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NCT02105766 | 8:16:chronic_disease,20:32:treatment | portal fibrosis by liver biopsy | 1 | [
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NCT03008070 | 22:34:treatment | Contra-indication to liver biopsy | 1 | [
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NCT03008070 | ,32:44:treatment,, | Have a stable weight since the liver biopsy was performed defined by no more than a 5 % loss of initial body weight | 1 | [
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NCT03008070 | 26:38:treatment, | Subject agrees to have a liver biopsy performed after 24 weeks of treatment | 1 | [
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NCT02515708 | ,43:55:treatment, | Liver steatosis (on visual estimate or on liver biopsy) > 30% | 1 | [
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NCT02474199 | 85:97:treatment,, | For subjects with elevated liver tests as defined above, local pathology reading of liver biopsy 6-10 days after darTregs infusion is without AR according to Banff criteria | 1 | [
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NCT02474199 | 11:23:treatment | Screening liver biopsy with any of the following histological criteria, as determined by the reading of a central pathologist | 1 | [
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NCT02412540 | ,,42:54:treatment, | Weight reduction of >5% between baseline liver biopsy and enrollment, as weight loss >5% may change NASH severity | 1 | [
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NCT02094794 | 1:22:treatment,26:61:treatment,, | Echocardiogram (ECHO) or multi gated acquisition scan (MUGA): ejection fraction of >= 50% | 1 | [
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NCT02257138 | 85:98:treatment,116:138:treatment | patients with newly diagnosed or previously treated disease are eligible as long as prior therapy does not include hypomethylating agents | 1 | [
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NCT03126110 | ,54:67:treatment | Has not recovered to ≤ Grade 1 from toxic effects of prior therapy | 1 | [
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NCT03104699 | 32:45:treatment,, | Persisting toxicity related to prior therapy of NCI CTCAE grade >1 severity | 1 | [
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NCT03007030 | 13:26:treatment | Any line of prior therapy | 1 | [
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NCT02942095 | 28:41:treatment,, | Patient who were receiving prior therapy will require wash out period of either more than 2 weeks or more than 5 half-lives whichever shorter | 1 | [
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NCT02932280 | 52:65:treatment, | have recovered from the acute toxic effects of all prior therapy to ≤ grade 1 before entering this study | 1 | [
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NCT02912572 | ,,42:55:treatment | Persisting Grade >=2 toxicity related to prior therapy | 1 | [
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NCT02584647 | 11:24:treatment | Allowable prior therapy | 1 | [
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NCT02553460 | 9:22:treatment | Limited prior therapy | 1 | [
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NCT02425904 | 49:62:treatment | There is no limitation of amount or the type of prior therapy or drugs | 1 | [
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NCT02392572 | 51:64:treatment, | Persistent clinically significant toxicities from prior therapy must not be greater than grade 1 | 1 | [
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NCT02383927 | 34:47:treatment | has relapsed or is refractory to prior therapy | 1 | [
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NCT02370693 | ,,,,58:71:treatment | Fall in FVC > 10% over 6 months on at least 12 months of prior therapy | 1 | [
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NCT02340156 | 61:74:treatment | Radiographic demonstration of disease progression following prior therapy | 1 | [
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NCT02315612 | 67:80:treatment | Subjects must have recovered from the acute side effects of their prior therapy, such that eligibility criteria are met | 1 | [
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NCT02302235 | ,,62:75:treatment | Failure to recover from <CTCAE grade 2 toxicities related to prior therapy | 1 | [
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NCT02192359 | 42:55:treatment | Any clinically significant toxicity from prior therapy must have improved to grade 0 or grade 1 | 1 | [
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NCT02159495 | 39:52:treatment, | Non hematological toxicity related to prior therapy must either have returned to =< grade 2, baseline, or deemed irreversible | 1 | [
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NCT02146924 | 39:52:treatment, | Non-hematological toxicity related to prior therapy must either have returned to =< grade 3, baseline, or deemed irreversible | 1 | [
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NCT02101034 | ,49:62:treatment | Minimum of 14 days elapsed since the end of any prior therapy | 1 | [
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NCT02013336 | 27:40:treatment | Disease progression after prior therapy in locally advanced or metastatic setting | 1 | [
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NCT01954576 | 36:49:treatment,, | Recovery from the toxic effects of prior therapy to not more than grade 1 or >3 weeks from prior therapy to registration, whichever is later | 1 | [
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NCT01906385 | 30:43:treatment,, | Recovered from toxicities of prior therapy to grade 0 or 1 | 1 | [
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NCT01896999 | 5:18:treatment, | All prior therapy must have been completed at least 21 days prior to enrollment | 1 | [
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NCT01371630 | 9:22:treatment | minimal prior therapy | 1 | [
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NCT01037790 | 74:87:treatment, | The subject has not recovered from clinically-meaningful toxicity due to prior therapy (i.e., back to baseline or Grade ≤ 1) | 1 | [
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NCT00412594 | 79:92:treatment | Patients with relapsed disease are eligible if they have had no more than one prior therapy | 1 | [
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NCT00004317 | ,25:38:treatment | No more than 1 month of prior therapy | 1 | [
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NCT02542202 | 18:21:chronic_disease,69:128:treatment,,, | patients who are HIV positive are eligible, provided they are under treatment with highly active antiretroviral therapy (HAART) and have a CD4 count >= 200 cells/microliter within 30 days prior to registration | 1 | [
