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      "title": "Safety and Immunogenicity of Typhax, a Typhoid Vaccine",
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      "title": "Pharmacokinetic and Tolerability Study of NFC-1 in Subjects Aged 6-17 Years With ADHD",
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      "nctId": "NCT03004768",
      "title": "Pharmacokinetics and Metabolism of [14C]BMS-986165 in Healthy Male Participants",
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    {
      "nctId": "NCT03025022",
      "title": "A Study to Investigate the Absorption, Distribution, Metabolism, and Excretion of 14C-JNJ-42847922 After a Single Oral Dose of 40 mg in Healthy Subjects",
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      "nctId": "NCT02984852",
      "title": "Study to Evaluate the Relative Bioavailability of Fixed-dose Combination Tablet Darunavir/Cobicistat/Emtricitabine/Tenofovir Alafenamide (D/C/F/TAF) as a Whole Tablet, as a Split Tablet, and as Crushed Tablet in Healthy Adult Participants",
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      "nctId": "NCT02998099",
      "title": "A Study to Evaluate the Effect of Age on the Pharmacokinetics, Safety and Tolerability of IV Rivipansel.",
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      "nctId": "NCT02626234",
      "title": "A Drug-drug Interaction (DDI) Study to Assess the Effect of INC280 on the Pharmacokinetics of Digoxin and Rosuvastatin in Patients With cMET-dysregulated Advanced Solid Tumors",
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      "nctId": "NCT03054194",
      "title": "Study to Assess the Safety, Tolerability, and Pharmacokinetics of E2730",
      "sponsor": "Eisai Inc.",
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      "title": "Effects of 2% IDL Lotion on Skin Hydration and Transepidermal Water Loss in Females With Dry Skin",
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      "nctId": "NCT02889367",
      "title": "A Study to Evaluate the Pharmacokinetics and the Effect on Cardiac Repolarization of Odalasvir Administered as a Single Dose Tablet Under Fed Conditions in Healthy Participants",
      "sponsor": "Janssen Research & Development, LLC",
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      "nctId": "NCT02244489",
      "title": "Momelotinib Combined With Capecitabine and Oxaliplatin in Adults With Relapsed/Refractory Metastatic Pancreatic Ductal Adenocarcinoma",
      "sponsor": "Sierra Oncology LLC - a GSK company",
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    {
      "nctId": "NCT03047317",
      "title": "A Pharmacokinetic Study of MABp1 in Healthy Volunteers",
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    {
      "nctId": "NCT03044873",
      "title": "Effect of BMS-986165 on the Pharmacokinetics of Rosuvastatin",
      "sponsor": "Bristol-Myers Squibb",
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        "Inflammatory Diseases"
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      "issuer": "BRISTOL MYERS SQUIBB CO",
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    {
      "nctId": "NCT02991261",
      "title": "Bioavailability Study of SPARC001 (Study 2) in Healthy Adult Volunteers",
      "sponsor": "Sun Pharma Advanced Research Company Limited",
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    {
      "nctId": "NCT02576457",
      "title": "Safety, Pharmacokinetics and Pharmacodynamics of BMS-936559 in Severe Sepsis",
      "sponsor": "Bristol-Myers Squibb",
      "sponsorClass": "INDUSTRY",
      "phases": [
        "PHASE1"
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    {
      "nctId": "NCT02593851",
      "title": "A Study to Assess the Pharmacokinetics, Safety, and Tolerability of Multiple Doses of Orally Administered JNJ-53718678 in Infants Hospitalized With Respiratory Syncytial Virus (RSV) Infection",
      "sponsor": "Janssen Sciences Ireland UC",
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    {
      "nctId": "NCT02882009",
      "title": "A Study to Assess the Impact of Speed and Site of Subcutaneous Injection on Pain, Tolerability, Safety, and Pharmacokinetics of Gantenerumab in Healthy Participants",
      "sponsor": "Hoffmann-La Roche",
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    {
      "nctId": "NCT04320173",
      "title": "Adhesion Performance Study of Lidocaine Topical System 1.8% Compared to Lidocaine Patch 5% and Lidocaine Medicated Plaster 5% in Healthy, Adult, Human Subjects",
      "sponsor": "Scilex Pharmaceuticals, Inc.",
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      "issuer": "Scilex Holding Co",
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    {
      "nctId": "NCT02439346",
      "title": "Phase I Dose Escalation and Expansion of Oral BAY 1143269 in Combination With Intravenous Docetaxel",
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    {
      "nctId": "NCT02593760",
      "title": "A Study to Evaluate the Efficacy and Safety of Vismodegib in Combination With Ruxolitinib for the Treatment of Intermediate- or High-Risk Myelofibrosis (MF)",
      "sponsor": "Hoffmann-La Roche",
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      "status": "COMPLETED",
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    {
      "nctId": "NCT03058822",
      "title": "Relative Bioavailability of BMS-931699 From Prefilled Syringe Compared to Drug in Vial",
      "sponsor": "Bristol-Myers Squibb",
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      "ticker": "BMY",
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      "issuer": "BRISTOL MYERS SQUIBB CO",
