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Phase 1 Study of CC-90005 in Healthy Subjects and Subjects With Moderate to Severe Plaque-type Psoriasis PHASE1 To evaluate the safety, tolerability, and pharmacokinetics of single and mu...
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PPD Development, LP
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A First Time in Human (FTIH) Study to Evaluate the Safety, Tolerability, Pharmacokinetics and Pharmacodynamics of Single and Repeat Doses of GSK3884464 in Healthy Participants PHASE1 This will be a FTIH study which aims to evaluate safety, tolerability, phar...
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GSK Investigational Site
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A First-in-human, 3-part Study of MRT-8102 in Healthy Participants and Participants at Cardiovascular Risk With Elevated CRP PHASE1 The principal aim of this study is to obtain safety and tolerability data w...
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Active Not Recruiting
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Clinical Pharmacology of Miami, LLC
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A Study to Learn About the Effects and Safety of RTA 408 (Omaveloxolone) in People Aged 16 to 40 With Friedreich's Ataxia PHASE2 In this study, researchers are learning more about RTA 408, also known as o...
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Study of Mechanism of Action of Ligelizumab (QGE031) in Patients With Chronic Urticaria PHASE1 The purpose of the study is to investigate the mechanism of action for lige...
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Novartis Investigative Site
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Single and Multiple Ascending Dose Study and Food Effect Study for AG181 PHASE1 The primary purpose of this study is to assess the safety and tolerability ...
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ICON 1255 East 3900 South
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A Study to Evaluate the Efficacy and Safety of GDC-8264 in Preventing Cardiac Surgery-Associated Acute Kidney Injury (AKI) and Major Adverse Kidney Events (MAKE) PHASE2 The aim of this study is to evaluate the efficacy and safety of GDC-8264 co...
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University of Stanford Medical Center
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A Study of Oral Calcitonin Given at Night to Healthy Postmenopausal Women PHASE2 This study is being conducted to assess the plasma CTx-1 concentrations whe...
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Bio-Kinetic Clinical Applications, Inc.
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A Pharmacokinetic And Bioavailability Study of Intravenous Danoprevir in Healthy Volunteers PHASE1 This three-part study will evaluate the pharmacokinetics and bioavailabilit...
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Multiple Locations
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Safety and Tolerability of FB-001 in Healthy Adult Volunteers and Adult Subjects With Enteric Hyperoxaluria PHASE1 This Phase 1, first-in-human, randomized, double-blinded, placebo controlle...
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Medpace Clinical Pharmacology Unit
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