Efficacy and Safety Study of Kedrion IVIG 10% to Treat Subjects With Primary Immunodeficiency (PID)

Completed · Phase 3

Conditions studied: Primary Immunodeficiency, Agammaglobulinemia, Hypogammaglobulinemia, Antibody Deficiency

In brief

The purpose of this study is to determine whether Kedrion IVIG 10% (an immunoglobulin solution) is effective in treating Primary Immunodeficiency (PID).

Key facts

Study ID: NCT01581593
Run by: Kedrion S.p.A.
People needed: 45
Starts: 2012-11-12
Expected to finish: 2014-08-27
Last updated by the study team: 2021-02-16

Who can join

Age: 2 and older, up to 70. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

Confirmed clinical diagnosis of a Primary Immunodeficiency Disease
Male or female, ages 2 to 70 years
Received 300-900 mg/kg of a licensed IVIG therapy at 21 or 28 day intervals for at least 3 months prior to this study
2 documented IgG trough levels of ≥ 5 g/L are obtained at two infusion cycles (21 or 28 days) within 12 months (one must be within 6 months) prior to study enrolment
Non-pregnant females of child-bearing potential who agree to use adequate birth control during the study
Subject is willing to comply with the protocol
Authorization to access personal health information.
Signed the informed consent form and a child assent form, if appropriate.
If currently participating in a clinical trial with another experimental IVIG may be enrolled if they have received stable IVIG therapy for at least 3 infusion cycles prior to receiving Kedrion IVIG 10% and all inclusion and exclusion criteria are satisfied
If currently participating in a trial of SCIG can be enrolled if they are switched to IVIG for three infusion cycles (21 or 28 days) prior to enrolment in this study

You may not qualify if…

Has secondary immunodeficiency.
Newly diagnosed and has not been treated with immunoglobulin or has been diagnosed with dysgammaglobulinemia or isolated IgG subclass deficiency.
Has a history of repeated reactions or hypersensitivity to IVIG or other injectable forms of IgG.
Has a history of thrombotic events defined by at least 1 event in subject's lifetime.
Has IgA deficiency and is known to have antibodies to IgA.
Has received blood products other than human albumin or human immunoglobulin within 12 months prior to enrolment.
Has significant protein losing enteropathy, nephrotic syndrome or lymphangiectasia.
Has an acute infection as documented by culture or diagnostic imaging and/or a body temperature exceeding 38.5 °C (101.3 °F) within 7 days prior to screening
Has a known history or is positive at enrolment for human immunodeficiency virus (HIV) type 1 by NAT, hepatitis B virus (HBsAg and NAT), hepatitis C virus (by NAT), or hepatitis A virus (by NAT).
Has levels of alanine aminotransferase (ALT) or aspartate aminotransferase (AST) > 2.5 times of the upper limit of normal for the laboratory designated for the study.
Has an implanted venous access device
Has profound anemia or persistent severe neutropenia (≤ 1000 neutrophils per mm3)or lymphopenia of less than 500 cells per microliter.
Has a severe chronic condition such as renal failure (creatinine concentration > 2.0 times the upper limit of normal) with proteinuria, congestive heart failure (New York Heart Association III/IV), cardiomyopathy, cardiac arrhythmia associated with thromboembolic events (e.g. atrial fibrillation), unstable or advanced ischemic heart disease, hyperviscosity, or any other condition that the investigator believes is likely to interfere with evaluation of the study drug or with satisfactory conduct of the trial.
Has a history of a malignant disease other than properly treated carcinoma in situ of the cervix or basal cell or squamous cell carcinoma of the skin within 24 months prior to enrolment.
Has history of epilepsy or multiple episodes of migraine (defined as at least one episode within 6 months of enrolment) not completely controlled by medication.
Is receiving steroids (oral or parenteral daily dose of ≥ 0.15 mg/kg/day of prednisone or equivalent) OR other immunosuppressive drugs or chemotherapy.
Females who are pregnant, breast feeding or planning a pregnancy during the course of the study. Women who become pregnant during the study will be withdrawn from the study.
Has participated in another clinical study within 3 weeks prior to study enrolment.

Where it is running

Arkansas Children's Hospital — Little Rock, Arkansas, United States
Allergy Associates of the Palm Beaches — North Palm Beach, Florida, United States
Family Allergy & Asthma Center, PC — Atlanta, Georgia, United States
Rush University — Chicago, Illinois, United States
University of Iowa Hospital and Clinics — Iowa City, Iowa, United States
Midwest Immunology Clinic — Plymouth, Minnesota, United States
AAIR Research Center — Rochester, New York, United States
Optimed Research, LTD — Columbus, Ohio, United States
Dallas Allergy Immunology Research — Dallas, Texas, United States
AARA Research Center — Dallas, Texas, United States
Virginia Commonwealth University Health Systems — Richmond, Virginia, United States
Marycliff Allergy Specialists — Spokane, Washington, United States
Gordon Sussman Clinical Research Inc. — Toronto, Ontario, Canada
Pediatric & Adult Allergy & Clinical Immunology — Toronto, Ontario, Canada
The Hospital for Sick Children — Toronto, Ontario, Canada

Full record on ClinicalTrials.gov

Trial information comes from ClinicalTrials.gov and is refreshed daily. TrialsForMe does not provide medical care and does not run the studies it lists.