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    {
      "nctId": "NCT03138759",
      "title": "Effect of Probenecid on Pexidartinib Pharmacokinetics",
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    {
      "nctId": "NCT03094403",
      "title": "To Evaluate the Therapeutic Equivalence and Safety of Azelaic Acid 15% Topical Gel",
      "sponsor": "Sun Pharmaceutical Industries, Inc.",
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      "daysOverdue": 3004,
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    {
      "nctId": "NCT04402112",
      "title": "Efficacy and Safety of Pitavastatin in a Real-world Setting",
      "sponsor": "JW Pharmaceutical",
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      "phases": [],
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      "daysOverdue": 3003,
      "startDate": "2012-04-02",
      "lastUpdate": "2021-04-19",
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      "fdaDrug": true,
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    {
      "nctId": "NCT03158506",
      "title": "Human Mass Balance Study of HMS5552 in Healthy Subjects",
      "sponsor": "Hua Medicine Limited",
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      "status": "COMPLETED",
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      "deadline": "2018-04-06",
      "daysOverdue": 2998,
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    {
      "nctId": "NCT02920398",
      "title": "A Multi-centre, Comparative, Double Blind, Randomised Cross-over Trial Investigating Single Dose Pharmacokinetics and Safety of Turoctocog Alfa Pegol From the Pivotal Process and Turoctocog Alfa Pegol From the Commercial Process in Patients With Severe Haemophilia A",
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      "status": "COMPLETED",
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      "daysOverdue": 2997,
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      "lastUpdate": "2017-12-15",
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        "Haemophilia A"
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      "ticker": "NVO",
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    {
      "nctId": "NCT03063645",
      "title": "Study to Compare the Pharmacokinetics of AC 1202 and Two Doses of AC-SD-01 on Ketone Body Production",
      "sponsor": "Cerecin",
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      "startDate": "2017-03-11",
      "lastUpdate": "2017-06-27",
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    {
      "nctId": "NCT02709850",
      "title": "Safety, Tolerability, Pharmacokinetics, and Pharmacodynamics of IONIS ANGPTL3-LRx in Healthy Volunteers With Elevated Triglycerides and Participants With Familial Hypercholesterolemia",
      "sponsor": "Ionis Pharmaceuticals, Inc.",
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      "status": "COMPLETED",
      "primaryCompletion": "2017-04-12",
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      "daysOverdue": 2992,
      "startDate": "2015-11-30",
      "lastUpdate": "2020-11-19",
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        "Familial Hypercholesterolemia"
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      "ticker": "IONS",
      "cik": "0000874015",
      "issuer": "IONIS PHARMACEUTICALS INC",
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    {
      "nctId": "NCT02696148",
      "title": "A Trial to Assess Safety, Tolerability, Pharmacokinetics and Pharmacodynamics of Liraglutide in Obese Children Aged 7 to 11 Years",
      "sponsor": "Novo Nordisk A/S",
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      "lastUpdate": "2019-03-18",
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      "ticker": "NVO",
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      "issuer": "NOVO NORDISK A S",
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    {
      "nctId": "NCT03643627",
      "title": "A Study of SYNT001 in Healthy Volunteers",
      "sponsor": "Syntimmune, Inc.",
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      "phases": [
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      "status": "COMPLETED",
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      "deadline": "2018-04-13",
      "daysOverdue": 2991,
      "startDate": "2016-08-17",
      "lastUpdate": "2018-08-24",
      "conditions": [
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      ],
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    {
      "nctId": "NCT00833963",
      "title": "A Study of Pregnancy and Pregnancy Outcomes in Women With Breast Cancer Treated With Trastuzumab, Pertuzumab in Combination With Trastuzumab, or Ado-Trastuzumab Emtansine",
      "sponsor": "Genentech, Inc.",
      "sponsorClass": "INDUSTRY",
      "phases": [],
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      "primaryCompletion": "2017-04-13",
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      "deadline": "2018-04-13",
      "daysOverdue": 2991,
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      "lastUpdate": "2019-05-16",
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        "Pregnancy"
      ],
      "fdaDrug": true,
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    {
      "nctId": "NCT01949324",
      "title": "A Phase 2 Multicenter Randomized Clinical Trial of CNTF for MacTel",
      "sponsor": "Neurotech Pharmaceuticals",
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        "PHASE2"
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      "status": "COMPLETED",
