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Currently, European Medicines
Agency and US Food and Drugs Administration has approved three adalimumab
biosimilars: AMJEVITA/Solymbic, Cyltezo and Imraldi for RA treatment.
As per the recent study of Current Rheumatology Reports, several biosimilars of Adalimumab will be in the pharmaceutical market soon. Introduction of adalimumab biosimilars offers exciting opportunities for improving treatment access and increasing treatment options for RA.
Adalimumab is a tumour necrosis factor (TNF) inhibitor involved to treat various types of arthritis states like ankylosing spondylitis and rheumatoid arthritis. It is the top-selling medication with $18 billion in sales in 2017 alone globally. The following license cessation of Adalimumab has glimpsed the emergence of the variously related biosimilar. The current study assessed the Adalimumab related biosimilars evidence in the treatment of rheumatoid arthritis (RA) from bio-originator trials to present context for critical review with relation to related biosimilars.
At present, three
Adalimumab biosimilars are present which are the EMA (European Medicines
Agency) and/or FDA (US Food and Drugs Administration) approved. The Samsung
Bioepis’s SB5, Amgen’s ABP 501 and Boehringer Ingelheim’s (BI0 695501 are the
three biosimilars. These all biosimilars meet up with their pre-specified
equality criteria. The noticed references and biosimilar products exhibited
subtle variations with regards to clinical responses and adverse events. The
induction of these biosimilars will provide excellent opportunities to enhance
treatment options for RA and other related issues. However, to certify safety
and efficacy, a real-world data assessment of these biosimilars is required.
Current Rheumatology Reports
Review of Biosimilar Trials and Data on Adalimumab in Rheumatoid Arthritis
Sizheng Zhao et al.
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