Sandoz introduces Hyrimoz® (adalimumab) high-dose variant in Europe to enhance patient treatment

Sandoz, the worldwide pioneer in generic and biosimilar medication, today publicizes the introduction of Hyrimoz® (adalimumab) without citrate high concentration version in Europe. The medication will gradually become accessible to patients throughout European nations, the process commences today.

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"Living with chronic inflammatory diseases can severely disrupt everyday life," said Rebecca Guntern, Europe President of Sandoz. “The roll out of Hyrimoz® HCF in Europe marks an important step in providing an alternative therapy for those in need, reflecting our ongoing dedication to broadening the availability of high-standard treatments."

Hyrimoz® citrate-free HCF, an improved formulation of the existing Hyrimoz® 50 mg/mL, reduces the injection volume by half, which may lessen the injection frequency for patients requiring an 80 mg/mL or higher dose. The HCF formulation is applied with the familiar Hyrimoz® SensoReady® pen, aiming to optimise the patient experience while keeping it recognisable.

The introduction of Hyrimoz ® HCF fortifies Sandoz's biosimilar selection in the field of immunology, which includes Erelzi® (biosimilar etanercept), Zessly® (biosimilar infliximab), and Rixathon® (biosimilar rituximab, including for the treatment of rheumatoid arthritis). The Hyrimoz® citrate-free HCF debuted in the US market in July 2023.

Dedicated to enabling millions of patients to access vital and possibly life-altering biologic treatments sustainably and economically, Sandoz operates in various fields including immunology, oncology, supportive care, and endocrinology. The company boasts a foremost international portfolio of eight marketed biosimilars, along with 25 additional assets at various developmental stages.

After launching the first European biosimilar in 2006, Sandoz has played a major part in facilitating early and widespread patient access to transformative treatments, leading to considerable healthcare cost savings and driving competition that spurs additional innovations.

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According to the data provided by the Synapse Database, As of November 28, 2023, there are 306 investigational drugs for the TNF-α target, including 215 indications, 391 R&D institutions involved, with related clinical trials reaching 4320, and as many as 53413 patents.

Adalimumab is a human immunoglobulin G1 monoclonal antibody targeting tumor necrosis factor alpha (TNF-α). The adalimumab reference medicine (Humira®*) was first approved with an adalimumab concentration of 50 mg/mL.1 In 2015, the EMA and US FDA approved Humira® HCF, which contains adalimumab at a concentration of 100 mg/mL.