      "primaryCompletion": "2017-04-14",
      "primaryCompletionType": "ACTUAL",
      "deadline": "2018-04-14",
      "daysOverdue": 2990,
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      "lastUpdate": "2018-09-12",
      "conditions": [
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      "fdaDrug": true,
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    {
      "nctId": "NCT02524782",
      "title": "A Phase 1, Single- and Multiple Dose Study to Evaluate the Safety, Tolerability, Pharmacokinetics, and Pharmacodynamics of MEDI4166 in Subjects With Type 2 Diabetes",
      "sponsor": "MedImmune LLC",
      "sponsorClass": "INDUSTRY",
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      "status": "COMPLETED",
      "primaryCompletion": "2017-04-14",
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      "deadline": "2018-04-14",
      "daysOverdue": 2990,
      "startDate": "2015-10-07",
      "lastUpdate": "2019-03-13",
      "conditions": [
        "Type 2 Diabetes"
      ],
      "fdaDrug": true,
      "fdaDevice": false,
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      "ctgovUrl": "https://clinicaltrials.gov/study/NCT02524782",
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    },
    {
      "nctId": "NCT04163783",
      "title": "Study to Investigate the Absorption, Metabolism, and Excretion of [14C]-BGB-3111 in Healthy Males",
      "sponsor": "BeiGene",
      "sponsorClass": "INDUSTRY",
      "phases": [
        "PHASE1"
      ],
      "status": "COMPLETED",
      "primaryCompletion": "2017-04-18",
      "primaryCompletionType": "ACTUAL",
      "deadline": "2018-04-18",
      "daysOverdue": 2986,
      "startDate": "2017-03-29",
      "lastUpdate": "2019-11-15",
      "conditions": [
        "Healthy Volunteers"
      ],
      "fdaDrug": true,
      "fdaDevice": false,
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      "ctgovUrl": "https://clinicaltrials.gov/study/NCT04163783",
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      "prov": "prov:fd0e126f35a3bb74"
    },
    {
      "nctId": "NCT03070678",
      "title": "Interaction Study to Evaluate the Effects of Mefenamic Acid on the Pharmacokinetics and Pharmacodynamics of Sotagliflozin in Healthy Male and Female Subjects",
      "sponsor": "Sanofi",
      "sponsorClass": "INDUSTRY",
      "phases": [
        "PHASE1"
      ],
      "status": "COMPLETED",
      "primaryCompletion": "2017-04-18",
      "primaryCompletionType": "ACTUAL",
      "deadline": "2018-04-18",
      "daysOverdue": 2986,
      "startDate": "2017-03-14",
      "lastUpdate": "2022-04-25",
      "conditions": [
        "Diabetes Mellitus"
      ],
      "fdaDrug": true,
      "fdaDevice": false,
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      "ctgovUrl": "https://clinicaltrials.gov/study/NCT03070678",
      "ctgovResultsUrl": "https://clinicaltrials.gov/study/NCT03070678?tab=results",
      "ticker": "SNY",
      "cik": "0001121404",
      "issuer": "Sanofi",
      "tickerConfidence": 0.95,
      "prov": "prov:f026ecd26b4f412a"
    },
    {
      "nctId": "NCT03059303",
      "title": "Study to Assess the Relative Bioavailability of Fixed-Dose Combination (FDC) Tablet (Simeprevir, Odalasvir and AL-335) Compared With Single Agents Administered Together, and to Assess the Effect of Multiple-Dose Lansoprazole or Omeprazole on Single-Dose Pharmacokinetics of SMV, ODV, and AL-335 (FDC)",
      "sponsor": "Janssen Research & Development, LLC",
      "sponsorClass": "INDUSTRY",
      "phases": [
        "PHASE1"
      ],
      "status": "TERMINATED",
      "primaryCompletion": "2017-04-24",
      "primaryCompletionType": "ACTUAL",
      "deadline": "2018-04-24",
      "daysOverdue": 2980,
      "startDate": "2017-02-20",
      "lastUpdate": "2017-12-22",
      "conditions": [
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      ],
      "fdaDrug": true,
      "fdaDevice": false,
      "resultsPosted": false,
      "ctgovUrl": "https://clinicaltrials.gov/study/NCT03059303",
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    },
    {
      "nctId": "NCT03931993",
      "title": "A Study of Tolerability and Safety of a New Cumulative Dose of Grass MATA MPL",
      "sponsor": "Allergy Therapeutics",
      "sponsorClass": "INDUSTRY",
      "phases": [
        "PHASE1"
      ],
      "status": "COMPLETED",
      "primaryCompletion": "2017-04-27",
      "primaryCompletionType": "ACTUAL",
      "deadline": "2018-04-27",
      "daysOverdue": 2977,
      "startDate": "2017-01-16",
      "lastUpdate": "2019-04-30",
      "conditions": [
        "Seasonal Allergic Rhinitis"
      ],
      "fdaDrug": true,
      "fdaDevice": false,
      "resultsPosted": false,
      "ctgovUrl": "https://clinicaltrials.gov/study/NCT03931993",
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      "prov": "prov:d141834239b7ab57"
    },
    {
      "nctId": "NCT03480997",
      "title": "Acute Bronchodilator Effect of Inhaled Albuterol Sulfate and Ipratropium Bromide in Patients With Stable COPD",
      "sponsor": "Pneuma Respiratory, Inc",
      "sponsorClass": "INDUSTRY",
      "phases": [
        "PHASE1"
      ],
      "status": "COMPLETED",
      "primaryCompletion": "2017-04-28",
      "primaryCompletionType": "ACTUAL",
      "deadline": "2018-04-28",
      "daysOverdue": 2976,
      "startDate": "2016-12-27",
      "lastUpdate": "2018-03-29",
      "conditions": [
        "COPD"
      ],
      "fdaDrug": true,
      "fdaDevice": true,
      "resultsPosted": false,
      "ctgovUrl": "https://clinicaltrials.gov/study/NCT03480997",
