Cutaquig® gives patients the flexibility to fit treatment around their individual lifestyle
Cutaquig® can be administered safely at flexible infusion regimens1
Cutaquig® can be administered safely at flexible infusion regimens1
Gupta S, et al. Subcutaneous Immunoglobulin 16.5 (Cutaquig®) in Primary Immunodeficiency Disease: Safety, Tolerability, Efficacy, and Patient Experience with Enhanced Infusion Regimens. J Clin Immunol. 2023; 43(6):1414-1425.
Cutaquig® Summary of Product Characteristics. November 2023.
Gardulf, A. Clinical experiences in primary and secondary immunodeficiencies and immune-mediated conditions using Gammanorm®. Immunotherapy, 2016. 8(5):633-647.
Kobayashi, R.H., et al., Clinical efficacy, safety and tolerability of a new subcutaneous immunoglobulin 16.5% (octanorm [cutaquig®]) in the treatment of patients with primary immunodeficiencies. Front Immunol, 2019. 10:40.
This is an international website for cutaquig® and is intended for healthcare professionals outside the US. The information on this site is not country-specific and may contain information that is outside the approved indications in the country in which you are located.
IMPORTANT: The information on this website is based on the European Summary of Product Characteristics (EU SmPC).
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