Safety, Tolerability, Efficacy, and Pharmacokinetic Study of ProMetic BioTherapeutics Immune Globulin Intravenous (Human) 10%
a study on Primary Immunodeficiency
This is a Phase 3, multicenter, open-label study of safety, tolerability, efficacy, and pharmacokinetics (PK) of ProMetic's Immune Globulin Intravenous (Human) 10% (Prometic IGIV 10%, the investigational medicinal product [IMP]), in Adults and Children with Primary Immunodeficiency Diseases (PIDD).
A Phase 3, Multinational, Multicenter, Open-Label Study of the Safety, Tolerability, Efficacy, and PK of ProMetic BioTherapeutics Immune Globulin Intravenous (Human) 10% in Adults and Children With Primary Immunodeficiency Diseases
This is a pivotal Phase 3, open-label, single-arm, multicenter study to assess the tolerability, safety, efficacy, and PK of the IMP in adults and children with PIDD. A total of approximately 75 subjects aged 2-80 years will be enrolled in the study. Subjects who switch from an investigational immune globulin or subcutaneous immune globulin (IGSC) are required to receive a stable dose of commercial product (CP), which is a licensed commercially available immune globulin intravenous (IGIV) product for at least 3 cycles before they can be given the IMP. This study schema will result in the CP Treatment Period and IMP Treatment Period. All subjects will be treated on an outpatient basis with the IMP for approximately 1 year, with the dose and schedule based on their previous IGIV treatment regimen (21-day or 28-day dosing interval). A subset of subjects will participate in a PK sub-study.
The primary objective of the study is to examine the rate of clinically documented serious bacterial infections (SBIs) in subjects treated with the IMP to achieve a rate of less than one SBI per year.
Primary Immunodeficiency Immunologic Deficiency Syndromes Immunoglobulins Antibodies gamma-Globulins Immunoglobulins, Intravenous Rho(D) Immune Globulin IMP
You can join if…
Open to people ages 2-80
- 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 CAN'T join 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.
- University of California, Irvine
Irvine California 92697 United States
- Children's Hospital Los Angeles
Los Angeles California 90027 United States
- in progress, not accepting new patients
- Start Date
- Completion Date
- Prometic Biotherapeutics, Inc.
- Phase 3
- Study Type
- Last Updated