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      "prov": "prov:bb4f223d7c1da7d1"
    },
    {
      "nctId": "NCT02138812",
      "title": "Phase I Dose Escalation of Oral BAY1161909 in Combination With Intravenous Paclitaxel",
      "sponsor": "Bayer",
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      "status": "TERMINATED",
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    {
      "nctId": "NCT03038971",
      "title": "Study Evaluating Safety of Ragweed Mix Given by Intralymphatic Node Injections",
      "sponsor": "Woodmont Pharmaceuticals, Inc.",
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    {
      "nctId": "NCT03168035",
      "title": "Study of NC-4016 in Patients With Advanced Solid Tumors or Lymphoma",
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    {
      "nctId": "NCT03107013",
      "title": "A Study to Investigate the Mass Balance of BTD-001",
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      "status": "COMPLETED",
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      "startDate": "2017-04-03",
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    {
      "nctId": "NCT01653470",
      "title": "Study to Evaluate Safety & Tolerability of BMS-906024 in Combination With Chemotherapy & to Define DLTs & MTD of BMS-906024 in Combination With One of the Following Chemotherapy Regimens; Weekly Paclitaxel, 5FU+Irinotecan or Carboplatin+Paclitaxel in Subjects With Advanced / Metastatic Solid Tumors",
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      "status": "COMPLETED",
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      "daysOverdue": 2971,
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      "lastUpdate": "2020-01-28",
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      "fdaDrug": true,
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      "ticker": "BMY",
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    {
      "nctId": "NCT03121339",
      "title": "Pharmacodynamic Open-Label Trial With VXA-A1.1 Oral H1 Vaccine in Healthy Adults",
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      "status": "COMPLETED",
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      "deadline": "2018-05-05",
      "daysOverdue": 2969,
      "startDate": "2017-03-31",
      "lastUpdate": "2018-05-30",
      "conditions": [
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      "fdaDrug": true,
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      "ticker": "VXRT",
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      "issuer": "Vaxart, Inc.",
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    {
      "nctId": "NCT03071770",
      "title": "Japanese Bridging Study of Ivosidenib (AG-120) in Healthy Subjects",
      "sponsor": "Agios Pharmaceuticals, Inc.",
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      "status": "COMPLETED",
      "primaryCompletion": "2017-05-09",
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      "daysOverdue": 2965,
      "startDate": "2017-03-31",
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      "ticker": "AGIO",
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    {
      "nctId": "NCT03063580",
      "title": "Effect of Rifampicin on the Pharmacokinetics and Pharmacodynamics of Sotagliflozin",
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      "status": "COMPLETED",
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      "daysOverdue": 2962,
      "startDate": "2017-02-27",
      "lastUpdate": "2022-04-25",
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      "fdaDrug": true,
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    {
      "nctId": "NCT03082300",
      "title": "A Study of ASP8273 in Subjects With Non-small Cell Lung Cancer (NSCLC) Harboring Epidermal Growth Factor Receptor (EGFR) Mutations",
      "sponsor": "Astellas Pharma Global Development, Inc.",
      "sponsorClass": "INDUSTRY",
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      "startDate": "2017-03-24",
      "lastUpdate": "2024-11-20",
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    {
      "nctId": "NCT03098953",
      "title": "Evaluation of the Safety, Systemic Pharmacokinetics, and Tolerability of Single and Repeat Ocular Installations",
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      "status": "COMPLETED",
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    {
      "nctId": "NCT03066687",
      "title": "A Study to Determine the Effect of Food on the Pharmacokinetics of Erdafitinib in Healthy Participants",
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    {
      "nctId": "NCT04039958",
      "title": "A Study of Sofosbuvir and Ledipasvir From Soviredia 90/400 mg Tablets (Minapharm, Egypt) Versus Harvoni 90/400 mg Tablets (Gilead Sciences, USA)",
      "sponsor": "Genuine Research Center, Egypt",
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      "status": "COMPLETED",
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      "daysOverdue": 2961,
      "startDate": "2017-04-05",
      "lastUpdate": "2019-07-31",
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    {
      "nctId": "NCT01473901",
      "title": "A Phase I Dose Escalation Study of BKM120 With Radiation Therapy and Temozolomide in Patients With Newly Diagnosed Glioblastoma",
      "sponsor": "Novartis Pharmaceuticals",
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      "status": "COMPLETED",
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      "lastUpdate": "2020-12-09",
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      "fdaDrug": true,
