Pharmacokinetics, Safety, and Tolerability of Subcutaneous GAMUNEX-C in Pediatric Subjects With Primary Immunodeficiency

Inclusion Criteria:

- Aged 2-16 years old, inclusive.

- Documented and confirmed pre-existing diagnosis of PI with features of
hypogammaglobulinemia requiring immunoglobulin replacement.

- Currently on IgG replacement therapy with a serum IgG trough concentration of ≥ 500
mg/dL at the Screening Visit.

- Adequate normal skin to allow for SC infusions.

- Signs an assent form, if applicable (per Institutional Review Board [IRB]
requirements). Parent or legal guardian must sign an informed consent form.

- Females of childbearing potential must have a negative urine pregnancy test result
and must practice an effective form of contraception (which may include abstinence).

Exclusion Criteria:

- History of anaphylaxis or severe systemic response to an immunoglobulin or blood
product.

- History of blistering skin disease, clinically significant thrombocytopenia, bleeding
disorder, recurrent skin infections or other disorders where subcutaneous therapy
could be contraindicated.

- Has a specific antibody deficiency disorder, IgG subclass deficiency, or transient
hypogammaglobulinemia of infancy.

- History of severe adverse reaction to parenteral products containing immunoglobulin A
(IgA).

- Significant proteinuria and/or has a history of acute renal failure and/or severe
renal impairment (serum creatinine more than 2.5 times the upper limit of normal
[ULN] for age and gender) and/or is on dialysis.

- Known substance or prescription drug abuse in the past 12 months.

- Acquired medical condition that is known to cause secondary immune deficiency.

- Receiving any of the following medications: systemic corticosteroids (long term
daily, >1 mg of prednisone equivalent/kg/day for >30 days) (intermittent courses
would not exclude subject); immunosuppressants (i.e., antimetabolites and systemic
calcineurin inhibitors; NOTE: inhaled steroids are allowed); or immunomodulators.

- Non-controlled arterial hypertension at a level of ≥ the 90th percentile blood
pressure (either systolic or diastolic) for age and height (based on
http://www.nhlbi.nih.gov/guidelines/hypertension/child_tbl.pdf ).

- History or current diagnosis of thrombotic episodes; venous thrombus that occurred in
association with a medical device > 2 years prior to screening are allowed.

- Currently receiving anti-coagulation therapy.

- History of Kawasaki disease.

- Participated in another clinical trial involving exposure to an investigational
product or device within 30 days prior to screening (imaging studies without
investigative treatments are permitted) or has received any investigational blood
product within the previous 3 months.

- Unable or unwilling to comply with any aspect of the protocol, including blood
sampling and completion of the Infusion Site Reactions pages in the SC Infusion
Diary.

- In the opinion of the Investigator the subject may have compliance problems with the
protocol and the procedures of the protocol.

- Pregnant or lactating.

- Clinical evidence of any significant acute or chronic disease that, in the opinion of
the Investigator, may interfere with successful completion of the study.