Date : 03 October 2025

The global intravenous immunoglobulin market size is calculated at USD 17.12 billion in 2024, grew to USD 18.68 billion in 2025, and is projected to reach around USD 40.78 billion by 2034. The market is expanding at a CAGR of 9.14% between 2025 and 2034.
Increasing Collaboration: Collaborations are made to access advanced technologies and expand their product portfolio, along with geographical presence.
FDA Approval: Regulatory agencies like the U.S. Food and Drug Administration (FDA) approve IVIG therapeutics for various disorders.
Research activities for IVIG include the development of innovative IVIG for a plethora of immunological and rare disorders.
Key Players: CSL Behring, Octapharma, and Grifols.
IVIGs are usually manufactured to prepare final liquid or lyophilized formulations to maintain sterility, integrity, and stability.
Key Players: Kedrion Biopharma, ADMA Biologics, and Takeda Pharmaceutical Company.
IVIG undergoes clinical trials after final preparation to assess its safety and efficacy against numerous disorders. Regulatory agencies approve an IVIG based on its human trials.
Key Players: Bio Products Laboratory, Grifols Therapeutics LLC, Octapharma
After an IVIG is approved for market use, it is distributed to hospitals and pharmacies in the respective countries where it is approved.
Patient support & services refer to providing clinical support, administration services, and care coordination for patients receiving IVIG treatment.
Kristina Allikmets, Senior Vice President and Head of R&D for Takeda’s Plasma-Derived Therapies Business Unit, commented that the approval of Gammagard Liquid ERC reinforces the company’s commitment to supporting individualized treatment approaches for people with primary immunodeficiency. The company aims to prioritize reliable supply while offering a broad range of IVIG therapies to address varied patient needs.
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