Study of ProMetic BioTherapeutics Immune Globulin Intravenous (Human) 10%

Completed · Phase 3

Conditions studied: Primary Immunodeficiency

In brief

Phase 3 multicenter, open-label study of safety, tolerability, efficacy, and pharmacokinetics (PK) of ProMetic's Immune Globulin Intravenous (Human) 10%, the investigational medicinal product \[IMP\]), in Adults and Children with Primary Immunodeficiency Diseases (PIDD).

Key facts

Study ID: NCT02269163
Run by: Prometic Biotherapeutics, Inc.
People needed: 82
Starts: 2016-01-26
Expected to finish: 2019-01-11
Last updated by the study team: 2021-11-05

Who can join

Age: 2 and older, up to 80. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

Subject is male or female between the ages of 2 and 80 years at Screening.
Female subjects of childbearing potential must agree to employ adequate birth control measures, as determined by their IRB/IEC, for the duration of the study.
The subject must have one of the following three diagnoses (isolated PIDD of other types will be excluded):
Common variable immunodeficiency
X-linked agammaglobulinemia
Hyper-IgM syndrome and documented low IgG levels (<4.5 mg/mL [450 mg/dL]).
Subjects must have been treated with a stable dose of immune globulin administered intravenously (IGIV) or subcutaneously (IGSC) and has documented trough or steady state IgG levels of ≥ 5 mg/mL.

You may not qualify if…

Subject has secondary immunodeficiency or has been diagnosed with dysgammaglobulinemia or isolated IgG subclass deficiency; has known hypoalbuminemia (<3 gm/dL), protein-losing enteropathy, or nephrotic syndrome.
Subject has ever had a history of severe anaphylactic or anaphylactoid reaction to immunoglobulins or other blood products.
Subject has a known history of immunoglobulin A (IgA) deficiency and known anti-IgA antibodies, thrombotic event, such as deep vein thrombosis, myocardial infarction, cerebrovascular accident, pulmonary embolism, at any time.
Subject has received blood products except IGIV, IGSC, or albumin within the previous 12 months or has participated in another study (except for IGIV, IGSC studies) within the previous 4 weeks.
Subject has had cancer in the past 5 years, except for basal cell or squamous cell cancers of the skin.
Subject has had a documented active infection within 7 days prior to Screening, or subject is on continuous prophylactic antibiotics.
Subject is positive for human immunodeficiency virus (HIV)-1 or HIV-2, a positive hepatitis C virus (HCV) or hepatitis B virus (HBV).
Subject has levels of alanine aminotransferase (ALT) or aspartate aminotransferase (AST) >2.5 times the upper limit of normal (ULN).
Subject has serum creatinine >1.5 times the ULN or a severe chronic condition such as renal failure with proteinuria.
Subject has anemia with a hemoglobin level ≤8 g/dL.
Subject has severe neutropenia with neutrophil count ≤1000 per mmᴧ3 or has lymphopenia with <500 per/ mmᴧ3.
Subject is taking prednisone at a dose ≥0.15 mg/kg/day and receiving other immunosuppressive drugs or chemotherapy.
Subject has known atrial fibrillation requiring anticoagulant therapy; congestive heart failure (New York Heart Association Class III/IV); cardiomyopathy; or cardiac arrhythmia associated with thromboembolic events, unstable or advanced ischemic heart disease, or hyperviscosity.
Subject has known decreased Protein C and/or Protein S levels.
Subject is positive for antibodies to β2GPI and/or β2GPI DI at Screening.
Female subject who is pregnant, breast-feeding, or planning a pregnancy during the course of the study.
A history of epilepsy or multiple episodes of migraine (defined as at least one episode within 6 months of enrolment) not completely controlled by medication, or any condition that is likely to interfere with evaluation of the IMP or satisfactory conduct of the study in the Investigator's opinion.

Where it is running

University of California, Irvine — Irvine, California, United States
Children's Hospital Los Angeles — Los Angeles, California, United States
Immunoe International Research — Centennial, Colorado, United States
National Jewish Hospital — Denver, Colorado, United States
Allergy Associates of the Palm Beaches — North Palm Beach, Florida, United States
Johns Hopkins All Children's Hospital — St. Petersburg, Florida, United States
Rush University Medical Center — Chicago, Illinois, United States
Fort Wayne Medical Institute — Fort Wayne, Indiana, United States
St. Louis University — St Louis, Missouri, United States
Duke University Medical Center — Durham, North Carolina, United States
Optimed Research — Columbus, Ohio, United States
Dallas Allergy Immunology — Dallas, Texas, United States
Bellingham Asthma, Allergy and Immunology Clinic — Bellingham, Washington, United States

Full record on ClinicalTrials.gov

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