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Characterisation of Relative Bioavailability With Bioequivalence Assessment of Deferiprone Tablets After Oral Single Dose Administration PHASE1 The present study will be conducted in order to compare the bioavailability...
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SocraTec R&D GmbH Clinical Pharmacology Unit
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Study of New Tablet Formulations and Suspension Formulation Compared to Current (1B) Formulation of BILR 355 BS in Healthy Male Volunteer Subjects PHASE1 1. To investigate the relative bioavailability (BA) of improved tablet form...
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Multiple Locations
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Tac, Mini-MTX, MMF Versus Tac, MTX for GVHD Prevention PHASE3 This randomized clinical trial studies standard GVHD prophylaxis with tacro...
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Cleveland Clinic Taussig Cancer Institute, Case Comprehensive Cancer Center
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CONSISTENT 1: Metabolic and Safety Outcomes of Hylenex Recombinant (Hyaluronidase Human Injection) Preadministered at CSII Infusion Site in Participants With Type 1 Diabetes Mellitus (T1DM) PHASE4 The primary objectives of this study are to compare the difference in glyco...
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For additional information regarding investigative sites for this trial, call (858) 794-8889 8 AM to 5 PM Mon-Fri Pacific Standard Time
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Safety and Efficacy of Dexlansoprazole Modified Release Formulation to Treat Gastroesophageal Reflux Disease PHASE3 The purpose of this study is to assess the efficacy and safety of Dexlansop...
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Multiple Locations
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Phase 1 Dose Escalation, Single Dose Study to Assess Safety and Pharmacokinetics of BAX930 in Hereditary Thrombotic Thrombocytopenic Purpura (TTP) PHASE1 The purpose of this Phase 1, prospective, uncontrolled, open-label, multice...
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Ohio State University Medical Center
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Study of the Influenza Vaccine (Split Virion, Inactivated) Northern Hemisphere 2009-2010 Formulation (Intradermal Route) PHASE2 This study is in support of the annual application for the variation of the...
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Multiple Locations
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Ketorolac Applied by Continuous IV Infusion for Treatment of Moderately Severe Postoperative Pain Following Bunionectomy PHASE3 This clinical study is a randomized, double-blind, double-dummy, parallel g...
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Sun City Clinical Research
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Conversion Pharmacodynamic Study in Stable Renal Transplant Patients Receiving Tacrolimus Two Times a Day to a New Formulation of Tacrolimus - LCP Tacro - 1 Time a Day. PHASE4 LCP-Tacro is an extended-release formulation of tacrolimus designed for onc...
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Nephrology Department- Hospital Universitari Bellvtge
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An Exploratory Rectal Safety Study of Three Tenofovir Gel Formulations PHASE1 This is a double-blinded, randomized, pharmacokinetic and safety study of 3...
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Johns Hopkins University, Division of Clinical Pharmacology, Drug Development Unit
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