Market Research Report
U.S. Intravenous Immunoglobulin Market, by Formulation, by Application, by Distribution Channel - Size, Share, Outlook, and Opportunity Analysis, 2021 - 2028
|U.S. Intravenous Immunoglobulin Market, by Formulation, by Application, by Distribution Channel - Size, Share, Outlook, and Opportunity Analysis, 2021 - 2028|
Published: December 22, 2021
Coherent Market Insights
Content info: 210 Pages
Delivery time: 2-3 business days
Intravenous immune globulin (IVIG) is an antibody-based product that can be administered intravenously (through a vein). Intravenous immunoglobulin (IVIG) is a blood product made from the serum of 1,000 to 15,000 donors per batch. It is a preferred treatment for the patients with antibody deficiencies. For this indication, IVIG is administered at a 'replacement dose' of 200-400 mg/kg body weight every three weeks.
Market players are involved in getting their products approved from regulatory authorities, which would contribute to the growth of the U.S. intravenous immunoglobulin market over the forecast period. For instance, on February 11, 2020, CSL Behring, a global biotherapeutics leader, announced that the U.S. Food and Drug Administration (FDA) designated Privigen (Immune Globulin Intravenous (Human), 10% Liquid) as an orphan-drug for the treatment of Systemic Sclerosis (SSc).
Market players and government authorities are involved in expanding their global presence by adopting strategies such as acquisitions and collaborations, which is expected to drive the growth of the U.S. intravenous immunoglobulin market. For instance, on April 27, 2020, Kamada Ltd. and Kedrion Biopharma, two prominent bio-pharmaceutical companies specializing in plasma-derived protein therapeutics, announced a global collaboration for the development, manufacturing, and distribution of a human plasma-derived Anti-SARS-CoV-2 (COVID-19) polyclonal immunoglobulin (IgG) product as a potential coronavirus treatment.
Increasing product launches and approvals is expected to boost the growth of US intravenous immunoglobulin market over the forecast period. For instance, on April 01, 2019, ADMA Biologics, Inc., a vertically integrated commercial biopharmaceutical and specialty immunoglobulin company, announced that the US Food and Drugs Administration (FDA) approved ASCENIV, Immune Globulin Intravenous, Human, 10% Liquid, formerly known as RI-002. ASCENIV is an Intravenous Immune Globulin (IVIG) drug product used to treat adults and adolescents with primary humoral immunodeficiency disease (PIDD or PI).
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Key pointers provided are also applicable to other companies covered in the scope of the report.