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The U.S. National Library of Medicine provides a database of clinical trials worldwide. Use the fields below to search the database. Expand your results and select terms or phrases and right-click to search using Google, MalaCards, MedlinePlus, PubMed, or Wikipedia.

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Clinical Trials Search Results

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Count: 1299
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NCT IDTitle
NCT01194999Evaluating the Change of Overactive Bladder Symptoms in Women Post Pubovaginal Sling Procedure for Stress Incontinence
NCT00815633A Pilot Study of Alefacept for the Treatment of Pityriasis Rubra Pilaris
NCT02685267Docetaxel/Prednisone Versus Docetaxel/Prednisone and Enzalutamide in Castration-Resistant Prostate Cancer
NCT02555787Global, Multicentre, Non Interventional Advagraf Conversion Registry in Kidney Transplant Patients
NCT00924014Comparing the Effects of Conivaptan and Diuretics on Plasma Neurohormones and Renal Blood Flow in Patients With Chronic Congestive Heart Failure
NCT00689104Study to Assess the Efficacy and Safety of the Beta-3 Agonist Mirabegron (YM178) in Patients With Symptoms of Overactive Bladder
NCT00379067A Phase 4 Study With Tamsulosin OCAS to Assess Nighttime Voiding.
NCT00451932A Study to Evaluate the Safety and Effectiveness of FK778 in Liver Transplant Patients
NCT02072967Ribomustin in the Second Line Therapy of Relapsed or Refractory Indolent B-cell Non-Hodgkin's Lymphoma
NCT02531204A Study of ASP1585 to Evaluate the Bioequivalence Between ASP1585 Granules and ASP1585 Capsules
NCT02531191Bioequivalence Evaluation of a New and Current Tablet of ASP015K
NCT00413218Isavuconazole (BAL8557) in the Treatment of Candidemia and Other Invasive Candida Infections
NCT04277624A Study to Assess Bioequivalence of Fezolinetant Formulations in Healthy Female Participants
NCT01294020Study to Compare the Pharmacokinetics of Tacrolimus in Stable Pediatric Allograft Recipients Converted From Prograf® to Advagraf®
NCT02752035A Study of ASP2215 (Gilteritinib) by Itself, ASP2215 Combined With Azacitidine or Azacitidine by Itself to Treat Adult Patients Who Have Recently Been Diagnosed With Acute Myeloid Leukemia With a FLT3 Gene Mutation and Who Cannot Receive Standard Chemotherapy
NCT02211846A Study to Evaluate the Pharmacokinetics, Safety and Tolerability of Mirabegron OCAS (Oral Controlled Absorption System) in Pediatric Subjects With Neurogenic Detrusor Overactivity or Overactive Bladder
NCT00837369Regadenoson R-T Perfusion Imaging Trial
NCT01964170A Study to Compare the Effect of ASP3550 With Goserelin in Patients With Prostate Cancer
NCT01090141Drug Concentration Analysis of Micafungin in Overweight, Obese, and Extremely Obese Volunteers
NCT01872039Post Marketing Study to Evaluate the Two Dose Regimens of Nicardipine Injection in Hypertensive Emergency Patients
NCT02377609To Validate an Analytical Method to Measure Concentration of Tacrolimus in Blood Taken From Finger Pricks
NCT01021332Long Term Study of Solifenacin Succinate and Tamsulosin Hydrochloride Oral Controlled Absorption System (OCAS) in Males With Lower Urinary Tract Symptoms
NCT00486200A Study With ASP2151 in Subjects With Recurrent Episodes of Genital Herpes
NCT01261572Study to Find Maintenance Dose for Periodic Administration of ASP3550
NCT05756777A Study of Gilteritinib in Combination With Ivosidenib or Enasidenib in People With Acute Myeloid Leukemia (AML)
NCT00852696Over Active Bladder Patients Having Sling Surgery
NCT01639794Vesitirim™ in Men Postmarketing Observational Study
NCT01457573Pilot Trial Of Urinary Nerve Growth Factor (NGF) As Biomarker for Male Lower Urinary Tract Symptoms
NCT03199469A Study of AT132 in Young Children With X-Linked Myotubular Myopathy (XLMTM)
NCT03737708A Study Comparing Biologics + Methotrexate With Biologics + Tacrolimus in Patients With Rheumatoid Arthritis (RA)
NCT01486017A Single Oral Dose Study of ASP015K in Healthy Volunteers Assessing the Relative Bioavailability Across Three Tablet Strengths From a New Formulation of ASP015K
NCT01339468A Study to Assess the Pharmacokinetics, Safety and Efficacy of Advagraf and Prograf in de Novo Liver Transplantation
NCT00691262Study to Evaluate the Response to Treatment and Safety of 0.03% Tacrolimus (FK506) Ointment Administered in Pediatric Patients With Moderate to Severe Atopic Dermatitis
NCT00534508Distribution of Tacrolimus in Skin, Atopic Dermatitis
NCT06206408A Study to Confirm if Fezolinetant Helps Reduce Hot Flashes in Japanese Women Going Through Menopause
NCT01655043Absolute Quantification of Coronary Flow Reserve by Stress Perfusion MRI
NCT01889238Safety and Efficacy Study of Enzalutamide in Patients With Advanced, Androgen Receptor-Positive, Triple Negative Breast Cancer
NCT00519233AGS-1C4D4 in Patients With Advanced Hormone Refractory Prostate Cancer
NCT02864290A Study to Evaluate Escalating Doses of ASP1235 (AGS62P1) Given as Monotherapy in Subjects With Acute Myeloid Leukemia (AML)
NCT01232413A Study of the Effect of ASP1941 on Cardiac Repolarization in Healthy Subjects
NCT03065959A Study to Assess the Anti-fatigability Effect of CK-2127107 in Elderly Male and Female Subjects With Limitations in Mobility
NCT00790660A Study to Assess the Safety and Tolerability of ASP1941 in Adults With Type 2 Diabetes Mellitus.
NCT00826280Caffeine's Effect on Regadenoson Administration With Single Photon Emission Computed Tomography (SPECT) Myocardial Perfusion Imaging (MPI)
NCT01775397A Post-marketing, Blinded Study to Investigate How Effective Fidaxomicin is Compared to Vancomycin in the Sustained Cure of Clostridium Difficile Infection in Adults That Are Receiving Therapy to Suppress the Immune System
NCT01373060A Study to Assess the Safety, Pharmacokinetics and Pharmacodynamics of ASP1941 in Healthy Male Taiwanese Subjects
NCT00794443ONO-5920/YM529 Confirmatory Study in Involutional Osteoporosis Patients
NCT00565331Rituximab for Prevention of Rejection After Renal Transplantation
NCT01057407A Comparative Study of ASP1585 in Chronic Kidney Disease Patients With Hyperphosphatemia on Hemodialysis
NCT00133172Effect of Rapid Steroid Withdrawal on Subclinical Markers of Rejection
NCT02963103A Study to Assess the Safety and Efficacy of a Tacrolimus Based Immunosuppressive Regimen in Stable Kidney Transplant Recipients Converted From Cyclosporine Based Immunosuppressive Regimen