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Clareo Health | Clinical Trials in Tennessee | 18,981 Studies Near You

Clinical TrialsTennessee

Clinical Trials in Tennessee

Discover 18,981 clinical trials near Tennessee. Find research studies in your area.

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Breast Cancer Lung Cancer Prostate Cancer Colorectal Cancer Melanoma Leukemia Lymphoma Pancreatic Cancer

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Early phase 1Phase 1Phase 1–2Phase 2Phase 2–3Phase 3Phase 4No phase

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Showing 6101-6120 of 18,981 trials

Active not recruitingPhase III Open Label First Line Therapy Study of MEDI 4736 (Durvalumab) With or Without Tremelimumab Versus SOC in Non Small-Cell Lung Cancer (NSCLC)This is a randomized, open-label, multi-center, global, Phase III study to determine the efficacy and safety of MEDI4736 + tremelimumab combination therapy and MEDI4736…NCT02453282·Scottsdale, Arizona and 195 others

Find Trials by Condition in Tennessee

Breast Cancerin Tennessee Lung Cancerin Tennessee Prostate Cancerin Tennessee Colorectal Cancerin Tennessee Melanomain Tennessee Leukemiain Tennessee Lymphomain Tennessee Pancreatic Cancerin Tennessee Ovarian Cancerin Tennessee Brain Cancerin Tennessee

Data from ClinicalTrials.govTerms

CompletedXenform Postmarket Surveillance StudyTo compare transvaginal repair with a biologic graft to traditional native tissue repair in women surgically treated for anterior and/or apical pelvic organ prolapse.NCT01945580·Orange, California and 24 others

TerminatedA Phase 2 Study Evaluating ABT-751 in Combination With Taxotere in Advanced Non-Small Cell Lung CancerTo determine the efficacy of ABT-751 when administered in combination with standard docetaxel in subjects with advanced or metastatic NSCLC.NCT00354562·Birmingham, Alabama and 31 others

Approved for marketingOlaratumab (LY3012207) Patient Access for Soft Tissue SarcomaThe purpose of this study is to continue to provide olaratumab to eligible patients who are currently receiving olaratumab commercially for the treatment of soft tissue sarcoma…NCT03994627·Glendale, Arizona and 88 others

CompletedSafety and Efficacy of Asacol 4.8 g/Day Versus Asacol 2.4 g/Day (ASCEND I)The purpose of this study is to evaluate the safety and efficacy of Asacol 4.8 g/day (800 mg tablet) versus Asacol 2.4 g/day (400 mg tabletNCT00577473·Birmingham, Alabama and 43 others

CompletedStudy to Compare Lefamulin to Moxifloxacin for the Treatment of Adults With PneumoniaThis study evaluates the safety and efficacy of lefamulin, a pleuromutilin, for the treatment of adults with moderate community-acquired bacterial pneumoniaNCT02813694·Beverly Hills, California and 154 others

CompletedHigher Dose Weekly Topotecan In The Treatment Of Patients With Extensive Stage Small-Cell Lung CancerThis proposed phase II trial will investigate weekly topotecan at a higher dose than was used in the previous trials in an attempt to achieve improved response rates and disease…NCT00294190·Jonesboro, Arkansas and 12 others

RecruitingNon-interventional Study of Patients With Transthyretin (ATTR) AmyloidosisThe MaesTTRo study aims to enroll a global cohort of patients with transthyretin (ATTR) amyloidosis to longitudinally observe the natural course of the disease and describe…NCT06465810·La Jolla, California and 88 others

CompletedBiology in Patients With Reflux EsophagitisGERD is a common condition in the western world. In most cases, the diagnostic is established by good response to empiric proton pump inhibitor (PPI) therapy.NCT01194323·Nashville, Tennessee

RecruitingReduction of Gastrointestinal Toxicity in Prostate Cancer by Proton Spot PlacementThis purpose of this study is to examine the placement of proton spots during pencil beam scanning proton therapy for low and intermediate risk prostate cancer.NCT06200259·Knoxville, Tennessee

CompletedPlacebo-Controlled Study of Perifosine + Single Agent Chemotherapy for Metastatic Cancer PatientsThis is an exploratory phase 2, randomized placebo-controlled trial with stratification for disease and chemotherapy type.NCT00398879·Tucson, Arizona and 48 others

CompletedA Multi-Center, Randomized, Double-Blind, Placebo-Controlled Study of the Efficacy and Safety of Adefovir Dipivoxil When Added to Standard Antiretroviral Therapy for the Treatment of HIV-Infected Patients With CD4 Cell Counts >= 200/mm3To evaluate the anti-HIV activity, safety, and tolerance of adefovir dipivoxil ( bis-POM PMEA ) in combination with standard antiretroviral therapy for 48 weeks.NCT00002161·Birmingham, Alabama and 26 others

CompletedMagnesium Treatment on Vitamin D Metabolism in Participants Completed Personalized Prevention of Colorectal Cancer TrialOne striking observation is that a large portion of the inter-person variation in serum 25-hydroxyvitamin D (25(OH)D) levels is unexplained.NCT03265483·Nashville, Tennessee

WithdrawnA Study of LY3314814 in Participants With Liver ImpairmentThe purpose of the study is to determine whether LY3314814 can be safely prescribed in participants with liver impairment without a dose adjustment.NCT03499041·Tustin, California and 3 others

UnknownInvestigate the Efficacy and Safety of Farudodstat Compared With Its Placebo in Adult Alopecia Areata ParticipantsThe main purpose of this study is to measure the efficacy of farudodstat compared to placebo at Week 12 from the treatment start, in adult participants with Alopecia Areata (AA)…NCT05865041·Birmingham, Alabama and 18 others

CompletedStudy of HemoCare™ Hemodialysis System for Home Nocturnal Dialysis in Patients With ESRDThis prospective multi-center, open-label, single-arm study intends to gather and evaluate safety data for the nocturnal use of the HemoCare™ Hemodialysis System.NCT04087213·Jackson, Mississippi and 7 others

CompletedEfficacy and Safety of Budesonide Foam for Participants With Active Mild to Moderate Ulcerative Proctitis or ProctosigmoiditisThe purpose of this study is to establish the efficacy profile of rectally administered budesonide foam, as compared to an equivalent volume of rectally administered placebo foam…NCT01008423·Dothan, Alabama and 61 others

Active not recruitingA Study in Adult Participants With EoE to Evaluate Vonoprazan 20 mg Compared to Placebo After 12 Weeks and to Evaluate Vonoprazan 20 mg Up to 24 WeeksThe primary objective of this study is to assess the efficacy of vonoprazan 20 mg once daily (QD) compared to placebo QD in the number of participants with a peak eosinophilic…NCT06851559·Little Rock, Arkansas and 40 others

UnknownCisplatin Plus Epinephrine in Treating Patients With Recurrent or Refractory Head and Neck CancerRATIONALE: Drugs used in chemotherapy use different ways to stop tumor cells from dividing so they stop growing or die. Combining more than one drug may kill more tumor cells.NCT00002659·Tucson, Arizona and 27 others

CompletedErlotinib (Tarceva) as a Single Agent or Intercalated With Combination Chemotherapy in Patients With EGFR Positive NSCLCThis will be the first prospective study where patients will be selected on the basis of two measures of the epidermal growth factor receptor (EGFR) pathway.NCT00294762·Alhambra, California and 42 others

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