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NCT02346253 | 1:4:chronic_disease,61:120:treatment,,, | HIV-positive patients are eligible, provided they are under treatment with highly active antiretroviral therapy (HAART) and have a CD4 count >= 200 cells/microliter no more than 30 days prior to registration | 1 | [
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NCT03175159 | 1:4:chronic_disease | HIV-uninfected | 1 | [
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NCT03175159 | 26:29:chronic_disease | Involvement in any other HIV Prevention study that may interfere with the ability to test major study outcomes | 1 | [
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NCT03167606 | 1:4:chronic_disease | HIV+ | 1 | [
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NCT03167606 | 13:16:chronic_disease | Self-report HIV-negative or unknown status | 1 | [
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NCT03157167 | 16:19:chronic_disease | The subject is HIV positive | 1 | [
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NCT03132415 | 16:19:chronic_disease | Self-report as HIV-negative or sero-status unaware | 1 | [
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NCT03109431 | 23:26:chronic_disease | Acutely infected with HIV | 1 | [
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NCT03109431 | 1:4:chronic_disease | HIV-positive serostatus | 1 | [
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NCT03088709 | 14:17:chronic_disease | Positive for HIV | 1 | [
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NCT03086057 | 1:4:chronic_disease | HIV Positive at baseline | 1 | [
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NCT03081559 | 38:41:chronic_disease | Evidence of suboptimal engagement in HIV care, as indicated by one or more | 1 | [
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NCT03081559 | 14:17:chronic_disease, | Reporting no HIV primary care appointments in the prior 6 months | 1 | [
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NCT03078153 | 1:4:chronic_disease | HIV negative | 1 | [
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NCT03078153 | 27:30:chronic_disease | Not enrolled in any other HIV prevention trial | 1 | [
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NCT03060772 | 1:4:chronic_disease | HIV-positive | 1 | [
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NCT03059355 | 23:26:chronic_disease | Be serum positive for HIV | 1 | [
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NCT03056339 | 29:32:chronic_disease | Known positive serology for HIV | 1 | [
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NCT03004170 | 96:99:chronic_disease, | Report engaging in one or more occasions of condomless anal and/or vaginal intercourse with an HIV-negative or unknown HIV serostatus sex partner in the 3 months prior to study enrollment | 1 | [
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NCT02979366 | 12:15:chronic_disease | arriers of HIV antibodies | 1 | [
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NCT02953509 | 1:4:chronic_disease | 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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NCT02907944 | 27:30:chronic_disease, | Employed at participating HIV clinic for at least 6 months | 1 | [
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NCT02907944 | 11:14:chronic_disease | Receiving HIV care in the index clinic | 1 | [
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NCT02895945 | 1:4:chronic_disease,, | HIV+ with stable disease and CD4+ count ≥ 200 cells/mm^3 at screening | 1 | [
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NCT02848417 | 1:4:chronic_disease | HIV | 1 | [
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NCT02835729 | 7:10:chronic_disease | Known HIV-infected patients | 1 | [
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NCT02833805 | 1:4:chronic_disease | HIV seropositivity | 1 | [
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NCT02820350 | 1:4:chronic_disease | HIV | 1 | [
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NCT02801747 | 27:30:chronic_disease,,, | Sub-optimal engagement in HIV care (assessed from the medical record, defined as less than 1 visit in every 4-mo. period in the past year [two of them at least 90 days apart], pro-rated for those diagnosed less than a year ago) or > 2 missed visits (without prior cancellation) in the past year | 1 | [
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NCT02797262 | 1:4:chronic_disease | HIV-infected individuals in HIV care | 1 | [
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NCT02796027 | 23:26:chronic_disease | positive confirmatory HIV test | 1 | [
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NCT02772562 | 51:54:chronic_disease | immunocompromised individuals, such as those with HIV | 1 | [
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NCT02770547 | 1:4:chronic_disease | HIV positive | 1 | [
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NCT02770326 | 1:4:chronic_disease,, | HIV infection with CD4 count <240 | 1 | [
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NCT02766998 | 1:4:chronic_disease | HIV positive mothers | 1 | [
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NCT02764853 | 1:4:chronic_disease | HIV-positive | 1 | [
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NCT02759575 | 1:4:chronic_disease | HIV | 1 | [
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NCT02734771 | 24:27:chronic_disease | Patient is known to be HIV positive (test result not required for enrollment) | 1 | [
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NCT02660528 | 1:4:chronic_disease | HIV | 1 | [
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NCT02641093 | 1:4:chronic_disease | HIV | 1 | [
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NCT02635360 | 18:21:chronic_disease | Known history of HIV | 1 | [
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NCT02629120 | 1:4:chronic_disease | HIV positive | 1 | [
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NCT02629120 | 9:12:chronic_disease | Must be HIV negative | 1 | [
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NCT02610374 | 1:4:chronic_disease | HIV-infected cohort (Cohort A) | 1 | [
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NCT02610374 | 1:4:chronic_disease | HIV-negative cohorts (Cohort B and C) | 1 | [
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NCT02600273 | 10:13:chronic_disease | Unstable HIV or associated comorbidities, as determined by a licensed medical professional | 1 | [
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