Influenza Clinical Trial
Official title:
A Phase 1, Open Label, Ascending Dose Cohort Study of the Pharmacokinetics of Anti-Influenza Hyperimmune Intravenous Immunoglobulin in Healthy Subjects
Despite currently available antivirals, influenza causes significant morbidity and mortality,
with 226,000 excess hospitalizations and 30,000-50,000 deaths each year in the United States
alone, and more therapies are needed in the armamentarium of anti-influenza medications
including humoral immunity-based agents.
This study will evaluate the pharmacokinetics of an anti-influenza hyperimmune intravenous
immunoglobulin. Beginning with a low dose, subjects will receive anti-influenza intravenous
immunoglobulin (FLU-IVIG) and evaluated on Study Days 0, 3, 7, 14, and 28. The safety and
tolerability is evaluated using symptoms, clinical laboratory tests, and pharmacokinetics.
Utilizing serum antibody responses as determined by hemagglutination inhibition (HAI) assays,
the dose will be escalated as immunogenicity is established....
Despite currently available antivirals, influenza causes significant morbidity and mortality,
with 226,000 excess hospitalizations and 30,000-50,000 deaths each year in the United States
alone, and more therapies are needed in the armamentarium of anti-influenza medications
including humoral immunity-based agents.
This study will evaluate the pharmacokinetics of an anti-influenza hyperimmune intravenous
immunoglobulin. Beginning with a low dose, subjects will receive anti-influenza intravenous
immunoglobulin (FLU-IVIG) and evaluated on Study Days 0, 3, 7, 14, and 28. The safety and
tolerability is evaluated using symptoms, clinical laboratory tests, and pharmacokinetics.
Utilizing serum antibody responses as determined by hemagglutination inhibition (HAI) assays,
the dose will be escalated as immunogenicity is established.
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