Immune globulin - Takeda
Alternative Names: 10% HyQ; 20% Solution with Recombinant Human Hyaluronidase (rHuPH20); 20% SubQ; CUVITRU; Cuvitru; DEQSIGA; Gammagard Liquid; GAMMAGARD LIQUID ERC; Gammagard S/D; Human Immune Globulin for Subcutaneous Administration; HyQ; HYQVIA; HyQvia; Ig20Gly; IGI 10% with rHuPH20; IGIV - Baxalta; IGSC - Baxalta; immune globulin intravenous; IVIG 10%; Kiovig; SCIG 20%; SHP-671; TAK 771; TAK-339; TAK-664; TAK-880; TAK-881Latest Information Update: 03 Sep 2025
At a glance
- Originator Baxter International
- Developer Baxter International; Halozyme Therapeutics; Shire; Takeda
- Class Anti-infectives; Anti-inflammatories; Antibacterials; Antidementias; Antifibrotics; Antivirals; Eye disorder therapies; Immunoglobulins; Immunoproteins; Polyethylene glycols; Serum globulins; Skin disorder therapies; Vascular disorder therapies
- Mechanism of Action Immunoglobulin replacements
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Orphan Drug Status
Orphan designation is assigned by a regulatory body to encourage companies to develop drugs for rare diseases.
- New Molecular Entity No
Highest Development Phases
- Marketed Allotransplant rejection; Chronic lymphocytic leukaemia; Guillain-Barre syndrome; HIV infections; Idiopathic thrombocytopenic purpura; Immunodeficiency disorders; Multifocal motor neuropathy
- Registered Agammaglobulinaemia; Chronic inflammatory demyelinating polyradiculoneuropathy
- Phase II Ataxia
- Discontinued Alzheimer's disease
Most Recent Events
- 30 Jul 2025 Registered for Chronic inflammatory demyelinating polyradiculoneuropathy in Japan (IV) (Takeda pipeline, July 2025)
- 30 Jul 2025 Registered for Multifocal motor neuropathy in Japan (SC) (Takeda pipeline, July 2025)
- 30 Jun 2025 Takeda anticipates commercialization of GAMMAGARD LIQUID ERC to begin in the EU in 2027