8 by local institution standard protocol. If an Allred Score is not reported on the diagnostic pathology report, ER positivity in > 66% cells | 1 | [
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NCT01912612 | ,,26:39:cancer, | Diagnosis of stage 0-III breast cancer within 12 years prior to enrollment | 1 | [
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NCT01912612 | 39:52:cancer | Pain that developed or worsened since breast cancer diagnosis and is not due to identifiable traumatic event or fracture | 1 | [
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NCT01905046 | 31:44:cancer | Must be at increased risk for breast cancer | 1 | [
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NCT01755208 | 22:35:cancer,,, | Participants who are breast cancer free (mammogram negative within 1 month of testing) with the absence of clinical suspicion of breast cancer on physical exam or with clinical stage II or stage III breast cancer | 1 | [
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NCT01622868 | 79:92:cancer | Pathologically (histologically or cytologically) proven diagnosis of invasive breast cancer | 1 | [
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NCT01591356 | 1:14:cancer | breast cancer are not exclusionary | 1 | [
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NCT01570998 | 30:43:cancer | Axillary lymph node positive breast cancer | 1 | [
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NCT00948285 | 17:30:cancer | Newly diagnosed breast cancer patients | 1 | [
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NCT00948285 | 15:28:cancer,,, | Patients with breast cancer diagnosis during pregnancy (women who could bear children must have a negative pregnancy test before beginning this study) | 1 | [
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NCT00924027 | ,20:33:cancer | male patients with breast cancer | 1 | [
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NCT00909909 | 26:39:cancer | Histologically confirmed breast cancer | 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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NCT02581982 | ,,,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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NCT02541565 | ,,,149:159:treatment | Female subject of childbearing potential should have a negative urine or serum pregnancy within 72 hours prior to receiving the first dose of study medication | 1 | [
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NCT02535533 | ,,71:81:treatment | Pre-existing uncontrolled hypertension defined as > 150/90 mm Hg with medication | 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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NCT02527265 | 32:42:treatment | Any disease or exposure to any medication which, in the judgment of the principal Investigator, may impact glucose metabolism | 1 | [
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NCT02502253 | 87:97:treatment | Deemed too unstable medically or neurologically to safely enroll in trial of research medication | 1 | [
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NCT02446457 | ,,106:116:treatment | have a negative urine or serum pregnancy test within 72 hours prior to receiving the first dose of study medication | 1 | [
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NCT02440815 | 42:52:treatment | Acute or uncontrolled medical illness or medication use impacting cognitive function | 1 | [
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NCT02437773 | 16:26:treatment | Not taking any medication, prescription or non-prescription, with psychotropic effects | 1 | [
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NCT02437370 | ,,,,149:159:treatment | Female subject of childbearing potential should have a negative urine or serum pregnancy within 72 hours prior to receiving the first dose of study medication; if the urine test is positive or cannot be confirmed as negative, a serum pregnancy test will be required | 1 | [
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NCT02433977 | 138:148:treatment | Any other condition and/or situation that causes the investigator to deem a subject unsuitable for the study (e.g. due to expected study medication non-compliance, inability to medically tolerate the study procedures, or a subject's unwillingness to comply with study-related procedures | 1 | [
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NCT02427997 | 1:11:treatment | medication regime is likely to change during the course of the study | 1 | [
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NCT02407171 | ,,131:141:treatment | childbearing potential should have a negative urine or serum pregnancy within 72 hours prior to receiving the first dose of study medication | 1 | [
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NCT02378714 | ,,171:181:treatment, | women of childbearing potential must agree to use a medically acceptable method of birth control or abstain from sexual intercourse during the time they are taking study medication and for at least one month after the medication period ends | 1 | [
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NCT02340156 | ,,73:83:treatment | Have diastolic blood pressure of > 90 mm Hg resting at baseline despite medication | 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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NCT02332668 | ,60:70:treatment | within 72 hours prior to receiving the first dose of study medication | 1 | [
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NCT02321501 | ,,,143:153:treatment,, | Negative serum or urine pregnancy test beta-Human Chorionic Gonadotropin (beta hCG) within 2 weeks prior to receiving the first dose of study medication for women of childbearing age | 1 | [
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NCT02302976 | 20:30:treatment | current use of any medication (prescription or over-the-counter) determined to cause potential drug interactions by the study physicians | 1 | [
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NCT02266004 | 8:18:treatment | Stable medication regimen | 1 | [
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NCT02234934 | 53:63:treatment | Contraindication for administration of conditioning medication | 1 | [
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NCT02234934 | 54:64:treatment | patients with a correctable deficiency controlled on medication | 1 | [