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      "ticker": "NVS",
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      "issuer": "NOVARTIS AG",
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    {
      "nctId": "NCT04032834",
      "title": "A Comparison of VR647 and Conventionally Nebulized Budesonide in Healthy Volunteers and Adult Asthma Subjects",
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      "status": "COMPLETED",
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      "deadline": "2018-05-22",
      "daysOverdue": 2952,
      "startDate": "2017-02-20",
      "lastUpdate": "2019-07-25",
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      "fdaDrug": true,
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    {
      "nctId": "NCT03198676",
      "title": "A Safety Study to Compare the Effect of Two PrEP-001 Nasal Powder Formulations on Nasal Mucosa and Serum Cytokine Production",
      "sponsor": "Prep Biopharm Limited",
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      "status": "COMPLETED",
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      "daysOverdue": 2950,
      "startDate": "2017-05-08",
      "lastUpdate": "2017-07-02",
      "conditions": [
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    {
      "nctId": "NCT03161015",
      "title": "Single-Dose PK Study of GBT440 in Subjects With Renal Impairment",
      "sponsor": "Global Blood Therapeutics",
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      "status": "COMPLETED",
      "primaryCompletion": "2017-05-25",
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      "deadline": "2018-05-25",
      "daysOverdue": 2949,
      "startDate": "2016-11",
      "lastUpdate": "2018-02-22",
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      ],
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    {
      "nctId": "NCT02993237",
      "title": "Study to Assess the Acceptability/Swallowability of DRV-Containing FDC Tablets in HIV-1 Infected Adolescents, Using Matching Placebo Tablets",
      "sponsor": "Janssen Research & Development, LLC",
      "sponsorClass": "INDUSTRY",
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      "status": "COMPLETED",
      "primaryCompletion": "2017-05-25",
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      "deadline": "2018-05-25",
      "daysOverdue": 2949,
      "startDate": "2017-01-23",
      "lastUpdate": "2019-05-13",
      "conditions": [
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    {
      "nctId": "NCT03126097",
      "title": "A Study to Investigate the Interaction Between JNJ-64155806 and Ethinylestradiol/Drospirenone in Healthy Females",
      "sponsor": "Janssen Research & Development, LLC",
      "sponsorClass": "INDUSTRY",
      "phases": [
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      ],
      "status": "TERMINATED",
      "primaryCompletion": "2017-05-26",
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      "deadline": "2018-05-26",
      "daysOverdue": 2948,
      "startDate": "2017-04-13",
      "lastUpdate": "2017-09-01",
      "conditions": [
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      ],
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    {
      "nctId": "NCT02480374",
      "title": "Study of Safety & Biological Activity of IP IMNN-001 (also Known As GEN-1) with Neoadjuvant Chemo in Ovarian Cancer",
      "sponsor": "Imunon",
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      "phases": [
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      "status": "COMPLETED",
      "primaryCompletion": "2017-05",
      "primaryCompletionType": "ACTUAL",
      "deadline": "2018-05-31",
      "daysOverdue": 2943,
      "startDate": "2015-09",
      "lastUpdate": "2024-10-02",
      "conditions": [
        "Epithelial Ovarian Cancer",
        "Fallopian Tube Cancer",
        "Primary Peritoneal Cancer"
      ],
      "fdaDrug": true,
      "fdaDevice": false,
      "resultsPosted": false,
      "ctgovUrl": "https://clinicaltrials.gov/study/NCT02480374",
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      "ticker": "IMNN",
      "cik": "0000749647",
      "issuer": "Imunon, Inc.",
      "tickerConfidence": 0.95,
      "prov": "prov:31d186e3a152c64f"
    },
    {
      "nctId": "NCT02860650",
      "title": "A Study to Evaluate Safety, Tolerability, and Immunogenicity of Heterologous Prime-boost Regimens Using the Multivalent Filovirus Vaccines Ad26.Filo and MVA-BN-Filo Administered in Different Sequences and Schedules in Healthy Adults",
      "sponsor": "Janssen Vaccines & Prevention B.V.",
      "sponsorClass": "INDUSTRY",
      "phases": [
        "PHASE1"
      ],
      "status": "COMPLETED",
      "primaryCompletion": "2017-05",
      "primaryCompletionType": "ACTUAL",
      "deadline": "2018-05-31",
      "daysOverdue": 2943,
      "startDate": "2016-08",
      "lastUpdate": "2018-02-05",
      "conditions": [
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      ],
      "fdaDrug": true,
      "fdaDevice": false,
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    {
      "nctId": "NCT03146013",
      "title": "Dual Algorithm Post Market Clinical Study",
      "sponsor": "MP Biomedicals, LLC",
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      "phases": [],
      "status": "COMPLETED",
      "primaryCompletion": "2017-05-31",
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      "deadline": "2018-05-31",
      "daysOverdue": 2943,
      "startDate": "2017-03-01",
      "lastUpdate": "2017-06-12",
      "conditions": [
        "HTLV-I Infections",
