Found 25 matching trials
A Pilot Trial To Assess The Feasibility And Efficacy Of SCIG In Patients With MG Exacerbation (SCIG-MG) PHASE3 This is a prospective open-label, uncontrolled, single-blind, pilot clinica...
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University of Alberta
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Prevalence of Humoral Dysfunction in Pts With Frequent Exacerbations of COPD, and the Effect of SCIgR for Prevention PHASE2 To examine the prevalence of humoral immunodeficiency in patients with Chro...
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Rochester Regional Health Ctr for Clinical Research - Alexander Park
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Study of Subcutaneous Immune Globulin in Patients Requiring IgG Replacement Therapy (Japan Study) PHASE3 The objective of this study is to assess the efficacy, safety, tolerability...
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Open Label Study of Subcutaneous Immunoglobulin (SCIg) in Myasthenia Gravis PHASE2 The purpose of this study is to determine whether Hizentra is a safe and ef...
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Phoenix Neurological Associates
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Safety and Tolerability of Higher Infusion Parameters of IgPro20 (Hizentra) in Subjects With Primary Immunodeficiency (PID) PHASE4 This multicenter, open-label, parallel-arm, non-randomized study is designe...
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Clinical Research Center of Alabama
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Study of Subcutaneous Immune Globulin in Patients Requiring IgG Replacement Therapy PHASE3 The objective of this study is to assess the efficacy, tolerability, safety...
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Double-blind, Randomized, Placebo-controlled Study Evaluating Efficacy and Safety of IgPro20 in Post-COVID-19 POTS PHASE3 This is a prospective, phase 3, multicenter, double-blind, randomized place...
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University of Alabama Hospital at Birmingham
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A Database Survey to Evaluate the Safety of Immune Globulin Subcutaneous (Human), 20% Solution in Participants With Primary Immunodeficiency N/A This study is a retrospective database study in Japan to evaluate the safet...
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Takeda selected site
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Real-world CANadian CUvitru Non-Interventional Study in Subjects Transitioning From Subcutaneous Immunoglobulin (CANCUN) N/A This study will provide insights on the infusion parameters, dosing, and ex...
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University of McMaster
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A Study to Evaluate the Pharmacokinetics and Safety of XEMBIFY Versus Gamunex-C in Participants With Chronic Inflammatory Demyelinating Polyradiculoneuropathy PHASE3 The main goal of the study is to find out whether XEMBIFY, given once a wee...
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GC2402 Study Site 104
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