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U.S. Intravenous Immunoglobulin Market Analysis Report 2021-2028: Robust Pipeline, Approval and Launch of Novel Products, and Increasing Government Initiatives – ResearchAndMarkets.com

DUBLIN–(BUSINESS WIRE)–The “U.S. Intravenous Immunoglobulin Market Size, Share & Trends Analysis Report by Application (Immunodeficiency Diseases, Multifocal Motor Neuropathy), by Distribution Channel, and Segment Forecasts, 2021-2028” report has been added to ResearchAndMarkets.com’s offering.

The U.S. intravenous immunoglobulin market size is expected to reach USD 10.24 billion by 2028. It is expected to expand at a CAGR of 6.8% from 2021 to 2028.

Robust pipeline, approval and launch of novel products, and increasing government initiatives are expected to be the major factors driving the market.

Robust pipeline and increasing approvals and launches of novel products are anticipated to support the market growth over the forecast period. For instance, in April 2019, U.S.-based ADMA Biologics, Inc. received U.S. FDA approval for its new drug Asceniv. It is an IVIG drug indicated for the treatment of primary humoral immunodeficiency disease.

Similarly, in December 2019, CSL Behring announced receiving orphan drug exclusivity for Hizentra from the U.S. FDA to treat Chronic Inflammatory Demyelinating Polyradiculoneuropathy (CIDP). In another instance, in February 2021, Biotest AG announced that it was the first in Germany to manufacture an investigational hyper immunoglobulin from plasma protein for the COVID-19 treatment.

Furthermore, increasing initiatives by various government organizations to boost the development of novel products are expected to support market growth over the forecast period. For instance, in January 2018, the National Institutes of Health (NIH) awarded a grant of USD 3 million to the U.S.-based GigaGen Inc. to develop novel recombinant intravenous immunoglobulin for patients with primary immunodeficiency diseases.

However, the manufacturing of IVIG requires a well-developed production facility and high capital investments, thereby leading to the high cost of the final product. Hence, this factor is anticipated to restrain the market growth. In addition, IVIG products undergo stringent regulations pertaining to safety and handling, which is another factor expected to impede the market growth

For instance, in 2018, the U.S. FDA delayed the approval of GC Pharma’s intravenous immunoglobulin product and demanded additional data related to the drug’s manufacturing process.

U.S. Intravenous Immunoglobulin Market Report Highlights

Market Dynamics

Market driver analysis

Market restraint analysis

U.S. Intravenous Immunoglobulin (IVIG) Market Analysis Tools

COVID-19 Impact on U.S. Intravenous Immunoglobulin (IVIG) Market

Companies Mentioned

For more information about this report visit https://www.researchandmarkets.com/r/od0m3

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