        "HTLV-II Infections",
        "Human T-lymphotropic Virus 1",
        "Human T-lymphotropic Virus 2",
        "HTLV I Associated T Cell Leukemia Lymphoma",
        "HTLV I Associated Myelopathies"
      ],
      "fdaDrug": true,
      "fdaDevice": true,
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      "ctgovUrl": "https://clinicaltrials.gov/study/NCT03146013",
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    {
      "nctId": "NCT03187496",
      "title": "Drug-drug Interaction Study Between EDP-305, Midazolam, Caffeine and Rosuvastatin in Healthy Volunteers.",
      "sponsor": "Enanta Pharmaceuticals, Inc",
      "sponsorClass": "INDUSTRY",
      "phases": [
        "PHASE1"
      ],
      "status": "COMPLETED",
      "primaryCompletion": "2017-06-01",
      "primaryCompletionType": "ACTUAL",
      "deadline": "2018-06-01",
      "daysOverdue": 2942,
      "startDate": "2017-05-11",
      "lastUpdate": "2017-08-21",
      "conditions": [
        "NASH"
      ],
      "fdaDrug": true,
      "fdaDevice": false,
      "resultsPosted": false,
      "ctgovUrl": "https://clinicaltrials.gov/study/NCT03187496",
      "ctgovResultsUrl": "https://clinicaltrials.gov/study/NCT03187496?tab=results",
      "ticker": "ENTA",
      "cik": "0001177648",
      "issuer": "ENANTA PHARMACEUTICALS INC",
      "tickerConfidence": 0.95,
      "prov": "prov:a548fcaacf97ea22"
    },
    {
      "nctId": "NCT05341102",
      "title": "A Study of Single and Repeated Doses of LY3556050 in Healthy Participants",
      "sponsor": "Eli Lilly and Company",
      "sponsorClass": "INDUSTRY",
      "phases": [
        "PHASE1"
      ],
      "status": "COMPLETED",
      "primaryCompletion": "2017-06-02",
      "primaryCompletionType": "ACTUAL",
      "deadline": "2018-06-02",
      "daysOverdue": 2941,
      "startDate": "2016-09-14",
      "lastUpdate": "2022-04-22",
      "conditions": [
        "Healthy"
      ],
      "fdaDrug": true,
      "fdaDevice": false,
      "resultsPosted": false,
      "ctgovUrl": "https://clinicaltrials.gov/study/NCT05341102",
      "ctgovResultsUrl": "https://clinicaltrials.gov/study/NCT05341102?tab=results",
      "ticker": "LLY",
      "cik": "0000059478",
      "issuer": "ELI LILLY & Co",
      "tickerConfidence": 0.8166666666666667,
      "prov": "prov:354a414948c55db4"
    },
    {
      "nctId": "NCT03206229",
      "title": "Study Comparing TPI-120 and Neulasta Administered Through Subcutaneous Route in Healthy Adult Subjects",
      "sponsor": "Adello Biologics, LLC",
      "sponsorClass": "INDUSTRY",
      "phases": [
        "PHASE1"
      ],
      "status": "COMPLETED",
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      "primaryCompletionType": "ACTUAL",
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    {
      "nctId": "NCT03108274",
      "title": "A Drug Interaction Study Between Danicopan and Midazolam, Fexofenadine, and Mycophenolate Mofetil in Healthy Participants",
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    {
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      "title": "A Study to Examine the Effects of Entinostat on Midazolam in Healthy Adult Subjects",
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    {
      "nctId": "NCT03554304",
      "title": "Evaluate the Effect of WCK 5222 on the QT/QTc Interval in Healthy Volunteers",
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    {
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      "title": "A First-in-Human Study of BNZ132-1-40",
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    {
      "nctId": "NCT02286219",
      "title": "Phase 1, Multiple Ascending Dose Study of Anti-HER2 FCAB FS102 in HER2 Positive Solid Tumors (Anti HER2 Fcab)",
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    {
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      "title": "A Trial of Intranasal Remimazolam Pharmacokinetics, Pharmacodynamics, Safety and Bioavailability",
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    {
      "nctId": "NCT01862081",
      "title": "A Dose-escalation Study to Assess the Safety, Tolerability, and Pharmacokinetics of GDC-0032 in Combination With Docetaxel or With Paclitaxel in Patients With HER2-negative Locally Recurrent or Metastatic Breast Cancer or Non-small Cell Lung Cancer",
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    {
      "nctId": "NCT02866227",
      "title": "TOL-463 Phase 2 Study for Vaginitis",
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    {
      "nctId": "NCT03229291",
      "title": "A Study Evaluating the Safety, Tolerability, and Pharmacokinetics of Multiple Ascending Doses of SM04755 Following Topical Administration to Healthy Subjects",
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    {
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      "title": "Safety and Tolerability of PF-06818883 in Healthy Subjects",
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      "ticker": "PFE",
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    {
      "nctId": "NCT05873907",
      "title": "A Study to Evaluate the Safety, Tolerability, Immunogenicity, Pharmacokinetics, and Pharmacodynamics of AMG 592 in Healthy Participants",
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    {
      "nctId": "NCT02941354",
      "title": "Evaluating the Pharmacokinetics of NovoEight® (Turoctocog Alfa) in Relation to BMI in Subjects With Haemophilia A",
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    {
      "nctId": "NCT02143635",
      "title": "Study to Determine and Evaluate a Safe and Tolerated Dose of HDM201 in Patients With Selected Advanced Tumors That Are TP53wt",
