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A Study to Assess the Relative Bioavailability of JNJ64041575 Administered as 2 Different New Concept Formulations (Oral Suspension and Tablet) Compared to Their Respective Current Formulations, and to Assess the Effect of Food on the Pharmacokinetics of the 2 New Concept Formulations PHASE1 The purpose of this study is to assess the rate and extent of absorption of...
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Clinical Pharmacology Unit
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Efficacy and Tolerability of an Innovative Formulation of BAK-free Latanoprost PHASE4 This study evaluates the efficacy and tolerability of a new formulation of ...
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Laboratoarios Poen
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Comparison of Pharmacokinetic Profiles of 3 New Nicotine Gum Formulations With a Reference Gum PHASE1 The purpose of the study is to compare the pharmacokinetic (PK) profiles an...
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Multiple Locations
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"Novo C Plus" Vitamin C Containing Dietary Supplement Bioavailability in Healthy Subjects PHASE1 The aim of this study is to evaluate the bioavailability of "Novo C Plus" v...
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Semmelweis University - 1st Departement of Internal Medicine
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A Study to Assess The Relative Bioavailability of New Tablet Formulations of GSK1265744 in Healthy Adult Subjects PHASE1 This study will evaluate two new GSK1265744 sodium salt tablet formulations...
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GSK Investigational Site
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Study to Evaluate Taste Profile of Different JNJ-53718678 Oral Liquid Formulations in Healthy Participants PHASE1 The primary objective is to evaluate in a double-blinded (neither physician...
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Multiple Locations
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A Comparison of the Bioavailability of OZ439 When Delivered Directly to the Small Intestine, or Via the Oral Route PHASE1 The purpose of this study is to determine the bioavailability of nanopartic...
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Quotient Clinical
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Immune Equivalence Between Multi-dose and Single Dose Formulation of Vi-DT and Their Overall Safety (Phase III) PHASE3 This is a multicenter, randomized, observer-blinded, controlled, immune equ...
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Lingga Health Research Center
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A Study of EDG-15400 in Healthy Adults PHASE1 The purposes of this Phase 1 study of EDG-15400 are to:
1. Learn about the...
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A Randomized, Double Blind Placebo-Controlled, Single Ascending Dose Study to Evaluate the Safety, Tolerability, Pharmacokinetics, and Pharmacodynamics of BMS-986166 in Healthy Subjects PHASE1 The primary purpose of this study is to determine if single doses of BMS-98...
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PPD Development, LLC
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