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NCT02193490 | ,,94:104:treatment | negative urine pregnancy test is required within 14 days of receiving her first dose of test medication (placebo/ study drug) along with definite evidence of contraceptive use during the duration of the study | 1 | [
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NCT02178566 | ,,,125:135:treatment | Women of childbearing potential must use a reliable method of contraception from screening until 1 month after end of study medication | 1 | [
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NCT02124772 | 98:108:treatment | Able to swallow and retain enterally (per oral [PO] or nasogastric or gastric tube) administered medication | 1 | [
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NCT02070549 | 29:39:treatment | Current use of a prohibited medication | 1 | [
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NCT02044120 | ,,,191:201:treatment | Females of childbearing potential as well as males and their partners must agree to use an effective form of contraception during the study and for 6 months following the last dose of study medication | 1 | [
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NCT02003222 | 64:74:treatment | Patients must be considered reliable enough to comply with the medication regimen and follow-up, and have social support necessary to allow this compliance | 1 | [
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NCT01954316 | ,,,194:204:treatment | Women and men of child producing potential must agree to use highly effective means of contraception during study participation, and for at least 30 days after the last administration of study medication | 1 | [
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NCT01943851 | ,,,102:112:treatment | Female subjects must agree to use contraception until at least 7 months after the last dose of study medication | 1 | [
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NCT01943851 | 67:77:treatment | This method must be used from the time of the first dose of study medication until 16 weeks after the last dose of study medication | 1 | [
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NCT01943851 | ,56:66:treatment | any subject who is expected to require a QT prolonging medication while on trial should not be enrolled | 1 | [
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NCT01676753 | ,,,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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NCT01438073 | 17:27:treatment | no history of a medication reaction requiring emergency medical care | 1 | [
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NCT00147056 | ,,23:33:treatment | diastolic BP > 100 on medication | 1 | [
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NCT02169739 | 1:33:treatment,,112:120:chronic_disease | Diffusion-weighted imaging (DWI) lesion < 2.0cm in size at largest dimension and corresponding to the clinical syndrome | 1 | [
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NCT02110992 | 1:8:treatment,12:24:treatment, | Surgery or chemotherapy within 4 weeks | 1 | [
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NCT03038620 | 1:8:treatment | Surgery scheduled for the trial duration period | 1 | [
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NCT02606045 | 1:8:treatment, | Surgery within the past 8 weeks | 1 | [
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NCT02204098 | 1:8:treatment | Surgery | 1 | [
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NCT03181126 | ,73:85:treatment | Refractory is defined as persistent disease after at least 2 courses of chemotherapy | 1 | [
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NCT03153410 | 33:45:treatment, | Must have received last dose of chemotherapy at least 14 days or longer prior to entry into the study | 1 | [
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NCT03139227 | ,,47:59:treatment | Must be > 1 year from pregnancy, lactation or chemotherapy | 1 | [
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NCT03088709 | ,78:90:treatment | Less than twenty-one days have elapsed since the subject's last radiation or chemotherapy prior to conditioning | 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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NCT02912572 | 33:45:treatment | patients who have only received chemotherapy in the adjuvant setting | 1 | [
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NCT02862938 | 19:31:treatment | Participant is on chemotherapy | 1 | [
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NCT02774421 | 28:40:treatment | who have been treated with chemotherapy at time of recurrence | 1 | [
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NCT02759146 | 12:24:treatment | Undergoing chemotherapy | 1 | [
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NCT02658565 | 23:35:treatment | Patients who received chemotherapy directed at the present disease | 1 | [
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NCT02639208 | 79:91:treatment | either in the context of standard treatment or a clinical trial and including chemotherapy | 1 | [
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NCT02603757 | 29:41:treatment | Patients who do not undergo chemotherapy | 1 | [
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NCT02589938 | 11:23:treatment | Receiving chemotherapy during study period | 1 | [
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NCT02565498 | 9:21:treatment | Planned chemotherapy for (neo)adjuvant treatment | 1 | [
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NCT02562716 | ,,,151:163:treatment | women/men of reproductive potential must have agreed to use an effective contraceptive method for up to 3 months after the final administered dose of chemotherapy | 1 | [
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NCT02536794 | 23:35:treatment | Patients who have had chemotherapy | 1 | [
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NCT02536794 | ,36:48:treatment | have received at least one line of chemotherapy in the metastatic setting | 1 | [
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NCT02492867 | 37:49:treatment | Patients cannot tolerate concurrent chemotherapy | 1 | [
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NCT02481765 | 66:78:treatment | Intensive medical treatment means that the subject is undergoing chemotherapy for a hematologic/oncologic condition, is carrying a pacemaker or has been diagnosed with a cardiac anomaly which causes cardiac insufficiency not compensated with medications | 1 | [
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