Found 150 matching trials
A Study Evaluating the Drug Levels of Iplimumab Given Under the Skin Alone and in Combination With Nivolumab in Multiple Tumor Types PHASE1 A study evaluating the drug levels of ipilimumab alone and in combination w...
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Local Institution - 0020
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A Study About the Long-Term Safety of TAK-881 in People With Primary Immunodeficiency Diseases PHASE3 The main aim of this study is to learn if TAK-881 is safe and well tolerate...
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Active Not Recruiting
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University of California, Irvine Medical Sciences I
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Gammagard Liquid and rHuPH20 in PID PHASE3 The purpose of the study is to develop a subcutaneous treatment option for ...
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Multiple Locations
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A Study to Evaluate the Safety, PK, and Immunogenicity of Recombinant Human Hyaluronidase in Healthy Subjects PHASE1 The study is being conducted to evaluate the safety, pharmacokinetics, and ...
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The Second Affiliated Hospital of Anhui Medical University
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A Study to Investigate the Safety, Tolerability, Pharmacokinetics, Immunogenicity, and Pharmacodynamics of a New Subcutaneous Formulation of Ocrelizumab in Participants With Multiple Sclerosis PHASE1 The main purpose of this study is to evaluate the safety and tolerability o...
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Active Not Recruiting
Location
Profound Research, LLC
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A Study of TAK-881 in Healthy Adults PHASE1 The main aims of this study are to check for side effects from TAK-881 in h...
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Clinical Pharmacology of Miami
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Study of Daratumumab in Patients With Mild to Moderate Alzheimer's Disease PHASE2 This is an open-label, pilot study designed to explore whether daratumumab ...
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The Litwin-Zucker Research Center
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Phase I, Open-Label, Dose-Escalation Study of a Human Monoclonal Antibody, VRC-HIVMAB091-00-AB (N6LS), Administered Intravenously or Subcutaneously With or Without Recombinant Human Hyaluronidase PH20 (rHuPH20) PHASE1 Background:
The experimental product in this study, N6LS, is a human monoc...
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National Institutes of Health Clinical Center
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A Study About How TAK-881 is Processed by the Body and Side Effects in People With Primary Immunodeficiency Diseases PHASE2 The main aim of this study is to evaluate the PK, safety, tolerability and ...
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University of California Irvine Medical Center
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Pharmacokinetic and Safety Study of HYLENEX Recombinant-Augmented Subcutaneous Ceftriaxone Administration PHASE1 The objectives of this study are:
* to establish the safety of subcutaneou...
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Multiple Locations
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