Found 32 matching trials
Study to Determine the Effects of Co-Administration of Alcohol on the Absorption of Oxycodone From a Proprietary Controlled-Release Formulation PHASE1 The study is designed to test whether or not the rate and extent of absorpt...
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Pfizer Investigational Site
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Oral Bio-equivalence Study PHASE1 Title of Study: An Open-Label, Balanced, Randomized, 2-Treatment, 2-Sequenc...
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Algorithme Pharma Inc.
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Bioequivalence Study of Sodium Valproate and Valproic Acid Tablets PHASE4 Bioavailability is the extent and rate to which the active drug ingredient ...
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Department of Pharmacy, Kathmandu University
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A Bioequivalence Study of SKF101804 Cefixime Versus Cefixime Reference Formulation in Healthy Adults Under Fasting Conditions PHASE1 Cefixime is an orally active third generation cephalosporin indicated for t...
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Multiple Locations
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A Clinical Study to Assess the Effect of Food and Gender on the Pharmacokinetics of SRT2104 Administered as an Oral Suspension or Capsule Formulation to Normal Healthy Volunteers PHASE1 The primary objective of this study is to assess the pharmacokinetic profil...
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GSK Investigational Site
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A Study to Test How Different Doses of Nerandomilast (BI 1015550) Are Taken up in the Body of Healthy Japanese Men PHASE1 The main objectives of this trial are to investigate pharmacokinetics (PK) ...
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SOUSEIKAI Sumida Hospital
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MitoQ for Early-phase Schizophrenia-spectrum Disorder and Mitochondrial Dysfunction PHASE2 The goal of this double-blind, placebo-controlled randomized clinical trial...
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Yale School of Medicine
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A Pharmacokinetic Study to Compare Sustained Release and Standard Paracetamol Formulations. PHASE1 This proof of principle study will evaluate an experimental formulation of ...
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Charles River Clinical Services Northwest, Inc.
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Comparative Bioavailability Study of Metformin/Sitagliptin 850 mg/50 mg Tablets in Healthy Male and Female Volunteers PHASE1 The objective of this study was to evaluate and compare the bioavailability...
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Algorithme Pharma
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Crossover, Single Dose, Two-stage Bioequivalence Study of SCMC-Lys Salt 1.35 g Powder vs SCMC-Lys Salt 90 mg/mL Syrup PHASE1 Objectives:
The objectives of the study was to investigate the bioequivale...
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CROSS Research S.A., Phase I Unit
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