      "sponsor": "Novartis Pharmaceuticals",
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      "nctId": "NCT01292655",
      "title": "Study to Evaluate the Safety and Tolerability of IV Doses of BMS-906024 in Subjects With Advanced or Metastatic Solid Tumors",
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      "nctId": "NCT03174041",
      "title": "A Drug-Drug Interaction Study Between GDC-0853 and Midazolam, Itraconazole, Rosuvastatin, and Simvastatin",
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    {
      "nctId": "NCT03327558",
      "title": "Randomized,Study of APRISO 375 mg Versus the Approved APRISO 375 mg Capsules in Healthy Male and Female Subjects",
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      "issuer": "Bausch Health Companies Inc.",
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    {
      "nctId": "NCT03257943",
      "title": "A Bioequivalence Study, Comparing Two Formulations of Ivermectin Lotion, 0.5%",
      "sponsor": "Sun Pharmaceutical Industries, Inc.",
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      "status": "COMPLETED",
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      "daysOverdue": 2916,
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      "lastUpdate": "2018-05-18",
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    {
      "nctId": "NCT03032536",
      "title": "Study of the Relative Oral Bioavailability of AL-3778 Tablets and Drug Interaction With Entecavir or Tenofovir Disoproxil Fumarate in Healthy Volunteers",
      "sponsor": "Alios Biopharma Inc.",
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      "status": "TERMINATED",
      "primaryCompletion": "2017-06-28",
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      "deadline": "2018-06-28",
      "daysOverdue": 2915,
      "startDate": "2017-01-31",
      "lastUpdate": "2017-10-16",
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        "Chronic Hepatitis B",
        "Viral Hepatitis B"
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    {
      "nctId": "NCT03135509",
      "title": "A Study to Assess the Relative Bioavailability of a New CC-220 Capsule Formulation, Compared to a Reference CC-220 Capsule Formulation, in Healthy Adult Subjects",
      "sponsor": "Celgene",
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      "status": "COMPLETED",
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      "startDate": "2017-05-24",
      "lastUpdate": "2017-07-02",
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    {
      "nctId": "NCT02223247",
      "title": "A Phase 1, First-In-Human Study of Escalating Doses of Oral TVB-2640 in Patients With Solid Tumors",
      "sponsor": "Sagimet Biosciences Inc.",
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      "status": "COMPLETED",
      "primaryCompletion": "2017-06",
      "primaryCompletionType": "ACTUAL",
      "deadline": "2018-06-30",
      "daysOverdue": 2913,
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      "lastUpdate": "2017-08-14",
      "conditions": [
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      "ticker": "SGMT",
      "cik": "0001400118",
      "issuer": "Sagimet Biosciences Inc.",
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    {
      "nctId": "NCT02475447",
      "title": "Safety, Pharmacokinetics and Preliminary Efficacy of Asimadoline in Pruritus Associated With Atopic Dermatitis",
      "sponsor": "Tioga Pharmaceuticals",
      "sponsorClass": "INDUSTRY",
      "phases": [
        "PHASE2"
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      "status": "COMPLETED",
      "primaryCompletion": "2017-06",
      "primaryCompletionType": "ACTUAL",
      "deadline": "2018-06-30",
      "daysOverdue": 2913,
      "startDate": "2015-07",
      "lastUpdate": "2017-12-13",
      "conditions": [
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        "Atopic Dermatitis"
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    {
      "nctId": "NCT03630094",
      "title": "Plasma and Intrapulmonary Concentrations Study of WCK 5222",
      "sponsor": "Wockhardt",
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        "PHASE1"
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      "status": "COMPLETED",
      "primaryCompletion": "2017-06-30",
      "primaryCompletionType": "ACTUAL",
      "deadline": "2018-06-30",
      "daysOverdue": 2913,
      "startDate": "2017-03-31",
      "lastUpdate": "2018-08-14",
      "conditions": [
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      ],
      "fdaDrug": true,
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    {
      "nctId": "NCT03125473",
      "title": "Dose-Optimization Trial of VXA-G1.1-NN in Healthy Volunteers",
      "sponsor": "Vaxart",
      "sponsorClass": "INDUSTRY",
      "phases": [
        "PHASE1"
      ],
      "status": "COMPLETED",
      "primaryCompletion": "2017-07-01",
      "primaryCompletionType": "ACTUAL",
      "deadline": "2018-07-01",
      "daysOverdue": 2912,
      "startDate": "2017-04-07",
      "lastUpdate": "2018-05-30",
      "conditions": [
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      ],
      "fdaDrug": true,
      "fdaDevice": false,
      "resultsPosted": false,
      "ctgovUrl": "https://clinicaltrials.gov/study/NCT03125473",
      "ctgovResultsUrl": "https://clinicaltrials.gov/study/NCT03125473?tab=results",
      "ticker": "VXRT",
      "cik": "0000072444",
      "issuer": "Vaxart, Inc.",
      "tickerConfidence": 0.95,
      "prov": "prov:1d1a1ebf9bb8bc2a"
