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Evaluation of an Oral Anti-TNF Antibody in Patients With Active Ulcerative Colitis PHASE1 The purpose of this study is to evaluate the safety and tolerability as wel...
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Anaheim Clinical Trials
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Holistic Healing for Knee Osteoarthritis NA This study is a single-center, three-arm, open-label randomized controlled ...
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All India Institute of Medical Sciences, Jodhpur
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Assessment of KM-001 - Safety, Tolerability, and Efficacy in Patients With PPPK1 or PC PHASE1 This Phase 1b, open-label, single-center, prospective trial will be assessi...
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Royal London Hospital-Clinical Research Facility-11D (11th Floor) Whitechapel, London, E1 1FR,
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Clinical Trial Using the Proteolytic Fraction P1G10 From V. Cundinamarcensis to Heal Diabetic Foot Ulcer PHASE2 The aim of the study was to investigate the role of the proteolytic fractio...
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Unidade de Referência Secundária (URS) Padre Eustáquio, do Distrito Sanitário Noroeste da Secretaria Municipal e Saúde de Belo Horizonte.
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Tricaprilin Phase 3 ALTER-AD (Alternative-Alzheimer Disease) Study PHASE3 The purpose of this study is to evaluate the effects of tricaprilin (20 g t...
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Multiple Locations
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Modified Dosage for Severe Acute Malnutrition NA Protocols for the community-based management of acute malnutrition (CMAM) h...
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Exploring Safety & Clinical Benefit of Anti-Influenza Immunoglobulin Intravenous in Hospitalized Adults With Influenza A PHASE2 Influenza, or the flu, is an infectious respiratory disease that can range ...
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University of Alabama at Birmingham
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A Study of Polatuzumab Vedotin (DCDS4501A) in Combination With Rituximab or Obinutuzumab Plus Bendamustine in Participants With Relapsed or Refractory Follicular or Diffuse Large B-Cell Lymphoma PHASE1 This study is a multicenter, open-label study of polatuzumab vedotin admini...
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University of Alabama at Birmingham
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Effect of a Synbiotic on the Gut Microbiota and Adiposity-related Markers in Healthy Overweight Subjects NA The purpose of this study is to investigate the effects of a synbiotic (Pro...
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Texas State University
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An Open Label, Randomised, Repeat Dose Study to Assess the Pharmacokinetic Performance of Five Ezogabine/Retigabine Modified Release (MR) Formulations at Steady State Compared to the Immediate Release (IR) Formulation. PHASE1 This is an open-label, single centre, repeat dose, up- titration study in h...
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GSK Investigational Site
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