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Immunologic Deficiency Syndromes clinical trials

View clinical trials related to Immunologic Deficiency Syndromes.

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NCT ID: NCT03961009 Completed - Clinical trials for Primary Immunodeficiency Disease

Clinical Assessment of Pharmacokinetics, Efficacy, and Safety of 10% IVIg in PID Patients

CARES10
Start date: April 30, 2019
Phase: Phase 3
Study type: Interventional

The purpose of this study was to assess efficacy and safety of Kedrion Immunoglobulin 10% (KIg10) in participants with Primary Immunodeficiency (PID).

NCT ID: NCT03939533 Completed - Clinical trials for Primary Immune Deficiency Disorder

Study to Monitor Subcutaneous Human Immunoglobulin Administered at Modified Dosing Regimens in Patients With Primary Immunodeficiency Diseases

Start date: October 17, 2019
Phase: Phase 3
Study type: Interventional

CLINICAL PHASE 3 STUDY TO MONITOR THE SAFETY, TOLERABILITY, AND EFFICACY OF SUBCUTANEOUS HUMAN IMMUNOGLOBULIN (CUTAQUIG®) ADMINISTERED AT MODIFIED DOSING REGIMENS IN PATIENTS WITH PRIMARY IMMUNODEFICIENCY DISEASES

NCT ID: NCT03922958 Terminated - Acute Kidney Injury Clinical Trials

Immunoparalysis in Acute Kidney Injury After Cardiac Surgery

Start date: February 22, 2019
Phase:
Study type: Observational

Infection and sepsis are common after acute kidney injury (AKI) and increase mortality. In this study, the investigators will determine whether patients with acute kidney injury after cardiac surgery have immunosuppression as judged by blood markers of immunoparalysis.

NCT ID: NCT03920735 Recruiting - Critical Illness Clinical Trials

Retrospective Non-interventional Analysis of Opportunistic Infections in Immunocompromised and Frail Patients

Start date: March 15, 2017
Phase:
Study type: Observational

The analysis of a cohort of consecutive non-selected patients from the Strasbourg University Hospital, and therefore representative of the real life, will allow better identifying the risk factors for these infections (by comparison with a cohort of patient with similar conditions of immunosuppression and no infection) and improving the diagnosis and therapeutic management. The primary objective is to identify prognosis factors affecting survival in patients with opportunistic infections

NCT ID: NCT03907241 Completed - Clinical trials for Primary Immunodeficiency

CLINICAL PHASE III STUDY TO MONITOR THE SAFETY, TOLERABILITY AND EFFICACY OF SUBCUTANEOUS HUMAN IMMUNOGLOBULIN (OCTANORM) IN PATIENTS WITH PRIMARY IMMUNODEFICIENCY DISEASES, INCLUDING (BUT NOT LIMITED TO) THOSE WHO HAVE COMPLETED THE SCGAM-01 TRIAL

Start date: March 1, 2016
Phase: Phase 3
Study type: Interventional

Summary for SCGAM-03: Clinical phase III study to monitor the safety, tolerability and efficacy of subcutaneous human immunoglobulin (Octanorm) in patients with primary immunodeficiency diseases who have completed the SCGAM-01 trial. Summary for SCGAM-03 in Canada: Clinical phase III study to monitor the safety, tolerability and efficacy of subcutaneous human immunoglobulin (octanorm) in patients with primary immunodeficiency diseases, including (but not limited to) those who have completed the SCGAM-01 trial

NCT ID: NCT03899480 Completed - HIV Infections Clinical Trials

Adoptive Transfer of Haploidentical NK Cells and N-803

Start date: May 1, 2019
Phase: Phase 1
Study type: Interventional

This is a pilot therapeutic study of related donor HLA-haploidentical NK-cell based therapy to determine if the treatment is safe and well-tolerated and if there is any measureable impact on virus reservoirs.

NCT ID: NCT03896932 Completed - Clinical trials for Primary Immunodeficiency

Minipooled-IVIG in Primary Immunodeficiency Disease

Start date: January 1, 2020
Phase: N/A
Study type: Interventional

1. study the pharmacokinetics of mini-pooled intravenous immunoglobulin( MP-IVIG) 2. Study the safety and efficacy of a newly developed preparation of MP-IVIG in children with primary immunodeficiency (PID) : - Adverse reaction of MP-IVIG(anaphylaxis and haemolysis)( no or mild or moderate) - Prevention of severe bacterial infection - Improvement of general health(weight gain and mentality) - Integration in to social live 3. Compare the efficacy of MP-IVIG to standard IVIG in children with primary immunodeficiency (PID).

NCT ID: NCT03894124 Completed - Clinical trials for Human Immunodeficiency Virus

Pharmacokinetics of Plasma Doravirine Once Daily Over 72 Hours Following Drug Intake Cessation in Healthy Volunteers

Start date: June 12, 2019
Phase: Phase 1
Study type: Interventional

Study to assess the pharmacokinetics of plasma doravirine once daily over 72 hours following drug intake cessation at steady-state in healthy volunteers

NCT ID: NCT03881566 Completed - Sepsis Clinical Trials

Presepsin as Detective Marker of Sepsis in Immunodeficiency ICU Patients

PREICU
Start date: March 1, 2019
Phase:
Study type: Observational

This is an observational study to evaluate the diagnostic and prognostic value of presepsin in the critically-ill immunocompromise patients.

NCT ID: NCT03836690 Recruiting - Lymphoma Clinical Trials

Transfer of Effector Memory T Cells (Tem) Following Allogeneic Stem Cell Transplantation

ToTem
Start date: October 21, 2019
Phase: Phase 1
Study type: Interventional

RATIONALE: Following stem cell transplantation, a major risk is graft-versus-host disease (GVHD). This occurs when donor immune cells that have been infused recognise the host's cells as 'foreign' and attack these cells. Prevention of GVHD relies upon depletion of donor immune T cells or drugs that block T cell function. However, these methods also increase the risk of life threatening infection. There is an important unmet need for better means of accelerating immune recovery following stem cell transplantation while avoiding GVHD. Pre-clinical studies have shown that infusion of donor CD62L- effector memory T cells (Tem) into the host improve immune recovery after allo-Stem Cell Transplant but do not cause GVHD. PURPOSE: This phase I dose escalation trial aims to determine the feasibility and safety of transfer of donor Tem following allogeneic stem cell transplantation.