The 7 major intravenous immunoglobulin markets reached a value of US$ 12.7 Billion in 2023. Looking forward, IMARC Group expects the 7MM to reach US$ 23.5 Billion by 2034, exhibiting a growth rate (CAGR) of 5.76% during 2024-2034.
Report Attribute
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Key Statistics
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Base Year | 2023 |
Forecast Years | 2024-2034 |
Historical Years |
2018-2023
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Market Size in 2023
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US$ 12.7 Billion |
Market Forecast in 2034
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US$ 23.5 Billion |
Market Growth Rate 2024-2034
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5.76% |
The intravenous immunoglobulin market has been comprehensively analyzed in IMARC's new report titled "Intravenous Immunoglobulin Market: Epidemiology, Industry Trends, Share, Size, Growth, Opportunity, and Forecast 2024-2034". Intravenous immunoglobulin (IVIG) refers to a pooled antibody and biological agent derived from human blood plasma. It is used to treat a wide range of medical conditions that affect the immune system and cause a deficiency of antibodies. The composition of IVIG products is similar to that of immunoglobulins found in normal human plasma, including IgG, IgA, traces of other Igs, soluble receptors, cytokines, etc. Based on the formulation, it is generally administered by injecting into a muscle, vein, or under the skin. IVIG can be utilized in various treatment protocols, including replacement therapy for patients with primary and secondary immunodeficiencies. It may also be used to aid in the prevention of infections in individuals who have undergone an organ or stem cell transplant. This therapy offers numerous advantages, such as low toxicity, targeted delivery, long-term effectiveness, quicker onset of action, etc. The dosage and frequency of IVIG treatment depend on the specific condition being treated and the patient's individual needs.
The rising incidence of immunodeficiency disorders, such as acquired immunodeficiency syndrome (AIDS) and primary immunodeficiency diseases (PIDs), is primarily driving the intravenous immunoglobulin market. In addition to this, the expanding geriatric population, who are more susceptible to infections and other immune-related ailments, is further creating a positive outlook for the market. Moreover, the emerging popularity of subcutaneous administration of IVIG on account of its several benefits over intravenous administration, such as a lower risk of infection, reduced incidence of infusion-related reactions, convenience, etc., is acting as another significant growth-inducing factor. Besides this, the escalating utilization of off-label IVIG for numerous indications, including inflammatory bowel disease, dermatological conditions, neurological disorders, etc., since it modulates the immune system and provides the body with antibodies, is also bolstering the market growth. Furthermore, the ongoing advancements in formulation and stabilization techniques that have increased the efficiency and scale of production, thereby lowering the cost of the therapy, are expected to drive the intravenous immunoglobulin market in the coming years.
IMARC Group's new report provides an exhaustive analysis of the intravenous immunoglobulin market in the United States, EU4 (Germany, Spain, Italy, and France), United Kingdom, and Japan. This includes treatment practices, in-market, and pipeline drugs, share of individual therapies, market performance across the seven major markets, market performance of key companies and their drugs, etc. The report also provides the current and future patient pool across the seven major markets. According to the report, the United States has the largest patient pool for intravenous immunoglobulin and also represents the largest market for its treatment. Furthermore, the current treatment practice/algorithm, market drivers, challenges, opportunities, reimbursement scenario, unmet medical needs, etc., have also been provided in the report. This report is a must-read for manufacturers, investors, business strategists, researchers, consultants, and all those who have any kind of stake or are planning to foray into the intravenous immunoglobulin market in any manner.
ASCENIV (immune globulin intravenous, human - slra) is a 10% immune globulin liquid for intravenous injection used to treat primary humoral immunodeficiency (PI) in adults and adolescents (12 to 17 years old). It is the only IVIG created by combining RSV plasma with normal source plasma.
GC5107 refers to a liquid solution containing 10% immunoglobulin G (100 mg/mL) for intravenous infusion, derived from pooled human plasma from US donors. The manufacturing method consists of three phases designed to decrease the possibility of virus transmission. The steps are the following: fractionation I and III, solvent/detergent (S/D) treatment, and nanofiltration.
BT-595 is under development by Biotest for the treatment of primary immune deficiency, idiopathic thrombocytopenic purpura and scleromyxedema (dermatology). The solution is injected intravenously. The drug candidate is a polyvalent human IgG.
Time Period of the Study
Countries Covered
Analysis Covered Across Each Country
This report also provides a detailed analysis of the current intravenous immunoglobulin marketed drugs and late-stage pipeline drugs.
In-Market Drugs
Late-Stage Pipeline Drugs
Drugs | Company Name |
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Asceniv (Immune globulin) | ADMA Biologics |
Bivigam (Immunoglobulin G) | ADMA Biologics |
Flebogamma (Immune globulin) | Grifols |
Gammagard Liquid (Immune globulin) | Takeda Pharmaceutical |
Panzyga (Immune globulin 10%) | Octapharma |
GC 5107 | GC Biopharma |
NPB-01 | Nihon Pharmaceutical |
GB 0998 | Mitsubishi Tanabe Pharma |
BT 595 | Biotest |
*Kindly note that the drugs in the above table only represent a partial list of marketed/pipeline drugs, and the complete list has been provided in the report.
Market Insights
Epidemiology Insights
Intravenous Immunoglobulin: Current Treatment Scenario, Marketed Drugs and Emerging Therapies