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Sandoz recently announced that the EMA (European Medicines Agency) has accepted its application for a 100 mg/ml citrate-free formulation of its biosimilar HYRIMOZ® (adalimumab). The indications covered in the application include rheumatoid arthritis, Crohn’s disease, ulcerative colitis, plaque psoriasis, and uveitis. According to the press release, Sandoz has conducted a Phase I pharmacokinetics (PK) bridging study comparing the high concentration formulation to the 50 mg/ml HYRIMOZ® product, which demonstrated comparable pharmacokinetics and showed similar safety and immunogenicity profiles between the two. The lower concentration HYRIMOZ® formulation was approved by the EMA on July 26, 2018.
The post Sandoz’s High Concentration Adalimumab Biosimilar Application Accepted by EMA appeared first on Big Molecule Watch.
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