    },
    {
      "nctId": "NCT03234699",
      "title": "Assess the Influence of Cenobamate on the PK of Cytochrome P450 (CYP) Probe Drugs As a Means of Predicting Drug-drug Interactions",
      "sponsor": "SK Life Science, Inc.",
      "sponsorClass": "INDUSTRY",
      "phases": [
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      "status": "COMPLETED",
      "primaryCompletion": "2017-07-03",
      "primaryCompletionType": "ACTUAL",
      "deadline": "2018-07-03",
      "daysOverdue": 2910,
      "startDate": "2017-02-22",
      "lastUpdate": "2024-09-19",
      "conditions": [
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      ],
      "fdaDrug": true,
      "fdaDevice": false,
      "resultsPosted": false,
      "ctgovUrl": "https://clinicaltrials.gov/study/NCT03234699",
      "ctgovResultsUrl": "https://clinicaltrials.gov/study/NCT03234699?tab=results",
      "prov": "prov:6825a29c6c2d835a"
    },
    {
      "nctId": "NCT01324479",
      "title": "Study of INC280 in Patients With c-MET Dependent Advanced Solid Tumors",
      "sponsor": "Novartis Pharmaceuticals",
      "sponsorClass": "INDUSTRY",
      "phases": [
        "PHASE1"
      ],
      "status": "COMPLETED",
      "primaryCompletion": "2017-07-04",
      "primaryCompletionType": "ACTUAL",
      "deadline": "2018-07-04",
      "daysOverdue": 2909,
      "startDate": "2012-02-29",
      "lastUpdate": "2020-12-19",
      "conditions": [
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      ],
      "fdaDrug": true,
      "fdaDevice": false,
      "resultsPosted": false,
      "ctgovUrl": "https://clinicaltrials.gov/study/NCT01324479",
      "ctgovResultsUrl": "https://clinicaltrials.gov/study/NCT01324479?tab=results",
      "ticker": "NVS",
      "cik": "0001114448",
      "issuer": "NOVARTIS AG",
      "tickerConfidence": 0.95,
      "prov": "prov:65aa556c9e0bc457"
    },
    {
      "nctId": "NCT03130556",
      "title": "A Study Of Glasdegib In Healthy Volunteers To Establish The Bioequivalence Of The Phase 2 Formulation To The ICH Formulation",
      "sponsor": "Pfizer",
      "sponsorClass": "INDUSTRY",
      "phases": [
        "PHASE1"
      ],
      "status": "COMPLETED",
      "primaryCompletion": "2017-07-06",
      "primaryCompletionType": "ACTUAL",
      "deadline": "2018-07-06",
      "daysOverdue": 2907,
      "startDate": "2017-05-01",
      "lastUpdate": "2017-08-01",
      "conditions": [
        "Healthy Volunteers"
      ],
      "fdaDrug": true,
      "fdaDevice": false,
      "resultsPosted": false,
      "ctgovUrl": "https://clinicaltrials.gov/study/NCT03130556",
      "ctgovResultsUrl": "https://clinicaltrials.gov/study/NCT03130556?tab=results",
      "ticker": "PFE",
      "cik": "0000078003",
      "issuer": "PFIZER INC",
      "tickerConfidence": 0.95,
      "prov": "prov:ddbad7b8ad73b7e8"
    },
    {
      "nctId": "NCT03065556",
      "title": "A Comparison of 188-0551 Solution Versus Vehicle Solution in Subjects With Plaque Psoriasis (Study 203)",
      "sponsor": "Therapeutics, Inc.",
      "sponsorClass": "INDUSTRY",
      "phases": [
        "PHASE2"
      ],
      "status": "COMPLETED",
      "primaryCompletion": "2017-07-06",
      "primaryCompletionType": "ACTUAL",
      "deadline": "2018-07-06",
      "daysOverdue": 2907,
      "startDate": "2017-01-26",
      "lastUpdate": "2018-08-10",
      "conditions": [
        "Plaque Psoriasis"
      ],
      "fdaDrug": true,
      "fdaDevice": false,
      "resultsPosted": false,
      "ctgovUrl": "https://clinicaltrials.gov/study/NCT03065556",
      "ctgovResultsUrl": "https://clinicaltrials.gov/study/NCT03065556?tab=results",
      "prov": "prov:21e7b26e26596dae"
    },
    {
      "nctId": "NCT03177278",
      "title": "A Study to Assess the Metabolism, Excretion, and Mass Balance of Radio-Labeled Plazomicin",
      "sponsor": "Achaogen, Inc.",
      "sponsorClass": "INDUSTRY",
      "phases": [
        "PHASE1"
      ],
      "status": "COMPLETED",
      "primaryCompletion": "2017-07-10",
      "primaryCompletionType": "ACTUAL",
      "deadline": "2018-07-10",
      "daysOverdue": 2903,
      "startDate": "2017-06-16",
      "lastUpdate": "2017-07-12",
      "conditions": [
        "Healthy Volunteers"
      ],
      "fdaDrug": true,
      "fdaDevice": false,
      "resultsPosted": false,
      "ctgovUrl": "https://clinicaltrials.gov/study/NCT03177278",
      "ctgovResultsUrl": "https://clinicaltrials.gov/study/NCT03177278?tab=results",
      "prov": "prov:0c2383d906d0d2fb"
    },
    {
      "nctId": "NCT03126721",
      "title": "The Study is to Evaluate the Effect of Multiple Doses PF-06751979 on the Pharmacokinetics of Midazolam in Healthy Adults",
      "sponsor": "Pfizer",
      "sponsorClass": "INDUSTRY",
      "phases": [
        "PHASE1"
      ],
      "status": "COMPLETED",
      "primaryCompletion": "2017-07-11",
      "primaryCompletionType": "ACTUAL",
      "deadline": "2018-07-11",
      "daysOverdue": 2902,
      "startDate": "2017-04-18",
      "lastUpdate": "2017-07-26",
      "conditions": [
        "Healthy"
      ],
      "fdaDrug": true,
      "fdaDevice": false,
      "resultsPosted": false,
      "ctgovUrl": "https://clinicaltrials.gov/study/NCT03126721",
      "ctgovResultsUrl": "https://clinicaltrials.gov/study/NCT03126721?tab=results",
      "ticker": "PFE",
      "cik": "0000078003",
      "issuer": "PFIZER INC",
      "tickerConfidence": 0.95,
      "prov": "prov:8a61d8ae7003ec8b"
    }
  ],
  "disclaimer": "Public-record facts derived from ClinicalTrials.gov. NOT a finding of violation, fraud, or non-compliance. NOT legal/investment advice."
}